State-of-the-art review: allogeneic stem cell transplantation for myelofibrosis in 2019

Abstract

Advances in understanding the pathogenesis and molecular landscape of myelofibrosis have occurred over the last decade. Treating physicians now have access to an ever-evolving armamentarium of novel agents to treat patients, although allogeneic hematopoietic stem cell transplantation remains the only curative approach. Improvements in donor selection, conditioning regimens, disease monitoring and supportive care have led to augmented survival after transplantation. Nowadays, there are comprehensive guidelines concerning allogeneic hematopoietic stem cell transplantation for patients with myelofibrosis. However, it commonly remains difficult for both physicians and patients alike to weigh up the risk-benefit ratio of transplantation given the inherent heterogeneity regarding both clinical course and therapeutic response. In this timely review, we provide an up-to-date synopsis of current transplantation recommendations, discuss usage of JAK inhibitors before and after transplantation, examine donor selection and compare conditioning platforms. Moreover, we discuss emerging data concerning the impact of the myelofibrosis mutational landscape on transplantation outcome, peritransplant management of splenomegaly, poor graft function and prevention/management of relapse.

Introduction

Myelofibrosis is a heterogeneous disease as regards both disease phenotype and mutational landscape. Following the discovery of the JAK2 mutation in 2005 and subsequent studies confirming the clinical efficacy of JAK inhibitors, the treatment paradigm has been revolutionized.61 Worldwide experience with JAK inhibitor therapy continues to grow and a considerable proportion of patients will gain beneficial symptom and/or splenic responses, albeit heterogeneous and of variable duration. Furthermore, given that many other novel therapeutics, such as anti-fibrotic and immunomodulatory agents, have been used to treat myelofibrosis,7 the majority of patients moving forward with allogeneic hematopoietic stem cell transplantation (SCT) have had at least one prior treatment, making ‘real-world’ transplant decisions increasingly complex. Data from the European Society for Blood and Marrow Transplantation (EBMT) suggest a year-on-year increase in transplants for myelofibrosis. In this review we focus on current indications for allogeneic SCT, prognostic scoring models to aid decision-making, donor selection, conditioning regimens, the role of splenectomy and prevention and management of relapse.

The transplant decision: how to decide who should be considered for allogeneic stem cell transplantation

Clinical prognostic scoring systems play a pivotal role in decisions regarding allogeneic SCT. Until recently, the most commonly applied was the International Prognostic Scoring System (IPSS) which estimates survival from time of diagnosis.8 The score is based upon five factors: age >65 years, hemoglobin <100 g/L, leukocyte count >25×10/L, circulating blasts ≥1% and constitutional symptoms, permitting stratification into four groups: low risk (0 risk factors; estimated median survival, 135 months), intermediate risk-1 (1 risk factor; median survival, 95 months), intermediate risk-2 (2 risk factors, median survival, 48 months) and high risk (3+ risk factors; median survival, 27 months). The Dynamic IPSS (DIPSS), utilizing the same five factors, permits application of the scoring system at any stage in the disease course.9 Finally, the DIPSS-plus incorporates three additional adverse factors – transfusion dependency; platelet count <100×10/L and unfavorable cytogenetics.1110 We follow current European LeukemiaNet/EBMT expert consensus whereby “Patients with intermediate-2- or high-risk disease according to the IPSS, DIPSS or DIPSS-plus and age <70 years should be considered potential candidates for allogeneic SCT”.12 Patients with “intermediate-1-risk disease and age <65 years should be considered as candidates if they present with either refractory, transfusion-dependent anemia, or a percentage of blasts in peripheral blood >2%, or adverse (as defined by the DIPSS-plus classification) cytogenetics”. Decisions regarding transplantation for intermediate-1-risk disease remain complex and are discussed below.

A retrospective, comparative multicenter outcome analysis of 438 patients with primary myelofibrosis aged <65 years at diagnosis who underwent allogeneic SCT (n=190) or conventional therapy in the era before JAK inhibitors (n=248), utilizing DIPSS scoring, demonstrated that allogeneic SCT clearly benefited intermediate-2 or high-risk patients whereas for low-risk disease, transplantation is not immediately indicated and is held in reserve for progressive disease.13 For intermediate-1 disease, individual counseling was recommended. Despite evident utility, marked heterogeneity may be observed within each allocated IPSS/DIPSS subgroup. Grinfeld et al. performed genomic and clinical phenotype analyses of 2,041 patients with myeloproliferative neoplasms, including 311 with myelofibrosis, and combined the findings into a unifying patient-specific predictive model.14 For myelofibrosis, this model predicted event-free survival better than did either the DIPSS or IPSS (81% versus 69% versus 77% concordance) and an online calculator is being developed for predicting patient-specific outcomes (https://jg738.shinyapps.io/mpn_app/). It will be of interest to apply this model to a population of myelofibrosis patients undergoing allogeneic SCT.

