Molecular Characterization and Treatment Approaches for Pediatric H3 K27-Altered Diffuse Midline Glioma: Integrated Systematic Review of Individual Clinical Trial Participant Data
1
Department of Pediatrics, Division of Pediatric Hematology, Oncology and Bone Marrow Transplant, School of Medicine & Public Health, University of Wisconsin, Madison, WI 53792, USA
2
Department of Neurosurgery, School of Medicine & Public Health, University of Wisconsin, UW Carbone Cancer Center, Madison, WI 53792, USA
3
Department of Biostatistics and Medical Informatics, School of Medicine and Public Health, University of Wisconsin, Madison, WI 53792, USA
*
Author to whom correspondence should be addressed.
Cancers 2023, 15(13), 3478; https://doi.org/10.3390/cancers15133478
Submission received: 2 June 2023
/
Revised: 30 June 2023
/
Accepted: 1 July 2023
/
Published: 3 July 2023
(This article belongs to the Section Systematic Review or Meta-Analysis in Cancer Research)
Abstract
:Simple Summary
Diffuse midline glioma, H3 K27-altered are central nervous system tumors that primarily affect the pediatric population. Currently, there are no curative therapies, with several completed and on-going clinical trials exploring many different therapeutic options. In this systematic review, we utilized individual participant data from published clinical trials to assess the effect of treatment options, molecular makeup and clinical characteristics on overall survival. These findings are intended to provide guidance for future interventions along with indicate the need to continue to assess results from clinical trials as they become available at a larger scale.
Abstract
Diffuse midline glioma (DMG), H3 K27-altered are highly aggressive, incurable central nervous system (CNS) tumors. The current standard palliative treatment is radiotherapy, with most children succumbing to the disease in less than one year from the time of diagnosis. Over the past decade, there have been significant advancements in our understanding of these heterogeneous tumors at the molecular level. As a result, most of the newer clinical trials offered utilize more targeted approaches with information derived from the tumor biopsy. In this systematic review, we used individual participant data from seven recent clinical trials published over the past five years that met our inclusion and exclusion criteria to analyze factors that influence overall survival (OS). We found that the most prominent genetic alterations H3.3 (H3F3A) and TP53 were associated with worse OS and that ACVR had a protective effect. In addition, re-irradiation was the only statistically significant treatment modality that showed any survival benefit. Our findings highlight some important characteristics of DMG, H3 K27-altered and their effects on OS along with the importance of continuing to review clinical trial data to improve our therapies for these fatal tumors.
1. Introduction
Diffuse midline glioma (DMG), H3 K27-altered are devastating central nervous system (CNS) tumors that affect both children and adults. The most common locations of these tumors are within the pons, thalamus or spinal cord of the CNS. These tumors are designated as World Health Organization (WHO) grade 4 regardless of their histology and anatomical location. The characteristic H3 K27M mutation that is the hallmark of these tumors comes in two primary genotypes with mutations in the HIST1H3B/C (H3.1) and H3F3A (H3.3) genes.
Our understanding of the pathogenesis and underlying molecular makeup of these tumors has improved over the past decade, yet there remains no cure. Conventional photon radiation therapy remains the standard treatment approach, with numerous clinical trials exploring more effective therapies. Over recent years, the clinical standard of DMG management has evolved to include regular biopsy and histological confirmation. In addition, with the increased use of next generation sequencing (NGS), numerous clinical trials have looked to assess the feasibility and efficacy of various targeted agents based on the molecular makeup of each individual patient’s tumors.
It is well known that those DMGs with the H3 K27M mutation have poorer outcomes as well as halted overall survival (OS) compared the unmutated type [1,2,3]. With newer therapies being utilized in clinical trials, we looked at more recently published literature to assess the efficacy of various treatments for pediatric patients with DMG, H3 K27-altered. Our primary objective was to investigate the impact of various treatment modalities and molecular alterations on OS. Our secondary analysis involved investigating other clinical factors, such as age, sex and tumor location, on DMG’s incidence as well as prognostic significance. This systematic analysis was performed by integrating the individual participant data (IPD) of recently published clinical trials that meet our inclusion/exclusion criteria. As newer therapies emerge, it will be important to continue to assess the response of these tumors in the context of their molecular makeup, given the significant heterogeneity of these tumors.
2. Materials and Methods
2.1. Study Selection Criteria
This systematic analysis was registered via the National Institute for Health and Care Research (NIHR) via identification number 432005. A search strategy was developed utilizing the Populations, Intervention, Comparison, Outcome, Study Type (PICOS) question format. In pediatric patients with diffuse midline glioma, H3 K27-altered (Population) who received targeted therapy as part of a clinical trial (Intervention and Study Type), the effects on overall survival based on the therapeutic modality along with the known molecular alterations, anatomic location of the tumor, sex and age of the patient (Comparison and Outcome) were determined. Though any H3 K27 mutation could be included within our study, all of the patients had the presence of the H3 K27M missense mutation.
A literature search in PUBMED was performed by three independent reviewers according to the Preferred Reporting Items for Systematic Reviews and Meta-Analysis (PRISMA) (Figure 1) guidelines. Our search included clinical trials, published from 1 January 2018 to 2 March 2023. The terms used for the literature search included “diffuse midline glioma” OR “diffuse intrinsic pontine glioma” OR “DMG” OR “DIPG” AND “targeted therapy” OR “clinical trial” OR “molecular”. These terms were specifically used in batch searches across both databases. All the articles resulting from our searches were analyzed for our inclusion and exclusion criteria and only articles that satisfied all our criteria were selected for the final analysis (Table 1).
2.2. Quality Evaluation of Clinical Trials
Publications included in this study were evaluated according to the Newcastle–Ottawa Scale (NOS) to assess for quality of the included study. This assessment tool has three domains: selection (maximum 4 stars), comparability (maximum 2 stars) and outcome (maximum 3 stars) [4]. Studies that were awarded fewer than 6 stars were considered low quality while those with at least 6 stars were regarded as moderate- to high-quality studies (Table 2).
