Next Article in Journal / Special Issue
The Utility of Proton Beam Therapy with Concurrent Chemotherapy for the Treatment of Esophageal Cancers
Previous Article in Journal / Special Issue
Carbon Ion Radiotherapy at the Gunma University Heavy Ion Medical Center: New Facility Set-up
Article Menu

Export Article

Cancers 2011, 3(4), 4061-4089;

A Review of the Role of Re-Irradiation in Recurrent High-Grade Glioma (HGG)
ATreP, Agenzia Provinciale per la Protonterapia, via Perini 181, 38122 Trento, Italy
Author to whom correspondence should be addressed.
Received: 5 August 2011; in revised form: 8 October 2011 / Accepted: 21 October 2011 / Published: 28 October 2011


: Despite the use of more effective multimodal treatments in high-grade glioma (HGG), the outcome of patients affected by this disease is still dismal and recurrence is a very common event. Many therapeutic approaches, alone or combined (surgery, drugs, targeted agents, immunotherapy, radiotherapy, supportive therapy), are available in the clinical armamentarium so far. The attitude of physicians is increasingly interventionist, but recurrent HGG still remains a very difficult scenario to be treated. Radiotherapy with different re-irradiation techniques is increasingly proposed as a therapeutic option with interesting results, even though the resulting duration of response is usually quite short. Most lesions re-recur locally, with inadequate identification and targeting of viable tumor being the most important cause of failure. Prognosis is affected by many patient-, tumor-, and treatment-associated prognostic factors. Radiotherapy is delivered with many advanced modalities: 3D-CRT, intensity-modulated radiation therapy, stereotactic fractionated radiotherapy, radiosurgery, and brachitherapy with or without chemotherapy administration. In order to evaluate the feasibility and efficacy of re-irradiation in this setting, we reviewed the PubMed and MEDLINE databases restricting the search to original reports published from January 1990 to June 2011. The search resulted in a total of 155 reports: 78 of them covering 2,688 patients treated with different irradiation modalities overall fulfilled the entry criteria. Radiation therapy demonstrated to be an acceptable option in recurrent HGG with good response rates and acceptable toxicity.
high-grade glioma; recurrence; radiotherapy

1. Introduction

High-grade glioma (HGG, WHO grade III-IV) is the most common primary central nervous system tumor in adults, accounting for more than 60% of all brain tumors [1]. Surgery and radiotherapy represent the cornerstones for their therapeutic management. Nevertheless, patients with HGG have a dismal prognosis and after initial treatment the majority relapse.

Tumor control and survival in patients with glioblastoma (GBM) have improved in the last ten years with the use of radiotherapy (RT) plus concomitant and adjuvant temozolomide (TMZ). In the recent EORTC/NCIC randomized trial, the reported median and 2-year survivals were 14.6 months and 27%, respectively; however, the majority of tumors recurred locally within a few months [2].

Most data suggest that in certain patients re-treatment will result in additional survival time and stabilization of neurologic deterioration [3,4]. Many approaches are currently available for the salvage treatment of patients with recurrent HGG after initial RT, including surgical re-resection, re-irradiation, or systemic agent(s) administration with chemotherapy probably being the most frequent treatment option, yet to date no standard of care exists.

A surgical approach can be employed in selected patients, but optimal resection is very difficult because of the extensive parenchymal infiltration of recurrent disease, and may be associated with a high risk of morbidity [5,6]. Reoperation may often be difficult due to the patient's medical condition and the potential for further neurological compromise [7]. Thus, only patients with well-accessible tumors and a good performance status are usually managed with this approach [8].

Chemotherapy has been the mainstay of treatment for patients with recurrent disease. However, available regimens are limited by the general poor conditions of these patients as well as the related development of side effects and mainly result in a modest palliation. Re-challenging with TMZ or switching to a non-conventional TMZ regimen has become a common practice [9]. More recently several targeted therapies such as anti-VEGF antibodies, EGFR, PKC/PI3K/AKT and integrin inhibitors have been introduced in clinical practice and in clinical trials with very preliminary results [10].

Re-irradiation is generally discussed controversially for the risk of toxicity. In fact, the high radiotherapy dose (about 60 Gy) usually applied to reduce the risk of in-field relapse, generally hampers the use of a second full-dose radiotherapy course. However, re-irradiation has been shown to be of value after local relapse. The literature provides consistent data supporting both the feasibility and the survival lengthening capability in comparison with supportive care only. Safe and effective re-irradiation of brain malignancies is challenging. Several approaches have been undertaken to improve the therapeutic ratio including external beam radiation therapy (RT), bi-dimensional (2D) or three-dimensional (3D) with/without combined hypoxic cell radiosensitizers, brachytherapy (BT), intensity-modulated radiation therapy (IMRT), fractionated stereotactic radiation therapy (FSRT) and stereotactic radiosurgery (SRS). Regardless of the treatment employed, the prognosis of this patient population is dismal; therefore, the treatment related toxicity and quality of life remains crucial when considering the therapeutic options. The aim of this review is to offer a survey on the efficacy of retreatment of HGG with different radiotherapy techniques.

2. Results and Discussion

2.1. Methods

Relevant articles regarding the irradiation re-treatment of high-grade gliomas were systematically searched in the PubMed and MEDLINE databases. The search was limited to articles in the English language and to those dealing with humans. Only studies published from the beginning of 1990 through the end of May 2011 and providing clinical results of ten or more patients were included. The selected keywords to accomplish the search included “high-grade glioma”, “glioblastoma”, “recurrent”, “radiotherapy”, “intensity-modulated radiation therapy”, “fractionated stereotactic radiotherapy”, “radiosurgery”, “brachytherapy”, “gliasite”, “boron neutron capture therapy”, “radioimmunotherapy”. The resulting papers were reviewed and prioritized by relevant content. Traditional reviews, editorials, case reports and letters of opinion were excluded. Data presented in abstract form were not included, even if they added valuable information. A secondary review was performed using the reference list of the selected articles in order to identify further relevant studies. In case of repeated publications from the same institution, only the most recent was used for the analysis. On the basis of the collected data, the possibility of undertaking a meta-analysis was evaluated.

2.2. Results

Overall, the search gathered 155 reports: 95 were retrieved from PubMed and MEDLINE while the article reference analysis provided a further 60 citations. According to the inclusion criteria, 78 updated papers were ultimately included in the analysis. The workflow used to generate the final number of studies is depicted in Figure 1

There were no prospective randomized trials and merely 17 (22%) prospective phase I-II studies. All the remaining papers were retrospective and only four had a control arm.

Considering that when randomized trials are not available and data mainly come from retrospective series pooling results is not recommended [93], the meta-analysis methodology was not applied. Hence, the following results are reported in the form of a narrative analysis.

Overall, the articles provided the clinical outcomes concerning 2,688 HGG patients. The techniques employed included conventional 2D/3D RT, FSRT, IMRT, SRS, BT, boron neutron capture therapy (BNCT), radio-immunotherapy (RIT), and pulsed reduced-dose-rate RT. The following sections provide an overview according to each technique.

2.2.1. External Beam Radiation Therapy

There were only retrospective reports and non-randomized studies. Seven series were published between 1996 and 2009 with single series of 10–32 treated patients for a total of 144 patients (74 GBM and 70 HGG) reported (Table 1).

The patients had a median age ranging from 10 to 50 years and a median Karnofsky performance status (KPS) between 60 and 90. In two studies [13,14] a chemotherapeutic regimen with CCNU (lomustine) was combined and in another two about half of patients received some types of concurrent drugs [11,17]. Re-irradiation started after a median interval time of 14–38 months after the first irradiation. A cumulative biologically effective dose (BED) of 163.1–197.5 is calculated to be received by the re-irradiated patients. About half (seventy-one) of the re-irradiated patients had previously received some form of second surgery. The treatment was quite well tolerated: only a minor number of radionecrosis was reported [11,15-17], in two studies [11,17] some patients were re-operated, and in two studies [13,16] the use of corticosteroid was increased or maintained for a long period. The mean overall survival (OS) was 9.4 months. Better results were reported with the use of combined chemotherapy by Arcicasa et al. [14] and Hayat et al. [13], with a median OS after irradiation of 13.7 and 13 months respectively in comparison to 7–10.2 months of the other studies not using chemotherapy [11,12,15-17]. In general, neurologic toxicity was mild. The radionecrosis rate ranged between 4.5% and 30% (median, 6.5%). The reoperation rate was only reported in three studies [11,15,17], with a rate of 30%, 15.6% and 19.3% respectively.

2.2.2. Fractionated Stereotactic Radiation Therapy

Twenty-four reports, published between 1993 and 2011, using FSRT as a method of re-irradiation, were retrieved; in 10/24 different types of chemotherapy were combined with radiotherapy (Table 2). A total of 773 patients were reported, with 575 cases of GBM and 198 of HGG. Median age was between 34 and 56 years and median KPS ranging between 60 and 90 (Table 2).

Dose of re-irradiation varied between a clear hypofractionated schedule with single doses ≥4 Gy [18-21,24,25,28-30,32,33,36,37], moderately hypofractionated schemes with the use of 3–3.5 Gy per fraction [22,23,35,39] or conventionally fractionated dose per fraction of 1.8 to 2.5 Gy [26,27,40-42]. Median total dose varied widely between 20 and 42 Gy, while median target volume, always defined by conventional morphologic imaging (CT/MR), was between 5.7 and 56.2 cc (median 24 cc). The mean OS for all the studies (radiotherapy and radiotherapy plus chemotherapy) was 9.9 months. Median OS was similar in patients treated with radiotherapy alone (range 6.7–16 months; median value 9.8 months) and with concomitant chemotherapy (range 7–14.5 months; median value 9.2 months). Overall, the concomitant administration of chemotherapy did not improve the results in comparison with radiotherapy alone. In five studies [21,24,28,30,33] some patients received salvage chemotherapy prior to re-irradiation. Only Vordemark et al. [28] reported no significant (p = 0.76) outcome difference between patients receiving re-irradiation up-front or after failed salvage chemotherapy; this issue was not evaluated in the remaining series.

Data regarding toxicity are available in 23 out of 24 studies. Thirteen series registered neither radionecrosis nor reoperation. Seven studies reported the occurrence of radionecrosis (range, 5–60%; median, 13.7%). Reoperation was registered in eight articles (range, 5.2–78%; median, 12%). Several prognostic factors present at the time of re-irradiation were individuated as statistically significant: age [39], PS [23,35], interval time to retreatment [29,39], dose of re-irradiation [22], tumor volume [21,27,32,39,42] and grade [23,28,31,32,34].

