Publication
Long-Term Sustained Disease Control in Patients With Mantle Cell Lymphoma With or Without Active Disease After Treatment With Allogeneic Hematopoietic Cell Transplantation After Nonmyeloablative Conditioning
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- Persistent URL
- Last modified
- 02/25/2025
- Type of Material
- Authors
- Language
- English
- Date
- 2015-07-24
- Publisher
- Wiley-Blackwell
- Publication Version
- Copyright Statement
- © 2015 American Cancer Society.
- Final Published Version (URL)
- Title of Journal or Parent Work
- Volume
- 121
- Issue
- 20
- Start Page
- 3709
- End Page
- 3716
- Grant/Funding Information
- This study was supported by grants CA018029, CA15704, CA078902, HL088021 and 5T32HL007093-38 from the National Heart Lung Blood Institute, the National Institutes of Health.
- M.L.S. is also supported by a Research Scholar Grant No. RSG-13- 084-01-CPHPS from the American Cancer Society; and by Patient-Centered Outcome Research Institute Contract No. CE-1304-7451.
- Abstract
- BACKGROUND Previously, early results were reported for allogeneic hematopoietic cell transplantation (HCT) after nonmyeloablative conditioning with 2 Gy of total body irradiation with or without fludarabine and/or rituximab in 33 patients with mantle cell lymphoma (MCL). METHODS This study examined the outcomes of 70 patients with MCL and included extended follow-up (median, 10 years) for the 33 initial patients. Grafts were obtained from human leukocyte antigen (HLA)-matched, related donors (47%), unrelated donors (41%), and HLA antigen-mismatched donors (11%). RESULTS The 5-year incidence of nonrelapse mortality was 28%. The relapse rate was 26%. The 5-year rates of overall survival (OS) and progression-free survival (PFS) were 55% and 46%, respectively. The 10-year rates of OS and PFS were 44% and 41%, respectively. Eighty percent of surviving patients were off immunosuppression at the last follow-up. The presence of relapsed or refractory disease at the time of HCT predicted a higher rate of relapse (hazard ratio [HR], 2.94; P =.05). Despite this, OS rates at 5 (51% vs 58%) and 10 years (43% vs 45%) were comparable between those with relapsed/refractory disease and those undergoing transplantation with partial or complete remission. A high-risk cytomegalovirus (CMV) status was the only independent predictor of worse OS (HR, 2.32; P =.02). A high-risk CMV status and a low CD3 dose predicted PFS (HR, 2.22; P =.03). CONCLUSIONS Nonmyeloablative allogeneic HCT provides a long-term survival benefit for patients with relapsed MCL, including those with refractory disease or multiple relapses.
- Author Notes
- Keywords
- MARROW TRANSPLANTATION
- CLINICAL-TRIAL
- VERSUS-HOST-DISEASE
- Science & Technology
- conditioning regimen
- NON-HODGKINS-LYMPHOMA
- GRAFT
- Life Sciences & Biomedicine
- BLOOD
- REDUCED-INTENSITY
- nonmyeloablative conditioning
- stem cell transplantation
- MOLECULAR REMISSIONS
- MALIGNANCY
- Oncology
- mantle cell lymphoma
- long-term follow-up
- FOLLOW-UP
- Research Categories
- Health Sciences, Oncology
- Health Sciences, General
- Biology, Cell
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