首页 | 本学科首页   官方微博 | 高级检索  
     


Interleukin-2 and interferon-alpha2b as a daily alternating schedule in advanced renal cell cancer
Authors:L. Bergmann  E. Weidmann  H. M. Enzinger  K. Fenchel  D. Jonas  P. S. Mitrou
Affiliation:(1) Division of Hematology, Department of Internal Medicine, J. W. Goethe University, Theodor-Stern-Kai 7, W-6000 Frankfurt/M., Federal Republic of Germany;(2) Division of Urology, Department of Surgery, J. W. Goethe University, Theodor-Stern-Kai 7, W-6000 Frankfurt/M., Federal Republic of Germany
Abstract:
Summary Interferon-alpha (IFN-agr) and interleukin-2 (Il-2) are effective as single agents in metastatic renal cell cancer (RCC) with response rates of 15–30%. Additionally, IFN-agr is assumed to act synergistically with Il-2 in the induction of lymphokine-activated killer cells. (LAK cells) in vitro. With the aims of increasing the response rate by combining both cytokines and of reducing side effects, we started a clinical trial with a daily alternating schedule of 10×106 units/m2 s.c. rIFN-agr2b (Essex, Munich, FRG) and 3×106 Cetus units/m2 rIL-2 (EuroCetus, Frankfurt, FRG) in the form of 1 h infusions over a period of 14 days. Patients found to have progressive disease after two cycles of therapy were withdrawn from the study; patients with stable disease or better received two further cycles.Of the 27 patients included in the study, 22 (16 male, 6 female) are evaluable for response. In 1 patient with multiple pulmonary metastases complete remission was achieved, in 5 patients partial remission, and in 2 a minor response. The schedule was practicable; the main side effects were influenza-like symptoms, fatigue and hypotension. Some patients suffered from arthralgias and erythemas up to 3 weeks after finishing the therapy cycle. On the whole, the side effects seem to be less severe than those arising from schedules using continuous Il-2 infusions.This work was supported by Grant No. 01GA8802 of the Bundesministerium für Forschung und Technologie (BMFT)
Keywords:
本文献已被 SpringerLink 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号