2.2.3. Stereotactic Radiosurgery

Ultimately, 15 articles published between 1992 and 2011 met the inclusion criteria and were included in the review (see Table 3). All but five [44,47,49,53,55] were retrospective and recruited 594 HGG patients; 75% (n = 443) were GBM.

The median age ranged between 43 and 58 years, while median KPS varied between 70 and 90. The patients were re-irradiated after a median time of 4 to 19.8 months. The median target volume, always defined by conventional morphologic imaging (CT/MR), was between 2.7 and 30 cc, while the median re-irradiation dose ranged between 12 and 18 Gy.

Considering the treatment was always delivered in a single fraction, there was no concomitant chemotherapy administration. However, chemotherapy was employed as part of a re-treatment strategy in two reports [36,49]. Only two studies [49,52] reported that some patients received salvage chemotherapy prior to re-irradiation. The issue regarding the outcome difference between patients receiving re-irradiation up-front or after failed salvage chemotherapy was not addressed.

Overall, the use of SRS translated into median OS rates from re-irradiation of 5.3 to 12 months. Two studies pointed out values of 26 [53] and 30 [47] months, respectively. Only six papers provided data concerning progression-free survival (PFS) from re-treatment with an overall value ranging between 3.4 and 8.6 months. When reported, both OS and PFS were usually worse for cases harboring GBM compared to non-GBM HGG patients. Even though the treatment-related neurological side effects were generally mild, the reoperation rate varied between 3.5 and 23% with the radionecrosis rate up to 31.3%.

2.2.4. Brachytherapy

The final selection provided 21 updated series employing BT as re-irradiation technique (see Table 4) published between 1991 and 2009. All but four [59,60,72,73] were retrospective, while merely two [68,71] had a control arm. The radiation sources included 125-I (13 studies), 192-Ir (4 studies) and 198-Au (1 study) with comparable results in terms of OS and PFS regardless the isotope used. The treatment was delivered with a high-dose or low-dose-rate. Depending on the article, implants were temporary or permanent. Three studies employed the so-called GliaSite system: it makes use of a silicone balloon catheter and an aqueous iodinated radiation source.

Overall, 877 HGGs were treated: median age of the patients ranged between 43 and 60 years, while median KPS varied between 70 and 90. In 11 series maximal safe resection mainly translating into gross/subtotal resection was attempted before re-irradiation. Only Patel et al. [70] pointed out a statistically significant better local control on multivariate analysis for patients who underwent a gross total resection. The median time before re-treatment ranged between 7.3 and 12.5 months. No studies demonstrated that such parameter could influence the prognosis. The median target volume, always defined by conventional morphologic imaging (CT/MR), was between 17 and 51 cc while the median re-irradiation dose ranged between 18 and 300 Gy. It is noteworthy that the latter total dose level was achieved by the means of a permanent low-activity 125-I source.

Chemotherapy was administered as part of a re-treatment strategy in two reports only [62,72]. Only in one study [60] some patients received salvage chemotherapy prior to re-irradiation. The issue regarding the outcome difference between patients receiving re-irradiation up-front or after failed salvage chemotherapy was not addressed. Overall, the use of brachytherapy translated into median OS from re-irradiation of 11.5 months (range, 5.5–18 months).

Only one study pointed out values above 24 months [69]. It is to note that such data deal with non-GBM HGG and that 92% of the patients received gross total resection before the implant. When reported, the PFS from re-irradiation ranged between 3.7 and 11 months, respectively. The comparison between GBM and non-GBM HGG patients was inconclusive due to the lack of consistency in the results.

In general, such results were achieved at the expense of mild neurologic toxicity. Nevertheless, the reoperation rate varied widely (9–56%) as well as the radionecrosis one (3–56%). Such results were comparable regardless the employed dose-rate as well as whether the type of implants was permanent or temporary.

2.2.5. Other Techniques

The literature search gathered 11 other updated articles fitting the inclusion criteria: one concerning pulsed reduced-dose-rate RT [76], seven dealing with RIT [77-83], and three regarding BNCT [84-86]. Eight series were organized as a formal phase I or phase I-II clinical trial [77-83,86].

Overall, 290 HGG patients were treated: 54 received pulsed reduced-dose-rate RT, 180 RIT and 56 BNCT. Median age ranged between 45.5 and 58 years, while most series did not provide any data concerning either KPS or re-irradiation volume. When reported, the median time before re-treatment ranged between 5.9 and 18.2 months.

In the series dealing with pulsed reduced-dose-rate RT [76], the delivery of a median dose of 50 Gy translated into a median OS since re-treatment of 5.6 and 5.1 months for grade 3 and 4 tumors, respectively.

In the studies employing RIT [77-83], the delivery of an activity ranging between 10 and 120 mCi achieved a median OS from re-treatment of 6.3 [82] to 23.1 [81] months.

Finally, in the reports regarding BNCT the use of a dose varying between 13 and 73.9 GyE translated into a median OS from re-irradiation of 7 to 10.8 months.

In general, all these techniques proved to be feasible and safe being the treatment-related toxicity usually mild. However, two out of seven studies employing RIT registered paresis [82] and severe neurotoxicity [83] in 16.6% and 18% of patients, respectively.

3. Discussion

3.1. External-Beam Radiation Therapy (EBRT)

The potential of three-dimensional conformal radiation therapy (3D-CRT) for re-irradiation of selected intracranial tumors was studied in current practice at the beginning of the Nineties. Before, clinicians were hesitant to offer external beam re-irradiation with conventional fractionation at radical doses to patients who have previously been treated with full doses of radiotherapy (50–60 Gy) as part of their initial treatment. At that time, retrospective analyses [87,88] reported a risk of radionecrosis (RN) of the brain at the 5% level with doses ≥45 Gy with most cases occurring at 60 Gy, with a fraction-size dependent effect. Cases of delayed cerebral RN correlate most strongly with doses greater than 60 Gy delivered in 200-cGy fractions. These analyses were performed using whole brain or large partial brain portals only; therefore, extrapolation of this toxicity data to limited conformal partial brain irradiation was not warranted. The development of new 3D technology allowed the practical integration of CT and/or MRI into treatment planning and with this 3D planning process, conformal blocking techniques were applied more frequently to the re-irradiation of patients with recurrent gliomas. At the present time, the relationship between irradiation dose and volume is well established [89] and there is an agreement on the fact that more dose can be delivered to limited volumes. Moreover, the old concept of non-reirradiation has been overcome, and a second course of irradiation can be delivered keeping in mind the maintenance of a dose-memoire of 50% of the initial irradiation [90]. The literature data presented in the series using EBRT in the re-irradiation phase confirm the feasibility of a second treatment performed on limited fields. Quite satisfying rates of median overall survival of 6.1–13.7 months were obtained at a price of a low rate of RN or reoperation and neurological side effects (see Table 1).

3.2. Fractionated Stereotactic Radiation Therapy

Compared with conventional EBRT, stereotactic techniques (given by linacs or Gamma units), given as single fraction SRS or as FSRT, can deliver more localized irradiation with a steeper dose gradient between the tumor and the surrounding normal tissues reducing the risk of radiation induced complications. FSRT is advantageous in treating recurrent, previously irradiated, tumors, particularly when located in critical/eloquent areas. Its ability to divide the dose allows the therapeutic dose to be delivered over a number of fractions, while minimizing potential normal tissue toxicity. The divided dose should permit normal brain tissue to repair and give time for the tumor to re-oxygenate. The use of FSRT translated into mean OS and PFS of 9.9 and 6.4 months respectively. Analyzing the published literature on this subject (24 reports) we can observe a series of factors related to patient, tumor and to treatment potentially related to the results obtained. Some of them are discussed thereafter.

3.2.1. Pre-Treatment Characteristics Interval Time

There is currently no consensus regarding the efficacy of salvage irradiation in patients who experience recurrence a short time after initial treatment. Grosu et al. [29] examining 44 patients with recurrent HGG found that an increased interval between initial diagnosis and recurrence was the most important prognostic factor associated with improved survival after re-irradiation. In contrast to this, Mayer and Sminia [91] reviewing ten years of re-irradiation studies did not find a correlation between time interval and prognosis. The study of Fogh et al. [39] did not demonstrate an inferior survival rate in patients who experienced a relapse within six months of primary treatment. The large number of patients examined in this study could have allowed to more accurately assessing this issue. This finding is of critical importance, considering that the eligibility in clinical trials is usually limited to patients who have survived at least six months from initial treatment. Patients' Performance Status

Karnofsky performance status (KPS) ≥70 at the time of recurrence was the strongest predictor for survival in some reports [23,35,92]. It is to note that KPS, (with tumor grade and age) is also a common independent variable predicting the longevity of patients with high-grade gliomas at initial diagnosis. Tumor Volume

Mixed findings regarding the influence of tumor volume on survival have been reported and are probably due to the different radiation doses, schedules and multimodal therapy used. Lederman et al. [21] showed that patients with tumor volumes <30 mL survived longer. In another study, tumor volumes <20 mL were associated with better response [22]. In other reports, tumor volume did not influence survival of patients after FSRT [23,35,92]. The volume is reported in different ways: as the tumor volume (GTV) in cm of diameter or in cc or as the irradiated volume (PTV). For this reason the values are not easily comparable. Target volume can also determine the risk of side effects. In the study of Ernst-Stecker et al. [32], some patients experienced an increase of edema with the need for an increase of steroid medication during the follow-up while GTV did not increase at imaging. The re-irradiated volumes in these cases were clearly higher than the median volumes treated. Tumor Grade

Grading is a well-known prognostic factor in the treatment of high-grade gliomas at diagnosis. The role of the grade of the primary tumor or at recurrence in re-irradiated patients is, instead, more controversial. WHO grading, both that determined at initial diagnosis of glioma and the most recent before SFRT, showed a significant impact on survival in the study of Vordemark et al. [28], while in other studies done by Shepherd et al. [20] and Cho et al. [23], only initial grade or grade at recurrence had a statistical significant value, respectively.

