Haploidentical BMT for severe aplastic anemia with intensive GVHD prophylaxis including posttransplant cyclophosphamide

Author:

DeZern Amy E.12,Zahurak Marianna L.13,Symons Heather J.14,Cooke Kenneth R.14,Rosner Gary L.3,Gladstone Douglas E.1,Huff Carol Ann1,Swinnen Lode J.1,Imus Philip1,Borrello Ivan1ORCID,Wagner-Johnston Nina1,Ambinder Richard F.1ORCID,Luznik Leo1,Bolaños-Meade Javier1,Fuchs Ephraim J.1,Jones Richard J.12,Brodsky Robert A.12

Affiliation:

1. Department of Oncology, Sidney Kimmel Cancer Center, Baltimore, MD;

2. Division of Hematology, Department of Medicine, Johns Hopkins University, Baltimore, MD; and

3. Department of Oncology Biostatistics and

4. Division of Pediatric Oncology, Sidney Kimmel Cancer Center, Baltimore, MD

Abstract

Abstract Severe aplastic anemia (SAA) is a stem cell disorder often treated with bone marrow transplantation (BMT) to reconstitute hematopoiesis. Outcomes of related HLA-haploidentical (haplo) donors after reduced-intensity conditioning with intensive graft-versus-host disease (GVHD) prophylaxis including posttransplantation cyclophosphamide are presented here from 37 SAA, 20 relapsed/refractory (R/R), and 17 treatment-naïve (TN) SAA patients. Median follow-up is 32 months (90% confidence interval [CI], 29-44). The median age was 25 (range, 4-69) years. The median time to neutrophil recovery was 17 days (range, 15-88). Four of 37 patients (11%) experienced graft failure (GF). There was 1 primary GF of 20 patients in the R/R group and 3 of 17 in the TN group at 200 cGy (1 primary, 2 secondary), but none in the 10 patients who received 400 cGy total body irradiation. Two patients with GF succumbed to infection and 2 were rescued with second haplo BMT. The overall survival for all patients is 94% (90% CI, 88-100) at 1 and 2 years. The cumulative incidence of grade II-IV acute GVHD at day 100 is 11%. The cumulative index of chronic GVHD at 2 years is 8%. Similar results were seen in 10 SAA patients who received the identical nonmyeloablative regimen with posttransplant cyclophosphamide but matched donor transplants. Haplo BMT with posttransplant cyclophosphamide represents a potential cure in SAA, with all 20 R/R currently alive, disease-free, and with no evidence of active GVHD. Extending this approach to TN patients was associated with higher GF rates, but an increase in total body irradiation dose to 400 cGy was associated with durable engraftment without greater early toxicity. Nonmyeloablative haplo BMT in TN SAA could lead to a paradigm shift, such that essentially all patients can proceed quickly to safe, curative BMT. These trials were registered at www.cincialtrials.gov as #NCT02224872) and #NCT02833805.

Publisher

American Society of Hematology

Subject

Hematology

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