Randomized Phase III Trial of ABVD Versus Stanford V With or Without Radiation Therapy in Locally Extensive and Advanced-Stage Hodgkin Lymphoma: An Intergroup Study Coordinated by the Eastern Cooperative Oncology Group (E2496)

Author:

Gordon Leo I.1,Hong Fangxin1,Fisher Richard I.1,Bartlett Nancy L.1,Connors Joseph M.1,Gascoyne Randy D.1,Wagner Henry1,Stiff Patrick J.1,Cheson Bruce D.1,Gospodarowicz Mary1,Advani Ranjana1,Kahl Brad S.1,Friedberg Jonathan W.1,Blum Kristie A.1,Habermann Thomas M.1,Tuscano Joseph M.1,Hoppe Richard T.1,Horning Sandra J.1

Affiliation:

1. Leo I. Gordon, Northwestern University Feinberg School of Medicine and Robert H. Lurie Comprehensive Cancer Center, Chicago; Patrick J. Stiff, Loyola University Cancer Center, Maywood, IL; Fangxin Hong, Dana-Farber Cancer Institute, Harvard School of Public Health, Boston, MA; Richard I. Fisher and Jonathan W. Friedberg, University of Rochester James P. Wilmot Cancer Center, Rochester, NY; Nancy L. Bartlett, Washington University Siteman Cancer Center, St Louis, MO; Joseph M. Connors and Randy D....

Abstract

Purpose Although ABVD (doxorubicin, bleomycin, vinblastine, and dacarbazine) has been established as the standard of care in patients with advanced Hodgkin lymphoma, newer regimens have been investigated, which have appeared superior in early phase II studies. Our aim was to determine if failure-free survival was superior in patients treated with the Stanford V regimen compared with ABVD. Patients and Methods The Eastern Cooperative Oncology Group, along with the Cancer and Leukemia Group B, the Southwest Oncology Group, and the Canadian NCIC Clinical Trials Group, conducted this randomized phase III trial in patients with advanced Hodgkin lymphoma. Stratification factors included extent of disease (localized v extensive) and International Prognostic Factors Project Score (0 to 2 v 3 to 7). The primary end point was failure-free survival (FFS), defined as the time from random assignment to progression, relapse, or death, whichever occurred first. Overall survival, a secondary end point, was measured from random assignment to death as a result of any cause. This design provided 87% power to detect a 33% reduction in FFS hazard rate, or a difference in 5-year FFS of 64% versus 74% at two-sided .05 significance level. Results There was no significant difference in the overall response rate between the two arms, with complete remission and clinical complete remission rates of 73% for ABVD and 69% for Stanford V. At a median follow-up of 6.4 years, there was no difference in FFS: 74% for ABVD and 71% for Stanford V at 5 years (P = .32). Conclusion ABVD remains the standard of care for patients with advanced Hodgkin lymphoma.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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