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Review

Allogeneic Hematopoietic Stem Cell Transplantation for Adults with Sickle Cell Disease

by
Santosh L. Saraf
* and
Damiano Rondelli
Division of Hematology & Oncology, Department of Medicine, University of Illinois at Chicago, Chicago, IL 60612, USA
*
Author to whom correspondence should be addressed.
J. Clin. Med. 2019, 8(10), 1565; https://doi.org/10.3390/jcm8101565
Submission received: 28 August 2019 / Revised: 17 September 2019 / Accepted: 23 September 2019 / Published: 1 October 2019
(This article belongs to the Special Issue Sickle Cell Anemia: From Genetic Epidemiology to New Therapeutic Strategies)
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Abstract

:
Sickle cell disease (SCD) is an inherited red blood cell disorder that leads to substantial morbidity and early mortality. Acute and chronic SCD-related complications increase with older age, and therapies are urgently needed to treat adults. Allogeneic hematopoietic stem cell transplantation (HSCT) is a curative therapy, but has been used less frequently in adults compared to children. This is, in part, due to (1) greater chronic organ damage, limiting tolerability to myeloablative conditioning regimens, (2) a higher rate of HSCT-related complications in adults versus children with SCD, and (3) limited coverage by public and private health insurance. Newer approaches using nonmyeloablative and reduced-intensity conditioning HSCT regimens have demonstrated better safety and tolerability, with high rates of stable engraftment in SCD adults. This review will focus on the impacts of HSCT, using more contemporary approaches to SCD-related complications in adults.

1. Morbidity and Mortality of Sickle Cell Disease

Sickle cell disease (SCD) is among the most common monogenetic disorders, affecting approximately 25 million people worldwide [1]. Sickle cell disease is due to homozygous inheritance of the hemoglobin S mutation (Hb SS) or compound heterozygous inheritance of the Hb S mutation with another β-globin chain abnormality, such as Hb C (Hb SC) or β-thalassemia (Hb Sβ+-thalassemia, Hb Sβ0-thalassemia). Under deoxygenated conditions, Hb S polymerizes, resulting in vaso-occlusion, chronic red blood cell hemolysis, acute and chronic organ complications, and reduced overall survival [2]. Allogeneic hematopoietic stem cell transplantation (HSCT) is a curative therapy that has been applied more frequently in children than adults with SCD [3].

1.1. Contemporary Survival Patterns in Sickle Cell Disease

The Comprehensive Study of Sickle Cell Disease (CSSCD) cohort study demonstrated that the median survival for men and women was 42 and 48 years in Hb SS SCD and 60 and 68 years in Hb SC SCD, respectively [4]. More recent cohorts have demonstrated that, with advances in care, such as newborn screening, penicillin prophylaxis, and effective vaccinations, the proportion of children surviving into adulthood has increased [5,6]. However, overall median survival remains substantially lower in SCD than in the general population. Based on mortality data from the Centers for Disease Control, mortality was highest in men 35–44 years of age and in women 45–54 years of age. The predominant causes of death were related to organ injury and included cardiac (32%), pulmonary (28%), renal (16%), and neurologic (12%) disease. Several other cohorts have demonstrated median survivals ranging between 38 and 67 years in Hb SS patients and 55 and 66 years in Hb SC or Hb Sβ+-thalassemia patients [7,8,9,10,11]. In a pooled analysis of SCD patients from two academic SCD centers in the USA, the median overall survival for Hb SS/Hb Sβ0-thalassemia/Hb SD and for Hb SC/HbSβ+-thalassemia was 48 and 55 years, respectively. These estimates are relatively unchanged from the median survivals observed in the CSSCD cohort approximately 25 years ago, highlighting the need for better interventions in SCD. Although improvements in some causes of mortality, such as from pneumococcal sepsis, have been observed, acute and chronic organ complications remain independent predictors for early mortality in SCD [4,10,11,12,13,14,15,16].

1.2. Acute Complications in Adults with Sickle Cell Disease

Acute pain is a hallmark feature of SCD that is a consequence of impaired oxygen delivery and ischemia‒reperfusion injury from vaso-occlusion. In a recent multicenter, prospective study of adults with SCD, 54% of patients with Hb SS and 46% with Hb SC had three or more vaso-occlusive crises (VOC) requiring medical attention [17]. In addition to being commonly observed, frequent VOC are associated with a 2.1–2.7-fold greater risk of early mortality compared to those with less frequent VOC [9,10]. Acute chest syndrome is defined by a new pulmonary infiltrate on chest radiograph, accompanied by fever and/or respiratory symptoms. It is the second most common cause of hospitalization, after VOC, and the leading cause of death in hospitalized SCD patients [4]. The occurrence of acute chest syndrome is associated with a 1.8–2.4-fold greater risk of mortality compared to those who do not develop an acute chest syndrome event [12,13].
The overall lifetime risk of a clinically overt or silent stroke is estimated at up to 30% and 43%, respectively, in patients with SCD [18,19]. In children, primary stroke prevention can be achieved by red blood cell transfusion therapy in those with elevated transcranial Doppler velocities [20]. In adults, stroke management is focused on secondary stroke prevention as cutoff values for stroke risk using transcranial Doppler velocities are less clear [21]. If untreated, SCD patients with an overt stroke have an approximately 50% risk of a recurrent stroke within the first two years after the initial event and up to a 66% risk on longer follow-up [22,23]. Red blood cell transfusion therapy, targeting a goal Hb concentration of 10 g/dL and Hb S < 30%, improves the risk of recurrence to 18% for an overt stroke and 28% for new silent infarcts [24]. The occurrence of stroke is also an independent risk factor for a 2-fold greater risk of death [12].

1.3. Cardiovascular Complications in Sickle Cell Disease

Chronic cardiovascular disease has been increasingly recognized as a leading cause of morbidity and mortality in adults with SCD. In one adult SCD cohort, 26% of deaths were attributed to cardiac causes [16]. The tricuspid regurgitant jet velocity (TRJV) is a noninvasive marker of systolic pulmonary artery blood pressure obtained by transthoracic echocardiography that is elevated in SCD patients with pulmonary hypertension or diastolic dysfunction. In a prospective cohort of SCD adults, a TRJV ≥ 2.5 m/s was observed in 32% of patients and was associated with a 10.1-fold increased risk of death [25]. Several other cohorts have reproduced the association of an elevated TRJV ≥ 2.5‒2.7 m/s as an independent predictor for mortality [26,27,28]. The plasma N-terminal-pro-brain natriuretic peptide (NT-proBNP) is a biomarker of cardiac wall stress that is released from myocytes in the left and right ventricles under conditions of pressure overload. An NT-proBNP > 160 pg/mL is observed in 24–30% of SCD adults and is associated with a 2.9–5.1-fold greater risk of death [29,30].

1.4. Health-Related Quality of Life

The impact of worsening acute and chronic SCD-related complications in adulthood leads to a reduced health-related quality of life (HRQOL). In a longitudinal cohort study of SCD adults, HRQOL was substantially lower in men and women compared to national norms for all SF-36 subscales, with the exception of the mental health scale [31]. Furthermore, when comparing the SF-36 subscale scores between adults with SCD versus age-matched patients with end-stage renal disease or cystic fibrosis, SCD patients scored significantly lower in several domains. This included lower scores for physical function, physical role, bodily pain, general health, and vitality.

1.5. Healthcare Utilization and Healthcare Costs

In parallel with the profound morbidity, SCD is associated with an increased burden on the healthcare system. It is currently estimated that medical care for treating SCD costs approximately $1.1 billion/year, with 81% of the costs being attributed to inpatient hospital care [32]. The total healthcare-related cost increases with age and is estimated between $34,266 and $231,050 per patient per year in adults with SCD [32,33].

