Abstract

Myelodysplastic syndromes (MDS) are a diverse group of hematological malignancies distinguished by a combination of dysplasia in the bone marrow, cytopenias and the risk of leukemic transformation. The hallmark of MDS is bone marrow failure which occurs due to selective growth of somatically mutated clonal hematopoietic stem cells. Multiple prognostic models have been developed to help predict survival and leukemic transformation, including the international prognostic scoring system (IPSS), revised international prognostic scoring system (IPSS-R), WHO prognostic scoring system (WPSS) and MD Anderson prognostic scoring system (MDAPSS). This risk stratification informs management as low risk (LR)-MDS treatment focuses on improving quality of life and cytopenias, while the treatment of high risk (HR)-MDS focuses on delaying disease progression and improving survival. While therapies such as erythropoiesis stimulating agents (ESAs), erythroid maturation agents (EMAs), immunomodulatory imide drugs (IMIDs), and hypomethylating agents (HMAs) may provide benefit, allogeneic blood or marrow transplant (alloBMT) is the only treatment that can offer cure for MDS. However, this therapy is marred, historically, by high rates of toxicity and transplant related mortality (TRM). Because of this, alloBMT is considered in a minority of MDS patients. With modern techniques, alloBMT has become a suitable option even for patients of advanced age or with significant comorbidities, many of whom who would not have been considered for transplant in prior years. Hence, a formal transplant evaluation to weigh the complex balance of patient and disease related factors and determine the potential benefit of transplant should be considered early in the disease course for most MDS patients. Once alloBMT is recommended, timing is a crucial consideration since delaying transplant can lead to disease progression and development of other comorbidities that may preclude transplant. Despite the success of alloBMT, relapse remains a major barrier to success and novel approaches are necessary to mitigate this risk and improve long term cure rates. This review describes various factors that should be considered when choosing patients with MDS who should pursue transplant, approaches and timing of transplant, and future directions of the field.

Highlights

  • Myelodysplastic syndromes (MDS) are a group of hematologic malignancies characterized by a combination of bone marrow (BM) dysplasia, cytopenias and risk of leukemic transformation [1]

  • The hallmark of MDS is bone marrow failure which occurs due to selective growth of somatically mutated clonal hematopoietic stem cells [6]

  • A critical deficiency of these predictive models is the absence of somatic mutations in the models; because of this, some patients deemed low risk (LR)-MDS by the international prognostic scoring system (IPSS)-R score may progress more rapidly than predicted

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Summary

INTRODUCTION

Myelodysplastic syndromes (MDS) are a group of hematologic malignancies characterized by a combination of bone marrow (BM) dysplasia, cytopenias and risk of leukemic transformation [1]. Other complications accompanying MDS include risk of infections, bleeding, iron overload, and cardio-pulmonary compromise [2]. The incidence of MDS increases with advancing age. The longterm overall survival (OS) of patients with MDS is 31.3% at 5 years [2]. There is a large disparity in OS of MDS patients based on specific prognostic disease characteristics. Allogeneic blood or marrow transplantation (alloBMT) remains the only potential curative treatment and offers an OS benefit in eligible high risk MDS patients. AlloBMT is associated with a risk of transplant related (TRM) due to infections, graft versus host disease (GVHD), chemotherapy related toxicities, rejection and relapse. The potential benefit of alloBMT may be negated in patients at high risk for TRM and relapse, so careful evaluation by a transplant specialist is necessary to identify suitable candidates. In this review we describe the indications and timing of transplant, transplant approaches, and post-transplant outcomes of patients with MDS

Cytopenias
Cytogenetics
Somatic Mutations
Prognostic Models
AlloBMT Indications
AlloBMT Eligibility
Disease Related Prognostic Factors
Donor Type
Treatment for MDS Preceding AlloBMT
Timing of Transplant
Conditioning for Transplant
Post-Transplant Maintenance Strategies
Relapse Post-AlloBMT
Therapy Related MDS
Hypoplastic MDS
MDS Originating From Germ Line Mutations
CONCLUSIONS
Findings
Results
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