TY - JOUR
T1 - Intensive conditioning regimen of etoposide (VP-16), cyclophosphamide and carmustine (VCB) followed by autologous hematopoietic stem cell transplantation for relapsed and refractory Hodgkin's lymphoma
AU - Benekli, M.
AU - Smiley, S. L.
AU - Younis, T.
AU - Czuczman, M. S.
AU - Hernandez-Ilizaliturri, F.
AU - Bambach, B.
AU - Battiwalla, M.
AU - Padmanabhan, S.
AU - McCarthy, P. L.
AU - Hahn, T.
PY - 2008/4
Y1 - 2008/4
N2 - 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) 2400mg/m2, cyclophosphamide 7200mg/m2 and carmustine (BCNU) 600mg/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.
AB - 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) 2400mg/m2, cyclophosphamide 7200mg/m2 and carmustine (BCNU) 600mg/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.
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U2 - 10.1038/sj.bmt.1705951
DO - 10.1038/sj.bmt.1705951
M3 - Article
C2 - 18071290
AN - SCOPUS:42149184655
SN - 0268-3369
VL - 41
SP - 613
EP - 619
JO - Bone Marrow Transplantation
JF - Bone Marrow Transplantation
IS - 7
ER -