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PCNU:晚期结直肠癌的II期评估。

PCNU: phase II evaluation in advanced colorectal carcinoma.

作者信息

Pazdur R, Samson M K, Baker L H

机构信息

Department of Internal Medicine, Wayne State University, Harper-Grace Hospitals, Detroit, MI 48201.

出版信息

Invest New Drugs. 1988 Jun;6(2):93-5. doi: 10.1007/BF00195366.

Abstract

PCNU, a N-(2-chloroethyl)-N-nitrosourea, was administered to 37 previously treated patients with metastatic adenocarcinoma of the colon and rectum. The drug dose was 100 mg/m2, intravenously, over one hour for good risk patients and 75 mg/m2 for poor risk patients. Poor risk patients were defined as patients over 65 years of age or having liver enzymes greater than twice normal. The infusion was repeated at 6 week intervals. Seventeen patients (median performance status 80%) received PCNU at the 100 mg/m2 dose; 20 patients (median performance status 70%) received PCNU at the 75 mg/m2 dose. Complete responses were not observed. One patient treated with 100 mg/m2 achieved a partial response. Toxicity was primarily hematological with life-threatening leukopenia and thrombocytopenia observed in six patients. PCNU administered in the described dose schedule demonstrated little therapeutic efficacy in this patient population.

摘要

PCNU(一种N-(2-氯乙基)-N-亚硝基脲)被用于37例先前接受过治疗的结肠和直肠转移性腺癌患者。对于风险较低的患者,药物剂量为100mg/m²,静脉滴注1小时;对于风险较高的患者,药物剂量为75mg/m²。风险较高的患者定义为年龄超过65岁或肝酶高于正常水平两倍的患者。每隔6周重复进行一次输注。17例患者(中位体能状态为80%)接受了100mg/m²剂量的PCNU治疗;20例患者(中位体能状态为70%)接受了75mg/m²剂量的PCNU治疗。未观察到完全缓解。1例接受100mg/m²治疗的患者达到部分缓解。毒性主要为血液学毒性,6例患者出现危及生命的白细胞减少和血小板减少。按照所述剂量方案给予PCNU在该患者群体中显示出几乎没有治疗效果。

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