A collaborative group recently studied 685 molecularly-annotated patients with secondary myelofibrosis to assess whether an independent prognostic scoring system could be derived.15 The so-called MYelofibrosis SECondary to PV and ET-Prognostic Model (MYSEC-PM) allocated individuals into four prognostic categories based on negative predictors of survival whereby two points were attributed to hemoglobin <110 g/dL, a CALR-unmutated phenotype and circulating blasts ≥3%, one point to thrombocytopenia <150×10/L and constitutional symptoms and 0.15 points to any year of age. Median survival estimates for each group ranged from not reached in the low-risk cohort to 2 years in high-risk cohorts. Akin to IPSS/DIPSS, recent analyses suggested that transplant-specific age-adjustment of the MYSEC-PM provided prognostic predictive power as regards overall survival following allogeneic SCT.1816

Comprehensive mutational profiling has helped identify heterogeneous somatic mutations in patients with myelofibrosis. Delineation of this mutational landscape confers prognostic significance as regards overall survival and risk of disease progression/transformation and increasingly influences therapeutic decisions (Table 1).2219 In the non-transplant setting, it is well established that myelofibrosis patients with CALR type-1/like mutations survive longer than patients with CALR type-2/like and MPL or JAK2 mutations.21 ‘Triple negativity’, i.e. lacking a detectable JAK2, MPL or CALR mutation, is associated with more adverse outcomes. Previous analyses of 617 myelofibrosis patients revealed that the median survival was only 3.2 years for those who were ‘triple negative’.19 Conventionally, high molecular risk myelofibrosis is defined by the presence of at least one of EZH2, ASXL1, IDH1/2 and SRSF2 mutations and is associated with worse overall and leukemia-free survival.22

Table 1.Key characteristics of pivotal non-JAK2/CALR or MPL mutations in myelofibrosis.

These data raise the question of whether earlier transplantation should be considered for those who have ‘triple negative’ disease, particularly with high molecular risk mutations, and need to be taken into consideration when counseling patients, particularly transplant-eligible individuals with intermediate-1-risk disease and ‘good’ donors. Recently, Guglielmelli and colleagues described the utility of both the mutation-enhanced IPSS ‘MIPSS70’ and ‘MIPSS70-plus’ (including cytogenetic evaluation) scoring systems for ‘transplant-age’ patients ≤70 years old with either pre-fibrotic or overt, primary myelofibrosis who were considered candidates for transplantation.23 Significant risk factors for overall survival were leukocyte count >25×10/L, platelet count <100×10/L, presence of >2 high molecular risk mutations, hemoglobin <100 g/L, peripheral blood blasts ≥2%, constitutional symptoms, high molecular risk category, fibrosis grade >2 and absence of CALR type-1/like mutations. These scoring systems enabled three discrete prognostic risk categories to be delineated: low-risk, intermediate-risk and high-risk with 5-year survival rates of 95%; 70% and 29%, respectively. The MIPSS70-plus included cytogenetics in the multivariable analysis. Recent updates to ‘MIPSS70-plus version 2’ occurred with recognition of U2AF1 as a high molecular risk mutation and the scoring system uses new sex- and severity-adjusted hemoglobin thresholds.24 Importantly these scores incorporate current molecular data and up-to-date WHO 2016 disease classification and will aid decisions regarding allogeneic SCT.

It can be difficult when a clinician is managing a young, fit patient with myelofibrosis who has intermediate risk-1 disease and a fully matched donor. Should we transplant upfront when the patient is fit, and the donor is available or should we wait for further disease upstaging before considering allogeneic SCT? Collectively, we feel that this is a very individualized choice, and has many strata including the patient’s wishes and donor type, disease-associated symptom burden and objective quality of life assessment. Given the marked intra-category heterogeneity, refinement of prognostication should occur with cytogenetic and mutational data and the patient should be counseled appropriately, particularly if high molecular risk features are present. Certainly, acquisition of high-risk karyotypes, transfusion dependence or steadily increasing peripheral blood blast counts would suggest a trigger to move towards allogeneic SCT.