2. Currently Accepted Indications for Allogeneic hematopoietic stem cell transplantation (HSCT) in Sickle Cell Disease

Based on the acute and chronic complications that lead to greater morbidity and mortality in SCD, several guidelines have been proposed for when to consider allogeneic HSCT [34,35,36,37]. Most of the earlier guidelines focused on acute complications (e.g., stroke, recurrent hospitalizations for VOC or acute chest syndrome), chronic organ complications (e.g., impaired neurocognitive function with abnormal brain MRI scan, early stages of sickle lung disease, nephropathy, retinopathy, or avascular necrosis of multiple joints), or red blood cell alloimmunization during long-term transfusion therapy [37]. More recent guidelines have included an elevated TRJV, removed sickle lung disease, and bilateral proliferative retinopathy as indications for HSCT. Table 1 provides criteria that have been proposed for HSCT using either HLA-matched related or alternative donors in SCD [34,35,36,37]. Due to the concern of greater HSCT-related complications when using an alternative donor as the graft source, guidelines recommend that hydroxyurea or chronic red blood cell transfusion therapy be tried prior to HSCT using an unrelated or haploidentical donor source [34].
The indications for HSCT should be carefully considered in the context of current and emerging therapies for SCD. Hydroxyurea is a ribonucleotide reductase inhibitor that increases hemoglobin F%. Hydroxyurea may also improve vascular endothelial damage in SCD by increasing nitric oxide generation by red blood cells and by lowering white blood cell and reticulocyte counts [38]. In the landmark Multicenter Study of Hydroxyurea, adult SCD patients randomized to hydroxyurea had significantly lower rates of VOC, acute chest syndrome, and red blood cell transfusions [39]. Several cohorts have demonstrated that long-term use of hydroxyurea may lead to improved survival patterns, particularly in those that have a high hemoglobin F response, although its effects on chronic organ damage are less clear [13,40,41]. l-glutamine is an essential amino acid that is required to synthesize nicotinamide adenine dinucloeotide (NAD), a redox cofactor in red blood cells that is deficient in SCD. In a multicenter, randomized, placebo-controlled phase 3 study, l-glutamine led to a modest reduction in VOC, with a median of 3.0 VOC in the l-glutamine group versus 4.0 VOC in the placebo group during a 48-week treatment period [42]. Newer therapies targeting P-selectin (crizanlizumab) or inhibiting hemoglobin S polymerization (voxelotor) have recently been tested in randomized, placebo-controlled, double-blind studies in adults with SCD. Crizanlizumab (5 mg/kg) led to a 45% decline in VOC rates compared to the placebo (2.98 vs. 1.63, respectively) over 52 weeks of therapy [43]. Voxelotor (1500 mg/day) improved hemolysis, reflected by improvements in mean change in hemoglobin concentrations (+1.1 g/dL vs. −0.1g/dL) and indirect bilirubin (−19.9% vs. +4.5%), compared to the placebo [44].

3. Allogeneic HSCT in Adults with Sickle Cell Disease

3.1. Global Experience

A combined analysis assessed outcomes in 1000 SCD patients undergoing allogeneic HSCT between 1986–2013 using data from the Center for International Blood and Marrow Transplant Research (CIBMTR), European Society for Blood and Marrow Transplantation (EBMT), and Eurocord databases [3]. In this study, only 154 (15%) of the SCD patients were adults (median age: 19 years, range: 16–54 years); 73% received a myeloablative conditioning regimen and 26% received a reduced-intensity conditioning regimen. Overall survival and event-free survival were significantly lower in patients 16 years or older (81% for each) versus those younger than 16 years (95% and 93%, respectively). The five-year probability of graft versus host disease (GVHD [22] was higher in patients 16 years or older (23%) versus those younger than 16 years (14%). Furthermore, for every one-year increment in age at transplantation, there was a 4% increase in the hazard ratio for acute GVHD, a 9% increased risk of graft failure, and a 10% increased risk of death. These results highlight the toxicity of myeloablative conditioning regimens in adult SCD patients, but did not include more recent series of adults undergoing HSCT using less intensive conditioning regimens.

3.2. Myeloablative Conditioning Regimens

Most of the earlier HSCT regimens in SCD used myeloablative doses of busulfan and cyclophosphamide and were predominantly performed in children [37,45,46,47]. One report on 15 young SCD adults with a median age of 19 years (range: 16–27) that underwent HSCT using a busulfan (485 mg/m2), cyclophosphamide (200 mg/kg), and anti-thymocyte globulin (ATG) (20 mg/kg) conditioning regimen and HLA-matched sibling donors demonstrated an overall survival and disease-free survival of 93% [48] Acute (≥grade 2) and chronic GVHD occurred in seven (47%) and two (14%) of the patients, respectively. Two of these patients had mixed chimerism (>75%), and all 14 living patients were tapered off immunosuppression.

3.3. Reduced-Intensity Conditioning Regimens

Reduced-intensity conditioning regimens have been studied in SCD adults in order to improve the tolerability for allogeneic HSCT. In one study, two SCD adults (40 and 56 years old) underwent allogeneic HSCT using a fludarabine‒melphalan conditioning regimen with ATG from a matched related donor [49]. Both patients tolerated the conditioning regimen reasonably, demonstrated stable engraftment, and had subsequent episodes of VOC. Unfortunately, the first patient developed chronic GVHD of the lung and passed away on day +335 and the second patient developed acute GVHD of the gut and liver and passed away on day +147.
More recent studies using fludarabine and lower doses of busulfan in SCD adults have demonstrated improvements in event-free and overall survival and in lower rates of acute and chronic GVHD, comparable to what has been observed in some pediatric cohorts (Table 2). In a retrospective study of 20 SCD adults (mean age of 33 years) undergoing HSCT using HLA-matched related donors at the University of Baskent, all 20 had stable engraftment at the last follow-up and 11 of 12 patients who completed one year of follow-up were off all immunosuppression [50]. In the prospective, multicenter STRIDE study of 22 adolescents and young adults (median age: 23 years) undergoing HSCT using either HLA-matched related or unrelated donors, two patients had secondary graft failures and two deaths were observed [35].

3.4. Nonmyeloablative Conditioning Regimens

Prior studies demonstrated that stable mixed chimerism, defined as a state wherein the lymphohematopoietic system is composed of a mixture of recipient and donor-derived blood cells, is sufficient to improve laboratory parameters and prevent SCD-related complications [51] Stable mixed chimerism is also associated with an induction of tolerance that leads to lower rates of GVHD compared to full donor chimerism [52]. A recent study [53] and a mathematical model [54] demonstrated that at least 20% myeloid donor chimerism is necessary to improve the SCD phenotype. In lethally irradiated mice transplanted with varying ratios of donor sickle and normal marrow, a myeloid chimerism >25% from normal marrow was sufficient to restore the Hb content to >90% normal, consistent with what has been observed in clinical studies [55].
Applying this concept, a nonmyeloablative approach using alemtuzumab/total body irradiation to achieve a stable mixed chimerism without substantial HSCT-related toxicity was developed at the National Institutes of Health (NIH) (Table 3). Initial reports demonstrated stable engraftment in nine out of 10 SCD adults, with no acute or chronic GVHD [56]. In a follow-up study of 30 SCD adults (median age: 29 years), four had secondary graft failure and there was one death [57]. No patients developed acute or chronic GVHD and 15 discontinued immunosuppression. Comparable outcomes were observed in another prospective study from the University of Illinois at Chicago, utilizing the same approach [58]. In this cohort of 13 SCD adults (median age: 30 years), one patient had secondary graft failure and no deaths or GVHD were observed. This same regimen has also been investigated at the King Saud Bin Abdulaziz University for Health Sciences in 17 adults with SCD (median age: 24 years). In this study, one secondary graft failure but no deaths or GVHD was observed [59].

3.5. Alternative Donor Approaches

The limited availability of an HLA-matched donor is a major barrier to HSCT in SCD. In one study, only 24 of 112 (21%) adult SCD patients meeting the eligibility criteria for HSCT had an HLA-matched related donor [56]. Similarly low rates of HLA-matched related donor availability have been observed in other adult and pediatric SCD cohorts [58,60,61]. Furthermore, in the National Marrow Donor Program donor registry, it is estimated that people of African descent have only a 16% probability of finding an HLA-matched donor [62]. The discovery that posttransplant immunosuppression with high doses of cyclophosphamide (PTCy) allows patients to engraft haploidentical donor cells without increasing the risk of GHVD has led to the rapid implementation of haploidentical HSCT for treating hematologic malignancies [63].
Transplantation using haploidentical related donors has also recently demonstrated encouraging results in adults with SCD (Table 4). A fludarabine/cyclophosphamide/total body irradiation (TBI) 200 cGy/ATG nonmyeloablative regimen with PTCy developed at Johns Hopkins University was first applied to 14 patients with SCD (median age: 30 years) [64]. In this study, the haploidentical regimen was well tolerated, with no observed transplant-related mortality or GVHD, but only 53% of patients achieved stable engraftment. Modifications to this regimen, including an increased dose of TBI to 300 cGy and using peripheral mobilized stem cells [65] or the addition of thiotepa [66] have improved the rates of stable engraftment. Another approach that has led to a high rate of stable engraftment in four children and young adults is the addition of two cycles of pre-HSCT immunosuppression using fludarabine and dexamethasone [67] To reduce the chemotherapy exposure in SCD adults with more advanced organ damage, the alemtuzumab/TBI regimen has been utilized as the conditioning regimen with PTCy using haploidentical donors [68]. SCD adults with more severe organ damage tolerated this regimen relatively well, but stable engraftment was observed in only 50% of patients; these patients continue on immunosuppression.