2.3. Data Extraction
All IPD were extracted from the main manuscript and supplementary text, tables and figures of the included articles. In total, 108 patients were identified from 7 published reports from published clinical trials (Table 3). Our primary outcome of interest was patients’ overall survival treated with the various therapies compared to one another. Secondary outcomes included assessing tumor anatomical location, sex, age and their prognostic impact. Two independent investigators (A.A. and K.K.) extracted the data, and confirmation of extracted data was also conducted by a third independent reviewer (S.D.). Cases that did not undergo an upfront biopsy or did not have the H3 K27M mutation were subsequently removed.
2.4. Statistical Analysis
The primary outcome from our study was impact of treatment modalities and molecular alterations on the OS of patients with DMG, H3 K27-altered. Additional factors were also assessed, including anatomic location of the tumor, sex and age of the patient, to determine their effects on OS along with co-incidence of one another. Statistical analysis was conducted using SAS software (SAS Institute Inc., Cary, NC, USA), version 9.4. All reported p-values are two-sided and a p < 0.05 was used to define statistical significance. Descriptive statistics such as count and frequency were generated for demographic variables. ANOVA and T-test were used to test difference of overall survival between different demographics, anatomical location, gene mutations and treatments. Fisher’s exact was used to test the association between gene mutations, treatments and anatomical location and sex.
3. Results
3.1. Study Characteristics
Our initial PubMed search resulted in 267 publications. The clinical trial article type was selected, which eliminated 116 articles. Due to duplicity, an additional 101 articles were eliminated. Forty-three articles were eliminated after the title/abstract were screened based upon our inclusion and exclusion criteria or if no IPD were available. In total, seven studies were selected for full-text review. By reading the full text of these papers, we integrated the IPD from all seven studies for the final analysis [5,6,7,8,9,10,11]. We identified a total of 108 pediatric cases with the available pertinent clinical data. Of note, 34 patients did not have NGS results available, either due to an inadequate sample or sampling not being performed. All included studies were rated as moderate- to high-quality based upon the NOS assessment tool. Table 2 presents the studies included in this analysis.
All patients included in our analysis underwent biopsy/partial resection of the initial tumor without any further surgeries conducted. The confirmation of the H3 K27M mutation was performed via IHC along with sequencing for all patients to delineate the H3.3 or H3.1 sub-type.
3.2. Survival Differences
We found overall survival differences stratified against molecular alterations and therapeutic interventions. Additional survival differences were seen in the age distribution of pediatric patients with DMG, H3 K27-altered. Patients aged <5 years had better OS (20.50 months) compared to patients aged >10 years (14.99 months) (p < 0.05). Tumors carrying the H3.3 (H3F3A) genotype had a worse OS compared to those with the H3.1 (HIST1H3B/C) (OS 14.25 months vs. 19.62 months; p < 0.001). Additionally, the tumors expressing the TP53 alteration also had a worse OS (13.71 months vs. 21.41 months; p < 0.0001), whereas those that expressed ACVR had an improved OS when compared against all the gene alterations that were assessed for (20.85 months vs. 14.89 months; p = 0.0081). Regarding therapeutic interventions, the only statistically significant treatment was tumor re-irradiation (18.62 months vs. 14.58 months; p = 0.0047). The use of any personalized treatment based upon the patients’ NGS alterations also showed a marginal benefit, though not statistically significant. The patients’ sex or anatomic location of the tumor had no effect on OS in our analysis (Table 4).
3.3. Genetic Alterations
Differences were observed in the type of genetic alterations seen when compared to the anatomic location of the tumor along with the sex of the patient. TP53 was identified frequently in both pontine and thalamic tumors (pons present in 58% vs. absent in 42% and thalamus present in 95% vs. absent in 5%; p 0.0018); however, it was proportionally more significant within thalamic tumors without any significant differences in sex. ACVR was solely identified in pontine tumors without any thalamic tumors showing expression for this and was more prevalent in female patients (31% vs. 9%; p = 0.0218). Thalamic tumors had a higher prevalence of ATRX mutations in comparison to tumors within the pons (48% vs. 10%; p = 0.0194). The H3.3 (H3F3A) alteration was more prevalent in both the pons and thalamus and in both male and female patients compared to H3.1 (HIST1H3B/C), without any statistical significance noted (Figure 2 and Table 5).
3.4. Treatment and Tumor Location
The type of treatments utilized when looking at the anatomical location of the tumor did show significant differences in the IPD analysis from the clinical trials. The use of a personalized treatment approach, based on an individual patient’s NGS sequencing, was more commonly utilized in pontine tumors compared to those within the thalamus (98% vs. 2%; p < 0.0001). This was also observed with patients who received a combination therapy of nimotuzumab and vinorelbine, where the combination therapy was only used for pontine tumors. On the other hand, the use of temozolomide was seen within both anatomic locations but was more prevalent in thalamic tumors. Immunotherapeutic approaches were also used for both anatomic locations but were more often used in pontine tumors (82% vs. 18%; p = 0.0015). Lastly, both re-irradiation and other chemotherapeutic therapies were used in patients with tumors in both locations but were more commonly seen in pontine tumors (Table 6).
4. Discussion
DMG, H3 K27-altered are fatal tumors located in midline CNS structures, primarily in the brainstem and thalamus but they can also be present within the spinal cord. The overall survival for pediatric patients is less than one year, generally ranging from 8–12 months after initial diagnosis [12,13]. Over the last decade, our understanding of the molecular makeup and biology of these tumors has expanded significantly. Now, biopsy is routinely conducted for tumors present within the pontine region (diffuse intrinsic pontine glioma or DIPG), and NGS testing is standard for the characteristic histone mutations associated with tumors present in other midline locations, such as the thalamus. With the advent of NGS, a more personalized approach to treatment has been the center of numerous clinical trials for these heterogeneous tumors, yet it is not certain how beneficial these treatments have been compared to the historical norm at a larger scale.
