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Differences in toxicity between men and women treated with 5-fluorouracil therapy for colorectal carcinoma
被引:103
|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
来源:
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.
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页码:1165 / 1171
页数:7
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