4. Evaluating Risks versus Benefits of Allogeneic HSCT in Adults with Sickle Cell Disease

Balancing the risks versus benefits for allogeneic HSCT can be challenging in a nonmalignant hematologic disorder with an unpredictable clinical course, such as SCD. The only way to prove the efficacy of allogeneic HSCT over the currently available therapies in SCD will be a prospective, randomized trial comparing HSCT with standard-of-care treatment.
The Hematopoietic Cell Transplant Comorbidity Index (HCT-CI) incorporates 17 comorbidities into a weight score that is used to predict relapse and overall mortality after HSCT [69] An intermediate or high score has been observed in 77% of SCD adults undergoing HSCT using a nonmyeloablative conditioning regimen [58] and in 30% using a reduced-intensity conditioning regimen [50]. Although this tool is useful in several malignant and nonmalignant hematologic conditions, an increasing HCT-CI score was not associated with lower survival when it was applied to patients with hemoglobinopathies [70]. This may be, in part, because this scoring system assigns three points for a total bilirubin > 1.5 times the upper limit of normal as an indicator of liver dysfunction. Because SCD is a chronic hemolytic disorder, the majority of patients will have an elevated total bilirubin, making this risk factor nondiscriminatory for HSCT outcome risk.
Understanding the risks that SCD patients are willing to accept is also important in the HSCT decision-making process. In a survey of 100 adults with SCD, 63% were willing to accept a 5% risk of HSCT-related mortality [71]. Interestingly, no significant differences in patient or disease characteristics were observed between those willing versus not willing to accept this level of risk. In a more recent survey of adults with SCD, 62% were willing to accept a HSCT-related mortality risk of 10% or greater, and 64% were willing to accept a risk of graft failure of 10% or greater [72]. In contrast, the majority (80%) were not willing to accept a risk of chronic GVHD. Findings from this survey are consistent with what we have observed in clinical practice [58]. Of 61 patients referred to our blood and marrow transplant clinic, 52 (87%) were interested in proceeding with workup for allogeneic HSCT using the alemtuzumab/TBI regimen. Based on these experiences, a large proportion of SCD adults are willing to accept the risk of HSCT-related mortality or graft failure.
While most of the clinical data on the benefits of HSCT have focused on pediatric cohorts, more recent studies have demonstrated similar improvements in acute and chronic SCD-related complications, as well as in HRQOL and healthcare utilization.

4.1. Acute Complications after HSCT

Several of the recent HSCT regimens in adults have demonstrated improvements in rates of VOC. In the reduced-intensity conditioning regimen developed by Ozdogu et al., the proportion of patients with ≥2 VOC/year improved from 90% pre-HSCT to no patients experiencing VOC after HSCT [50]. In the NIH cohort, pain-related admissions improved from a median of three/year pre-HSCT to zero/year at one year post-HSCT in those with stable long-term engraftment using the alemtuzumab/TBI regimen [73]. Improvements in the rates of VOC from a median of four/year pre-HSCT to a median of two/year at one year post-HSCT and to zero/year at two years post-HSCT have also been observed using the alemtuzumab/TBI regimen in the UIC cohort [74]. In this cohort, rates of acute chest syndrome also improved from 31% in the year prior to HSCT to 6% in the first year post-HSCT and 0% by the second year post-HSCT. In parallel with the improvement in VOC crises, opioid use has also gradually improved. In the study by Ozdogu et al., opioid use improved from 85% pre-HSCT to 10% at day +100, 5% at day +180, and 0% at one year post-HSCT in this study [50]. The NIH also demonstrated a gradual improvement in opioid use after HSCT [57].
Low rates of stroke recurrence and stable brain MRI imaging findings have been consistently demonstrated in several different HSCT approaches (Table 5). In a combined analysis of six different studies for HSCT in adults, only one stroke recurrence out of 33 patients (3%) with stable engraftment has been observed [35,57,58,64,65,66]. This rate of stroke recurrence is substantially lower than what is observed with chronic red blood cell transfusion therapy (18%). Furthermore, stable brain MRI and angiography findings have been demonstrated in those patients that had pre- and post-HSCT brain imaging studies and stable engraftment [35,57].

4.2. Cardiovascular Function after HSCT

In two separate studies using the alemtuzumab/TBI nonmyeloablative conditioning regimen, improvements in the TRJV, a strong predictor for mortality, have been observed from pre-HSCT values to values at one or two years post-HSCT (Figure 1) [57,58]. In the STRIDE study, two SCD patients with a TRJV ≥ 2.7 m/s pre-HSCT had normalization of their TRJV, while one patient with a TRJV = 2.4 m/s pre-HSCT had an increase to 2.7 m/s at one year post-HSCT [35]. An improvement in BNP, a marker of cardiac myocyte stress, has also been observed in SCD adults from median values pre-HSCT (21 pg/mL, range: 5–92 pg/mL) to one year post-HSCT (9 pg/mL, range: 1–26 pg/mL) [58]. Right heart catheter-defined pulmonary hypertension is a strong predictor of early mortality in adults with SCD [75]. One report of a 32-year-old woman with SCD and pulmonary hypertension requiring supplemental oxygen demonstrated a dramatic improvement after haploidentical HSCT [76]. This patient’s TRJV improved from 2.8 m/s pre-HSCT to 2.4 m/s at two years post-HSCT, with normalization of her pulmonary artery pressures and being completely weaned off supplemental oxygen.

4.3. Health-Related Quality of Life after HSCT

Until recently, the benefits of HSCT on HRQOL were not as clear in adults undergoing HSCT. Pediatric cohorts using primarily myeloablative regimens have demonstrated that HRQOL may initially decline within the first three months post-HSCT, followed by an improvement at one year post-HSCT compared to pre-HSCT scores [77,78]. More current experience with reduced-intensity and nonmyeloablative regimens have demonstrated that adults with SCD, who have more chronic SCD-related complications, still see a benefit to their HRQOL after allogeneic HSCT (Figure 2). In adults who underwent HSCT using the alemtuzumab/TBI regimen, improvements in bodily pain, general health, vitality, and social function scores were observed from pre-HSCT to one year post-HSCT according to the short form (SF)-36 HRQOL questionnaire [58]. In this study, both bodily pain and general health progressively improved starting as early as day +30 post-HSCT. Furthermore, the SF-6D summary score, which provides an overall utility score based on societal weights derived from items in the SF-36 questionnaire, demonstrated clinically meaningful improvements in HRQOL starting at day +30 and progressively increasing at day + 90 and one year post-HSCT. Improvements at one year post-HSCT have also been demonstrated in adults undergoing reduced-intensity conditioning regimens. In the study by Ozdogu et al., significant improvements in the SF-36 score were observed for role physical, general health, and bodily domains while trends in improvement were observed for energy/vitality, social functioning, role emotional, and mental health from pre-HSCT to one year post-HSCT [50]. In the STRIDE study, improvements in pain interference were observed at six months and one year post-HSCT, while physical function was improved at one year post-HSCT compared to pre-HSCT values using the PROMIS-57 profile [35].