In this study, we integrated IPD from 108 biopsied or resected DMG, H3 K27-altered patients that participated in a clinical trial. Our study represents the first meta-analysis assessing the integrated response of DMG, H3 K27-altered patients enrolled in clinical trials published within the last 5 years. All patients in our study had confirmed presence of the H3 K27M mutation and the specific variant confirmed via sequencing. Most of the patients had NGS run on their tumor tissue, though many had inadequate or insufficient tissue for this to be assessed (34 in total). We primarily looked at the use of various treatment options and molecular alterations and their effect on OS in our patient cohort. We also assessed further available clinical data including age, sex and anatomical location for their effect on OS along with the incidence of molecular alterations and use of therapeutic strategies.
Our analysis showed that molecular characteristics of the tumor have significant impacts on patients’ overall outcome, with patients who had the H3.3 (H3F3A) genotype and TP53 mutation carrying a worse OS. Conversely, patients with an ACVR mutation had an improved OS compared to the rest. It has been well described that patients who carry the H3.3 genotype of DMG, H3 K27-altered have a halted OS and more protracted course [14,15,16]. The exact reasoning for this is not known, but irrespective of anatomical location has been found to be true [17,18]. Similarly, the TP53 mutation has also portrayed a poorer prognosis along with a high occurrence in patients with the H3.3 genotype [19,20]. It has been thought that TP53 may play a role in radio resistance in these tumors, leading to a halted OS compared to those without it [21,22]. The prevalence of TP53 was seen in thalamic tumors at a higher percentage compared to those in the pons in our study. Within the literature, the incidence of TP53 has not been well established with the anatomical location of the tumor but has been shown to be prevalent within all midline locations [1,23]. The ACVR mutation showed a protective effect on OS in our analysis. As a single gene alteration level, this has not been looked at in this regard, and further analysis is warranted to better understand and validate it given the fatality of the tumor. The prevalence of ACVR was seen only in the pontine location in our study, which is true considering what has also been described in similar studies of DMG, H3 K27-altered [18,24,25]. Sex differences have not been well described for this tumor, and aside from a higher incidence of ACVR in female patients compared to male in our analysis, no other differences were seen.
Previous studies have refuted the notion that anatomical location had an impact on the OS of DMG, H3 K27-altered in pediatric patients [18,26]. This was also the case in our study. However, more recent literature suggests this to not be true, with tumors within the brainstem and pons region having a decreased OS compared to tumors located in other midline areas [18,27,28]. The literature suggests that older patients typically have a more prolonged OS [29,30,31]. This was different from what was seen in our analysis, with patients <5yo having the longest OS and patients between 5–10yo having the worst OS. This is limited by the number of patients accounting for the <5yo and >10yo groups in our study, which limits the clinical significance to this. Therapeutically, only irradiation was found to have a significant benefit on OS. The literature also corroborates this, but the toxicity and poor quality of life associated with repeated radiation and its marginal improvement on OS has made this treatment modality unappealing [32,33]. The use of personalized therapeutic strategies showed a marginal benefit in our analysis, and this is likely the approach that will be needed at a combination level to combat these highly heterogeneous tumors. The use of most therapeutic interventions assessed in our study were seen to a higher degree in pontine tumors compared to thalamic. This is confounded by the increased number of pontine tumors in our study, but also proportionally seen within the literature with the pons being the primary location of DMG, H3 K27-altered in the pediatric population.
Conventional photon radiation therapy remains the standard palliative treatment offered to patients, but currently there are 11 interventional clinical trials enrolling with the majority utilizing a targeted therapy or combination approach (Table 7). As shown in previous studies, the use of oral chemotherapy agents such as temozolomide along with immunotherapeutic options such as bevacizumab did not seem to make a difference in OS while also adding more adverse effects for patients [34,35,36,37]. As shown from our study, the use of these treatments showed similar results, highlighting the need for further improvement for a sustained response while minimizing toxicity. One avenue that has shown promise is the use of other immunotherapeutic options such as CAR T cell therapy, with further research needed to explore this as a sustainable treatment [38,39,40,41]. Continued research looking into novel therapeutic targets along with more combinatorial therapeutic approaches is on-going.
The results of our study add to the existing current knowledge known for pediatric patients with DMG, H3 K27-altered. By utilizing patients who had been enrolled in clinical trials, we were able to assess the response of various therapeutic options and genetic alterations on OS. Additional factors including age, sex and anatomical location of tumor were also analyzed for their impact on OS. The limitations of our study include the overall small sample size and higher proportion of pontine tumors and patients aged 5–10yo. As shown in Table 3, many patients from the utilized studies were also excluded from analysis as they did not have a biopsy performed, which contributed to the heterogeneity of our cohort. As more results from on-going and completed clinical trials come about with the use of targeted, immunotherapeutic and personalized approaches using molecular characterization, it will be prudent to re-analyze this topic for further differences or notable changes at a larger scale.
5. Conclusions
Our study demonstrated that the molecular characteristics of pediatric DMG, H3 K27-altered influences on overall outcome, though the tumor still remains universally fatal. Additional analysis showed that the ACVR mutation was associated with a prolonged OS compared to patients without this and that those with an H3.3 genotype and TP53 mutation were associated with worse survival. No sex differences were observed in our study regarding OS. Personalized therapeutic interventions showed a marginal benefit in our cohort, with more investigation warranted. With the increased use of targeted and combination therapies currently and in upcoming clinical trials, further research and evaluation of clinical trial data are needed to continue to help advance our understanding and management of these fatal tumors.
Author Contributions
S.D.: Conception and design, data input, data analysis, manuscript writing. A.A.: Data input, manuscript writing. K.K.: Data input, manuscript writing. Q.Z.: Data input, data analysis, manuscript writing. M.D.: Conception and design, manuscript writing. All authors have read and agreed to the published version of the manuscript.
Funding
This work was supported by the NIH K08NS092895 grant (M.D.).
Conflicts of Interest
The authors declare no conflict of interest.
