PHASE-II EVALUATION OF MENOGARIL IN PATIENTS WITH ADVANCED CERVICAL-CARCINOMA - A COLLABORATIVE TRIAL OF THE NORTH-CENTRAL-CANCER-TREATMENT-GROUP AND MAYO-CLINIC

被引:0
|
作者
LONG, HJ
WIEAND, HS
FOLEY, JF
NIEDRINGHAUS, RD
LAURIE, JA
MORTON, RF
GOLDBERG, RM
MAILLIARD, JA
MALKASIAN, GD
EDMONSON, JH
机构
[1] MAYO CLIN & MAYO FDN,CTR CANC,STAT UNIT,ROCHESTER,MN 55905
[2] MAYO CLIN & MAYO FDN,DEPT OBSTET & GYNECOL,ROCHESTER,MN 55905
[3] CREIGHTON UNIV,NEBRASKA ONCOL GRP,OMAHA,NE 68178
[4] UNIV NEBRASKA,MED CTR,OMAHA,NE 68105
[5] DULUTH CLIN CCOP,DULUTH,MN 55805
[6] GRAND FORKS CLIN LTD,GRAND FORKS,ND 58201
[7] IOWA ONCOL RES ASSOC CCOP,DES MOINES,IA 50314
[8] GEISINGER CLIN & MED CTR CCOP,DANVILLE,PA 17822
关键词
MENOGARIL; CERVIX CANCER; SQUAMOUS CELL CARCINOMA; PHASE-II TRIAL;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Fourteen patients with advanced/recurrent squamous cell carcinoma of the uterine cervix received menogaril, 200 mg/m2 by one hour intravenous infusion at four-week intervals. No objective regressions were observed. Median time to progression was less than two months and median survival was seven months. All patients experienced neutropenia. Platelet toxicity was negligible. Venous irritation and phlebitis occurred at the infusion site in 43% of patients. Menogaril as administered in this protocol is ineffective in treating previously irradiated advanced/recurrent squamous cell carcinoma of the uterine cervix and warrants no further investigation in this disease at the dosage and administration schedule used in this protocol.
引用
收藏
页码:349 / 351
页数:3
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