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Volume 14, Issue 7, Pages 775-782 (July 2008)


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Favorable Overall Survival with Fully Myeloablative Allogeneic Stem Cell Transplantation for Follicular Lymphoma

John Kuruvilla12Corresponding Author Informationemail address, Gregory Pond3, Richard Tsang4, Vikas Gupta12, Jeffrey H. Lipton12, Hans A. Messner12

Received 24 October 2007; accepted 13 April 2008.

Abstract 

Allogeneic stem cell transplantation (Allo-SCT) remains an option for patients with follicular lymphoma (FL). We performed a retrospective analysis to examine long-term disease control and treatment-related mortality (TRM) in a group of patients that underwent transplant for clinically high-risk disease. Thirty-seven patients with indolent FL (follicular small cleaved [FSC], follicular mixed [FM] or FL grades 1 or 2 by WHO criteria) underwent allo-SCT. Patients were in a chemosensitive remission at the time of SCT. The conditioning regimen was typically busulfan-cyclophosphamide (BuCy). Cyclophosphamide-total body irradiation (TBI) was used for unrelated donor SCT. The median age at the time of transplant was 45 years (range: 24-58). The median number of prior chemotherapy regimens was 3 (range: 1-6). Thirty-seven patients received BuCy conditioning and 2 patients underwent reduced intensity conditioning SCT. Seventy-two percent of patients had a matched sibling donor. With a median follow-up of 63.5 months in survivors, the 5-year overall survival is 79.1% (95% confidence interval 66.3%-94.4%). TRM was 15.4%, with an additional case of mortality from breast cancer. These results demonstrate that in selected younger patients, a fully myeloablative allo-SCT utilizing BuCy conditioning provides excellent OS and disease control with low TRM.

1 Allogeneic Blood and Marrow Transplant Programme, Princess Margaret Hospital, Toronto, Canada

2 Division of Medical Oncology and Hematology, Princess Margaret Hospital, Toronto, Canada

3 Clinical Study Coordination and Biostatistics, Princess Margaret Hospital, Toronto, Canada

4 Department of Radiation Oncology, Princess Margaret Hospital, Toronto, Canada

Corresponding Author InformationCorrespondence and reprint requests: John Kuruvilla, MD, FRCPC, Princess Margaret Hospital, Division of Medical Oncology & Hematology, 610 University Avenie, Room 5-108, Toronto, Canada M5G 2M9.

PII: S1083-8791(08)00151-1

doi:10.1016/j.bbmt.2008.04.007


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