References
- Wang, Y.; Feng, L.L.; Ji, P.G.; Liu, J.H.; Guo, S.C.; Zhai, Y.L.; Sankey, E.W.; Wang, Y.; Xue, Y.R.; Wang, N.; et al. Clinical Features and Molecular Markers on Diffuse Midline Gliomas with H3K27M Mutations: A 43 Cases Retrospective Cohort Study. Front. Oncol. 2020, 10, 602553. [Google Scholar] [CrossRef]
- Zheng, L.; Gong, J.; Yu, T.; Zou, Y.; Zhang, M.; Nie, L.; Chen, X.; Yue, Q.; Liu, Y.; Mao, Q.; et al. Diffuse Midline Gliomas with Histone H3 K27M Mutation in Adults and Children: A Retrospective Series of 164 Cases. Am. J. Surg. Pathol. 2022, 46, 863–871. [Google Scholar] [CrossRef]
- Karremann, M.; Gielen, G.H.; Hoffmann, M.; Wiese, M.; Colditz, N.; Warmuth-Metz, M.; Bison, B.; Claviez, A.; van Vuurden, D.G.; von Bueren, A.O.; et al. Diffuse high-grade gliomas with H3 K27M mutations carry a dismal prognosis independent of tumor location. Neuro Oncol. 2018, 20, 123–131. [Google Scholar] [CrossRef] [Green Version]
- Stang, A. Critical evaluation of the Newcastle-Ottawa scale for the assessment of the quality of nonrandomized studies in meta-analyses. Eur. J. Epidemiol. 2010, 25, 603–605. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Del Baldo, G.; Carai, A.; Abbas, R.; Cacchione, A.; Vinci, M.; Di Ruscio, V.; Colafati, G.S.; Rossi, S.; Diomedi Camassei, F.; Maestro, N.; et al. Targeted therapy for pediatric diffuse intrinsic pontine glioma: A single-center experience. Ther. Adv. Med. Oncol. 2022, 14, 17588359221113693. [Google Scholar] [CrossRef] [PubMed]
- DeWire, M.; Fuller, C.; Hummel, T.R.; Chow, L.M.L.; Salloum, R.; de Blank, P.; Pater, L.; Lawson, S.; Zhu, X.; Dexheimer, P.; et al. A phase I/II study of ribociclib following radiation therapy in children with newly diagnosed diffuse intrinsic pontine glioma (DIPG). J. Neurooncol. 2020, 149, 511–522. [Google Scholar] [CrossRef]
- El-Khouly, F.E.; Veldhuijzen van Zanten, S.E.M.; Jansen, M.H.A.; Bakker, D.P.; Sanchez Aliaga, E.; Hendrikse, N.H.; Vandertop, W.P.; van Vuurden, D.G.; Kaspers, G.J.L. A phase I/II study of bevacizumab, irinotecan and erlotinib in children with progressive diffuse intrinsic pontine glioma. J. Neurooncol. 2021, 153, 263–271. [Google Scholar] [CrossRef]
- Gallego Perez-Larraya, J.; Garcia-Moure, M.; Labiano, S.; Patino-Garcia, A.; Dobbs, J.; Gonzalez-Huarriz, M.; Zalacain, M.; Marrodan, L.; Martinez-Velez, N.; Puigdelloses, M.; et al. Oncolytic DNX-2401 Virus for Pediatric Diffuse Intrinsic Pontine Glioma. N. Engl. J. Med. 2022, 386, 2471–2481. [Google Scholar] [CrossRef]
- Gojo, J.; Pavelka, Z.; Zapletalova, D.; Schmook, M.T.; Mayr, L.; Madlener, S.; Kyr, M.; Vejmelkova, K.; Smrcka, M.; Czech, T.; et al. Personalized Treatment of H3K27M-Mutant Pediatric Diffuse Gliomas Provides Improved Therapeutic Opportunities. Front. Oncol. 2019, 9, 1436. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Mueller, S.; Jain, P.; Liang, W.S.; Kilburn, L.; Kline, C.; Gupta, N.; Panditharatna, E.; Magge, S.N.; Zhang, B.; Zhu, Y.; et al. A pilot precision medicine trial for children with diffuse intrinsic pontine glioma-PNOC003: A report from the Pacific Pediatric Neuro-Oncology Consortium. Int. J. Cancer 2019, 145, 1889–1901. [Google Scholar] [CrossRef] [Green Version]
- Rodriguez, D.; Calmon, R.; Aliaga, E.S.; Warren, D.; Warmuth-Metz, M.; Jones, C.; Mackay, A.; Varlet, P.; Le Deley, M.C.; Hargrave, D.; et al. MRI and Molecular Characterization of Pediatric High-Grade Midline Thalamic Gliomas: The HERBY Phase II Trial. Radiology 2022, 304, 174–182. [Google Scholar] [CrossRef]
- Di Ruscio, V.; Del Baldo, G.; Fabozzi, F.; Vinci, M.; Cacchione, A.; de Billy, E.; Megaro, G.; Carai, A.; Mastronuzzi, A. Pediatric Diffuse Midline Gliomas: An Unfinished Puzzle. Diagnostics 2022, 12, 2064. [Google Scholar] [CrossRef]
- Jovanovich, N.; Habib, A.; Head, J.; Hameed, F.; Agnihotri, S.; Zinn, P.O. Pediatric diffuse midline glioma: Understanding the mechanisms and assessing the next generation of personalized therapeutics. Neurooncol. Adv. 2023, 5, vdad040. [Google Scholar] [CrossRef]
- Castel, D.; Philippe, C.; Calmon, R.; Le Dret, L.; Truffaux, N.; Boddaert, N.; Pagès, M.; Taylor, K.R.; Saulnier, P.; Lacroix, L.; et al. Histone H3F3A and HIST1H3B K27M mutations define two subgroups of diffuse intrinsic pontine gliomas with different prognosis and phenotypes. Acta Neuropathol. 2015, 130, 815–827. [Google Scholar] [CrossRef] [Green Version]