The majority of prognostic scoring systems incorporate age as a risk factor; however, multiple dynamic factors determine post-transplant outcome (Figure 1). One of the most common questions is how old is ‘too old’? Transplantation may be more challenging for elderly recipients and there is marked variation globally in the arbitrary age ‘cut-off’ for allogeneic SCT for myelofibrosis. Historically, many earlier studies suggested worse outcome with increasing age. For example, early myeloablative conditioning (MAC) studies involving total body irradiation demonstrated worse outcome for those patients >45 years old, and other small studies suggested worse outcomes for those >50 and >60 years old.2725 In contrast, the Seattle group reported on a highly selected group of myelofibrosis patients undergoing allogeneic SCT with a median age of 65 years (range, 60–78 years), many of whom had multiple co-morbidities.28 Time to engraftment and graft-versus-host-disease (GvHD) rates did not differ significantly from those in younger cohorts. Moreover, no significant outcome differences were identified when comparing patients <65 years old with those >65 years old. Focusing on chronological age alone may not be correct and well-selected elderly patients with minimal co-morbidities and good organ function can benefit significantly from allogeneic SCT. However, real-life decisions can be more difficult in those >70 years old or in those individuals aged 65–70 years who have co-morbidities. In some cases, potential candidates may be frail because of disease symptom burden and have a worse Performance Status, a history of thrombosis or significant potential for hepatic dysfunction. These factors need careful consideration and optimization where possible. As described above, an upper age limit of 70 years was cautiously suggested but this does not mean that ‘fit’ individuals within a few years above this threshold should be excluded. In general, the transplant decision is heavily influenced by careful assessment of the patient and a multi-disciplinary approach. Moreover, factors incorporated in the comprehensive geriatric assessment should be considered and this requires validation in the setting of patients with myelofibrosis undergoing allogeneic SCT.29

Figure 1.Factors determining outcomes following allogeneic stem cell transplantation in myelofibrosis. The determinants of outcomes following allogeneic stem cell transplantation can be divided into: pre-transplantation, transplant-specific, and post-transplant strategies and relapse management. IPSS: International Prognostic Scoring System; DIPSS: dynamic IPSS; IST: immunosuppressive therapy; DLI: donor lymphocyte infusion; MRD: minimal residual disease; Sib: sibling; MUD: matched unrelated donor; MMUD: mismatched unrelated donor; MAC: myeloablative conditioning; RIC: reduced Intensity conditioning; CMV: cytomegalovirus

Is there a role for splenectomy before transplantation for myelofibrosis?

Evidence on the beneficial role of splenectomy prior to allogeneic SCT remains somewhat sparse although in theory splenectomy may be an attractive strategy as it could aid engraftment and perhaps be associated with improved post-transplant outcome.30 However, this procedure is not without risk. Over a decade ago, the Mayo clinic group reported on 314 myelofibrosis patients, albeit not transplant candidates, undergoing elective splenectomy: the intervention was associated with significant perioperative complications in nearly 28% of cases.31 Despite major improvements with minimally invasive approaches, there are still potential risks of both thrombosis and hemorrhage. Although a prospective study of 103 patients undergoing allogeneic SCT coordinated by the Chronic Malignancies Working Party of the EBMT suggested more rapid neutrophil engraftment in those who had undergone splenectomy (n=14) compared to those who had not, both univariate and multivariate analyses suggested a significantly higher rate of relapse at 3 years for the former.32 Moreover, effects on immune reconstitution and GvHD modulation are unclear. In contrast, a French group retrospectively reported on 85 myelofibrosis allogeneic SCT patients from a single center, 39 of whom had undergone pre-transplant splenectomy.33 Of note, one half of those patients undergoing splenectomy had surgical or post-surgical complications, most frequently of a thrombotic or hemorrhagic nature. Following Cox adjustment analyses, there was no association between pre-transplant splenectomy and either non-relapse mortality (NRM) or relapse risk, in fact there was a suggestion towards improved overall survival and event-free survival. This evidently requires evaluation in a larger cohort and ideally in a controlled study as suggested by the authors. In contrast to these findings, initial analyses by McLornan et al. found no significant effect of splenectomy on overall survival or NRM in a large cohort of splenectomized patients undergoing allogeneic SCT with either reduced intensity conditioning (RIC) or MAC (n=180) registered in the EBMT registry database and nor did the retrospective Center for International Blood and Marrow Transplant Research (CIBMTR) study.3534 Moreover, given the potential splenic effects of JAK inhibitor therapy, alternative methods of reducing bulky splenomegaly are possible. Lastly, it is unknown what effect pre-transplant spleen removal will have on immune reconstitution. In general, it is the view of the authors that pre-transplant splenectomy cannot be routinely recommended although it is clear that individual patient-stratified assessment should occur. Low-dose splenic irradiation prior to transplantation has been explored in small cohorts of patients, but overall there is insufficient evidence on this strategy.3736

