TY - JOUR
T1 - Cisplatin-CBV with autologous bone marrow transplantation for relapsed hodgkin's disease
AU - Spinolo, Jorge A.
AU - Jagannath, Sundar
AU - Velásquez, William
AU - Spitzer, Gary
AU - Cabanillas, Fernando
AU - Hagemeister, Fredrick
AU - Horwitz, Leonard J.
AU - Dicke, Karel A.
PY - 1993
Y1 - 1993
N2 - The use of high-dose cyclophosphamide, carmustine, and etoposide (CBV) with autologous bone marrow transplantation (ABMT) results in long-term disease-free survival of about 30% in patients with relapsed Hodgkin's disease. Laboratory and clinical data show that cisplatin is synergistic with etoposide and carmustine, with non-overlapping extramedullary toxicity. Twenty-one patients with relapsed Hodgkin's disease that had progressed after both MOPP-like and ABVD-like regimens were treated with CBV plus cisplatin (90 mg/m2) and ABMT. The CR rate was 55%; the three-year disease-free and overall survival were 29% and 38% respectively; these results are comparable to prior experience with CBV. Performance status was strongly correlated with achievement of CR, survival, and time to treatment failure. Nephrotoxicity was seen in 3 patients, and ototoxicity in 1 patient. Although cisplatin could be added to CBV with minimal additional toxicity, the results obtained in this small patient population were not better than those of the earlier regimen. A larger trial in patients not previously exposed to cisplatin may better define the role of its addition to CBV.
AB - The use of high-dose cyclophosphamide, carmustine, and etoposide (CBV) with autologous bone marrow transplantation (ABMT) results in long-term disease-free survival of about 30% in patients with relapsed Hodgkin's disease. Laboratory and clinical data show that cisplatin is synergistic with etoposide and carmustine, with non-overlapping extramedullary toxicity. Twenty-one patients with relapsed Hodgkin's disease that had progressed after both MOPP-like and ABVD-like regimens were treated with CBV plus cisplatin (90 mg/m2) and ABMT. The CR rate was 55%; the three-year disease-free and overall survival were 29% and 38% respectively; these results are comparable to prior experience with CBV. Performance status was strongly correlated with achievement of CR, survival, and time to treatment failure. Nephrotoxicity was seen in 3 patients, and ototoxicity in 1 patient. Although cisplatin could be added to CBV with minimal additional toxicity, the results obtained in this small patient population were not better than those of the earlier regimen. A larger trial in patients not previously exposed to cisplatin may better define the role of its addition to CBV.
KW - Autologous bone marrow transplant
KW - Cisplatinum/CBV
KW - Relapsed Hodgkin's disease
UR - http://www.scopus.com/inward/record.url?scp=0027162633&partnerID=8YFLogxK
U2 - 10.3109/10428199309148506
DO - 10.3109/10428199309148506
M3 - Article
C2 - 8477204
AN - SCOPUS:0027162633
SN - 1042-8194
VL - 9
SP - 71
EP - 77
JO - Leukemia and Lymphoma
JF - Leukemia and Lymphoma
IS - 1-2
ER -