- Buczkowicz, P.; Hoeman, C.; Rakopoulos, P.; Pajovic, S.; Letourneau, L.; Dzamba, M.; Morrison, A.; Lewis, P.; Bouffet, E.; Bartels, U.; et al. Genomic analysis of diffuse intrinsic pontine gliomas identifies three molecular subgroups and recurrent activating ACVR1 mutations. Nat. Genet. 2014, 46, 451–456. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Haag, D.; Mack, N.; Benites Goncalves da Silva, P.; Statz, B.; Clark, J.; Tanabe, K.; Sharma, T.; Jager, N.; Jones, D.T.W.; Kawauchi, D.; et al. H3.3-K27M drives neural stem cell-specific gliomagenesis in a human iPSC-derived model. Cancer Cell 2021, 39, 407–422. [Google Scholar] [CrossRef]
- Solomon, D.A.; Wood, M.D.; Tihan, T.; Bollen, A.W.; Gupta, N.; Phillips, J.J.; Perry, A. Diffuse Midline Gliomas with Histone H3-K27M Mutation: A Series of 47 Cases Assessing the Spectrum of Morphologic Variation and Associated Genetic Alterations. Brain Pathol. 2016, 26, 569–580. [Google Scholar] [CrossRef] [PubMed]
- Vuong, H.G.; Le, H.T.; Jea, A.; McNall-Knapp, R.; Dunn, I.F. Risk stratification of H3 K27M-mutant diffuse midline gliomas based on anatomical locations: An integrated systematic review of individual participant data. J. Neurosurg. Pediatr. 2022, 30, 99–106. [Google Scholar] [CrossRef] [PubMed]
- Yuen, B.T.; Knoepfler, P.S. Histone H3.3 mutations: A variant path to cancer. Cancer Cell 2013, 24, 567–574. [Google Scholar] [CrossRef] [Green Version]
- Buccoliero, A.M.; Giunti, L.; Moscardi, S.; Castiglione, F.; Provenzano, A.; Sardi, I.; Scagnet, M.; Genitori, L.; Caporalini, C. Pediatric High Grade Glioma Classification Criteria and Molecular Features of a Case Series. Genes 2022, 13, 624. [Google Scholar] [CrossRef]
- Werbrouck, C.; Evangelista, C.C.S.; Lobón-Iglesias, M.J.; Barret, E.; Le Teuff, G.; Merlevede, J.; Brusini, R.; Kergrohen, T.; Mondini, M.; Bolle, S.; et al. TP53 Pathway Alterations Drive Radioresistance in Diffuse Intrinsic Pontine Gliomas (DIPG). Clin. Cancer Res. 2019, 25, 6788–6800. [Google Scholar] [CrossRef] [Green Version]
- Pedersen, H.; Schmiegelow, K.; Hamerlik, P. Radio-Resistance and DNA Repair in Pediatric Diffuse Midline Gliomas. Cancers 2020, 12, 2813. [Google Scholar] [CrossRef]
- Kazarian, E.; Marks, A.; Cui, J.; Darbinyan, A.; Tong, E.; Mueller, S.; Cha, S.; Aboian, M.S. Topographic correlates of driver mutations and endogenous gene expression in pediatric diffuse midline gliomas and hemispheric high-grade gliomas. Sci. Rep. 2021, 11, 14377. [Google Scholar] [CrossRef] [PubMed]
- Han, H.J.; Jain, P.; Resnick, A.C. Shared ACVR1 mutations in FOP and DIPG: Opportunities and challenges in extending biological and clinical implications across rare diseases. Bone 2018, 109, 91–100. [Google Scholar] [CrossRef] [PubMed]
- Fontebasso, A.M.; Papillon-Cavanagh, S.; Schwartzentruber, J.; Nikbakht, H.; Gerges, N.; Fiset, P.O.; Bechet, D.; Faury, D.; De Jay, N.; Ramkissoon, L.A.; et al. Recurrent somatic mutations in ACVR1 in pediatric midline high-grade astrocytoma. Nat. Genet. 2014, 46, 462–466. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Jang, S.W.; Song, S.W.; Kim, Y.H.; Cho, Y.H.; Hong, S.H.; Kim, J.H.; Ra, Y.S.; Chong, S. Clinical Features and Prognosis of Diffuse Midline Glioma: A Series of 24 Cases. Brain Tumor Res. Treat. 2022, 10, 255–264. [Google Scholar] [CrossRef] [PubMed]
- Kramm, C.M.; Butenhoff, S.; Rausche, U.; Warmuth-Metz, M.; Kortmann, R.D.; Pietsch, T.; Gnekow, A.; Jorch, N.; Janssen, G.; Berthold, F.; et al. Thalamic high-grade gliomas in children: A distinct clinical subset? Neuro Oncol. 2011, 13, 680–689. [Google Scholar] [CrossRef]
- Liu, H.; Qin, X.; Zhao, L.; Zhao, G.; Wang, Y. Epidemiology and Survival of Patients with Brainstem Gliomas: A Population-Based Study Using the SEER Database. Front. Oncol. 2021, 11, 692097. [Google Scholar] [CrossRef]
- Dono, A.; Takayasu, T.; Ballester, L.Y.; Esquenazi, Y. Adult diffuse midline gliomas: Clinical, radiological, and genetic characteristics. J. Clin. Neurosci. 2020, 82, 1–8. [Google Scholar] [CrossRef]
- Hu, J.; Western, S.; Kesari, S. Brainstem Glioma in Adults. Front. Oncol. 2016, 6, 180. [Google Scholar] [CrossRef] [Green Version]
- Enomoto, T.; Aoki, M.; Hamasaki, M.; Abe, H.; Nonaka, M.; Inoue, T.; Nabeshima, K. Midline Glioma in Adults: Clinicopathological, Genetic, and Epigenetic Analysis. Neurol. Med.-Chir. 2020, 60, 136–146. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Cacciotti, C.; Liu, K.X.; Haas-Kogan, D.A.; Warren, K.E. Reirradiation practices for children with diffuse intrinsic pontine glioma. Neurooncol. Pract. 2021, 8, 68–74. [Google Scholar] [CrossRef] [PubMed]
- Chavaz, L.; Janssens, G.O.; Bolle, S.; Mandeville, H.; Ramos-Albiac, M.; Van Beek, K.; Benghiat, H.; Hoeben, B.; Morales La Madrid, A.; Seidel, C.; et al. Neurological Symptom Improvement After Re-Irradiation in Patients With Diffuse Intrinsic Pontine Glioma: A Retrospective Analysis of the SIOP-E-HGG/DIPG Project. Front. Oncol. 2022, 12, 926196. [Google Scholar] [CrossRef] [PubMed]