What is the role of JAK inhibitors before transplantation for myelofibrosis?

Many questions arise from the use of JAK inhibitors in the myelofibrosis transplant algorithm. Following the phase III trials, COMFORT-I and –II, confirming the efficacy of the JAK1/JAK2 inhibitor ruxolitinib (Novartis, Switzerland) in myelofibrosis, many potential allogeneic SCT recipients have been treated with this agent.65 JAK inhibitors collectively are attractive agents given that they may improve Performance Status, reduce splenomegaly and potentially shorten time to engraftment and may dampen an inherently pro-inflammatory milieu. Earlier and more recent studies demonstrated that, in general, there were no serious adverse effects following the use of JAK inhibitors prior to allogeneic SCT with appropriate tapering.4038 Of note the French phase II JAK ALLO trial, investigating the use of ruxolitinib before allogeneic SCT, was temporarily halted because of two cases of febrile cardiogenic shock and one of tumor lysis syndrome following ruxolitinib discontinuation.41 Subsequent experience has not demonstrated that either of these adverse events is common. Outcomes of 100 patients who had been exposed to JAK inhibitor therapy and underwent allogeneic SCT, between 2009–2014, were determined in a retrospective, multicenter study.42 The cohort was divided into five groups defined by clinical status/response to JAK inhibition: groups (i) clinical improvement (n=23), (ii) stable disease (n=31), (iii) new cytopenia/increasing blasts/JAK inhibitor intolerance (n=15), (iv) progressive disease: splenomegaly (n=18), and (v) leukemic transformation (n=13). The overall survival rate at 2 years after allogeneic SCT for the entire cohort was 61% (95% CI: 49–71%). The cumulative incidence of grade II-IV acute GvHD by day 100 was 37% (95% CI: 27–47%) and that of chronic GvHD by 2 years was 48%. Survival analyses performed based on response to JAK inhibition prior to allogeneic SCT revealed a 2-year overall survival rate of 91% (95% CI: 69–97%) for patients with clinical improvement. However, it remains unclear whether the better post-transplant outcome in those achieving a clinical improvement was drug-related or simply reflected the presence of an inherently more favorable disease phenotype. A multicenter, German study reported on 159 patients, 46 of whom had received pre-transplant ruxolitinib at any point with a median treatment duration of 4.9 months (range, 0.4-39.1 months).43 There was a trend towards a lower rate of relapse in the ruxolitinib group (9% versus 17%, P=0.2), with similar disease-free and overall survival rates. The hypothesis that pre-exposure to JAK inhibitors may modulate the relapse risk requires further exploration. In a recently published study of a small cohort of patients (n=12) undergoing allogeneic SCT for myelofibrosis, ruxolitinib (5 mg BID) was continued until stable engraftment.44 There was no graft failure and timely neutrophil engraftment, although the drug had to be discontinued in two patients, on days +17 and +18, because of post-engraftment cytopenia. Of particular relevance, the rate of grade II-IV acute GvHD within the first 100 days was low at 8% although the cytomegalovirus reactivation rate was 41%. The use of peri-transplantation JAK inhibition to reduce the risk of GvHD remains an area of great interest. In conclusion, the majority of patients in 2018 who proceeded to allogeneic SCT had been exposed to JAK inhibitor therapy. The JAK inhibitor should be tapered down over a 10- to 14-day period so that JAK inhibition therapy is ceased just before the commencement of conditioning or prior to stem cell return. Whether the best strategy for patients receiving JAK inhibitor therapy with a view to allogeneic SCT is to undergo the transplant at the time of best response or whether the procedure should be delayed until a further trigger occurs remains difficult to determine and hence patient-stratified approaches are required. Of note, JAK inhibitors are additionally becoming established in the treatment of steroid refractory GvHD, although this is outside the purpose of this review.45

Conditioning intensity and regimen?