4.4. Healthcare Utilization after HSCT

Adults require more healthcare, determined by emergency room visits, frequency of inpatient hospitalization, and inpatient hospital days, than children with SCD [32]. Two studies using the alemtuzumab/TBI regimen demonstrated that HSCT in adults reduced healthcare utilization (Figure 3). In the NIH cohort, the rate of hospitalizations progressively improved from pre-HSCT to one year and two years post-HSCT. In adults treated at the University of Illinois at Chicago, there was a trend for an increase in the median number of inpatient hospital days from the year pre-HSCT (22 days/year) to the year of the HSCT (38 days/year), which included the number of days hospitalized for the HSCT procedure [74]. By the second year post-HSCT, the median number of inpatient hospital days (one day/year) was significantly lower than pre-HSCT values. Median rates of emergency room visits were significantly lower at both one year (two visits/year) and two years (one visit/year) post-HSCT compared to the year pre-HSCT (four visits/year).

5. Future Directions

Current guidelines in symptomatic children with SCD advocate for HSCT as early as possible if an HLA-matched related donor is available [79]. As safer and more effective conditioning regimens are emerging, guidelines and recommendations will need to be updated for when to consider HSCT in adults with SCD. Current data suggest that nonmyeloablative transplants from either matched-related or haploidentical donors may represent relatively safe options for adult patients with advanced SCD. Prediction models, based on clinical complications [80]. Genetic risk modifiers [81], or gene expression patterns [82], may help identify high-risk SCD patients for HLA-matched and alternative donor HSCT, but will require validation in future studies. The long-term risks and benefits of HSCT, such as on fertility and overall survival, will also need to be better understood, particularly in the context of emerging therapies, such as selectin inhibitors (crizanlizumab), small-molecule inhibitors of sickle hemoglobin polymerization (voxelotor), and gene therapy to treat SCD.