- Bailey, S.; Howman, A.; Wheatley, K.; Wherton, D.; Boota, N.; Pizer, B.; Fisher, D.; Kearns, P.; Picton, S.; Saran, F.; et al. Diffuse intrinsic pontine glioma treated with prolonged temozolomide and radiotherapy--results of a United Kingdom phase II trial (CNS 2007 04). Eur. J. Cancer 2013, 49, 3856–3862. [Google Scholar] [CrossRef] [Green Version]
- Cohen, K.J.; Heideman, R.L.; Zhou, T.; Holmes, E.J.; Lavey, R.S.; Bouffet, E.; Pollack, I.F. Temozolomide in the treatment of children with newly diagnosed diffuse intrinsic pontine gliomas: A report from the Children’s Oncology Group. Neuro Oncol. 2011, 13, 410–416. [Google Scholar] [CrossRef] [Green Version]
- Evans, M.; Gill, R.; Bull, K.S. Does a Bevacizumab-based regime have a role in the treatment of children with diffuse intrinsic pontine glioma? A systematic review. Neurooncol. Adv. 2022, 4, vdac100. [Google Scholar] [CrossRef]
- Jing, L.; Qian, Z.; Gao, Q.; Sun, R.; Zhen, Z.; Wang, G.; Yang, X.; Li, H.; Guo, T.; Zhang, W. Diffuse midline glioma treated with epigenetic agent-based immunotherapy. Signal Transduct. Target. Ther. 2023, 8, 23. [Google Scholar] [CrossRef]
- Majzner, R.G.; Ramakrishna, S.; Yeom, K.W.; Patel, S.; Chinnasamy, H.; Schultz, L.M.; Richards, R.M.; Jiang, L.; Barsan, V.; Mancusi, R.; et al. GD2-CAR T cell therapy for H3K27M-mutated diffuse midline gliomas. Nature 2022, 603, 934–941. [Google Scholar] [CrossRef]
- Bernstock, J.D.; Hoffman, S.E.; Kappel, A.D.; Valdes, P.A.; Essayed, W.; Klinger, N.V.; Kang, K.D.; Totsch, S.K.; Olsen, H.E.; Schlappi, C.W.; et al. Immunotherapy approaches for the treatment of diffuse midline gliomas. Oncoimmunology 2022, 11, 2124058. [Google Scholar] [CrossRef]
- Majzner, R.G.; Theruvath, J.L.; Nellan, A.; Heitzeneder, S.; Cui, Y.; Mount, C.W.; Rietberg, S.P.; Linde, M.H.; Xu, P.; Rota, C.; et al. CAR T Cells Targeting B7-H3, a Pan-Cancer Antigen, Demonstrate Potent Preclinical Activity Against Pediatric Solid Tumors and Brain Tumors. Clin. Cancer Res. 2019, 25, 2560–2574. [Google Scholar] [CrossRef]
- Chen, Y.; Zhao, C.; Li, S.; Wang, J.; Zhang, H. Immune Microenvironment and Immunotherapies for Diffuse Intrinsic Pontine Glioma. Cancers 2023, 15, 602. [Google Scholar] [CrossRef] [PubMed]
Figure 1.
Flow diagram of systematic review according to PRISMA guidelines.
Figure 2.
Significant molecular alterations by anatomical location.
Table 1.
Inclusion and exclusion criteria.
| Inclusion | Exclusion |
|---|---|
| (1) patients >18yo |
| (2) non-clinical trial publications |
| (3) published in languages different than English |
| (4) published prior to 2018 |
| (5) upfront tumor biopsy/resection not done |
| (6) histone mutation status not available |
| (7) IPD unavailable |
Table 2.
Included studies and quality assessment.
| Authors & Year | Country | NOS (No. of Stars) | ||
|---|---|---|---|---|
| Selection | Comparability | Outcome | ||
| Del Baldo et al., 2022 [5] | Italy | 4 | 0 | 3 |
| DeWire et al., 2020 [6] | USA | 4 | 0 | 3 |
| El-Khouly et al., 2021 [7] | Netherlands | 4 | 0 | 2 |
| Pérez-Larraya et al., 2022 [8] | Spain | 4 | 0 | 2 |
| Gojo et al., 2020 [9] | Austria | 4 | 0 | 3 |
| Mueller et al., 2019 [10] | USA | 4 | 0 | 3 |
| Rodriguez et al., 2022 [11] | Italy | 4 | 0 | 3 |
Table 3.
Characteristics of included studies.
| Articles | Country | Trial Overview/Intervention | Total Number Participants | Participants Included in Analysis |
|---|---|---|---|---|
| Del Baldo et al., 2022 [5] | Italy | Targeted therapies combined with standard of care for pediatric DMG. | 25 | 25 |
| DeWire et al., 2020 [6] | USA | Addition of ribociclib following standard-of-care radiotherapy for DMG. | 10 | 10 |
| El-Khouly et al., 2021 [7] | Netherlands | Combined treatment with bevacizumab, irinotecan and erlotinib for DMG. | 9 | 4 |
| Gojo et al., 2020 [9] | Austria | Feasibility and outcomes of including personalized treatment via molecular tumor analysis with focal irradiation and backbone therapy for DMG. | 18 | 17 |
| Mueller et al., 2019 [10] | USA | Evaluated whether whole-exome sequencing and RNA sequencing of paired normal and tumor tissues could be incorporated into personalized treatment of DMG. | 17 | 13 |
| Pérez-Larraya et al., 2022 [8] | Spain | Dose-escalation study of DNX-2401, an oncolytic adenovirus, followed by radiotherapy for DMG. | 12 | 10 |
| Rodriguez et al., 2022 [11] | Italy | Bevacizumab in combination with temozolomide and radiotherapy in pediatric patients with high-grade glioma. | 121 | 29 |
Table 4.