3.2.2. Treatment Characteristics Dose of Radiation

In the majority of studies published in the literature investigating the effectiveness of FSRT, a relatively large dose per fraction (usually ≥5 Gy/fraction) is used in the hypofractionated regimens. Data showed that higher total doses of FSRT result in an improved survival [19,23,26,31]; but at the same time, doses greater than 40 Gy have been associated with increased toxicity with higher rates of re-operation [18,20], indicating a small therapeutic window. Similar data are reported with the use of high-dose single fractions of 5- to 6-Gy [21,25] with increased long-term toxicity in late-responding tissue in other disease sites. Fogh et al. [39] used 3.5 Gy fractions to 35 Gy and reported no grade 3 toxicities or re-operation secondary to toxicity, providing additional support that this moderate level of dose and fraction size is well tolerated [22,23].

FSRT given in small fractions of 2–3 Gy enables the precision and accuracy of SRS, while maintaining the radiobiological advantages of fractionation in terms of tumor control and protection of surrounding normal brain tissue [23,41]. Combination with Chemotherapy

Although the role of chemotherapy combined with irradiation has been well established for patients with newly diagnosed primary GBM [1,2], there is a paucity of data reporting on the combination of chemotherapy and conventional [13,14] or SFRT [19,21,29, 30,33,34,37,40,41] for recurrent gliomas.

In the study of Fogh et al. [39], SFRT was associated with favourable survival benefit independent of second surgery or concomitant chemotherapy. Although it was not a randomized trial, the study did not demonstrate a survival advantage in combining chemotherapy with FSRT at recurrence compared with patients who received FSRT alone.

SFRT plus concomitant TMZ for patients with recurrent GBM is a feasible treatment associated with low toxicity; however, the survival benefits are modest [41]. In the study of Minniti et al. [41] patients with methylated MGMT and longer stable disease after primary standard chemoradiation have the better outcome, suggesting that methylation status of MGMT promoter also retains its prognostic value in recurrent GBM.

In general, the data of our review show similar median overall survival, comparing studies using FSRT alone or in combination with different schemes of chemotherapy, ranging between seven and fourteen months, considering also the different grades (III and IV) reported together in some series. The potential advantages of combined chemoradiation schedules to further improve outcome in patients with recurrent GBM and HGG need to be further explored. Toxicity

Because of the high total dose applied during the initial irradiation (usually near 60 Gy), the role of re-irradiation is largely debated regarding the risk of acute or late toxicity.

Radionecrosis, based on clinical features that included deterioration of neurologic deficits (without tumor progression) associated with abnormal findings on imaging such as positron emission tomography (PET), magnetic resonance spectroscopy (MRS), and/or other imaging studies (MRI or CT), is the most important side effect in this sense.

Many studies reported the development of RN after re-irradiation [19-21,25,31,41]. In several series patients were also reoperated after FSRT [20,21,23,25,31,37]. Patients who underwent surgical resection after FSRT often demonstrated radiographic progression confirmed by pathology, indicating these patients underwent re-operation mainly because of tumor progression rather than treatment-related effects.

3.3. Stereotactic Radiosurgery

Stereotactic radiosurgery is a non-invasive irradiation modality that can be delivered with gamma knife (Elekta, Stockholm, Sweden), Cyberknife (Accuracy, Sunnyvale, CA, USA), or specially adapted linear accelerators without relevant dosimetrical differences. It is a highly conformal, precise and accurate technique. Thanks to its features, stereotactic radiosurgery allows delivery of steep dose gradients, which translates into the sparing of the surrounding tissues. However, considering that treatment-related toxicity increases with target size as well as increased delivered dose, the lesions amenable by SRS are usually small.

These features best fit with small and round shaped relapsed HGGs, and automatically limit its wide use in this clinical scenario. Therefore, the large number of series we retrieved on its use is not surprising. However, due to the above-mentioned features, it is noteworthy the strict application clinical setting. In general, suitable patients were fairly young, with a high KPS and small relapses while the prescribed dose had very limited variations. From this standpoint, it is not surprising that all the series provided very consistent outcomes. Accordingly, such homogeneity hampered the detection of well-defined prognostic factors. Concerning OS, only few series pointed out the prognostic value of WHO grade [23,46,53], younger age [23,45,46] as well as KPS [23,46,47] while only four articles [23,45,47,53] revealed the role played by the treatment volume. However, with this respect, a clear volume-cutoff cannot be defined from literature data. Interestingly, the timing of re-irradiation does not seem to be of prognostic value. Based on the reported data, the risk of radionecrosis (up to 31%) should not be underestimated, hence the patient should be carefully selected.

3.4. Brachitherapy

Interstitial brachytherapy employing radioactive sources has been performed in recurrent HGGs because its higher spatial dose localization can improve the therapeutic ratio. Several sources such as 125-I, 192-Ir and 198-Au were employed to deliver high-dose or low-dose-rate irradiation as well as permanent or temporary implants ultimately generating great intra-modality variability. Regardless of the dose-rate and type of implant, the placement of multiple sources in the proximity of a resection cavity or relapsed tumor is challenging, and optimal dose distribution may be consequently difficult to be achieved [94]. However, the use of low-dose-rate interstitial BT could reduce the rate of severe complications in comparison with high-dose-rate implants. From this standpoint, a novel alternative temporary BT system (Gliasite, Cytic Surgical Products, Palo Alto, CA, USA) can overcome the limiting factors of conventional interstitial BT. In fact, working as a single spherical source of low-dose-rate radiation it can homogenously deliver a steep dose gradient around the surgical cavity.

This relevant variability, on the one hand significantly increased the volume of experience on BT re-irradiation of HGG; on the other hand, it decreased the possibility to address all the issues dealing with this technique. As a consequence, several topics such as the optimum prescribed dose, dose-rate, isotope, and implant modality have yet to be properly clarified.

In general, BT treatment of relapsed HGG can improve the survival with the high cost of radionecrosis. The capability of larger target irradiation with respect to SRS can only in part justify these data, while the promising results have to be interpreted in the light of the relevant reoperation rate before BT.

Moreover, it must be noted that, similarly to SRS, patients offered BT represent a highly selected population due to their favourable features (age, performance status, target volume). Considering the consequent patient homogeneity, the reviewed studies provided consistent results that ultimately hampered the detection of well-defined prognostic factors. With this regard, age [45,63,69,70,72], KPS [59,60,63,64,66,71,72,74,75] and treatment volume [64,69,71] demonstrated again the strongest predictive value.

3.5. Other Techniques

The literature search also provided data concerning three further techniques: pulsed reduced-dose-rate radiotherapy, radioimmunotherapy, and boron neutron capture therapy.

Regarding the first modality, the reduction in the delivery dose-rate might exploit differences between normal and malignant cells, allowing normal tissues to repair sublethal damage [76]. Moreover, splitting each fraction into a number of subfractions takes advantage of a second radiation phenomenon known as low-dose hyper-radiosensitivity [76].

Conversely, RIT achieves elevated local drugs concentration for a protracted time by locally delivering the chemotherapy compounds. Moreover, tissue-specific monoclonal antibodies labelled with high-energy β-emitting radionuclides can destroy a large number of tumor cells [80].

BNCT is based on the nuclear capture reaction that occurs when nonradioactive boron is irradiated with neutrons of sufficient thermal energy to yield high-energy α particles and lithium nuclei. The effect of α and lithium is limited primarily to boron-containing cells. The modality success is dependant upon a selective uptake of sufficient amounts of boron into cancer cells compared with normal tissues. Preferential uptake of boron into cancerous tissue is achieved using boron carriers [86]. Apart from these theoretical considerations only few data (overall, 290 patients) exist on the use of such techniques in recurrent HGG. Each modality proved to be safe and feasible while clinical outcomes are consistent with the series employing “conventional” re-irradiation modalities. However, considering that enrolled patients often received such techniques at their second or third relapse, they deserve further investigation as first-line re-treatment.

3.6. Considerations on Different Re-Irraddiation Techniques

Conventional fractionated radiotherapy using 3D-CRT is an outpatient-based, non-invasive approach that takes advantage of the properties of a standard fractionation schedule as well as of non-complex technique. However, it cannot best decrease the dose to neighbouring tissue. Therefore, the use of 3D-CRT, either alone or combined with chemotherapy, allows the delivery of relatively low dose in this clinical scenario and is not able to shorten the number of weeks of treatment. The few published data concerning patient re-irradiated by this technique pointed out acceptable side effect rates, whereas the clinical outcomes were not meaningful. To date, this technique should be employed to deliver short-course palliative re-irradiation in patients with worse prognostic factors.

With the advent of relocatable frames, it is possible to exploit the radiobiological advantages of fractionation with the possibility of improving the therapeutic ratio. FSRT can be delivered as an outpatient-based, non-invasive approach that takes advantage of the stereotactic precision. Hence, large tumors, which might be technically ineligible for implantation or SRS, can be safely and effectively treated. FSRT can be delivered with standard fractionation regimens or with hypofractionated schedules. The latter possibility is not only more beneficial to patients with respect to quality of life and convenience, but it may also represent a decrease in cost associated with retreatment.

Radiosurgery requires a single day of outpatient therapy, limiting treatment and hospitalization times. The main advantage of SRS is the capability of relevant dose delivery to the tumor volume while sparing surrounding normal tissues. This non-invasive approach enables the local application of radiation without surgical intervention. As a consequence, many of the risks involved with brachytherapy (such as infection, haemorrhage, exposure of the personnel to radiation) do not apply to radiosurgery. However, the potential advantage of radiation delivery over multiple cell-cycle times (as achieved in brachytherapy) is not provided. The argument for the use of radiosurgery is the relevant radiobiological effect of single-session radiation cell kill or cell division capability arrest, regardless of mitotic phase. Moreover, when the treatment volume is small and contains little functioning brain tissue, the need for fractionation may not apply. However, its high-dose focal radiation delivery may encounter in a high risk for side effects, when the treatment volume becomes larger or the tumor is at or close to eloquent structures (e.g., optic pathway, basal ganglia, speech or motor area). Due to the above-mentioned features, the application clinical setting is limited to patients with small, round shaped lesions and with good prognostic factors. However, also deep-sited lesions (usually considered not implantable) can be managed.

Brachytherapy also allows delivery of a large dose to the tumor volume while sparing surrounding normal tissue. However, the corresponding invasive procedures involve some surgical risks and require the patient's hospitalization. Considering that the radiation dose is usually delivered during 4 to 6 days, the radiobiological advantages include reoxygenation and the phase-specific cell sensitivity. Unfortunately, all BT implants generally produce inhomogenous dose distribution. Hence, the implantation of large tumors (even though feasible) should be avoided. Albeit the results obtained with this modality are encouraging, the technical complexity in performing brachytherapy implants limits its use in current clinical practice. Moreover, it could be offered to selected patients who are young and have good functional status and no-deep lesions.