Author Contributions

S.L.S. and D.R. reviewed the literature and wrote the manuscript.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Modell, B.; Darlison, M. Global epidemiology of haemoglobin disorders and derived service indicators. Bull. World Health Organ. 2008, 86, 480–487. [Google Scholar] [CrossRef] [PubMed]
  2. Piel, F.B.; Steinberg, M.H.; Rees, D.C. Sickle Cell Disease. N. Engl. J. Med. 2017, 376, 1561–1573. [Google Scholar] [CrossRef] [PubMed]
  3. Gluckman, E.; Cappelli, B.; Bernaudin, F.; Labopin, M.; Volt, F.; Carreras, J.; Simões, B.P.; Ferster, A.; Dupont, S.; de la Fuente, J.; et al. Sickle cell disease: An international survey of results of HLA-identical sibling hematopoietic stem cell transplantation. Blood 2017, 129, 1548–1556. [Google Scholar] [CrossRef] [PubMed]
  4. Platt, O.S.; Brambilla, D.J.; Rosse, W.F.; Milner, P.F.; Castro, O.; Klug, P.P.; Steinberg, M.H. Mortality In Sickle Cell Disease—Life Expectancy and Risk Factors for Early Death. N. Engl. J. Med. 1994, 330, 1639–1644. [Google Scholar] [CrossRef] [PubMed]
  5. Quinn, C.T.; Rogers, Z.R.; McCavit, T.L.; Buchanan, G.R. Improved survival of children and adolescents with sickle cell disease. Blood 2010, 115, 3447–3452. [Google Scholar] [CrossRef] [PubMed]
  6. Hamideh, D.; Alvarez, O. Sickle cell disease related mortality in the United States (1999–2009). Pediatr. Blood Cancer 2013, 60, 1482–1486. [Google Scholar] [CrossRef]
  7. Lanzkron, S.; Carroll, C.P.; Haywood, C., Jr. Mortality Rates and Age at Death from Sickle Cell Disease: U.S.; 1979–2005. Public Health Rep. 2013, 128, 110–116. [Google Scholar] [CrossRef] [PubMed]
  8. DeBaun, M.R.; Ghafuri, D.L.; Rodeghier, M.; Maitra, P.; Chaturvedi, S.; Kassim, A.; Ataga, K.I. Decreased median survival of adults with sickle cell disease after adjusting for left truncation bias: A pooled analysis. Blood 2019, 133, 615–617. [Google Scholar] [CrossRef]
  9. Elmariah, H.; Garrett, M.E.; De Castro, L.M.; Jonassaint, J.C.; Ataga, K.I.; Eckman, J.R.; Ashley-Koch, A.E.; Telen, M.J. Factors associated with survival in a contemporary adult sickle cell disease cohort. Am. J. Hematol. 2014, 89, 530–535. [Google Scholar] [CrossRef] [Green Version]
  10. Gardner, K.; Douiri, A.; Drasar, E.; Allman, M.; Mwirigi, A.; Awogbade, M.; Thein, S.L. Survival in adults with sickle cell disease in a high-income setting. Blood 2016, 128, 1436–1438. [Google Scholar] [CrossRef] [Green Version]
  11. Lobo, C.L.C.; Nascimento, E.M.D.; Jesus, L.J.C.; Freitas, T.G.; Lugon, J.R.; Ballas, S.K. Mortality in children, adolescents and adults with sickle cell anemia in Rio de Janeiro, Brazil. Hematol. Transfus. Cell Ther. 2018, 40, 37–42. [Google Scholar] [CrossRef] [PubMed]
  12. Powars, D.R.; Chan, L.S.; Hiti, A.; Ramicone, E.; Johnson, C. Outcome of sickle cell anemia: A 4-decade observational study of 1056 patients. Medicine 2005, 84, 363–376. [Google Scholar] [CrossRef] [PubMed]
  13. Steinberg, M.H.; Barton, F.; Castro, O.; Pegelow, C.H.; Ballas, S.K.; Kutlar, A.; Orringer, E.; Bellevue, R.; Olivieri, N.; Eckman, J.; et al. Effect of hydroxyurea on mortality and morbidity in adult sickle cell anemia: Risks and benefits up to 9 years of treatment. JAMA 2003, 289, 1645–1651. [Google Scholar] [CrossRef] [PubMed]
  14. Darbari, D.S.; Wang, Z.; Kwak, M.; Hildesheim, M.; Nichols, J.; Allen, D.; Seamon, C.; Peters-Lawrence, M.; Conrey, A.; Hall, M.K.; et al. Severe Painful Vaso-Occlusive Crises and Mortality in a Contemporary Adult Sickle Cell Anemia Cohort Study. PLoS ONE 2013, 8, e79923. [Google Scholar] [CrossRef] [PubMed]
  15. Maitra, P.; Caughey, M.; Robinson, L.; Desai, P.C.; Jones, S.; Nouraie, M.; Gladwin, M.T.; Hinderliter, A.; Cai, J.; Ataga, K.I. Risk factors for mortality in adult patients with sickle cell disease: A meta-analysis of studies in North America and Europe. Haematologica 2017, 102, 626–636. [Google Scholar] [CrossRef] [PubMed]
  16. Fitzhugh, C.D.; Lauder, N.; Jonassaint, J.C.; Telen, M.J.; Zhao, X.; Wright, E.C.; Gilliam, F.R.; De Castro, L.M. Cardiopulmonary complications leading to premature deaths in adult patients with sickle cell disease. Am. J. Hematol. 2010, 85, 36–40. [Google Scholar] [CrossRef]
  17. Lanzkron, S.; Little, J.; Field, J.; Shows, J.R.; Wang, H.; Seufert, R.; Brooks, J.; Varadhan, R.; Haywood, C.; Saheed, M.; et al. Increased acute care utilization in a prospective cohort of adults with sickle cell disease. Blood Adv. 2018, 2, 2412–2417. [Google Scholar] [CrossRef]
  18. Jordan, L.C.; Kassim, A.A.; Donahue, M.J.; Juttukonda, M.R.; Pruthi, S.; Davis, L.T.; Rodeghier, M.; Lee, C.A.; Patel, N.J.; DeBaun, M.R. Silent infarct is a risk factor for infarct recurrence in adults with sickle cell anemia. Neurology 2018, 91, e781–e784. [Google Scholar] [CrossRef]
  19. Wong, W.-Y.; Powars, D.R. Overt and Incomplete (Silent) Cerebral Infarction in Sickle Cell Anemia: Diagnosis and Management. Hematol. Clin. N. Am. 2005, 19, 839–855. [Google Scholar] [CrossRef]
  20. Adams, R.J.; McKie, V.C.; Hsu, L.; Files, B.; Vichinsky, E.; Pegelow, C.; Abboud, M.; Gallagher, D.; Kutlar, A.; Nichols, F.T.; et al. Prevention of a First Stroke by Transfusions in Children with Sickle Cell Anemia and Abnormal Results on Transcranial Doppler Ultrasonography. N. Engl. J. Med. 1998, 339, 5–11. [Google Scholar] [CrossRef]
  21. Valadi, N.; Silva, G.S.; Bowman, L.S.; Ramsingh, D.; Vicari, P.; Filho, A.C.; Massaro, A.R.; Kutlar, A.; Nichols, F.T.; Adams, R.J. Transcranial Doppler ultrasonography in adults with sickle cell disease. Neurology 2006, 67, 572–574. [Google Scholar] [CrossRef] [PubMed]
  22. Powars, D.; Wilson, B.; Imbus, C.; Pegelow, C.; Allen, J. The natural history of stroke in sickle cell disease. Am. J. Med. 1978, 65, 461–471. [Google Scholar] [CrossRef]
  23. Kassim, A.A.; Galadanci, N.A.; Pruthi, S.; DeBaun, M.R. How I treat and manage strokes in sickle cell disease. Blood 2015, 125, 3401–3410. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  24. Hulbert, M.L.; McKinstry, R.C.; Lacey, J.L.; Moran, C.J.; Panepinto, J.A.; Thompson, A.A.; Sarnaik, S.A.; Woods, G.M.; Casella, J.F.; Inusa, B.; et al. Silent cerebral infarcts occur despite regular blood transfusion therapy after first strokes in children with sickle cell disease. Blood 2011, 117, 772–779. [Google Scholar] [CrossRef] [Green Version]
  25. Gladwin, M.T.; Sachdev, V.; Jison, M.L.; Minter, K.; Brown, B.; Coles, W.A.; Nichols, J.S.; Ernst, I.; Hunter, L.A.; Ognibene, F.P.; et al. Pulmonary Hypertension as a Risk Factor for Death in Patients with Sickle Cell Disease. N. Engl. J. Med. 2004, 350, 886–895. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  26. De Castro, L.M.; Jonassaint, J.C.; Graham, F.L.; Ashley-Koch, A.; Telen, M.J. Pulmonary hypertension associated with sickle cell disease: Clinical and laboratory endpoints and disease outcomes. Am. J. Hematol. 2008, 83, 19–25. [Google Scholar] [CrossRef]
  27. Ataga, K.I.; Moore, C.G.; Jones, S.; Olajide, O.; Strayhorn, D.; Hinderliter, A.; Orringer, E.P. Pulmonary hypertension in patients with sickle cell disease: A longitudinal study. Br. J. Haematol. 2006, 134, 109–115. [Google Scholar] [CrossRef]
  28. Damy, T.; Bodez, D.; Habibi, A.; Guellich, A.; Rappeneau, S.; Inamo, J.; Guendouz, S.; Gellen-Dautremer, J.; Pissard, S.; Loric, S. Haematological determinants of cardiac involvement in adults with sickle cell disease. Eur. Heart J. 2016, 37, 1158–1167. [Google Scholar] [CrossRef]
  29. Machado, R.F.; Hildesheim, M.; Mendelsohn, L.; Remaley, A.T.; Kato, G.J.; Gladwin, M.T. NT-pro brain natriuretic peptide levels and the risk of death in the cooperative study of sickle cell disease. Br. J. Haematol. 2011, 154, 512–520. [Google Scholar] [CrossRef]