Characteristics, molecular alterations and treatments used in pediatric DMG, H3 K27-altered.
Table 4.
Characteristics, molecular alterations and treatments used in pediatric DMG, H3 K27-altered.
| Parameters | Number of Patients | Overall Survival | p-Value | ||
|---|---|---|---|---|---|
| Mean | STD | ||||
| Age | <5 | 16 | 20.50 | 9.72 | 0.0163 * |
| 5–10 | 52 | 14.54 | 6.07 | ||
| 10+ | 40 | 14.99 | 7.69 | ||
| Sex | Female | 57 | 15.61 | 6.84 | 0.9845 |
| Male | 51 | 15.58 | 8.30 | ||
| Anatomical location | pons | 77 | 16.30 | 7.41 | 0.1229 |
| thalamus | 31 | 13.83 | 7.63 | ||
| Histone Mutation | H3.1 (HIST1H3B/C) | 27 | 19.62 | 7.67 | 0.0011 * |
| H3.3 (H3F3A) | 18 | 14.25 | 7.02 | ||
| TP53 | N | 23 | 21.41 | 8.38 | <0.0001 * |
| Y | 51 | 13.71 | 6.40 | ||
| ACVR | N | 59 | 14.89 | 7.16 | 0.0081 * |
| Y | 15 | 20.85 | 9.03 | ||
| ATRX | N | 54 | 16.26 | 7.94 | 0.7698 |
| Y | 20 | 15.66 | 7.91 | ||
| PIK3CA | N | 63 | 15.59 | 7.29 | 0.1824 |
| Y | 11 | 19.04 | 10.63 | ||
| mTOR | N | 63 | 15.52 | 7.95 | 0.1275 |
| Y | 11 | 19.45 | 6.84 | ||
| BRAF | N | 71 | 15.87 | 7.72 | 0.2311 |
| Y | 3 | 21.47 | 11.59 | ||
| PDGFRA | N | 60 | 16.87 | 8.22 | 0.0838 |
| Y | 14 | 12.82 | 5.27 | ||
| FGFR3 | N | 70 | 16.19 | 8.04 | 0.6855 |
| Y | 4 | 14.53 | 4.56 | ||
| Personalized treatment approach | N | 59 | 14.33 | 6.57 | 0.0548 |
| Y | 49 | 17.12 | 8.35 | ||
| Nimotuzumab/vinorelbine | N | 74 | 14.86 | 7.36 | 0.1368 |
| Y | 34 | 17.19 | 7.74 | ||
| Temozolomide | N | 49 | 14.68 | 7.76 | 0.2539 |
| Y | 59 | 16.35 | 7.30 | ||
| Bevacizumab | N | 61 | 14.89 | 8.08 | 0.2683 |
| Y | 47 | 16.51 | 6.71 | ||
| Panobinostat | N | 101 | 15.65 | 7.64 | 0.7551 |
| Y | 7 | 14.73 | 6.08 | ||
| Immunotherapy | N | 37 | 14.17 | 7.77 | 0.1576 |
| Y | 71 | 16.33 | 7.34 | ||
| Other chemotherapy | N | 66 | 14.88 | 6.90 | 0.2163 |
| Y | 42 | 16.72 | 8.38 | ||
| Re-irradiation | N | 81 | 14.58 | 7.86 | 0.0047 * |
| Y | 27 | 18.62 | 5.52 | ||
| Radiation | N | 9 | 17.69 | 8.80 | 0.3843 |
| Y | 99 | 15.40 | 7.42 | ||
Y = yes; N = no; * = statistical significance; other chemotherapy = systemic chemotherapy regimens not otherwise assessed as above.
Table 5.
Gene alteration by tumor location and sex.
| Gene | Anatomical Location | Sex | |||||
|---|---|---|---|---|---|---|---|
| Pons | Thalamus | p-Value | Female | Male | p-Value | ||
| TP53 | N | 22 (42%) | 1 (5%) | 0.0018 * | 14 (36%) | 9 (26%) | 0.4519 |
| Y | 31 (58%) | 20 (95%) | 25 (64%) | 26 (74%) | |||
| ACVR | N | 38 (72%) | 21 (100%) | 0.004 * | 27 (69%) | 32 (91%) | 0.0218 * |
| Y | 15 (28%) | 0 (0%) | 12 (31%) | 3 (9%) | |||
| ATRX | N | 43 (81%) | 11 (52%) | 0.0194 * | 28 (72%) | 26 (74%) | 1.0000 |
| Y | 10 (19%) | 10 (48%) | 11 (28%) | 9 (26%) | |||
| PIK3CA | N | 46 (87%) | 17 (81%) | 0.4953 | 33 (85%) | 30 (86%) | 1.0000 |
| Y | 7 (13%) | 4 (19%) | 6 (15%) | 5 (14%) | |||
| mTOR | N | 43 (81%) | 20 (95%) | 0.1628 | 31 (79%) | 32 (91%) | 0.1980 |
| Y | 10 (19%) | 1 (5%) | 8 (21%) | 3 (9%) | |||
| BRAF | N | 51 (96%) | 20 (95%) | 1.0000 | 39 (100%) | 32 (91%) | 0.1010 |
| Y | 2 (4%) | 1 (5%) | 0 (0%) | 3 (9%) | |||
| PDGFRA | N | 43 (81%) | 17 (81%) | 1.0000 | 31 (79%) | 29 (83%) | 0.7732 |
| Y | 10 (19%) | 4 (19%) | 8 (21%) | 6 (17%) | |||
| FGFR3 | N | 51 (96%) | 19 (90%) | 0.3180 | 37 (95%) | 33 (94%) | 1.0000 |
| Y | 2 (4%) | 2 (10%) | 2 (5%) | 2 (6%) | |||
| Histone Mutation | H3.1 (HIST1H3B/C) | 23 (30%) | 4 (13%) | 0.0861 | 15 (26%) | 12 (24%) | 0.8254 |
| H3.3 (H3F3A) | 54 (70%) | 27 (87%) | 42 (74%) | 39 (76%) | |||
Y = yes; N = no; * = statistical significance.
