Journal of Clinical Oncology, Vol 22, No 12 (June 15), 2004: pp. 2419-2423
© 2004 American Society of Clinical Oncology.
DOI: 10.1200/JCO.2004.09.092
Nonmyeloablative Allogeneic Hematopoietic Transplantation: A Promising Salvage Therapy for Patients With Non-Hodgkin's Lymphoma Whose Disease Has Failed a Prior Autologous Transplantation
Maricer P. Escalón,
Richard E. Champlin,
Rima M. Saliba,
Sandra A. Acholonu,
Chitra Hosing,
Luis Fayad,
Sergio Giralt,
Naoto T. Ueno,
Farzaneh Maadani,
Barbara Pro,
Michele Donato,
Peter McLaughlin,
Issa F. Khouri
From the Departments of Blood and Marrow Transplantation and Lymphoma, Division of Cancer Medicine, The University of Texas M.D. Anderson Cancer Center, Houston, TX
Address reprint requests to Issa F. Khouri, MD, Department of Blood and Marrow Transplantation, Box 423, The University of Texas M.D. Anderson Cancer Center, 1515 Holcombe Blvd, Houston, TX 77030; e-mail: ikhouri{at}mdanderson.org
PURPOSE: Allogeneic transplantation for patients with lymphoma who experience a recurrence after an autologous transplantation has been considered a hazardous therapeutic choice. We investigated the safety and efficacy of nonmyeloablative stem-cell transplantation in these patients.
PATIENTS AND METHODS: Patients were required to have chemosensitive or stable disease. Twenty consecutive patients were treated in two sequential trials. Fifteen patients underwent a preparative regimen of fludarabine (30 mg/m2 daily for 3 days), intravenous cyclophosphamide (750 mg/m2 daily for 3 days), and rituximab. For the remaining five patients, the conditioning regimen consisted of cisplatin (25 mg/m2 continuous infusion daily for 4 days), fludarabine (30 mg/m2 daily for 2 days), and cytarabine (1,000 mg/m2 daily for 2 days). Tacrolimus and methotrexate were used for graft-versus-host disease prophylaxis.
RESULTS: All patients experienced engraftment of donor cells. One patient (5%) experienced grade 2 acute graft-versus-host disease, and no patients experienced a higher grade. One patient experienced disease progression at 115 days post-transplantation and responded to donor lymphocyte infusion. The remaining patients remained disease-free. One patient died at 10.5 months from a fungal infection. With a median follow-up time of 25 months, the estimated 3-year current progression-free survival rate was 95%.
CONCLUSION: These data suggest that nonmyeloablative allogeneic stem-cell transplantation is an effective option in lymphoma patients with chemosensitive or stable disease who experience disease recurrence following autologous transplantation.
Supported in part by research grants from The G & P Foundation for Cancer Research.
Authors' disclosures of potential conflicts of interest are found at the end of this article.

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