  30. Gladwin, M.T.; Barst, R.J.; Gibbs, J.S.R.; Hildesheim, M.; Sachdev, V.; Nouraie, M.; Hassell, K.L.; Little, J.A.; Schraufnagel, D.E.; Krishnamurti, L.; et al. Risk Factors for Death in 632 Patients with Sickle Cell Disease in the United States and United Kingdom. PLoS ONE 2014, 9, e99489. [Google Scholar] [CrossRef]
  31. McClish, D.K.; Penberthy, L.T.; Bovbjerg, V.E.; Roberts, J.D.; Aisiku, I.P.; Levenson, J.L.; Roseff, S.D.; Smith, W.R. Health related quality of life in sickle cell patients: The PiSCES project. Health Qual. Life Outcomes 2005, 3, 50. [Google Scholar] [CrossRef] [PubMed]
  32. Kauf, T.L.; Coates, T.D.; Huazhi, L.; Hartzema, A.G.; Mody-Patel, N.; Mody-Patel, N. The cost of health care for children and adults with sickle cell disease. Am. J. Hematol. 2009, 84, 323–327. [Google Scholar] [CrossRef] [PubMed]
  33. Ballas, S.K. The cost of health care for patients with sickle cell disease. Am. J. Hematol. 2009, 84, 320–322. [Google Scholar] [CrossRef] [PubMed]
  34. Gluckman, E. Allogeneic transplantation strategies including haploidentical transplantation in sickle cell disease. Hematology 2013, 2013, 370–376. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  35. Krishnamurti, L.; Neuberg, D.S.; Sullivan, K.M.; Kamani, N.R.; Abraham, A.; Campigotto, F.; Zhang, W.; Dahdoul, T.; De Castro, L.; Parikh, S.; et al. Bone Marrow Transplantation for Adolescents and Young Adults with Sickle Cell Disease: Results of a Prospective Multicenter Pilot Study. Am. J. Hematol. 2019, 94, 446–454. [Google Scholar] [CrossRef] [PubMed]
  36. Guilcher, G.M.; Truong, T.H.; Saraf, S.L.; Joseph, J.J.; Rondelli, D.; Hsieh, M.M. Curative therapies - allogeneic hematopoietic cell transplantation from matched related donors using myeloablative, reduced intensity, and non-myeloablative conditioning in sickle cell disease. Semin. Hematol. 2018, 55, 87–93. [Google Scholar] [CrossRef]
  37. Walters, M.C.; Patience, M.; Leisenring, W.; Eckman, J.R.; Scott, J.P.; Mentzer, W.C.; Davies, S.C.; Ohene-Frempong, K.; Bernaudin, F.; Matthews, D.C.; et al. Bone Marrow Transplantation for Sickle Cell Disease. N. Engl. J. Med. 1996, 335, 369–376. [Google Scholar] [CrossRef]
  38. McGann, P.T.; Ware, R.E. Hydroxyurea therapy for sickle cell anemia. Expert Opin. Drug Saf. 2015, 14, 1749–1758. [Google Scholar] [CrossRef]
  39. Charache, S.; Terrin, M.L.; Moore, R.D.; Barton, F.B.; Eckert, S.V.; Bonds, D.R.; Dover, G.J.; McMahon, R.P. Effect of Hydroxyurea on the Frequency of Painful Crises in Sickle Cell Anemia. N. Engl. J. Med. 1995, 332, 1317–1322. [Google Scholar] [CrossRef]
  40. Fitzhugh, C.D.; Hsieh, M.M.; Allen, D.; Coles, W.A.; Seamon, C.; Ring, M.; Zhao, X.; Minniti, C.P.; Rodgers, G.P.; Schechter, A.N.; et al. Hydroxyurea-Increased Fetal Hemoglobin Is Associated with Less Organ Damage and Longer Survival in Adults with Sickle Cell Anemia. PLoS ONE 2015, 10, e0141706. [Google Scholar] [CrossRef]
  41. Voskaridou, E.; Christoulas, D.; Bilalis, A.; Plata, E.; Varvagiannis, K.; Stamatopoulos, G.; Sinopoulou, K.; Balassopoulou, A.; Loukopoulos, D.; Terpos, E. The effect of prolonged administration of hydroxyurea on morbidity and mortality in adult patients with sickle cell syndromes: Results of a 17-year, single-center trial (LaSHS). Blood 2010, 115, 2354–2363. [Google Scholar] [CrossRef] [PubMed]
  42. Niihara, Y.; Miller, S.T.; Kanter, J.; Lanzkron, S.; Smith, W.R.; Hsu, L.L.; Gordeuk, V.R.; Viswanathan, K.; Sarnaik, S.; Osunkwo, I.; et al. A Phase 3 Trial of l-Glutamine in Sickle Cell Disease. N. Engl. J. Med. 2018, 379, 226–235. [Google Scholar] [CrossRef] [PubMed]
  43. Ataga, K.I.; Kutlar, A.; Kanter, J.; Kutlar, A.; Kanter, J.; Liles, D.; Cancado, R.; Friedrisch, J.; Guthrie, T.H.; Knight-Madden, J.; et al. Crizanlizumab for the Prevention of Pain Crises in Sickle Cell Disease. N. Engl. J. Med. 2017, 376, 429–439. [Google Scholar] [CrossRef] [PubMed]
  44. Vichinsky, E.; Hoppe, C.C.; Ataga, K.I.; Ware, R.E.; Nduba, V.; El-Beshlawy, A.; Hassab, H.; Achebe, M.M.; Alkindi, S.; Brown, R.C.; et al. A Phase 3 Randomized Trial of Voxelotor in Sickle Cell Disease. N. Engl. J. Med. 2019, 381, 509–519. [Google Scholar] [CrossRef] [PubMed]
  45. Bernaudin, F.; Socie, G.; Kuentz, M.; Chevret, S.; Duval, M.; Bertrand, Y.; Vannier, J.-P.; Yakouben, K.; Thuret, I.; Bordigoni, P.; et al. Long-term results of related myeloablative stem-cell transplantation to cure sickle cell disease. Blood 2007, 110, 2749–2756. [Google Scholar] [CrossRef] [PubMed]
  46. Panepinto, J.A.; Walters, M.C.; Carreras, J.; Marsh, J.; Bredeson, C.N.; Gale, R.P.; Hale, G.A.; Horan, J.; Hows, J.M.; Klein, J.P.; et al. Matched-related donor transplantation for sickle cell disease: Report from the Center for International Blood and Transplant Research. Br. J. Haematol. 2007, 137, 479–485. [Google Scholar] [CrossRef] [PubMed]
  47. Vermylen, C.; Cornu, G.; Ferster, A.; Brichard, B.; Ninane, J.; Ferrant, A.; Zenebergh, A.; Maes, P.; Dhooge, C.; Benoit, Y.; et al. Haematopoietic stem cell transplantation for sickle cell anaemia: The first 50 patients transplanted in Belgium. Bone Marrow Transplant. 1998, 22, 1–6. [Google Scholar] [CrossRef]
  48. Kuentz, M.; Robin, M.; Dhedin, N.; Hicheri, Y.; de Latour, R.P.; Rohrlich, P.; Bordigoni, P.; Bruno, B.; Socié, G.; Bernaudin, F. Is there still a place for myeloablative regimen to transplant young adults with sickle cell disease? Blood 2011, 118, 4491–4492. [Google Scholar] [CrossRef] [PubMed]
  49. Van Besien, K.; Bartholomew, A.; Stock, W.; Peace, D.; Devine, S.; Sher, D.; Sosman, J.; Chen, Y.; Koshy, M.; Hoffman, R. Fludarabine-based conditioning for allogeneic transplantation in adults with sickle cell disease. Bone Marrow Transplant. 2000, 26, 445–449. [Google Scholar] [CrossRef] [Green Version]
  50. Özdoğu, H.; Boga, C.; Yeral, M.; Kozanoglu, I.; Gereklioglu, Ç.; Aytan, P.; Kasar, M.; Asma, S.; Buyukkurt, N.; Solmaz, S.; et al. Allogenic peripheral stem cell transplantation from HLA-matched related donors for adult sickle cell disease: Remarkable outcomes from a single-center trial. Bone Marrow Transplant. 2018, 53, 880–890. [Google Scholar] [CrossRef]
  51. Walters, M.; Patience, M.; Leisenring, W.; Rogers, Z.; Aquino, V.; Buchanan, G.; Roberts, I.; Yeager, A.; Hsu, L.; Adamkiewicz, T.; et al. Stable mixed hematopoietic chimerism after bone marrow transplantation for sickle cell anemia. Biol. Blood Marrow Transplant. 2001, 7, 665–673. [Google Scholar] [CrossRef] [PubMed]
  52. Sachs, D.H.; Kawai, T.; Sykes, M. Induction of Tolerance through Mixed Chimerism. Cold Spring Harb. Perspect. Med. 2014, 4, a015529. [Google Scholar] [CrossRef] [PubMed]
  53. Abraham, A.; Hsieh, M.; Eapen, M.; Fitzhugh, C.; Carreras, J.; Keesler, D.; Guilcher, G.; Kamani, N.; Walters, M.C.; Boelens, J.J.; et al. Relationship between Mixed Donor–Recipient Chimerism and Disease Recurrence after Hematopoietic Cell Transplantation for Sickle Cell Disease. Biol. Blood Marrow Transplant. 2017, 23, 2178–2183. [Google Scholar] [CrossRef] [PubMed]
  54. Fitzhugh, C.D.; Cordes, S.; Taylor, T.; Coles, W.; Roskom, K.; Link, M.; Hsieh, M.M.; Tisdale, J.F. At least 20% donor myeloid chimerism is necessary to reverse the sickle phenotype after allogeneic HSCT. Blood 2017, 130, 1946–1948. [Google Scholar] [CrossRef] [Green Version]
  55. Iannone, R.; Luznik, L.; Engstrom, L.W.; Tennessee, S.L.; Askin, F.B.; Casella, J.F.; Kickler, T.S.; Goodman, S.N.; Hawkins, A.L.; Griffin, C.A.; et al. Effects of mixed hematopoietic chimerism in a mouse model of bone marrow transplantation for sickle cell anemia. Blood 2001, 97, 3960–3965. [Google Scholar] [CrossRef] [Green Version]
