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A Gynecologic Oncology Group phase II study of amonafide (NSC #308847) in squamous cell carcinoma of the cervix.

作者信息

Asbury R F, Blessing J A, Soper J T

机构信息

Department of Medicine in Oncology, University of Rochester School of Medicine, New York.

出版信息

Am J Clin Oncol. 1994 Apr;17(2):125-8. doi: 10.1097/00000421-199404000-00007.

DOI:10.1097/00000421-199404000-00007
PMID:8141104
Abstract

Twenty evaluable patients with squamous cell carcinoma of the cervix, who had previously received a cisplatin-containing regimen, were treated with amonafide 300 mg/m2 over 1 hour for 5 consecutive days every 3 weeks. One partial response (5%) was seen. Hematologic toxicity was substantial with severe or life-threatening events occurring as follows: leukopenia, 5 patients (25%); thrombocytopenia, 4 patients (20%); granulocytopenia, 2 patients (10%). One patient experienced acute bilateral open-angle glaucoma immediately after treatment, and another developed gastric ulceration with life-threatening gastrointestinal bleeding. In view of the low response rate and high toxicity, amonafide does not warrant further investigation as second-line chemotherapy in squamous cell carcinoma of the cervix.

摘要

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