Historically, the majority of MAC platforms consisted of total body irradiation with or without high-dose cyclophosphamide and early toxicity, NRM and GvHD rates were high, especially for older individuals.3525 (Table 2). The large CIBMTR study reported on 289 patients who underwent allogeneic SCT between 1989 and 2002, 79% of whom received MAC – predominantly busulfan + cyclophosphamide and total body irradiation with or without cyclophosphamide.25 The day +100 transplant-related mortality rate was 18% for those undergoing allogeneic SCT from an HLA-matched sibling and 35% for those receiving a graft from an unrelated donor. Approximately one-third of the patients achieved long-term (5 years) relapse-free survival. Kerbauy et al. reported on 104 patients, with a median age of 45 years (range, 18–70 years), 95 of whom received MAC. The NRM rate at 5 years was 34% and there were significant rates of acute grade II-IV GvHD (64%) and chronic GvHD (84%).46 The estimated 5-year survival rate was 61% (95% CI: 43–65%) for the entire cohort. Those undergoing MAC with targeted levels of busulfan in combination with cyclophosphamide (120 mg/kg) had a significantly higher probability of overall survival (68%). For younger recipients planned for MAC allogeneic SCT, our preference is towards busulfan + cyclophosphamide in an attempt to reduce therapy-related morbidity.

Table 2.Summary of outcomes in the main studies on reduced intensity and myeloablative conditioning in myelofibrosis.

Due to age distribution, the vast majority of patients undergoing transplantation will receive RIC. However, the term RIC covers a highly heterogeneous group of treatments as regards both immunosuppressive and moderate myeloablative properties. According to the EBMT consensus, RIC regimens are strictly defined as those which do not fit the definition for MAC or non-myeloablative regimens.47 Historically, published RIC platforms were admixed and reflected local practice (Table 2). The first prospective, EBMT multicenter phase II trial of RIC allogeneic SCT in myelofibrosis enrolled 103 patients between 2002–2007.32 Conditioning was uniform and consisted of busulfan (10 mg/kg) orally (or equivalent IV dose)/fludarabine (180 mg/m) and T-cell depletion achieved with antithymocyte globulin (Fresenius, Graefeling, Germany) at a dose of 3 × 10 mg/kg (for related transplantation) or 3 x 20 mg/kg (for unrelated donor transplantation). Primary graft failure rates were low (~2%) and timely engraftment of both neutrophils (median, 18 days; range, 10–84 days) and platelets >20 × 10/L occurred (median, 22 days; range, 8 -145 days). Rates of acute GvHD were acceptable at 27% for grade II-IV and 11% for grade III-IV. The cumulative incidence of NRM at 1 year was 16% (95% CI: 9–23%) and was significantly higher in the mismatched donor setting than in the fully matched donor setting (38% versus 12%; P=0.003). The cumulative incidences of relapse at 3 and 5 years were acceptable at 22% and 29%, respectively. Multivariate analysis suggested a higher 3-year relapse incidence with splenectomy (HR: 3.6) and Lille HR score (HR: 5.23). HLA-mismatched transplantation was a risk factor for both therapy-related mortality and adverse overall survival. Updated survival analyses revealed estimated 5- and 8-year overall survival rates of 68% and 65%, respectively. More recently, the two most frequently used RIC regimens for myelofibrosis - fludarabine-busulfan (FB) and fludarabine-melphalan (FM) were compared in a retrospective study of 160 patients (FB: n=105, FM: n=55) with a median follow up >5 years.48 Conditioning protocols were uniform, the FM regimen consisted of fludarabine 90 mg/m and melphalan 140 mg/m and the FB regimen consisted of intravenous busulfan (or oral equivalent) 8 mg/kg, fludarabine 180 mg/m and antithymocyte globulin-Fresenius. After statistical weighting, the incidence of acute GvHD was 62% for the FM group and 31% for the FB group while chronic GvHD rates were 49% and 53%, respectively. Although the FM regimen had more pronounced early toxicity, the long-term outcome of patients treated with the two regimens was similar. Multivariate analysis failed to demonstrate significant differences regarding overall survival or disease-free survival although individuals undergoing FM conditioning had relapse rates of <5%. In both groups, the use of a HLA-mismatched unrelated donor was associated with worse outcomes as regards NRM, overall survival and progression-free survival. A prospective, multicenter, phase II MPD-RC study investigated the use of FM conditioning in 66 patients recruited between 2007–2011.49 Those with sibling donors (n=32) received FM whereas those with unrelated donors (n=34) received FM + antithymocyte globulin. Significantly inferior results were seen with unrelated donors than with sibling donors: with a median follow up of 25 months, the overall survival rate was 75% in the sibling group compared to only 32% in the unrelated donor group (HR: 3.9; 95% CI: 1.8-8.9; P<0.001). Moreover, considerable NRM rates were observed in the unrelated donor setting. Of note, this small study did not determine outcome differences between matched or mismatched unrelated donors, in contrast to other studies.3432

