Reduced-Intensity Conditioning with Fludarabine, Cyclophosphamide, and High-Dose Rituximab for Allogeneic Hematopoietic Cell Transplantation for Follicular Lymphoma: A Phase Two Multicenter Trial from the Blood and Marrow Transplant Clinical Trials Networ

TitleReduced-Intensity Conditioning with Fludarabine, Cyclophosphamide, and High-Dose Rituximab for Allogeneic Hematopoietic Cell Transplantation for Follicular Lymphoma: A Phase Two Multicenter Trial from the Blood and Marrow Transplant Clinical Trials Networ
Publication TypeJournal Article
Year of Publication2016
AuthorsLaport, GG, Wu, J, Logan, B, Bachanova, V, Hosing, C, Fenske, T, Longo, W, Devine, SM, Nademanee, A, Gersten, I, Horowitz, M, Lazarus, HM, Riches, ML
Corporate AuthorsBlood and Marrow Transplant Clinical Trials Network
JournalBiol Blood Marrow Transplant
Volume22
Issue8
Pagination1440-1448
Date Published2016 08
ISSN1523-6536
KeywordsAdult, Aged, Antineoplastic Agents, Immunological, Cyclophosphamide, Graft vs Host Disease, Hematopoietic Stem Cell Transplantation, Humans, Lymphoma, Follicular, Middle Aged, Myeloablative Agonists, Recurrence, Remission Induction, Rituximab, Salvage Therapy, Survival Analysis, Transplantation Conditioning, Transplantation, Homologous, Treatment Outcome, Vidarabine
Abstract

Allogeneic (allo) hematopoietic cell transplantation (HCT) can induce long-term remissions in chemosensitive relapsed follicular lymphoma (FL). The Blood and Marrow Transplant Clinical Trials Network conducted a multicenter phase 2 trial to examine the efficacy of alloHCT using reduced-intensity conditioning with rituximab (RTX) in multiply relapsed, chemosensitive FL. The primary endpoint was 2-year progression-free survival (PFS). The conditioning regimen consisted of fludarabine, cyclophosphamide, and high-dose RTX (FCR), in which 3 of the 4 doses of RTX were administered at a dose of 1 gm/m(2). Graft-versus-host disease (GVHD) prophylaxis was with tacrolimus and methotrexate. Sixty-five patients were enrolled and 62 were evaluable. Median age was 55 years (range, 29 to 74). This group was heavily pretreated: 77% had received ≥ 3 prior regimens, 32% had received ≥ 5 prior regimens, and 11% had received prior autologous HCT. Donors were HLA-matched siblings (n = 33) or HLA-matched unrelated adults (n = 29). No graft failures occurred. The overall response rate after HCT was 94% with 90% in complete remission (CR), including 24 patients not in CR before alloHCT. With a median follow-up of 47 months (range, 30 to 73), 3-year PFS and overall survival rates were 71% (95% confidence interval, 58% to 81%) and 82% (95% confidence interval, 70% to 90%), respectively. Three-year cumulative incidences of relapse/progression and nonrelapse mortality were 13% and 16%, respectively. Two-year cumulative incidences of grades 2 to 4 and grades 3 or 4 acute GVHD were 27% and 10%, respectively, and extensive chronic GVHD incidence was 55%. Serum RTX concentrations peaked at day +28 and remained detectable as late as 1 year in 59% of patients with available data. In conclusion, alloHCT with FCR conditioning confers high CR rates, a low incidence of relapse/progression, and excellent survival probabilities in heavily pretreated FL patients.

DOI10.1016/j.bbmt.2016.04.014
Alternate JournalBiol Blood Marrow Transplant
PubMed ID27118571
PubMed Central IDPMC4949103
Grant ListU10 HL069294 / HL / NHLBI NIH HHS / United States
U10 HL069290 / HL / NHLBI NIH HHS / United States
U10 HL069278 / HL / NHLBI NIH HHS / United States
U24 CA076518 / CA / NCI NIH HHS / United States
UL1 TR000114 / TR / NCATS NIH HHS / United States
KL2 TR000113 / TR / NCATS NIH HHS / United States
UG1 HL069278 / HL / NHLBI NIH HHS / United States
U10 HL069334 / HL / NHLBI NIH HHS / United States
U10 HL109137 / HL / NHLBI NIH HHS / United States
U10 CA180820 / CA / NCI NIH HHS / United States
U10 CA180799 / CA / NCI NIH HHS / United States
U10 CA180888 / CA / NCI NIH HHS / United States
U10 CA180853 / CA / NCI NIH HHS / United States