Given that FSRT patients had comparable survival to SRS/BT patients, FSRT may be a better option for patients with larger tumors or tumors in eloquent structures.

The inherent variation of tumor and patient characteristics, as well as therapeutic interventions for recurrent HGG patients make comparison of patient groups from different studies unreliable. The series are mainly retrospective and feature several selection bias:

  • BT candidates had lobar tumors without involvement of midline structures, no ventricular disease, small tumor diameter and high KPS. Moreover, the surgical procedure allowed for maximal safe re-resection;

  • SRS series usually included patients with potentially adverse prognostic factors not amenable with BT;

  • Patients with larger recurrent tumors or tumor in eloquent structures were selected to receive FSRT compared with those treated with SRS/BT. As a consequence, potential prognostic variables predicting longer survival were preferentially distributed in favour of SRS/BT;

  • Many patients received additional and different therapies at the time of failure, making it difficult to properly interpret the results. In this regard, the end point of survival is a relatively poor measure of treatment efficacy, whereas time to failure after treatment is potentially less subject to the effects of selection bias. Unfortunately, time to failure data was generally not available for most series.

4. Conclusions

The standard of care for patients with recurrent HGG has not yet been clearly defined. Reoperation can only be performed in selected patients of younger age and with good performance status. Indeed, the infiltrative nature of the disease does not always allow a total resection without compromising neurologic functions.

The chemotherapy administration (especially TMZ), is probably the most frequent salvage treatment employed for recurrent HGG.

Considering the risk of acute and late side effects, re-irradiation of the same tumor site with conventional technique (EBRT) is considered to be troublesome.

Hypofractionated stereotactic radiotherapy as a salvage therapy is a non-invasive approach to deliver a precisely localized high radiation dose into a small volume. This technique is characterized by a steep dose fall-off to the periphery and may be a valuable re-treatment option after high-dose percutaneous radiotherapy. Further therapy options include BT and SRS but they are limited to smaller tumor volumes. In addition, BT and SRS show a higher risk of toxicities (e.g., radionecrosis).

Re-irradiation using these high precision techniques allows the survival prolongation and delays disease progression or recurrence. However, it is not a curative treatment and it is limited to selected subgroups of patients. Therefore, a further therapeutic improvement is needed. The radiochemotherapy combination as well as alternative treatment modalities are worthy of investigation.

Figure 1. Study selection for inclusion into the review.
Figure 1. Study selection for inclusion into the review.
Cancers 03 04061f1 1024
Table 1. Re-irradiation with external beam radiotherapy with or without chemotherapy.
Table 1. Re-irradiation with external beam radiotherapy with or without chemotherapy.
Author [ref.]≠ PtsMed. age (years)Med. KPSSurgery before re-irr.Med. total dose (Gy)Med. time to re-irr. (mos.)Med. re-irr. total dose (Gy)CHTMed. survival (mos.)Neurol. side effects

Bauman et al. [11]1020801/1054– 7215.518–745/10
RT+CHT (various)
OS 8.3
PFS 3.3
RN 3
Deterioration 2
Reop 3
Kim et al. [12]14 (7 GBM)21–52607/1459.43836RT aloneOS 7RN 1
Hayat et al. [13]114180NR453130/2.5RT+CHT (CCNU)OS 13Cort prolonged
Arcicasa et al. [14]2444704 total
8 subtot
601434.5RT+CHT (CCNU)OS 13.7No
Nieder et al. [15]32 (21 GBM)44701458.62045.5 bidRT aloneOS 8.5
Reop 5
RN 2
Late neurotox.
Verninga et al. [16]22 (17 GBM)34WHO ≤ 221/42 (+other)6032.846RT aloneOS
GBM 6.1
HGG 8.2
RN 1
Cognitive decline 1
Cort 8/10 increased, 18/32 started
Henke et al. [17]31 (29 GBM)509016/31 12 total59NR2015/31
RT+CHT (various)
OS 10.2RN 2
Reop 6

GBM: glioblastoma; Med.: median; NR: not reported; Gy: Gray; bid: bis in die; OS: overall survival; PFS: progression-free survival; HGG: high-grade glioma; re-irr.: re-irradiation; CHT: chemotherapy; mos.: months; CCNU: lomustine; KPS: Karnofsky performance status; Cort: corticosteroids; Neurol.: neurologic; RN: radionecrosis; Reop: reoperation.

Table 2. Re-irradiation with fractionated stereotactic radiation therapy with or without chemotherapy.
Table 2. Re-irradiation with fractionated stereotactic radiation therapy with or without chemotherapy.
Author [ref. ]≠ Pts.Med. age (years)Med. KPSSurgery before re-irr.Med. total dose (Gy)Med. time to re-irr. (mos.)Med. re-irr. total dose (Gy)Med. vol. (cc)CHTMed. surv. (mos.)Neurol. side effects

Laing et al. [18]19 (12 GBM)34706 STR55204025--OS 9.85 neurol. deterioration
Glass et al. [19]20 (13 GBM)4490NRNR84214.3Cis-DDPOS 13.73 RN
1 somnolence
1 confusion
1 seizure
Shepherd et al. [20]2937806/29552920–5024--OS 10.74 RN
2 Reop
1 steroid increase
Lederman et al. [21]14 (GBM)5670NR607.82432.7TAXOS 77 RN
11 Reop
Hudes et al. [22]20 (19 GBM)5280NR603.124–3512.6--OS 10.53 steroid increase
Cho et al. [23]20 (15 GBM)5360NR59.41937.525--OS 121 RN
3 Reop
41 steroid start
Selch et al. [24]21 (14 GBM)54804 STR60112512--OS 6.7
Voynov et al. [25]10 (4 GBM)48805/10 STR59.7193034.75/10 variousOS 10.12 Reop
6 RN
Combs et al. [26]4042≥80: 389 STR59.434.53656.2 (PTV)--OS 16
No > G2
Combs et al. [27]50 (GBM)55≥80: 46NR57103649 (PTV)OS 8
No > G2
Vordemark et al. [28]19 (14 GBM)509012/1945– 61193015--OS 9.3
GBM 7.3
HGG 15.4
PFS 4.9
1 reop
Grosu et al. [29]44 (33 GBM)5080NR6016301529/44 TMZOS 86 steroid increase
Wurm et al. [30]25 (20 GBM)4580NR54.4 bid/6012.825–3016.5TopoOS 14.5
PFS 10.5
(PFS6 42%)
Kohshi et al. [31]25 (11 GBM)4670NR601128.1– 68.28.7--OS
GBM 11
HGG 19
7 Reop (partial RN)
Ernst-Stecken et al. [32]15 (11 GBM)4980NR57.7510355.7--1 year
OS 43%
PFS 53%
(PFS6 75%)
3 steroid increase
Schwer et al. [33]15 (11 GBM)47704 GTR
6011.918–3641.3GefOS 10
(PFS6 63%)
3 seizure
2 deterioration
Combs et al. [34]25 (GBM)39≥70 92%5 GTR
13 STR
60363650TMZOS 8
(PFS6 48%)
Fokas et al. [35]53 (GBM)537023/5354NR3035--OS 9No
Patel et al. [36]10 (GBM)44902 GTR
50– 6014.93651.1--OS 7.41 RN
1 Reop

Gutin et al. [37]25 (20 GBM)5680NR59.4153034BevaOS 12.5
PFS 7.5
(PFS6 64%)
3 Reop
1 hemorrhage
1 wound deiscence
Villaceincio et al. [38]26 (GBM)568015 GTR
59.413207--OS 7NR
Fogh et al. [39]147 (105 GBM)NRNR24 GTR
60 STR
609352248/147 variousOS
GBM 11
HGG 10
15 steroid increase
Torcuator et al. [40]1655.790NoNRNR36NR12/16 Beva+TMZ or otherOS 7.2
PFS 2.6
Minniti et al. [41]36 (GBM)5670NR601437.513.1TMZOS 9.7
(PFS6 42%)
3 RN
Hauff et al. [42]59 (GBM)55.79011/59Dose
NR30 + HT46.5--OS 13.4No

Pts.: patients; GBM: glioblastoma; NR: not reported; tot: total; subtot: subtotal; vol.: volume; mos.: months; GTR: gross total resection; STR: subtotal resection; RN: radionecrosis; re-irr: reirradiation; Gy: Gray; OS: overall survival; PFS: progression free survival; PFS6: 6-month progression-free survival; CHT: chemotherapy; KPS: Karnofsky performance status; RN: radionecrosis; Reop: reoperation; TMZ: temozolamide; cis-DDP: cisplatin; Beva: bevacizumab; Topo: topotecan; Gef: gefitinib; TAX: paclitaxel; HT: thermotherapy; G: grade; RTOG: Radiation Therapy Oncology Group; PTV: planning target volume.

Table 3. Series of high-grade gliomas treated by stereotactic radiosurgery.
Table 3. Series of high-grade gliomas treated by stereotactic radiosurgery.
Author [ref. ]≠ Pts.Med. age (years)Med. KPSMed. TD before re-irr. (Gy)Med. re-irr. TD (Gy)Med. time to re-irr. (mos.)Med. Vol. (cc)Med. survival from re-irr. (mos.)Neurol. side effects

Alexander et al. [43]25 (16 GBM)458059.413 to 70% isodose (Linac)1410OS 9RN 12%
Chamberlain et al. [44]13 (5 GBM)Mean 42 (GBM)
Mean 34 (HGG)
Mean 60 (GBM)
Mean 80 (HGG)
Mean 62 (GBM
Mean 58 (HGG)
Mean 12 (GBM)
Mean 14 (HGG) (Linac)
Mean 10.4 (GBM)
Mean 36.3 (HGG)
Mean 34.3 mL (GBM)
Mean 16 mL (HGG)
OS 8 *
PFS 4 *
Shrieve et al. [45]86 (GBM)4680NR13 to med. 80% isodose (Linac)10.310.1OS 10.2Seizures 3.5%hosp. 2.5% exitus 1% cr. nerve deficit 1%
Reop 22%
Larson et al. [46]63 (46 GBM)53 (GBM)
43 (HGG)
90NRMed. min. 16 to med. 50% isodose (GK)>16 weeks6.2 (GBM)
7.5 (HGG)
OS 57 weeks (GBM) not reached (HGG; 1y OS 68%)NR
Kondziolka et al. [47]42 (19 GBM)Mean 51 (GBM)
Mean 45 (HGG)§
Mean 90§Mean 60Mean 15.5 (GBM)
Mean 15.2 (HGG) to 50% isodose (GK)
18.9 (GBM)
19.8 (HGG)
Mean 6.5 mL (GBM)
Mean 6 mL (HGG)§
30 (GBM)
31 (HGG)
Reop 19%
RN 1.6%(GBM)
Reop 23%
RN 4.7% (HGG)§

