Gemcitabine in hematologic malignancies

被引:43
作者
Nabhan, C
Krett, N
Gandhi, V
Rosen, S
机构
[1] Northwestern Univ, Sch Med, Div Hematol Oncol, Robert H Lurie Comprehens Canc Ctr, Chicago, IL 60611 USA
[2] Univ Texas, MD Anderson Canc Ctr, Dept Expt Therapeut, Houston, TX 77030 USA
关键词
D O I
10.1097/00001622-200111000-00015
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Gemcitabine is a pyrimidine analogue that showed significant activity in solid malignancies. Gemcitabine acts by inhibiting DNA synthesis through chain termination and ribonucleotide reductase inhibition. During initial phase I and II studies, gemcitabine had a low toxicity profile and was well tolerated as a single agent and in combination therapy. Recently, there has been more interest in studying the activity of gemcitabine in hematologic malignancies. Gemcitabine demonstrated good activity in refractory Hodgkin disease patients, non-Hodgkin lymphoma, cutaneous T-cell lymphoma, and acute leukemias. There is a preponderance of evidence on the activity of gemcitabine in vitro in myeloma and leukemic cell lines. The activity of gemcitabine in these disorders will pave the way for incorporating this agent into the early phases of therapy. Curr Opin Oncol 2001, 13:514-521 (C) 2001 Lippincott Williams & Wilkins, Inc.
引用
收藏
页码:514 / 521
页数:8
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