NEUROTOXICITY OF PURINE ANALOGS - A REVIEW

被引:145
作者
CHESON, BD
VENA, DA
FOSS, FM
SORENSEN, JM
机构
[1] EMMES CORP,POTOMAC,MD
[2] BOSTON UNIV,MED CTR,MED ONCOL SECT,BOSTON,MA
关键词
D O I
10.1200/JCO.1994.12.10.2216
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: The purine analogs, fludarabine, cladribine, and pentostatin, are active against a broad spectrum of indolent lymphoid malignancies. They also have similar toxicities, including myelosuppression, immunosuppression, and sporadic neurotoxicity. This review compares the spectrum of neurotoxicity of each of these agents. Now that these drugs are commercially available and are being widely used, physicians should be aware of potentially serious side effects that may be encountered. Methods: The literature was searched using MedLine and Cancerline, as well as the bibliographies of published reports through the fail of 1993. In addition, case records from National Cancer Institute (NCI) Group C protocols were reviewed for fludarabine in chronic lymphocytic leukemia (CLL), and cladribine and pentostatin in hairy cell leukemia (HCL), as well as adverse drug reactions reported to the NCI from January 1980 through September 1993. Results: At higher than recommended doses, life-threatening and fatal neurotoxicity were encountered with all three drugs. At the recommended doses, each agent induced neurotoxicity in approximately 15% of patients, mostly mild and reversible. However, severe neurologic complications were reported; these were occasionally delayed, sometimes fatal, but often at least partially reversible. Conclusion: The doses of these three agents should not be increased above the recommended levels. Development of moderate or worse neurotoxicity should result in discontinuation of that drug. (C) 1994 by American Society of Clinical Oncology.
引用
收藏
页码:2216 / 2228
页数:13
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