Cho et al. [23]46 (27 GBM)48706017 to med.
50% isodose (Linac)
1030 mLOS 11Initiation or steroids increase 41%
Reop 14%
RN 4.3%
Park et al. [48]23 (GBM)5380NR15 to 60% isodose (Linac/GK)NR9.9OS 10.3
PFS 4.7
Larson et al. [49]26 (14 WHO 4)53 (WHO 4)
44 (HGG)
90NRMed min. 15 (WHO 4)
16.5 (HGG)(GK) #
12 (WHO 4)
43 (HGG)
8 (WHO 4)
2.7 (HGG)
OS 38 weeks PFS
15 weeks (WHO 4)
OS 68 weeks PFS
29 weeks (HGG)
Combs et al. [50]32 (GBM)56≥705415 to 80% isodose (Linac)1010 mLOS 10
PFS 5 (PFS6 33%)
No > G2 (acute)
Hsieh et al. [51]26 (GBM)58Mean 706012 to 50% isodose (GK)NRMean 21.6OS 10RN 31.3% §
Mahajan et al. [52]41 (GBM)549060NR (Linac)104.7OS 11Reop 22%
Kong et al. [53]114 (65 GBM)49806016 to 50% (GK) or 80% (linac) isodose (Linac/GK)NR10.6 mLOS 13 PFS
4.6 (GBM)
OS 26
PFS 8.6 (HGG)
Reop 3.5%
RN 24%
Biswas et al. [54]18 (GBM)57.8 §≥706015 to the isocenter (Linac)12.18.4 mLOS 5.3
PFS 3.4
No > G2 (acute)
Patel et al. [36]26 (GBM)5380Range 50-6018 to 90% isodose (Linac) 1210.4OS 8.4NS
Maranzano et al. [55]13 (GBM)55906017 to the isocenter (Linac)95.3OS 11RN 23%

Med.: median; GBM: glioblastoma; HGG: high-grade glioma; surg.: surgery; TD: total dose; re-irr.: re-irradiation; min.: minimum; mos.: months; GK: gamma-knife; Linac: linear accelerator; NR: not reported; NS: not specified; OS: overall survival; PFS: progression-free survival; PFS6: 6-month progression-free survival; Reop: reoperation; hosp: hospitalization; cr.: cranial; RN: radionecrosis; Gy: Gray; CHT: chemotherapy; KPS: Karnofsky performance status; Neurol.: neurological;°:some patients included in different publications;*:this series also includes some LGG;§:data refer both to newly and recurrent HGG;#:delivered before marimastat (10 mg b.i.d.);¶:delivered before not specified chemotherapy.

Table 4. Series of high-grade gliomas treated by brachytherapy.
Table 4. Series of high-grade gliomas treated by brachytherapy.
Author [ref. ]≠PtsMed. age (years)Med. KPSSurg. before re-irr. (%)Med. TD before re-irr.(Gy)Med re-irr. TD (Gy)Med. interval to re-irr. (mos.)Med. volume (cc)Med. survival from re-irr. (mos.)Side effects

Lucas et al. [56]20 (7 GBM)Mean 43 (GBM)
Mean 32 (HGG)
NRNRMean 58.2Mean 50
HDR 192-Ir sources
OS 18 (HGG)
Seizures 6% wound inf 6%
CSF leak 3%
Reop 9%
RN 3%
Scharfen et al. [57]111 (65 GBM)Mean 46§90 §NR60 §64.4
LDR 125-I sources
NRNROS 49 weeks (GBM)
OS 52 weeks
G3 6%
G4 1%
G5 < 1% (Acute) §
Reop 38% (GBM)
47% (HGG)
RN 5% §

Malkin et al. [58]36NRMean 75NRNR60
LDR 125-I sources
NRMean 41OS 10Misplacement 9%
Reop 43%
RN 9%
Sneed et al. [59]42 (26 GBM)4390NRNRRange 50-60 Temp
LDR 125-I sources + HT
NR17OS 47 weeks (GBM)
OS not achieved 1y OS 81% (HGG)
Reop 43%
RN 5%
Bernstein et al. [60]44 (32 GBM)46≥60NRRange 50–60Mean 70.17
LDR 125-I sources
12.550.3OS 46 weeks *IPI 6.5%catheter migration 2.1% (Acute) steroid-dep.
Reop 26.1%
RN 4.3%
Kitchen et al. [61]23Mean 45Mean 69NRNR50 (DP)
LDR 125-I
51 weeksMean 28OS 25 weeksNS
Shrieve et al. [45]32 (GBM)4580NRNR50 Temp
LDR 125-I sources
7.329OS 11.5Scalp inf 6% (Acute) visual deficit 6%
Reop 44%
RN 6%
Chamberl ain et al. [62]1547NRNRNR50
LDR 125-I sources
25% P
Steroid-dep. 62% dementia 6%
Reop 56%
RN 56%
Mayr et al. [63]41 (28 GBM)52 §80 §NRNRMean 59 §
LDR 125-I sources
NRMean 28 §41.2 weeks (GBM)
32.6 weeks (HGG)
RN 16% other compl. 13%
Simon et al. [64]42 (GBM)4980B 100Range 46–6050
LDR 192-Ir sources
NR23OS 50 weeksSkin necrosis 4.7%men. 9.5%
Reop 24%
RN 7%

Tselis et al. [65]84 (GBM)5780NRUp to 6040
HDR 192-Ir sources
NR51OS 37 weeksIntracerebral bleeding 2.3%men. 1.1%
RN 2.3% (Acute)
Fabrini et al. [66]216080GTR/ STR 10060 (all pts)18
HDR 192-Ir sources
NRNROS 5.5G1 headache 100%
G2 CFS leak 4.7%
G3 CFS leak 4.7%
G5 4.7% (Acute) asymptomatic
RN 9.5%
Larson et al. [67]33 (13 GBM)55 (GBM)
40 (HGG)
NRMax. safe res. 100NRRange 40–50
Perm LDR 198-Au seeds
OS 17 (HGG)
Halligan et al. [68]21NR≥50GTR 86
STR 14
Range 54–64.8210 (DP)
Perm LDR
125-I seeds
NRNROS 65 weeks
PFS 29 weeks
Gaspar et al. [69]60 (37 GBM)47≥60Max. safe res. 92 B 8Range 50–66103.68 (DP)
Perm LDR 125-I seeds
NR17OS 10.8 (GBM)
OS 24.4 (HGG)
Reop 40%
RN 5%
Patel et al. [70]40 (GBM)5070GTR 55
STR 45
60 (all pts)Range 120-160
Perm LDR 125-I seeds
NR47.3OS 47 weeks
PFS 25 weeks
Healing compl. 5%
Larson et al. [71]38 (GBM)4790STR 60 (resid. ≥0.5 cm) STR 40 (resid. <0.5 cm)60 (all but 2 pts)300
Perm LDR 125-I seeds
39 weeks21 Pre-implantOS 52 weeks
PFS 16 weeks
Reop 10.5%
RN 2.6%

Darakchiev et al. [72]34 (GBM)5380GTR 85
STR 15
NS120 (DP) @
Perm LDR 125-I seeds
NR34 before surgeryOS 69 weeks
PFS 47 weeks (PFS6 67%)
Healing compl. 11.7%
Reop 29.4%
RN 23.5%
Tatter et al. [73]21 (15 GBM)Mean 48.480Max. safe res. 100NSRange 40–60
OS 17.9 (HGG)
Pseudo-meningocele 4.7%wound inf 4.7%chemical men.4.7%
Chan et al. [74]24 (GBM)4880Max. safe res. 100Mean 59.8Mean 53.1
NRNROS 9.1G1-2 headache 42%nausea-vomiting 4%wound inf 6%(Acute) neurological deficit 4%RN 8%
Gabayan et al. [75]95 (80 GBM)5180Max. safe res. 1006060
40.6 weeksNROS 35.9 weeks (GBM)
OS 43.6 weeks (HGG)
G1 1.1%
G2 8.4%
G3 2.1% (RN)

Med.: median; GBM: glioblastoma; HGG: high-grade glioma; surg.: surgery; TD: total dose; re-irr.: re-irradiation; mos.: months; NR: not reported; NS not specified; OS: overall survival; PFS: progression-free survival; PFS6: 6-month progression-free survival; reop: reoperation; RN: radionecrosis; IPI: intracranial pressure increase; inf: infection; compl.: complication; men.: meningitis; dep.: dependent; Gy: Gray; CHT: chemotherapy; KPS: Karnofsky performance status; DP: dose prescription; max.: maximal; res.: resection; GTR: gross total resection; STR: sub-total resection; B: biopsy; BCNU: carmustine; Perm: permanent; Temp: temporary; LDR: low-dose rate; HDR: high-dose rate; HT: hyperthermia; CSF: cerebrospinal fluid; pts: patients; I: iodium; Ir: iridium; C.E.: contrast enhancement.*:data also include 2 LGGs;§:data refer both to newly diagnosed and recurrent HGG;¶:delivered in combination with cisplatin (20 mg/m2 × 5 gg);@:delivered in combination with BCNU wafers (Med. 61.6 mg).


