1. ¹Department of Medical Oncology, Gazi University Faculty of Medicine, Ankara, Turkey
2. ²Department of Medicine, Roswell Park Cancer Institute, Buffalo, NY, USA
3. ³Blood and Marrow Transplantation Program, Roswell Park Cancer Institute, Buffalo, NY, USA
4. ⁴Department of Pediatrics, Roswell Park Cancer Institute, Buffalo, NY, USA

Correspondence: Dr SL Smiley, Department of Medicine, Roswell Park Cancer Institute, Elm and Carlton Streets, Buffalo, NY 14263, USA. E-mail: shannon.smiley@roswellpark.org

⁵These authors contributed equally to this work.

Received 17 May 2007; Revised 15 October 2007; Accepted 24 October 2007; Published online 10 December 2007.

Abstract

Several high-dose therapy regimens are used for autologous hematopoietic stem cell transplantation (auto-HSCT) for relapsed and refractory Hodgkin's lymphoma (HL) with variable disease response. An intensified regimen of etoposide (VP-16) 2400 mg/m², cyclophosphamide 7200 mg/m² and carmustine (BCNU) 600 mg/m² (VCB) pre-auto-HSCT was developed to overcome disease recurrence. A total of 43 relapsed and refractory HL patients underwent auto-HSCT between January 1992 and December 2004. At day 100 there were 37 (86%) complete responses. A total of 40 patients survived beyond day 100, 14 of whom subsequently relapsed/progressed. At a median follow-up of 4.9 years (range 1.5–11.4 years), 26 patients (60%) are alive and disease free. Five-year actuarial event-free survival (EFS) was 53% (95% CI 35–70%) and median EFS was 5.9 years. Median progression-free and overall survivals have not been reached. EFS was reduced with an increasing number of prognostic factors (Karnofsky performance status, KPS <90, chemotherapy-resistant disease and 3 chemotherapy regimens prior to transplant 1 vs 2; P=0.049). Grade III–IV regimen-related toxicity was 9% (n=4). The 1-year cumulative incidence of interstitial pneumonitis (IP) was 36%, however only two patients died of IP complications. Disease progression was the most common cause of death (n=10, 23%). Intensive VCB is an effective and well-tolerated preparative regimen for relapsed and refractory HL auto-HSCT.