Gefitinib treatment affects androgen levels in non-small-cell lung cancer patients

被引:24
作者
Nishio, M
Ohyanagi, F
Horiike, A
Ishikawa, Y
Satoh, Y
Okumura, S
Nakagawa, K
Nishio, K
Horai, T
机构
[1] Japanese Fdn Canc Res, Canc Inst Hosp, Div Internal Med, Koto Ku, Tokyo 1358550, Japan
[2] Japanese Fdn Canc Res, Canc Inst Hosp, Dept Chest Surg, Tokyo, Japan
[3] Japanese Fdn Canc Res, Inst Canc, Dept Pathol, Tokyo 170, Japan
[4] Natl Canc Ctr, Res Inst, Div Pharmacol, Tokyo 104, Japan
关键词
sex hormone; epidermal growth factor receptor; tyrosine kinase inhibitor;
D O I
10.1038/sj.bjc.6602585
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Gefitinib, an inhibitor of the epidermal growth factor receptor (EGFR, HER1/ErbB1) tyrosine kinase, has been shown to have clinical activity against non-small-cell lung cancers (NSCLCs), especially in women nonsmokers with adenocarcinomas. The aim of the present study was to clarify the relationship between androgen levels and gefitinib treatment in patients with advanced NSCLCs. Sera from 67 cases ( 36 men and 31 women) were obtained pretreatment and during treatment with gefitinib monotherapy (days 14-18) for examination of testosterone, dehydroepiandrosterone sulphate ( DHEA), and dehydroepiandrosterone sulphate (DHEAS) levels. Testosterone and DHEA during treatment were significantly lower than the pretreatment values in both women and men, and the DHEAS levels during treatment were also significantly lowered in women. Gefitinib treatment significantly suppressed androgen levels, especially in women who had no smoking history. In addition, hormone levels in women responding to gefitinib were significantly lower during the treatment than in women who did not respond. Gefitinib-associated decrease in serum androgen levels may play a role in its clinical efficacy.
引用
收藏
页码:1877 / 1880
页数:4
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