  1. Wen, P.Y.; Kesari, S. Malignant gliomas in adults. N. Engl. J. Med. 2008, 9, 492–507. [Google Scholar]
  2. Stupp, R.; Mason, W.P.; van den Bent, M.J.; Weller, M.; Fisher, B.; Taphoorn, M.J.; Belanger, K.; Brandes, A.A.; Marosi, C.; Bogdahn, U.; et al. Radiotherapy plus concomitant and adjuvant temozolomide for glioblastoma. N. Engl. J. Med. 2005, 352, 987–996. [Google Scholar]
  3. Nieder, C.; Adam, M.; Molls, M.; Grosu, A.L. Therapeutic options for recurrent high-grade glioma in adult patients: Recent advances. Crit. Rev. Oncol. Hematol. 2006, 60, 181–193. [Google Scholar]
  4. Butowski, N.A.; Sneed, P.K.; Chang, S.M. Diagnosis and treatment of recurrent high-grade astrocytoma. J. Clin. Oncol. 2006, 24, 1273–1280. [Google Scholar]
  5. Soults, C.B.; Canute, G.S.; Ryken, T.C. Evidence-based review of the role of reoperation in the management of malignant glioma. Neurosurg. Focus 1998, 4, e11. [Google Scholar]
  6. Barbagallo, G.M.; Jenkinson, M.D.; Brodbelt, A.R. “Recurrent” glioblastoma multiforme, when should we reoperate? Br. J. Neurosurg. 2008, 22, 452–455. [Google Scholar]
  7. Harsh, G.R., IV; Levin, V.A.; Gutin, P.H.; Seager, M.; Silver, P.; Wilson, C.B. Reoperation for recurrent glioblastoma and anaplastic astrocytoma. Neurosurgery 1987, 21, 615–621. [Google Scholar]
  8. Guyotat, J.; Signorelli, F.; Frappaz, D.; Madarassy, G.; Ricci, A.C.; Bret, P. Is reoperation for recurrence of glioblastoma justified? Oncol. Rep. 2000, 7, 899–904. [Google Scholar]
  9. Wick, A.; Pasher, C.; Wick, W.; Jauch, T.; Weller, M.; Bogdahn, U.; Hau, P. Rechallenge with temozolomide in patients with recurrent gliomas. J. Neurol. 2009, 256, 734–741. [Google Scholar]
  10. Wick, W.; Wller, M.; Weiler, M.; Batchelor, T.; Yung, W.K.A.; Platten, M. Pathway inhibition: Emerging molecular targets for treating glioblastoma. Neuro-Oncology 2011, 13, 566–579. [Google Scholar]
  11. Bauman, G.S.; Sneed, P.K.; Wara, W.M.; Stalpers, L.J.; Chang, S.M.; McDermott, M.W.; Gutin, P.H.; Larson, D.A. Reirradiation of primary CNS tumors. Int. J. Radiat. Oncol. Biol. Phys. 1996, 36, 433–441. [Google Scholar]
  12. Kim, H.K.; Thornton, A.F.; Greenberg, H.S.; Page, M.A.; Junck, L.; Sandler, H.M. Results of re-irradiation of primary intracranial neoplasms with three-dimensional conformal therapy. Am. J. Clin. Oncol. 1997, 20, 358–363. [Google Scholar]
  13. Hayat, K.; Jones, B.; Bisbrown, G.; Baria, K.; Pigott, T. Retreatment of patients with intracranial gliomas by external beam radiotherapy and cytotoxic chemotherapy. Clin. Oncol. (R. Coll. Radiol.) 1997, 9, 158–163. [Google Scholar]
  14. Arcicasa, M.; Roncadin, M.; Bidoli, E.; Dedkov, A.; Gigante, M.; Trovò, M.G. Reirradiation and lomustine in patients with relapsed high-grade gliomas. Int. J. Radiat. Oncol. Biol. Phys. 1999, 43, 789–793. [Google Scholar]
  15. Nieder, C.; Nestle, U.; Ketter, R.; Kolles, H.; Gentner, S.J.; Steudel, W.I.; Schnabel, K. Hyperfractionated and accelerated-hyperfractionated radiotherapy for glioblastoma multiforme. Radiat. Oncol. Investig. 1999, 7, 36–41. [Google Scholar]
  16. Veninga, T.; Langendijk, H.A.; Slotman, B.J.; Rutten, E.H.; van der Kogel, A.J.; Prick, M.J.; Keyser, A.; van der Maazen, R.W. Reirradiation of primary brain tumours: Survival, clinical response and prognostic factors. Radiother. Oncol. 2001, 59, 127–137. [Google Scholar]
  17. Henke, G.; Paulsen, F.; Steinbach, J.P.; Ganswindt, U.; Isijanov, H.; Kortmann, R.D.; Bamberg, M.; Belka, C. Hypofractionated reirradiation for recurrent malignant glioma. Strahlenther. Onkol. 2009, 185, 113–119. [Google Scholar]
  18. Laing, R.W.; Warrington, A.P.; Graham, J.; Britton, J.; Hines, F.; Brada, M. Efficacy and toxicity of fractionated stereotactic radiotherapy in the treatment of recurrent gliomas (phase I/II study). Radiother. Oncol. 1993, 27, 22–29. [Google Scholar]
  19. Glass, J.; Silverman, C.L.; Axelrod, R.; Corn, B.W.; Andrews, D.W. Fractionated stereotactic radiotherapy with cis-platinum radiosensitization in the treatment of recurrent, progressive, or persistent malignant astrocytoma. Am. J. Clin. Oncol. 1997, 20, 226–229. [Google Scholar]
  20. Shepherd, S.F.; Laing, R.W.; Cosgrove, V.P.; Warrington, A.P.; Hines, F.; Ashley, S.E.; Brada, M. Hypofractionated stereotactic radiotherapy in the management of recurrent glioma. Int. J. Radiat. Oncol. Biol. Phys. 1997, 37, 393–398. [Google Scholar]
  21. Lederman, G.; Wronski, M.; Arbit, E.; Odaimi, M.; Wertheim, S.; Lombardi, E.; Wrzolek, M. Treatment of recurrent glioblastoma multiforme using fractionated stereotactic radiosurgery and concurrent paclitaxel. Am. J. Clin. Oncol. 2000, 23, 155–159. [Google Scholar]
  22. Hudes, R.S.; Corn, B.W.; Werner-Wasik, M.; Andrews, D.; Rosenstock, J.; Thoron, L.; Downes, B.; Curran, W.J., Jr. A phase I dose escalation study of hypofractionated stereotactic radiotherapy as salvage therapy for persistent or recurrent malignant glioma. Int. J. Radiat. Oncol. Biol. Phys. 1999, 43, 293–298. [Google Scholar]
  23. Cho, K.H.; Hall, W.A.; Gerbi, B.J.; Higgins, P.D.; McGuire, W.A.; Clark, H.B. Single dose versus fractionated stereotactic radiotherapy for recurrent high-grade gliomas. Int. J. Radiat. Oncol. Biol. Phys. 1999, 45, 1133–1141. [Google Scholar]
  24. Selch, M.T.; DeSalles, A.A.F.; Solberg, T.D.; Wallace, R.E.; Do, T.M.; Ford, J.; Cabatan-Awang, C.; Withers, H.R. Hypofractionated stereotactic radiotherapy for Recurrent Malignant Gliomas. J. Radiosurg. 2000, 3, 3–12. [Google Scholar]
  25. Voynov, G.; Kaufman, S.; Hong, T.; Pinkerton, A.; Simon, R.; Dowsett, R. Treatment of recurrent malignant gliomas with stereotactic intensity modulated radiation therapy. Am. J. Clin. Oncol. 2002, 25, 606–611. [Google Scholar]
  26. Combs, S.E.; Gutwein, S.; Thilmann, D.; Debus, J.; Schulz-Ertner, D. Reirradiation of recurrent WHO Grade III astrocytomas using fractionated stereotactic radiotherapy (FSRT). Strahlenther. Onkol. 2005, 181, 768–773. [Google Scholar]
  27. Combs, S.E.; Gutwein, S.; Thilmann, D.; Huber, P.; Debus, J.; Schulz-Ertner, D. Stereotactically guided fractionated re-irradiation in recurrent glioblastoma multiforme. J. Neurooncol. 2005, 74, 167–171. [Google Scholar]
  28. Vordermark, D.; Kolbl, O.; Ruprecht, K.; Vince, G.H.; Bratengeier, K.; Flentje, M.; Vince, G.H.; Bratengeier, K. Hypofractionated stereotactic re-irradiation: Treatment option in recurrent malignant glioma. BMC Cancer 2005, 5, 55. [Google Scholar]
  29. Grosu, A.L.; Weber, W.A.; Franz, M.; Stärk, S.; Piert, M.; Thamm, R.; Gumprecht, H.; Schwaiger, M.; Molls, M.; Nieder, C. Reirradiation of recurrent high-grade gliomas using amino acid PET (SPECT)/CT/MRI image fusion to determine gross tumor volume for stereotactic fractionated radiotherapy. Int. J. Radiat. Oncol. Biol. Phys. 2005, 63, 511–519. [Google Scholar]
  30. Wurm, R.E.; Kuczer, D.A.; Schlenger, L.; Matniani, G.; Scheffler, D.; Cosgrove, V.P.; Ahlswede, J.; Woiciechowski, C.; Budach, V. Hypofractionated stereotactic radiosurgery combined with topotecan in recurrent malignant glioma. Int. J. Radiat. Oncol. Biol. Phys. 2006, 66, S26–S32. [Google Scholar]
  31. Kohshi, K.; Yamamoto, H.; Nakahara, A.; Katoh, T.; Takagi, M. Fractionated stereotactic radiotherapy using gamma unit after hyperbaric oxygenation on recurrent high-grade gliomas. J. Neurooncol. 2007, 82, 297–303. [Google Scholar]
  32. Ernst-Stecken, A.; Ganslandt, O.; Lambrecht, U.; Sauer, R.; Grabenbauer, G. Survival and quality of life after hypofractionated stereotactic radiotherapy for recurrent malignant glioma. J. Neurooncol. 2007, 81, 287–294. [Google Scholar]
  33. Schwer, A.L.; Damek, D.M.; Kavanagh, B.D.; Gaspar, L.E.; Lillehei, K.; Stuhr, K.; Chen, C. A phase I dose-escalation study of fractionated stereotactic radiosurgery in combination with gefitinib in patients with recurrent malignant gliomas. Int. J. Radiat. Oncol. Biol. Phys. 2008, 70, 993–1001. [Google Scholar]
  34. Combs, S.E.; Bischof, M.; Welzel, T.; Hof, H.; Oertel, S.; Debus, J.; Schulz-Ertner, D. Radiochemotherapy with temozolomide as reirradiation using high precision fractionated stereotactic radiotherapy (FSRT) in patients with recurrent gliomas. J. Neurooncol. 2008, 89, 205–210. [Google Scholar]