Table 6.
Treatment use by tumor anatomical location.
| Treatment | Anatomical Location | |||
|---|---|---|---|---|
| Pons | Thalamus | p-Value | ||
| Personalized treatment approach | N | 29 (49%) | 30 (51%) | <0.0001 * |
| Y | 48 (98%) | 1 (2%) | ||
| Nimotuzumab/vinorelbine | N | 43 (58%) | 31 (42%) | <0.0001 * |
| Y | 34 (100%) | 0 (0%) | ||
| Temozolomide | N | 48 (98%) | 1 (2%) | <0.0001 * |
| Y | 29 (49%) | 30 (51%) | ||
| Bevacizumab | N | 43 (70%) | 18 (30%) | 1.0000 |
| Y | 34 (72%) | 13 (28%) | ||
| Panobinostat | N | 70 (69%) | 31 (31%) | 0.1887 |
| Y | 7 (100%) | 0 (0%) | ||
| Immunotherapy | N | 19 (51%) | 18 (49%) | 0.0015 * |
| Y | 58 (82%) | 13 (18%) | ||
| Other chemotherapy | N | 36 (55%) | 30 (45%) | <0.0001 * |
| Y | 41 (98%) | 1 (2%) | ||
| Re-irradiation | N | 51 (63%) | 30 (37%) | 0.0005 * |
| Y | 26 (96%) | 1 (4%) | ||
| Radiation | N | 8 (89%) | 1 (11%) | 0.4416 |
| Y | 69 (70%) | 30 (30%) | ||
Y = yes; N = no; * = statistical significance.
Table 7.
Available clinical trials for pediatric DMG, H3 K27-altered.
| Study Title | NCT Number | Therapeutic Intervention | Country |
|---|---|---|---|
| Stereotactic Biopsy Split-Course Radiation Therapy in Diffuse Midline Glioma, SPORT-DMG Study | NCT05077735 | Radiation: hypofractionated radiation therapy | USA |
| A Study of BXQ-350 in Children with Newly Diagnosed Diffuse Intrinsic Pontine Glioma (DIPG) or Diffuse Midline Glioma (DMG) | NCT04771897 | Drug: BXQ-350 | USA |
| FUS Etoposide for DMG—A Feasibility Study | NCT05762419 | Drug: etoposide and device: focused ultrasound with neuro-navigator-controlled sonication | USA |
| rHSC-DIPGVax Plus Checkpoint Blockade for the Treatment of Newly Diagnosed DIPG and DMG | NCT04943848 | Biological: rHSC-DIPGVax; drug: balstilimab; and drug: zalifrelimab | USA |
| Biological Medicine for Diffuse Intrinsic Pontine Glioma (DIPG) Eradication 2.0 | NCT05476939 | Drug: everolimus; drug: ONC201; and radiation: radiotherapy | France |
| Combination Therapy for the Treatment of Diffuse Midline Gliomas | NCT05009992 | Drug: ONC201; radiation: radiation therapy; and drug: paxalisib | USA |
| A Study of the Drug Selinexor with Radiation Therapy in Patients with Newly-Diagnosed Diffuse Intrinsic Pontine (DIPG) Glioma and High-Grade Glioma (HGG) | NCT05099003 | Radiation: radiation therapy and drug: selinexor | USA |
| Loc3CAR: Locoregional Delivery of B7-H3-CAR T Cells for Pediatric Patients with Primary CNS Tumors | NCT05835687 | Drug: B7-H3-CAR T cells | USA |
| Phase I Study of Oral ONC206 in Recurrent and Rare Primary Central Nervous System Neoplasms | NCT04541082 | Drug: ONC206 | USA |
| Oral AMXT 1501 Dicaprate in Combination with IV DFMO | NCT05500508 | Drug: AMXT1501 and drug: DFMO | USA |
| ONC206 for Treatment of Newly Diagnosed, or Recurrent Diffuse Midline Gliomas, and Other Recurrent Malignant CNS Tumors (PNOC 023) | NCT04732065 | Drug: ONC206 and radiation: radiation therapy | USA and Switzerland |
Clinical trials found on www.clinicaltrials.gov as of 25 May 2023.
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content. |
© 2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
Share and Cite
MDPI and ACS Style
Damodharan, S.; Abbott, A.; Kellar, K.; Zhao, Q.; Dey, M. Molecular Characterization and Treatment Approaches for Pediatric H3 K27-Altered Diffuse Midline Glioma: Integrated Systematic Review of Individual Clinical Trial Participant Data. Cancers 2023, 15, 3478. https://doi.org/10.3390/cancers15133478
AMA Style
Damodharan S, Abbott A, Kellar K, Zhao Q, Dey M. Molecular Characterization and Treatment Approaches for Pediatric H3 K27-Altered Diffuse Midline Glioma: Integrated Systematic Review of Individual Clinical Trial Participant Data. Cancers. 2023; 15(13):3478. https://doi.org/10.3390/cancers15133478
Chicago/Turabian StyleDamodharan, Sudarshawn, Alexandra Abbott, Kaitlyn Kellar, Qianqian Zhao, and Mahua Dey. 2023. "Molecular Characterization and Treatment Approaches for Pediatric H3 K27-Altered Diffuse Midline Glioma: Integrated Systematic Review of Individual Clinical Trial Participant Data" Cancers 15, no. 13: 3478. https://doi.org/10.3390/cancers15133478
APA StyleDamodharan, S., Abbott, A., Kellar, K., Zhao, Q., & Dey, M. (2023). Molecular Characterization and Treatment Approaches for Pediatric H3 K27-Altered Diffuse Midline Glioma: Integrated Systematic Review of Individual Clinical Trial Participant Data. Cancers, 15(13), 3478. https://doi.org/10.3390/cancers15133478
Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.