There are no current, prospective trials comparing RIC with MAC for myelofibrosis and conclusions from retrospective studies are not always straight forward. In a well-described cohort of 92 patients undergoing allogeneic SCT between 1982–2009, 40 patients received MAC and 52 RIC regimens.27 No differences existed with regards to day +100 transplant-related mortality. The probability of survival at 5 years was 49% for patients given MAC and 59% for those given RIC (P=0.125). However, RIC platforms were associated with markedly improved outcome for those <60 years old compared to those who were older (estimated 5-year survival of 75% versus 20%) and there was a lower incidence of acute GvHD with RIC regimens than with MAC. Almost 10 years ago, Patriarca et al. reported on the 20-year experience of the Gruppo Italiano Trapianto Di Midollo Osseo (GITMO) in which 48 patients underwent MAC and 52 were given RIC regimens.50 Intensity of the conditioning regimen did not significantly influence either overall survival or relapse incidence. More recently, a preliminary analysis from the CMWP of the EBMT by McLornan et al. reported on a total of 2,183 patients who underwent allogeneic SCT for myelofibrosis; regimen intensity was assessed by standard EBMT criteria.34 Conventional MAC regimens were utilized in 760 patients while 1,423 received RIC regimens. Donor sources were similar: MAC cohort, 309 (41%) matched sibling donors and 451 (59%) unrelated donors; RIC cohort, 543 (38%) matched sibling donors and 880 (62%) unrelated donors. In the preliminary analyses, no statistically significant differences in engraftment, GvHD, NRM, progression-free survival and overall survival rates were found between these two large RIC and MAC cohorts; the final multivariate analysis is awaited. Lastly, the exact role of T-cell depletion strategies in allogeneic SCT for myelofibrosis requires clarification. In addition to the above discussions, retrospective analyses by Robin et al., on behalf of EBMT, have demonstrated that in the matched sibling donor setting, use of antithymocyte globulin decreased acute GvHD rates without increasing the relapse risk.51

Alternative donors

Until recently, overall experience remained restricted because of historical fears of graft rejection and GvHD and exclusion from clinical trials. The EBMT group recently described a retrospective study of 56 myelofibrosis patients (median age, 57 years; range, 38–72 years) who underwent mismatched related donor transplantation.52 In this cohort, 70% received MAC and 30% received RIC; the source of hematopoietic stem cells was bone marrow in 66% of cases and peripheral blood in 34%. Conditioning approaches varied, reflecting the heterogeneous nature of this cohort, but the most commonly used was thiotepa, busulfan and fludarabine (TBF) and post-transplant cyclophosphamide. Encouragingly, neutrophil engraftment by day 28 was achieved by 82% of the cohort, at a median time of 21 (range, 19–23) days. Primary graft failure occurred in five patients and secondary graft failure in seven, with two patients dying before engraftment. The cumulative incidence of acute GvHD at day +100 was 28% for grade II-IV and 9% for grade III-IV disease. The cumulative incidence of chronic GvHD at 1 year was 45%. The 1- and 2-year overall survival rates were 61% (range, 48–74%) and 56% (range, 41–70%), respectively. The cumulative incidence of relapse was 19% (range, 7–31%) and the NRM was 38% (range, 24–51%) at 2 years. The exact role of transplantation from mismatched related donors in myelofibrosis does, therefore, require further clarification but this study demonstrates that engraftment is feasible with acceptable rates of GvHD and overall survival, although cumulative NRM rates remain somewhat high.