  35. Fokas, E.; Wacker, U.; Gross, M.W.; Henzel, M.; Encheva, E.; Engenhart-Cabillic, R. Hypofractionated stereotactic reirradiation of recurrent glioblastomas: A beneficial treatment option after high-dose radiotherapy? Strahlenther. Onkol. 2009, 185, 235–240. [Google Scholar]
  36. Patel, M.; Siddiqui, F.; Jin, J.Y.; Mikkelsen, T.; Rosenblum, M.; Movsas, B.; Ryu, S. Salvage reirradiation for recurrent glioblastoma with radiosurgery: Radiographic response and improved survival. J. Neurooncol. 2009, 92, 185–191. [Google Scholar]
  37. Gutin, P.H.; Iwamoto, F.M.; Beal, K.; Mohile, N.A.; Karimi, S.; Hou, B.L.; Lymberis, S.; Yamada, Y.; Chang, J.; Abrey, L. Safety and efficacy of bevacizumab with hypofractionated stereotactic irradiation for recurrent malignant gliomas. Int. J. Radiat. Oncol. Biol. Phys. 2008, 75, 156–163. [Google Scholar]
  38. Villavicencio, A.T.; Burneikiene, S.; Romanelli, P.; Fariselli, L.; McNeely, L.; Lipani, J.D.; Chang, S.D.; Nelson, E.L.; McIntyre, M.; Broggi, G.; et al. Survival following stereotactic radiosurgery for newly diagnosed and recurrent glioblastoma multiforme: A multicenter experience. Neurosurg. Rev. 2009, 32, 417–424. [Google Scholar]
  39. Fogh, S.E.; Andrews, D.W.; Glass, J.; Curran, W.; Glass, C.; Champ, C.; Evans, J.J.; Hyslop, T.; Pequignot, E.; Downes, B.; et al. Hypofractionated stereotactic radiation therapy: An effective therapy for recurrent high-grade gliomas. J. Clin. Oncol. 2010, 28, 3048–3053. [Google Scholar]
  40. Torcuator, R.G.; Thind, R.; Patel, M.; Mohan, Y.S.; Anderson, J.; Doyle, T.; Ryu, S.; Jain, R.; Schultz, L.; Rosenblum, M.; et al. The role of salvage reirradiation for malignant gliomas that progress on bevacizumab. J. Neurooncol. 2010, 97, 401–407. [Google Scholar]
  41. Minniti, G.; Armosini, V.; Salvati, M.; Lanzetta, G.; Caporello, P.; Mei, M.; Osti, M.F.; Maurizi, R.E. Fractionated stereotactic reirradiation and concurrent temozolomide in patients with recurrent glioblastoma. J. Neurooncol. 2011, 103, 683–691. [Google Scholar]
  42. Maier-Hauff, K.; Ulrich, F.; Nestler, D.; Niehoff, H.; Wust, P.; Thiesen, B.; Orawa, H.; Budach, V.; Jordan, A. Efficacy and safety of intratumoral thermotherapy using magnetic iron-oxide nanoparticles combined with external beam radiotherapy on patients with recurrent glioblastoma multiforme. J. Neurooncol. 2011, 103, 317–324. [Google Scholar]
  43. Alexander, E., 3rd; Loeffler, J.S. Radiosurgery using a modified linear accelerator. Neurosurg. Clin. N. Am. 1992, 3, 167–190. [Google Scholar]
  44. Chamberlain, M.C.; Barba, D.; Kormanik, R.N.; Shea, M.C. Stereotactic radiosurgery for recurrent gliomas. Cancer 1994, 74, 1342–1347. [Google Scholar]
  45. Shrieve, D.C.; Alexander, E., 3rd; Wen, P.Y.; Fine, H.A.; Kooy, H.M.; Black, P.McL.; Loeffler, J.S. Comparison of stereotactic radiosurgery and brachytherapy in the treatment of recurrent glioblastoma multiforme. Neurosurgery 1995, 36, 275–284. [Google Scholar]
  46. Larson, D.A.; Gutin, P.H.; McDermott, M.; Lamborn, K.; Sneed, P.K.; Wara, W.M.; Flickinger, J.; Kondziolka, D.; Lunsford, L.D.; Hudgins, W.R.; et al. Gamma knife for glioma: Selection factors and survival. Int. J. Radiat. Oncol. Biol. Phys. 1996, 36, 1045–1053. [Google Scholar]
  47. Kondziolka, D.; Flickinger, J.; Jonh, C.; Bisonette, D.J.; Bozik, M.; Lunsford, L.D. Survival benefit of stereotactic radiosurgery for patients with malignant glial neoplasm. Neurosurgery 1997, 41, 776–785. [Google Scholar]
  48. Park, J.L.; Suh, J.H.; Barnett, G.H.; Reddy, C.A.; Peereboom, D.M.; Stevens, G.H.J.; Cohen, B.H. Survival after stereotactic radiosurgery for recurrent glioblastoma multiforme. J. Radiosurg. 2000, 3, 169–175. [Google Scholar]
  49. Larson, D.A.; Prodos, M.; Lamborn, K.R.; Smith, V.; Sneed, P.K.; Chang, S.; Nicholas, K.M.; Wara, W.M.; Devriendt, D.; Kunvar, S.; et al. Phase II study of high central dose gamma knife radiosurgery and marimastat in patients with recurrent malignant glioma. Int. J. Radiat. Oncol. Biol. Phys. 2002, 54, 1397–1304. [Google Scholar]
  50. Combs, S.E.; Widmer, V.; Thilmann, C.; Holger, H.; Debus, J.; Schulz-Ertner, D. Stereotactic radiosurgery (SRS). Treatment option for recurrent glioblastoma multiforme (GBM). Cancer 2005, 104, 2168–2173. [Google Scholar]
  51. Hsieh, P.C.; Chandler, J.P.; Bhangoo, S.; Panagiotopoulos, K.; Kalapurakal, J.A.; Maymont, M.H.; Cozzens, J.W.; Levy, R.M.; Salehi, S. Adjuvant gamma knife stereotactic radiosurgery at the time of tumor progression potentially improves survival for patients with glioblastoma multiforme. Neurosurgery 2005, 57, 684–691. [Google Scholar]
  52. Mahajan, A.; McCutcheon, I.E.; Suki, D.; Chang, E.L.; Hassenbach, S.J.; Weinberg, J.S.; Shiu, A.; Maor, M.H.; Woo, S.Y. Case-control study of stereotactic radiosurgery for recurrent glioblastoma multiforme. J. Neurosurg. 2005, 103, 210–217. [Google Scholar]
  53. Kong, D.S.; Lee, J.I.; Park, K.; Kim, J.H.; Lim, D.H.; Nam, D.H. Efficacy of stereotactic radiosurgery as a salvage treatment for recurrent malignant gliomas. Cancer 2008, 112, 2046–2051. [Google Scholar]
  54. Biswas, T.; Okunieff, P.; Schell, M.C.; Smudzin, T.; Pilcher, W.H.; Bakos, R.S.; Vates, G.E.; Walter, K.A.; Wensel, A.; Korones, D.N.; et al. Stereotactic radiosurgery for glioblastoma: Retrospective analysis. Radiat. Oncol. 2009, 4, 11. [Google Scholar]
  55. Maranzano, E.; Anselmo, P.; Casale, M.; Trippa, F.; Carletti, S.; Principi, M.; Loreti, F.; Italiani, M.; Caserta, C.; Giorgi, C. Treatment of recurrent glioblastoma with stereotactic radiotherapy: Long-term results of a mono-institutional trial. Tumori 2011, 97, 56–61. [Google Scholar]
  56. Lucas, G.L.; Luxton, G.; Cohen, D.; Petrovich, Z.; Langholz, B.; Apuzzo, M.L.J.; Sapozink, M.D. Treatment results of stereotactic interstial brachytherapy for primary and metastatic brain tumors. Int. J. Radiat. Oncol. Biol. Phys. 1991, 21, 715–721. [Google Scholar]
  57. Scharfen, C.O.; Sneed, P.K.; Wara, W.M.; Larson, D.A.; Phillips, T.L.; Prados, M.D.; Weaver, K.A.; Malec, M.M.; Acord, P.; Lamborn, K.R.; et al. High activity iodine-125 interstitial implant for gliomas. Int. J. Radiat. Oncol. Biol. Phys. 1992, 24, 583–591. [Google Scholar]
  58. Malkin, M.G. Interstitial irradiation of malignant gliomas. Rev. Neurol. 1992, 148, 448–453. [Google Scholar]
  59. Sneed, P.K.; Gutin, P.H.; Stauffer, P.R.; Phillips, T.L.; Prados, M.D.; Weaver, K.A.; Suen, S.; Lamb, S.A.; Ham, B.; Ahn, D.K.; et al. Thermoradiotherapy of recurrent malignant brain tumors. Int. J. Radiat. Oncol. Biol. Phys. 1992, 23, 853–861. [Google Scholar]
  60. Bernstain, M.; Laperriere, N.; Glen, J.; Leung, P.; Thomason, C.; Landon, A. Brachytherapy for recurrent malignant astrocytoma. Int. J. Radiat. Oncol. Biol. Phys. 1994, 30, 1213–1217. [Google Scholar]
  61. Kitchen, N.D.; Hughes, S.W.; Taub, N.A.; Sofat, A.; Beaney, R.P.; Thomas, D.G.T. Survival following interstitial brachytherapy for recurrent malignant glioma. J. Neurooncol. 1994, 18, 33–39. [Google Scholar]
  62. Chamberlain, M.C.; Barba, D.; Komanik, P.; Berson, A.M.; Saunders, W.M.; Shea, M.C. Concurrent cisplatin therapy and iodine 125 brachytherapy for recurrent malignant brain tumors. Arch. Neurol. 1995, 52, 162–167. [Google Scholar]
  63. Mayr, M.T.; Crocker, J.R.; Butker, E.K.; Williams, H.; Cotsonis, G.A.; Olson, J. Results of interstitial brachytherapy for malignant brain tumors. Int. J. Oncol. 2002, 21, 817–823. [Google Scholar]
  64. Simon, J.M.; Cornu, P.; Boisserie, G.; Hasboun, D.; Tep, B.; Hardiman, C.; Valery, C.A.; Delattre, J.Y.; Dormont, D.; Baillet, F.; et al. Brachytherapy of glioblastoma recurring in previously irradiated territory: Predictive value of tumor volume. Int. J. Radiat. Oncol. Biol. Phys. 2002, 53, 67–74. [Google Scholar]
  65. Tselis, N.; Kolotas, C.; Birn, G.; Röddiger, S.; Filipowicz, I.; Kontova, M.; Fountzilas, G.; Selviaridis, P.; Baltas, D.; Heyd, R.; et al. CT-guided interstial HDR brachytherapy for recurrent glioblastoma multiforme. Long-term results. Strahlenther. Onkol. 2007, 183, 563–570. [Google Scholar]
