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Phase II trial of amonafide in patients with stage III and IV non-small-cell lung cancer.

作者信息

Berger M Z, Kris M G, Gralla R J, Marks L D, Potanovich L M, Dimaggio J J, Heelan R T

机构信息

Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York, NY 10021.

出版信息

Am J Clin Oncol. 1991 Apr;14(2):124-6. doi: 10.1097/00000421-199104000-00006.

Abstract

Amonafide (benzisoquinolinedione, nafidimide, NSC 308847) is an anticancer agent that functions as a DNA intercalator. Sixteen patients with stage III or IV non-small-cell lung cancer who had not previously received chemotherapy were given amonafide at an initial dose of 300 mg/m2 i.v. daily for 5 days every 21 days. No major objective responses were observed among the 14 patients adequately treated (95% confidence limits 0-20%). Local reactions at the injection site or phlebitis were seen in 14 of the 16 patients. Leukopenia (44%), nausea or vomiting (38%), and thrombocytopenia and rash (each 25%) were also noted. With the low response rate and the toxicity observed, amonafide at this dosage and schedule has limited use in the treatment of non-small-cell lung cancer.

摘要

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