In the setting of myelofibrosis, Takagi et al. initially reported on 14 patients who had undergone RIC umbilical cord blood transplantation, predominantly high-risk candidates with secondary acute myeloid leukemia.53 Neutrophil engraftment was achieved in the vast majority (92%) at a median of 23 days and full donor chimerism, where evaluable, was rapidly achieved. Survival was poor with a 4-year overall survival rate of only 28%, perhaps not surprisingly given the high-risk population. More recently, a series of 35 umbilical cord blood transplant recipients (median age, 54 years), registered under EUROCORD, was reported: seven had developed blast phase myelofibrosis and almost half underwent splenectomy.54 The most common conditioning regimen was total body irradiation, cyclophosphamide and fludarabine (TCF). Cord blood units were 5/6 (23%) and 4/6 (77%) HLA-matched. Neutrophil engraftment was achieved in 28/35 patients at a median time of 30 days and a total of 14 patients displayed graft failure (4 underwent a second transplant procedure). The 2-year overall and event-free survival rates were 44% and 30% respectively. In the RIC setting, all recipients undergoing TCF conditioning achieved both neutrophil and platelet engraftment and there was an association between utilization of this regimen and improved event-free survival.

Blast phase myelofibrosis and allogeneic stem cell transplantation

Historically, the outcome of patients with blast phase myeloproliferative neoplasms has been extremely poor. A recent retrospective analysis of 410 patients with blast phase myeloproliferative neoplasms, not focusing on allogeneic SCT, revealed a sobering median survival of 3.5 months.55 Intensive chemotherapy resulted in complete remission or complete remission with incomplete count recovery rates of 35% and 24%, respectively, and even following allogeneic SCT the 3-year survival rate was 32%. This retrospective work suggested that allogeneic SCT has a role in improving short-term survival but durability of response remains under question although the authors did acknowledge that the overall cohort of patients who underwent allogeneic SCT was small. The EBMT group published data on 46 patients who underwent allogeneic SCT for blast phase myelofibrosis and confirmed the importance of achieving complete remission prior to transplantation, which was also demonstrated in a retrospective collaborative French study.5756 The transplant-related mortality rate at 1 year was acceptable at 28% and the 3-year progression-free and overall survival rates were 26% and 33%, respectively. The impact of both karyotype and mutational landscape on determining outcomes following transplantation for blast phase myelofibrosis is an area of active research and consideration should be given to post-transplant maintenance strategies.

Post-transplant outcomes and complications

Early studies investigating the impact of the mutational landscape on the outcomes of allogeneic SCT yielded conflicting results.5832 Retrospective studies revealed a significant adverse impact of lack of the JAK2 mutation on overall survival after allogeneic SCT for myelofibrosis whereas a CALR mutation was associated with improved overall survival and less NRM.6059 The impact of more extensive mutational profiling was recently investigated in a large retrospective study.61 A targeted 16-gene panel was used to analyze a total of 169 patients (110 with primary myelofibrosis, 46 with secondary myelofibrosis and 13 in transformation). Multivariate analysis revealed that the presence of a CALR mutation was associated with favorable overall survival (HR: 0.448; P=0.03) and progression-free survival (HR: 0.393; P=0.01), and reduced NRM (HR, 0.415; P=0.05). Additionally, both IDH2 and ASXL1 mutations were independent prognostic risk factors for reduced progression-free survival (HR: 5.451; P=0.002 and HR: 1.53; P=0.008, respectively). Interestingly, ‘triple negativity’ did not appear to have a significant effect on post-transplant outcomes in this cohort although the numbers analyzed were small. Overall, where possible and dependent on local facilities, we recommend that a targeted gene panel is used to determine the mutational risk profile.

Despite initial engraftment, it is well established that poor graft function can be problematic and patients may remain transfusion dependent and/or require growth factor support for a considerable period. Alchalby et al. reported that the cumulative incidence of poor graft function was 17% in a cohort of 100 RIC allogeneic SCT patients and that the median onset of this complication was day +49 (range, 24–99 days).62 Poor graft function was defined by either two or three cytopenias (hemoglobin <100 g/L, neutrophil count <1.0×10/L, platelet count <30×10/L) at day +30 after allogeneic SCT, with transfusion requirements in the presence of complete donor chimerism and an absence of severe GvHD/disease relapse. Persistence of significant splenomegaly at day +30 remained a significant risk factor for poor graft function and univariate analysis revealed an association with older recipient age, perhaps reflecting age-related changes in a hostile bone marrow niche. Poor graft function did not appear to influence survival. Of relevance, Hart et al. recently compared engraftment kinetics in a small cohort of acute myeloid leukemia and myelofibrosis allogeneic SCT recipients.63 Compared to the group with acute myeloid leukemia, the myelofibrosis patients had marked early clearance of hematopoietic stem cells due to early splenic pooling accompanied by a significant reduction in VCAM1 expression in the bone marrow niche which may well explain, in part, the observed early poor graft function. Whether JAK inhibitor-mediated reductions in splenomegaly will result in lower incidences of poor graft function remains undetermined. Judicious monitoring of chimerism and appropriate growth factor and transfusion support are necessitated by the recognition that some patients may require stem cell top up or consideration given to splenectomy if bulky splenomegaly persists.