  66. Fabrini, M.G.; Perrone, F.; de Franco, L.; Pasqualetti, F.; Grespi, S.; Vannozzi, R.; Cionini, L. Perioperitive high-dose-rate brachytherapy in the treatment of recurrent malignant gliomas. Strahlenther. Onkol. 2009, 185, 524–529. [Google Scholar]
  67. Larson, G.L.; Wilbanks, J.H.; Dennis, W.S.; Permenter, W.D.; Easley, J.D. Interstial radiogold implantation for the treatment of recurrent high-grade gliomas. Cancer 1990, 66, 27–29. [Google Scholar]
  68. Halligan, J.B.; Stelzer, K.J.; Rostomily, R.C.; Spence, A.M.; Griffin, T.W.; Berger, M.S. Operation and permanent low activity 125I brachytherapy for recurrent high-grade astrocytomas. Int. J. Radiat. Oncol. Biol. Phys. 1996, 35, 541–547. [Google Scholar]
  69. Gaspar, L.E.; Zamorano, L.J.; Shamsa, F.; Fontanesi, J.; Ezzel, G.E.; Yakar, D.A. Permanent 125iodine implants for recurrent malignant gliomas. Int. J. Radiat. Oncol. Biol. Phys. 1999, 43, 977–982. [Google Scholar]
  70. Patel, S.; Breneman, J.C.; Warnick, R.E.; Albright, R.E.; Tobler, W.D.; van Loveren, H.R.; Tew, J.M. Permanent iodine-125 interstial implants for the treatment of recurrent glioblastoma multiforme. Neurosurgery 2000, 46, 1123–1130. [Google Scholar]
  71. Larson, D.A.; Suplica, J.M.; Chang, S.M.; Lamborn, K.R.; McDermott, M.W.; Sneed, P.K.; Prados, M.D.; Wara, W.M.; Nicholas, M.K.; Berger, M.S. Permanent iodine 125 brachytherapy in patients with progressive or recurrent glioblastoma multiforme. Neuro-oncol 2004, 6, 119–126. [Google Scholar]
  72. Darakchiev, B.J.; Albright, R.E.; Breneman, J.C.; Warnick, R. Safety and efficacy of permanent iodine-125 implants and carmustine wafers in patients with recurrent glioblastoma multiforme. J. Neurosurg. 2008, 108, 236–242. [Google Scholar]
  73. Tatter, S.B.; Shaw, E.G.; Rosenblum, M.L.; Karvelis, K.C.; Kleinberg, L.; Weingart, J.; Olson, J.J.; Crocker, I.R.; Brem, S.; Perarlman, J.L.; et al. An inflatable balloon catheter and liquid 125I radiation source (GliaSite radiation therapy system) for treatment of recurrent malignant glioma: Multicenter safety and feasibility trial. J. Neurosurg. 2003, 99, 297–303. [Google Scholar]
  74. Chan, T.A.; Weingart, J.D.; Parisi, M.; Hughes, M.A.; Olivi, A.; Borzillary, S.; Alahakone, D.; Detorie, N.A.; Wharam, M.D.; Kleinberg, L. Treatment of recurrent glioblastoma multiforme with gliasite brachytherapy. Int. J. Radiat. Oncol. Biol. Phys. 2005, 62, 1133–1139. [Google Scholar]
  75. Gabayan, A.J.; Green, S.B.; Sanan, A.; Jenrette, J.; Schultz, C.; Papagikos, M.; Tatter, S.P.; Patel, A.; Amin, P.; Lustig, R.; et al. Gliasite brachytherapy for treatment of recurrent malignant gliomas: A retrospective multi-institutional analysis. Neurosurgery 2006, 58, 701–708. [Google Scholar]
  76. Adkinson, J.B.; Tomè, W.; Seo, S.; Richards, G.M.; Robins, H.I.; Rassmussen, K.; Welsh, J.S.; Mahler, P.A.; Howard, S.P. Reirradiation of large-volume recurrent glioma with pulsed reduced-dose-rate radiotherapy. Int. J. Radiat. Oncol. Biol. Phys. 2011, 79, 835–841. [Google Scholar]
  77. Riva, P.; Arista, A.; Tison, V.; Sturiale, C.; Franceschi, G.; Spinelli, A.; Riva, N.; Casi, M.; Moscatelli, G.; Frattarelli, M. Intralesional radioimmunotherapy of malignant gliomas. An effective treatment in recurrent tumors. Cancer 1994, 73, 1076–1082. [Google Scholar]
  78. Bigner, D.D.; Brown, M.T.; Friedman, A.H.; Coleman, R.E.; Akabani, G.; Friedman, H.S.; Thorstadt, W.L.; McLendon, R.E.; Bigner, S.H.; Zhao, X.G.; et al. Iodine-131-labeled antitenascin monoclonal antibody 81C6 treatment of patients with recurrent malignant gliomas: Phase I trial results. J. Clin. Oncol. 1998, 16, 2202–2212. [Google Scholar]
  79. Paganelli, G.; Bartolomei, M.; Ferrari, M.; Cremonesi, M.; Broggi, G.; Maira, G.; Sturiale, C.; Grana, C.; Prisco, G.; Gatti, M.; et al. Pre-targeted locoregional radioimmunotherapy with 90Y-biotin in glioma patients: Phase I study and preliminary therapeutic results. Cancer Biother. Radiopharm. 2001, 16, 227–235. [Google Scholar]
  80. Boiardi, A.; Bartolomei, M.; Silvani, A.; Eoli, M.; Salmaggi, A.; Lamperti, E.; Milanesi, I.; Botturi, A.; Rocca, P.; Bodei, L.; et al. Intratumoral delivery of mitoxantrone in association with 90-Y radioimmunotherapy (RIT) in recurrent glioblastoma. J. Neurooncol. 2005, 72, 125–131. [Google Scholar]
  81. Reardon, D.A.; Akabani, G.; Coleman, R.E.; Friedman, A.H.; Friedman, H.S.; Herndon, J.E., 2nd; McLendon, R.E.; Pegram, C.N.; Provenzale, J.M.; Quinn, J.A.; et al. Salvage radioimmunotherapy with murine iodine-131-labeled antitenascin monoclonal antibody 81C6 for patients with recurrent primary and metastatic malignant brain tumors: Phase II study results. J. Clin. Oncol. 2006, 24, 115–122. [Google Scholar]
  82. Mamelak, A.N.; Rosenfeld, S.; Bucholz, R.; Raubitschek, A.; Nabors, L.B.; Fiveash, J.B.; Shen, S.; Khazaeli, M.B.; Colcher, D.; Liu, A.; et al. Phase I single-dose study of intracavitary-administered iodine-131-TM-601 in adults with recurrent high-grade glioma. J. Clin. Oncol. 2006, 24, 3644–3650. [Google Scholar]
  83. Casaco, A.; Lopez, G.; Garcia, I.; Rodriguez, J.A.; Fernandez, R.; Figueredo, J.; Torres, L.; Perera, A.; Batista, J.; Leyva, R.; et al. Phase I single-dose of intracavitary-administered nimotuzumab labeled with 188Re in adult recurrent high-grade glioma. Cancer Biol. Ther. 2008, 7, 333–339. [Google Scholar]
  84. Pellettieri, L.; H-Stenstam, B.; Rezaei, A.; Giusti, V.; Skold, K. An investigation of boron neutron capture therapy for recurrent glioblastoma multiforme. Acta Neurol. Scand. 2008, 117, 191–197. [Google Scholar]
  85. Miyatake, S.I.; Kawabata, S.; Yokoyama, K.; Kuroiwa, T.; Michiue, H.; Sakurai, Y.; Kumada, H.; Suzuki, M.; Maruhashi, A.; Kirihata, M.; et al. Survival benefit of boron neutron capture therapy for recurrent malignant gliomas. J. Neurooncol. 2009, 91, 199–206. [Google Scholar]
  86. Kankaanranta, L.; Seppala, T.; Koivunoro, H.; Valimaki, P.; Beule, A.; Collan, J.; Kortesniemi, M.; Uusi-Simola, J.; Kotiluoto, P.; Auterinen, I.; et al. L-boronophenylalanine-mediated boron neutron capture therapy for malignant glioma progressing after external beam radiation therapy: A phase I study. Int. J. Radiat. Oncol. Biol. Phys. Phys. 2011, 80, 369–376. [Google Scholar]
  87. Marks, J.E.; Baglan, R.J.; Prassad, S.C. Cerebral radionecrosis incidence and risk in relation to dose, time, fractionation, and volume. Int. J. Radiat. Oncol. Biol. Phys. 1981, 7, 243–252. [Google Scholar]
  88. Sheline, G.E. Irradiation injury of the human brain: A review of clinical experience. In Radiation Damage to the Nervous System; Gilbert, H.A., Kagan, A.R., Eds.; Raven Press: New York, NY, USA, 1980; pp. 39–58. [Google Scholar]
  89. Lawrence, Y.R.; Li, X.A.; El-Naqa, I.; Hahn, C.A.; Marks, L.B.; Merchant, T.E.; Dicker, A.P. Radiation dose-volume effect in the brain. Int. J. Radiat. Oncol. Biol. Phys. 2010, 76, S20–S27. [Google Scholar]
  90. Flickinger, J.C.; Deutsch, M.; Lunsford, L.D. Repeat megavoltage irradiation of pituitary and suprasellar tumors. Int. J. Radiat. Oncol. Biol. Phys. 1989, 17, 171–175. [Google Scholar]
  91. Mayer, R.; Sminia, P. Reirradiation tolerance of the human brain. Int. J. Radiat. Oncol. Biol. Phys. 2008, 70, 1350–1360. [Google Scholar]
  92. Nieder, C.; Astner, S.T.; Mehta, M.P.; Grosu, A.L.; Molls, M. Improvement, clinical course, and quality of life after palliative radiotherapy for recurrent glioblastoma. Am. J. Clin. Oncol. 2008, 31, 300–305. [Google Scholar]
  93. Higgins, J.P.T., Green, S., Eds.; Cochrane Handbook for Systematic Reviews of Interventions, Version 5.0.2. Available online: (accessed on 8 October 2011).
  94. Liu, B.L.; Cheng, J.X.; Zhang, X.; Zang, W. Controversies concerning the application of brachytherapy in central nervous system tumors. J. Cancer Res. Clin. Oncol. 2010, 136, 173–185. [Google Scholar]
Cancers EISSN 2072-6694 Published by MDPI AG, Basel, Switzerland RSS E-Mail Table of Contents Alert
Back to Top