Gemcitabine, vinorelbine, and pegylated liposomal doxorubicin (GVD), a salvage regimen in relapsed Hodgkin's lymphoma: CALGB 59804

被引:204
作者
Bartlett, N. L.
Niedzwiecki, D.
Johnson, J. L.
Friedberg, J. W.
Johnson, K. B.
van Besien, K.
Zelenetz, A. D.
Cheson, B. D.
Canellos, G. P.
机构
[1] Washington Univ, Sch Med, Siteman Canc Ctr, St Louis, MO 63110 USA
[2] Duke Univ, Med Ctr, CALGB Stat Ctr, Durham, NC USA
[3] Dana Farber Partners, Boston, MA USA
[4] Univ Calif San Diego, San Diego, CA 92103 USA
[5] Univ Chicago, Chicago, IL 60637 USA
[6] Mem Sloan Kettering Canc Ctr, New York, NY 10021 USA
[7] Georgetown Univ, Med Ctr, Washington, DC 20007 USA
关键词
gemcitabine; Hodgkin's lymphoma; liposomal doxorubicin; recurrent; salvage therapy; vinorelbine;
D O I
10.1093/annonc/mdm090
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Because of high single-agent activity and modest toxicity, we hypothesized the combination of gemcitabine (G), vinorelbine M, and pegylated liposomal doxorubicin (D) would be an effective salvage therapy for Hodgkin's lymphoma (HL). Patients and methods: A total of 91 patients participated. GVD was administered on days 1 and 8 every 21 days at doses of G 1000 mg/m2, V 20 mg/m2, and D 15 mg/m2 for transplant-naive patients, and G 800 mg/m2, V 15 mg/m2, and D 10 mg/m2 for post-transplant patients. Results: The dose-limiting toxicity was mucositis for the transplant-naive patients and febrile neutropenia for posttransplant patients. The overall response rate (RR) for all patients was 70% [95% confidence interval (CI) 59.8, 79.7], with 19% complete remissions. The 4-year event-free and overall survival rates in transplant-naive patients treated with GVD followed by autologous transplant were 52% (95% CI 0.34, 0.68) and 70% (95% CI 0.49, 0.84), and in the patients in whom prior transplant failed, these were 10% (95% CI 0.03, 0.22) and 34% (95% CI 0.17, 0.52), respectively. Conclusions: GVD is a well-tolerated, active regimen for relapsed HL with results similar to those reported for more toxic regimens. High RRs in patients in whom prior transplant failed confirms this regimen's activity even in heavily pretreated patients.
引用
收藏
页码:1071 / 1079
页数:9
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