  56. Hsieh, M.M.; Kang, E.M.; Fitzhugh, C.D.; Link, M.B.; Bolan, C.D.; Kurlander, R.; Childs, R.W.; Rodgers, G.P.; Powell, J.D.; Tisdale, J.F. Allogeneic hematopoietic stem-cell transplantation for sickle cell disease. N. Engl. J. Med. 2009, 361, 2309–2317. [Google Scholar] [CrossRef]
  57. Hsieh, M.M.; Fitzhugh, C.D.; Weitzel, R.P.; Link, M.E.; Coles, W.A.; Zhao, X.; Rodgers, G.P.; Powell, J.D.; Tisdale, J.F. Nonmyeloablative HLA-matched sibling allogeneic hematopoietic stem cell transplantation for severe sickle cell phenotype. JAMA 2014, 312, 48–56. [Google Scholar] [CrossRef]
  58. Saraf, S.L.; Oh, A.L.; Patel, P.R.; Jalundhwala, Y.; Sweiss, K.; Koshy, M.; Campbell-Lee, S.; Gowhari, M.; Hassan, J.; Peace, D.; et al. Nonmyeloablative Stem Cell Transplantation with Alemtuzumab/Low-Dose Irradiation to Cure and Improve the Quality of Life of Adults with Sickle Cell Disease. Biol. Blood Marrow Transplant. 2016, 22, 441–448. [Google Scholar] [CrossRef] [Green Version]
  59. Al-Zahrani, M.; Alaskar, A.; Damlaj, M.; Abuelgasim, K.; Gmati, G.; Salama, H.A.; Ghazi, S.; Ali, O.; Alahmari, B.; Hejazi, A. Non-myeloablative transplant in severe sickel cell disease is safe & effective. Single center experience from Saudi Arabia. Blood 2017, 130, 5549. [Google Scholar]
  60. Walters, M.C.; Patience, M.; Leisenring, W.; Eckman, J.R.; Buchanan, G.R.; Rogers, Z.R.; Olivieri, N.E.; Vichinsky, E.; Davies, S.C.; Mentzer, W.C.; et al. Barriers to bone marrow transplantation for sickle cell anemia. Biol. Blood Marrow Transplant. 1996, 2, 100–104. [Google Scholar]
  61. Mentzer, W.C.; Heller, S.; Pearle, P.R.; Hackney, E.; Vichinsky, E. Availability of related donors for bone marrow transplantation in sickle cell anemia. J. Pediatr. Hematol. 1994, 16, 27–29. [Google Scholar]
  62. Gragert, L.; Eapen, M.; Williams, E.; Freeman, J.; Spellman, S.; Baitty, R.; Hartzman, R.; Rizzo, J.D.; Horowitz, M.; Confer, D.; et al. HLA Match Likelihoods for Hematopoietic Stem-Cell Grafts in the U.S. Registry. N. Engl. J. Med. 2014, 371, 339–348. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  63. Luznik, L.; Engstrom, L.W.; Iannone, R.; Fuchs, E.J. Posttransplantation cyclophosphamide facilitates engraftment of major histocompatibility complex-identical allogeneic marrow in mice conditioned with low-dose total body irradiation. Biol. Blood Marrow Transplant. 2002, 8, 131–138. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  64. Bolaños-Meade, J.; Fuchs, E.J.; Luznik, L.; Lanzkron, S.M.; Gamper, C.J.; Jones, R.J.; Brodsky, R.A. HLA-haploidentical bone marrow transplantation with posttransplant cyclophosphamide expands the donor pool for patients with sickle cell disease. Blood 2012, 120, 4285–4291. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  65. Saraf, S.L.; Oh, A.L.; Patel, P.R.; Sweiss, K.; Koshy, M.; Campbell-Lee, S.; Gowhari, M.; Jain, S.; Peace, D.; Quigley, J.G.; et al. Haploidentical Peripheral Blood Stem Cell Transplantation Demonstrates Stable Engraftment in Adults with Sickle Cell Disease. Biol. Blood Marrow Transplant. 2018, 24, 1759–1765. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  66. de la Fuente, J.; Dhedin, N.; Koyama, T.; Bernaudin, F.; Kuentz, M.; Karnik, L.; Socié, G.; Culos, K.A.; Brodsky, R.A.; DeBaun, M.R.; et al. Haploidentical Bone Marrow Transplantation with Post-Transplantation Cyclophosphamide Plus Thiotepa Improves Donor Engraftment in Patients with Sickle Cell Anemia: Results of an International Learning Collaborative. Biol. Blood Marrow Transplant. 2019, 25, 1197–1209. [Google Scholar] [CrossRef]
  67. Pawlowska, A.B.; Cheng, J.C.; Karras, N.A.; Sun, W.; Wang, L.D.; Bell, A.D.; Gutierrez, L.; Rosenthal, J. HLA Haploidentical Stem Cell Transplant with Pretransplant Immunosuppression for Patients with Sickle Cell Disease. Biol. Blood Marrow Transplant. 2018, 24, 185–189. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  68. Fitzhugh, C.D.; Hsieh, M.M.; Taylor, T.; Coles, W.; Roskom, K.; Wilson, D.; Wright, E.; Jeffries, N.; Gamper, C.J.; Powell, J.; et al. Cyclophosphamide improves engraftment in patients with SCD and severe organ damage who undergo haploidentical PBSCT. Blood Adv. 2017, 1, 652–661. [Google Scholar] [CrossRef]
  69. Sorror, M.; Maris, M.; Storb, R.; Baron, F.; Sandmaier, B.; Maloney, D.; Barry, S. Hematopoietic cell transplantation (HCT)-specific comorbidity index: A new tool for risk assessment before allogeneic HCT. Blood 2005, 106, 2912–2919. [Google Scholar] [CrossRef]
  70. Thakar, M.S.; Broglie, L.; Logan, B.; Artz, A.; Bunin, N.; Burroughs, L.M.; Fretham, C.; Jacobsohn, D.A.; Loren, A.W.; Kurtzberg, J.; et al. The Hematopoietic Cell Transplant Comorbidity Index predicts survival after allogeneic transplant for nonmalignant diseases. Blood 2019, 133, 754–762. [Google Scholar] [CrossRef] [Green Version]
  71. Van Besien, K.; Koshy, M.; Anderson-Shaw, L.; Talishy, N.; Dorn, L.; Devine, S.; Yassine, M.; Kodish, E. Allogeneic stem cell transplantation for sickle cell disease. A study of patients’ decisions. Bone Marrow Transplant. 2001, 28, 545–549. [Google Scholar] [CrossRef] [PubMed]
  72. Chakrabarti, S.; Bareford, D. A survey on patient perception of reduced-intensity transplantation in adults with sickle cell disease. Bone Marrow Transplant. 2007, 39, 447–451. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  73. Darbari, D.S.; Liljencrantz, A.I.J.; Martin, S.; Roderick, M.C.; Fitzhugh, C.D.; Tisdale, J.F.; Thein, S.L.; Hsieh, M. Pain and opioid use after reversal of sickle cell disease following HLA-matched sibling haematopoietic stem cell transplant. Br. J. Haematol. 2019, 184, 690–693. [Google Scholar] [CrossRef] [PubMed]
  74. Saraf, S.L.; Ghimire, K.; Patel, P.; Sweiss, K.; Quigley, J.G.; Khan, I.; Peace, D.; Gowhari, M.; Jain, S.; Galvin, J.P.; et al. Health care utilization in transplanted versus non-transplanted sickle cell disease patients. Blood 2018, 132, 313. [Google Scholar]
  75. Mehari, A.; Gladwin, M.T.; Tian, X.; Machado, R.F.; Kato, G.J. Mortality in adults with sickle cell disease and pulmonary hypertension. JAMA 2012, 307, 1254–1256. [Google Scholar] [CrossRef] [PubMed]
  76. Pittman, C.; Hsieh, M.M.; Coles, W.; Tisdale, J.F.; Weir, N.A.; Fitzhugh, C.D. Reversal of pre-capillary pulmonary hypertension in a patient with sickle cell anemia who underwent haploidentical peripheral blood stem cell transplantation. Bone Marrow Transplant. 2017, 52, 641–642. [Google Scholar] [CrossRef]
  77. Kelly, M.J.; Pennarola, B.W.; Rodday, A.M.; Parsons, S.K. Journeys to Recovery Study H-CS. Health-related quality of life (HRQL) in children with sickle cell disease and thalassemia following hematopoietic stem cell transplant (HSCT). Pediatr. Blood Cancer 2012, 59, 725–731. [Google Scholar] [CrossRef] [PubMed]
  78. Bhatia, M.; Kolva, E.; Cimini, L.; Jin, Z.; Satwani, P.; Savone, M.; George, D.; Garvin, J.; Paz, M.L.; Briamonte, C.; et al. Health-Related Quality of Life after Allogeneic Hematopoietic Stem Cell Transplantation for Sickle Cell Disease. Biol. Blood Marrow Transplant. 2015, 21, 666–672. [Google Scholar] [CrossRef] [Green Version]
  79. Angelucci, E.; Matthes-Martin, S.; Baronciani, D.; Bernaudin, F.; Bonanomi, S.; Cappellini, M.D.; Dalle, J.-H.; Di Bartolomeo, P.; De Heredia, C.D.; Dickerhoff, R.; et al. Hematopoietic stem cell transplantation in thalassemia major and sickle cell disease: Indications and management recommendations from an international expert panel. Haematologica 2014, 99, 811–820. [Google Scholar] [CrossRef]
  80. Rotz, S.J.; O’Riordan, M.A.; Kim, C.; De Lima, M.; Gladwin, M.T.; Little, J.A.; Rotz, S. Traffic Light: Prognosis-based eligibility for clinical trials of hematopoietic SCT in adults with sickle cell anemia. Bone Marrow Transplant. 2015, 50, 918–923. [Google Scholar] [CrossRef]