Measurable residual disease (MRD) monitoring to guide weaning of immunosuppression with or without utilization of immunotherapeutic strategies has become well established in the setting of allogeneic SCT for myelofibrosis. Alchalby et al. demonstrated that clearance of detectable JAK2 after allogeneic SCT was associated with a significantly reduced risk of relapse.59 Both MPL and CALR mutations can be used as markers of MRD.6564 More recently, the significance of MRD was evaluated in a large, single-center cohort (n=136), in which pre-transplant molecular profiling revealed JAK2 (n=101), MPL (n=4) and CALR (n=31) mutations.66 Individuals with a detectable mutation at either day +100 or day +180 had a significantly higher risk of clinical relapse at 5 years compared to those in whom molecular studies were negative (62% versus 10%, P<0.001 and 70% versus 10%, P<0.001, respectively). Multivariate modeling revealed that detectable MRD at day +180 and high-risk disease status were significant factors associated with higher relapse rates. MRD status and chimerism studies should be used in tandem to determine whether donor lymphocyte infusions are required. Kroger et al. described the use of both pre-emptive (n=8) and salvage donor lymphocyte infusion (n=9) regimens in 17 myelofibrosis patients undergoing allogeneic SCT, highlighting the utility of MRD monitoring for guiding donor lymphocyte infusions and that pre-emptive strategies take precedence over salvage approaches.67

Relapse remains a significant issue following allogeneic SCT for myelofibrosis. Longer term follow-up of the EBMT prospective study described above suggested relapse rates of up to 25% at 5 years.32 A more recent EBMT retrospective study by McLornan et al. investigated the management and outcomes of 202 relapsed patients.68 The overall median time to relapse was relatively short at 7 months (range, 1.4-111). Patients who relapsed early had significantly worse outcomes than those of patients who relapsed later. Management approaches to the relapse episode were heterogeneous and direct comparisons were not possible; however, there was a suggested benefit from adoptive immunotherapeutic approaches with donor lymphocyte infusions and/or a second allograft. There is some experience on the use of using JAK inhibitors following relapse to bridge to a second transplant and for symptom control but no improvements in donor chimerism or reductions in JAK2 allelic burden, where applicable, were seen.69 Pre-emptive use of JAK inhibitors in the post-transplant setting to reduce relapse incidence is of interest and requires prospective studies.

Conclusions

Rapid advances in the availability of novel therapeutic agents for myelofibrosis has made it increasingly complex to gauge the timing and sequencing of allogeneic SCT in the patient’s care process. Nonetheless, allogeneic SCT remains the only curative approach for transplant-eligible patients. All available prognostic information and recent scoring systems should be utilized, including comprehensive mutational profiling where available, to stratify realistic patient-specific prognostic outcomes and assess the risk-benefit ratio. Changes in practice are required so that potential candidates are assessed by transplant physicians at an earlier stage, even if this is only to discuss and provide information about the procedure, assess fitness and identify potential donors. JAK inhibitors have become an integral part of the pre-allogeneic SCT pathway for many patients and increasing data on outcome analysis are now available. Overall, the use of these drugs prior to allogeneic SCT appears to be safe, with no adverse effects on engraftment; tapering is appropriate leading up to conditioning therapy and there is emerging data concerning potential reductions in the risks of GvHD and relapse, although these need confirmation. Alertness to potential infectious complications is warranted. How the role of other novel agents will fit into the transplant paradigm remains unknown. Current challenges regarding allogeneic SCT are to reduce the relapse risk and rates of NRM, particularly when using alternative donors, and optimization of graft function.

Footnotes

• ↵* CNH and NK: joint senior authors
• Check the online version for the most updated information on this article, online supplements, and information on authorship & disclosures: www.haematologica.org/content/104/4/659

• Received September 9, 2018.
• Accepted November 16, 2018.