Abstract 833

HLA-identical siblings (MRD) or 10 of 10 HLA - A, B, C, DRB1 and DQB1 matched unrelated volunteers (MUD) are considered optimal donors for patients who may benefit from allogeneic hematopoietic cell transplantation (allo-HCT). However, many patients, particularly those from ethnic minorities and mixed race backgrounds, will lack such donors.

HLA-haploidentical (Haplo) relatives are available for virtually all patients. Traditional approaches to allo-HCT using Haplo donors have entailed stringent ex-vivo T-cell depletion and intense preparative regimens. Such transplants have been associated with slow immune reconstitution and a high-risk of opportunistic infections and non-relapse mortality (NRM). Recently, another approach to haploidentical transplantation using T-replete grafts and post-transplant cyclophosphamide (Cy) to prevent graft versus host disease (GVHD) and rejection has demonstrated promising results (Brunstein et al Blood 2011, vol118, p 282).

Forty-Five patients underwent first allografts with a Haplo donor at our center between 02/05 and 08/10 (median age=46, range 20–73; diagnoses were AML 14, ALL 6, CML 4, MDS 4, CLL 7, NHL 4, HD 6; median KPS 90, range 70–90; CIBMTR disease risk score low 14, intermediate 7, high 24; median hematopoietic cell transplant co-morbidity index (HCTCI) score = 1, range 0–5; prior autotransplant = 7). Twenty-seven patients received a reduced-intensity conditioning regimen (RIC): fludarabine 30 mg/m2/d d −6 to −2; TBI 200cGy d-1, Cy 14.5 mg/kg/d on d-6,-5 and 50mg/kg/d on d+3,+4 with a bone marrow graft. Eighteen patients received myeloablative conditioning where the above regimen was modified by replacing low-dose TBI with iv busulfan 110–130 mg/m2/d × 4 days and bone marrow was replaced with G-CSF mobilized PBSC as the graft. Two patients receiving RIC failed to engraft and developed autologous hematopoietic recovery. All other patients engrafted with median 100% donor T-cell chimerism from initial testing at d+30. Outcomes of the Haplo transplants were compared to contemporaneous first allografts from MRD (n=115) and MUD (n=99) at our center. Median follow-up for surviving patients was 36 months (range 9–74.5 months). Cumulative probability of NRM at 36 months was 16%, 19% and 8% for MRD, MUD and Haplo respectively (p=NS) (see Fig). For both overall survival (OS) and disease-free survival (DFS), the effects of patient and disease characteristics were evaluated in Cox models with three transplant groups as strata. HCTCI score, CIBMTR risk category, type of diagnosis were identified as significant covariates on both OS and DFS, while age was significant on DFS only. The adjusted probabilities of OS and DFS were estimated from the stratified Cox models, weighted by the proportions of the significant covariates in the pooled sample. MRD had statistically superior OS to Haplo at 18 months (79% vs. 61%, p=0.033 in point wise comparison). However, adjusted OS was not significantly different between the three types of transplant at 36 months (71%, 58% and 58% for MRD, MUD and Haplo respectively (p=NS)). Adjusted DFS at 36 months was 47%, 46% and 55% respectively (p=NS) (see Fig). Ninety-three patients (35.7%) suffered relapse or progression of their malignancy at a median of 154 days post transplant (range 12–1445 days). Estimated cumulative incidence of relapse at 36 months was 35%, 38% and 36% respectively for MRD, MUD and Haplo (p=NS) (see Fig). The inverse probability of censoring weighted (IPCW) method was used to determine survival following relapse/progression in each group. Estimated survival at 1 year following relapse was 71%, 64% and 15% (p<0.0001 pointwise comparison for MRD vs. Haplo and MUD vs. Haplo).

This study demonstrates that excellent NRM and DFS can be achieved using haploidentical donor transplantation with the above regimens. These outcomes are equivalent to those obtained in contemporaneously transplanted MRD and MUD at our center. T-cell replete haploidentical transplant is therefore a valid alternative for patients who lack a conventional donor. Survival following relapse/progression is inferior following haploidentical than conventional donor transplants. This may at least partly be related to the difficulty in using DLI following relapse in haploidentical transplants. Future strategies to improve outcomes following haploidentical transplants should focus on treatment approaches following relapse.
graphic
View largeDownload slide
graphic
View largeDownload slide
Disclosures:

Bashey:Otsuka America Pharmaceuticals, Inc: Research Funding. Sizemore:Otsuka America Pharmaceuticals, Inc: Research Funding. Manion:Otsuka America Pharmaceuticals, Inc: Research Funding. Brown:Otsuka America Pharmaceuticals, Inc: Research Funding. Holland:Otsuka America Pharmaceuticals, Inc.: Research Funding. Solomon:Otsuka America Pharmaceuticals, Inc: Research Funding. Morris:Otsuka America Pharmaceuticals, Inc: Research Funding.

Topics:
cyclophosphamide, donors, haploidentical transplantation, human leukocyte antigens, relationship - sibling, t-lymphocytes, transplantation, allografting, allopurinol, graft-versus-host disease

Author notes

*

Asterisk with author names denotes non-ASH members.

© 2011 by The American Society of Hematology
2011
Sign in via your Institution