  81. Saraf, S.L.; Akingbola, T.S.; Shah, B.N.; Ezekekwu, C.A.; Sonubi, O.; Zhang, X.; Hsu, L.L.; Gladwin, M.T.; Machado, R.F.; Cooper, R.S.; et al. Associations of alpha-thalassemia and BCL11A with stroke in Nigerian, United States, and United Kingdom sickle cell anemia cohorts. Blood Adv. 2017, 1, 693–698. [Google Scholar] [CrossRef] [PubMed]
  82. Desai, A.A.; Lei, Z.; Bahroos, N.; Maienschein-Cline, M.; Saraf, S.L.; Zhang, X.; Shah, B.N.; Nouraie, S.M.; Abbasi, T.; Patel, A.R.; et al. Association of circulating transcriptomic profiles with mortality in sickle cell disease. Blood 2017, 129, 3009–3016. [Google Scholar] [CrossRef] [PubMed]
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Figure 1. Improvements in the tricuspid regurgitant jet velocity (TRJV) after hematopoietic stem cell transplantation in adults with sickle cell disease from (A) the National Institutes of Health (n = 13) and (B) University of Illinois at Chicago (pre-HSCT mean = 2.3 ± 0.5 m/s, post-HSCT mean = 2.0 ± 0.4 m/s) (n = 12) cohorts, using an alemtuzumab and total body irradiation conditioning regimen.
Figure 1. Improvements in the tricuspid regurgitant jet velocity (TRJV) after hematopoietic stem cell transplantation in adults with sickle cell disease from (A) the National Institutes of Health (n = 13) and (B) University of Illinois at Chicago (pre-HSCT mean = 2.3 ± 0.5 m/s, post-HSCT mean = 2.0 ± 0.4 m/s) (n = 12) cohorts, using an alemtuzumab and total body irradiation conditioning regimen.
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Figure 2. Increased health-related quality of life after hematopoietic stem cell transplantation in adults with sickle cell disease from (A) the University of Illinois (n = 9), (B) University of Baskent (n = 20), and (C) the multi-center STRIDE study (n = 17).
Figure 2. Increased health-related quality of life after hematopoietic stem cell transplantation in adults with sickle cell disease from (A) the University of Illinois (n = 9), (B) University of Baskent (n = 20), and (C) the multi-center STRIDE study (n = 17).
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Figure 3. Lower healthcare utilization in adults with sickle cell disease after allogeneic hematopoietic stem cell transplantation from (A) the National Institutes of Health and (B) the University of Illinois at Chicago cohorts, using an alemtuzumab and total body irradiation conditioning regimen.
Figure 3. Lower healthcare utilization in adults with sickle cell disease after allogeneic hematopoietic stem cell transplantation from (A) the National Institutes of Health and (B) the University of Illinois at Chicago cohorts, using an alemtuzumab and total body irradiation conditioning regimen.
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Table
Table 1. Indications for allogeneic hematopoietic stem cell transplantation in sickle cell disease [34,35,36,37].
Table 1. Indications for allogeneic hematopoietic stem cell transplantation in sickle cell disease [34,35,36,37].
IndicationHLA-Matched Related DonorAlternative Donor*
Predictors for Increased Mortality≥2 VOC/yearXX
Recurrent acute chest syndromeXX
StrokeXX
Cognitive impairment + Abnormal cerebral MRI XX
TRJV ≥ 2.7 m/sXX
Sickle nephropathyX
Predictors for Increased MorbidityRed blood cell alloimmunizationX
Recurrent priapismX
Osteonecrosis of multiple jointsX
HLA, human leukocyte antigen; VOC, vaso-occlusive crisis; MRI, magnetic resonance imaging: TRJV, tricuspid regurgitant jet velocity. * Despite hydroxyurea and/or chronic red blood cell transfusion therapy.
Table
Table 2. Reduced-intensity conditioning regimens in adults with SCD.
Table 2. Reduced-intensity conditioning regimens in adults with SCD.
Conditioning RegimenGVHD ProphylaxisNAge
(years)		Graft
Source		Event-free
Survival		Overall
Survival		aGVHD
(≥grade 2)		cGVHD
(≥moderate)		Reference
Fludarabine (150 mg/kg)
Busulfan (3.2 mg/kg)
Cy (29 mg/kg)
ATG (15 mg/kg)
Total body irradiation (200 cGy)
  • Cy 33 mg/kg/day on day +3, 4
  • Sirolimus
2020–4520 MRD100%100%5%0%[50]
Fludarabine (175 mg/m2)
Busulfan (13.2 mg/kg)
ATG (6 mg/kg)
  • MTX 7.5 mg/m2/day on day +1, 3, 6, 11
  • Cyclosporine or tacrolimus
2217–3617 MRD
5 MUD		82%91%18%14%[35]
SCD, sickle cell disease; aGVHD, acute graft versus host disease; cGVHD, chronic graft versus host disease; Cy, cyclophosphamide; ATG, antithymocyte globulin; cGy, centigray; MRD, matched related donors; MUD, matched unrelated donors.
Table
Table 3. Nonmyeloablative alemtuzumab/TBI conditioning regimens in adults with SCD.
Table 3. Nonmyeloablative alemtuzumab/TBI conditioning regimens in adults with SCD.
Conditioning RegimenGVHD ProphylaxisNAge
(years)		Graft
Source		Event-free
Survival		Overall
Survival		aGVHD
(≥grade 2)		cGVHD
(≥moderate)		Reference
Alemtuzumab 1 mg/kg
Total body irradiation (300 cGy)		Sirolimus3017–65MRD87%97%0%0%[57]
1317–4092%100%0%0%[58]
1714–3989%100%0%0%[59]
Table
Table 4. Haploidentical hematopoietic stem cell transplantation (HSCT) in adults with SCD.
Table 4. Haploidentical hematopoietic stem cell transplantation (HSCT) in adults with SCD.
Conditioning RegimenGVHD ProphylaxisNAge
(years)		Graft
Source		Event-free
Survival		Overall
Survival		aGVHD
(≥grade2)		cGVHD
(≥moderate)		Reference
Fludarabine (150 mg/m2)
Cy (29 mg/kg)
ATG (4.5 mg/kg)
Total body irradiation (200 cGy)
  • Cy 50 mg/kg/day on day +3, 4
  • MMF until day +35
  • Tacrolimus or Sirolimus
1415–42Bone
Marrow		57%100%0%0%[64]
Alemtuzumab (1 mg/kg)
Total body irradiation (400 cGy)
  • Cy 50 mg/kg/day on day +3, 4
  • Sirolimus
1220–56PBSC50%92%0%0%[68]
Fludarabine (150 mg/m2)
Cy (29 mg/kg)
ATG (4.5 mg/kg)
Total body irradiation (300 cGy)
  • Cy 50 mg/kg/day on day +3, 4
  • MMF until day +35
  • Sirolimus
820–38PBSC75%88%25%13%[65]
Pre-HSCT Immunosuppression:
Fludarabine (200 mg/m2)
Dexamethasone (125 mg/m2)
Conditioning:
Fludarabine (210 mg/m2)
Busulfan (520 mg/m2)
ATG (4.5 mg/kg)
  • Cy 50 mg/kg/day on day +3, 4
  • MMF until day +28
  • Tacrolimus
412–24Bone Marrow
(n = 3)
PBSC
(n = 1)		100%100%0%0%[67]
Fludarabine (150 mg/m2)
Cy (29 mg/kg)
Thiotepa (10 mg/kg)
ATG (4.5 mg/kg)
Total body irradiation (300 cGy)
  • Cy 50 mg/kg/day on day +3, 4
  • MMF until day +35
  • Sirolimus
157–40Bone Marrow93%100%13%0%[66]
Table
Table 5. Stroke recurrence and brain imaging findings in adults with sickle cell disease after allogeneic hematopoietic stem cell transplantation (HSCT).
Table 5. Stroke recurrence and brain imaging findings in adults with sickle cell disease after allogeneic hematopoietic stem cell transplantation (HSCT).
HSCT TypeStroke RecurrenceBrain MRI FindingsReference
• Nonmyeloablative,
• Matched-related donor		0 out of 9Stable brain MRI and angiography findings[57]
• Nonmyeloablative
• Haploidentical related donor		0 out of 3–[64]
• Nonmyeloablative
• Matched-related donor		1 out of 4–[58]
• Nonmyeloablative
• Haploidentical		0 out of 2–[65]
• Nonmyeloablative
• Haploidentical		0 out of 9–[66]
• Reduced-intensity
• Matched-related and unrelated donor		0 out of 2Stable brain MRI in 17 patients[35]
TOTAL1 out of 29 (3%)

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Saraf, S.L.; Rondelli, D. Allogeneic Hematopoietic Stem Cell Transplantation for Adults with Sickle Cell Disease. J. Clin. Med. 2019, 8, 1565. https://doi.org/10.3390/jcm8101565

AMA Style

Saraf SL, Rondelli D. Allogeneic Hematopoietic Stem Cell Transplantation for Adults with Sickle Cell Disease. Journal of Clinical Medicine. 2019; 8(10):1565. https://doi.org/10.3390/jcm8101565

Chicago/Turabian Style

Saraf, Santosh L., and Damiano Rondelli. 2019. "Allogeneic Hematopoietic Stem Cell Transplantation for Adults with Sickle Cell Disease" Journal of Clinical Medicine 8, no. 10: 1565. https://doi.org/10.3390/jcm8101565

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