Differences in toxicity between men and women treated with 5-fluorouracil therapy for colorectal carcinoma

被引:108
作者
Chansky, K
Benedetti, J
Macdonald, JS
机构
[1] SW Oncol Grp, Ctr Stat, Seattle, WA USA
[2] St Vincents Comprehens Canc Ctr, Div Med Oncol, New York, NY USA
关键词
5-fluorouracil; colorectal carcinoma; toxicity; gender; classification trees; clinical trials;
D O I
10.1002/cncr.20878
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND. Recent explorations suggest that women may experience more severe 5-fluorouracil (5-FU)-related toxicity than men. The patient Populations from 4 Southwest Oncology Group colorectal carcinoma trials with 5-FU-containing regimens were examined for toxicity differences between the genders. METHODS. The current Study included 1074 patients froin 4 trials. Hypotheses regarding differences in specific toxicities were generated via exploratory analyses on the data from the 2 earlier trials (n = 505 patients), using basic univariate techniques and classification tree methods. Validation of these hypotheses was performed on data from the 2 later trials (n = 569 patients) using logistic regression models for dichotomous toxicity outcomes and rank-SLIM tests for comparisons of overall toxicity grade. RESULTS. 5-FU toxicity was more extensive in women than in men in terms of average maximum toxicity grade (P = 0.005), number of different types of toxicity experienced (P = 0.009), and incidence of severe toxicities (P = 0.02). The incidence of greater than or equal to Grade 2 hematologic toxicity in the 2 later trials was higher in women than in men and women experienced more frequent moderate to severe mucositis compared with men. CONCLUSIONS. Differences in 5-FU toxicity profiles between men and women were hypothesized after an exploratory analysis, and then verified by an independent confirmatory analysis using data from the 2 later trials. This process provided Substantial evidence for gender differences in specific aspects of 5-FU toxicity that persist across a range of treatment regimens, patient characteristics, and cancer trial settings.
引用
收藏
页码:1165 / 1171
页数:7
相关论文
共 20 条
[11]  
KONISHI T, 1994, ANTICANCER RES, V14, P1277
[12]   INFLUENCE OF SEX AND AGE ON FLUOROURACIL CLEARANCE [J].
MILANO, G ;
ETIENNE, MC ;
CASSUTOVIGUIER, E ;
THYSS, A ;
SANTINI, J ;
FRENAY, M ;
RENEE, N ;
SCHNEIDER, M ;
DEMARD, F .
JOURNAL OF CLINICAL ONCOLOGY, 1992, 10 (07) :1171-1175
[13]   FLUOROURACIL PLUS LEVAMISOLE AS EFFECTIVE ADJUVANT THERAPY AFTER RESECTION OF STAGE-III COLON-CARCINOMA - A FINAL REPORT [J].
MOERTEL, CG ;
FLEMING, TR ;
MACDONALD, JS ;
HALLER, DG ;
LAURIE, JA ;
TANGEN, CM ;
UNGERLEIDER, JS ;
EMERSON, WA ;
TORMEY, DC ;
GLICK, JH ;
VEEDER, MH ;
MAILLIARD, JA .
ANNALS OF INTERNAL MEDICINE, 1995, 122 (05) :321-326
[14]  
National Cancer Institute, 1999, COMM TOX CRIT CTC
[15]  
PORT RE, 1991, ONCOLOGY, V48, P277
[16]  
Ries L., 1997, SEER CANC STAT REV 1
[17]   Sex differences in fluorouracil-induced stomatitis [J].
Sloan, JA ;
Loprinzi, CL ;
Novotny, PJ ;
Okuno, S ;
Nair, S ;
Barton, DL .
JOURNAL OF CLINICAL ONCOLOGY, 2000, 18 (02) :412-420
[18]   Women experience greater toxicity with fluorouracil-based chemotherapy for colorectal cancer [J].
Sloan, JA ;
Goldberg, RM ;
Sargent, DJ ;
Vargas-Chanes, D ;
Nair, S ;
Cha, SS ;
Novotny, PJ ;
Poon, MA ;
O'Connell, MJ ;
Loprinzi, CL .
JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (06) :1491-1498
[19]  
STEIN BN, 1995, CANCER-AM CANCER SOC, V75, P11, DOI 10.1002/1097-0142(19950101)75:1<11::AID-CNCR2820750104>3.0.CO
[20]  
2-N