Clinical Allogeneic Transplantation: Conditioning Regimens, Engraftment and Acute Transplant Toxicities
Oral and Poster Abstracts
721. Clinical Allogeneic Transplantation: Conditioning Regimens, Engraftment and Acute Transplant Toxicities: Poster I
Hall A, Level 2
(Orange County Convention Center)
Moaath Mustafa Ali, MD1*, Donna M Abounader2*, Lisa A. Rybicki, MS3*, Melissa A Yurch2*, Jamie Starn, RN, BSN2*, Christina Ferraro, RN, BSN2*, Victoria Winslow, RN, BSN2*, Betty K. Hamilton, MD2,4, Aaron T. Gerds, MD, MS5, Hien Liu, MD2*, Robert Dean2, Brian T. Hill, MD. PhD2, Brad Pohlman, MD2, Steven Andresen, DO2*, Rabi Hanna, MD6, Matt Kalaycio, MD5, Brian J. Bolwell, MD2, Navneet S. Majhail, MD, MS2 and Ronald Sobecks, MD2
1Internal Medicine, Cleveland Clinic, Cleveland, OH
2Blood and Marrow Transplant, Department of Hematology and Medical Oncology, Cleveland Clinic Taussig Cancer Institute, Cleveland Clinic, Cleveland, OH
3Quantitative Health Sciences, Cleveland Clinic Lerner Research Institute, Cleveland, OH
4Blood and Marrow Transplant Program, Department of Hematology and Medical Oncology, Cleveland Clinic Taussig Cancer Institute, Cleveland, OH
5Leukemia Program, Cleveland Clinic, Cleveland, OH
6Pediatric Hematology/Oncology, Cleveland Clinic, Cleveland, OH
Reduced intensity conditioning for allogeneic hematopoietic cell transplantation (alloHCT) has become a standard approach for older patients and for those with co-morbidities that prohibit myeloablative conditioning. The optimal conditioning regimen for patients with AML or MDS undergoing such transplants is not clear. Therefore we performed a single center, retrospective analysis comparing busulfan (100 mg/m
2/day on days -5, -4, -3, -2) and fludarabine (40 mg/m
2/day on days -5, -4, -3, -2) (BuFlu) versus fludarabine (30 m
2/day on days -5, -4, -3) and 400 cGy total body irradiation (200 cGy on days -1 and 0) (FluTBI) conditioning. All of the BuFlu transplants were performed as inpatient hospitalizations while all of those with FluTBI were performed as an outpatient. A total of 71 patients in two cohorts were included. The first study cohort consisted of 38 patients (23 AML, 15 MDS) who received FluTBI from 3/2004-4/2010, and the second included 33 (20 AML, 13 MDS) patients conditioned with FluBu from 6/2010-12/2013. The groups had similar disease risk and HCT comorbidity index scores. The BuFlu patients were older (median age 65 [range, 34-73] vs. 61[range, 44-70] years, P=0.03), but there were no other differences in patient or disease characteristics. All patients received peripheral blood stem cells as the graft source. The donor sources were 53% matched related (MRD) and 47% matched unrelated (MUD) for FluTBI patients and 58% MRD and 42% MUD for BuFlu patients. The BuFlu group received more red blood cell (RBC) transfusions (median 4 vs. 2, P=0.02), but there were no differences in platelet transfusion requirements. Platelet recovery was longer for patients receiving BuFlu than FluTBI (median 16 vs. 12 days, P=0.004), but there was no difference in cumulative incidence of neutrophil recovery. The respective median number of days hospitalized in the first 100 days post-transplant was 22 vs. 10 days (P<0.001) and in the first year was 40 vs. 16 days (P<0.001). Post-transplant outcomes are shown in the Table. The most common causes of death were relapse and infection for both the FluTBI (44% and 13%) and BuFlu (57% and 14%) groups. Quality of life assessments using the FACT-BMT were performed pre-alloHCT, at day 100, 6 months and 1 year. There was no difference in physical, social, emotional, and functional well-beings, additional concerns, trial outcome index or total score between the two groups at baseline or any of the follow-up timepoints. We conclude that alloHCT using FluTBI or BuFlu reduced intensity conditioning regimens results in comparable outcomes in patients with AML/MDS. The greater RBC transfusion requirement and need for inpatient hospitalization with the BuFlu regimen have implications for healthcare resource utilization. Future prospective investigation comparing these regimens with larger patient cohorts and cost-effectiveness analyses are warranted.
Table: Patient outcomes
Variable
|
FluTBI
N (%)
|
BuFlu
N (%)
|
P-value
|
T-cell complete donor chimerism
|
29 (78)
|
26 (81)
|
0.83
|
Graft failure/rejection
|
3 (8)
|
3 (9)
|
0.87
|
Grade II-IV acute GvHD
|
13 (34)
|
17 (52)
|
0.24
|
Grade III-IV acute GvHD
|
3 (8)
|
6 (18)
|
0.21
|
Any Chronic GvHD
|
16 (42)
|
14 (42)
|
0.91
|
Extensive chronic GvHD
|
8 (21)
|
13 (39)
|
0.06
|
CMV reactivation
|
12 (32)
|
13 (39)
|
0.66
|
Fungal Infection
|
2 (5)
|
1 (3)
|
0.83
|
Relapse (2-years)
|
20 (53)
|
17 (52)
|
0.96
|
100 day mortality
|
13 (95% CI 6-29 )
|
9 (95% CI 3-26 )
|
0.59
|
Non-relapse mortality (2-years)
|
29 (95% CI 15-44)
|
29 (95% CI 14-45)
|
0.56
|
Relapse mortality (2-years)
|
34 (95% CI 20-49)
|
36 (95% CI 20-53)
|
0.86
|
Overall survival (2-years)
|
37 (95% CI 22-52)
|
35 (95% CI 19-51)
|
0.73
|
Disclosures: Majhail: Gamida Cell Ltd.:
Consultancy
; Anthem Inc.:
Consultancy
.
*signifies non-member of ASH