Cancer Research UK UK, Queen Mary University of London, London, United Kingdom.
J Clin Oncol. 2010 Jul 20;28(21):3411-5. doi: 10.1200/JCO.2009.27.2021. Epub 2010 Jun 14.
Third-generation aromatase inhibitors have been widely used in postmenopausal women for the adjuvant treatment of hormone receptor-positive breast cancer. As aromatase inhibitors work by inhibiting the conversion of androgens to estrogens in adipose tissue, we hypothesized that anastrozole may be more effective in women with a high body mass index (BMI).
The Arimidex, Tamoxifen Alone or in Combination (ATAC) study was a double-blind randomized clinical trial in which postmenopausal women with early-stage breast cancer were randomly assigned to receive oral daily anastrozole (1 mg) alone, tamoxifen (20 mg) alone, or the combination in a double-blind fashion. Analyses were based on the 100-month median follow-up for women with hormone receptor-positive breast cancers (estrogen [ER] and/or progesterone [PgR] positive). Here, we investigate the impact of BMI on recurrence and the relative benefit of anastrozole versus tamoxifen according to baseline BMI. Results Overall, women with a high BMI (BMI > 35 kg/m(2)) at baseline had more recurrences than those women with a low BMI (BMI < 23 kg/m(2); adjusted hazard ratio [HR], 1.39; 95% CI, 1.06 to 1.82; P(heterogeneity) = .03) and significantly more distant recurrences (adjusted HR, 1.46; 95% CI, 1.07 to 1.61; P(heterogeneity) = .01). Overall, the relative benefit of anastrozole versus tamoxifen was nonsignificantly better in thin women compared to overweight women.
These results confirm the poorer prognosis of obese women with early-stage breast cancer. Recurrence rates were lower for anastrozole than tamoxifen for all BMI quintiles. Our results suggest that the relative efficacy of anastrozole compared to tamoxifen is greater in thin postmenopausal women and higher doses or more complete inhibitors might be more effective in overweight women, but this requires independent confirmation.
第三代芳香酶抑制剂已广泛用于绝经后妇女的激素受体阳性乳腺癌的辅助治疗。由于芳香酶抑制剂通过抑制脂肪组织中雄激素向雌激素的转化而起作用,我们假设阿那曲唑在体重指数(BMI)较高的女性中可能更有效。
阿那曲唑、他莫昔芬单独或联合(ATAC)研究是一项双盲随机临床试验,其中绝经后早期乳腺癌患者被随机分配接受口服每日阿那曲唑(1 毫克)、他莫昔芬(20 毫克)或两者联合的双盲治疗。分析基于激素受体阳性乳腺癌(雌激素[ER]和/或孕激素[PgR]阳性)女性的 100 个月中位数随访。在这里,我们根据基线 BMI 研究 BMI 对复发的影响以及阿那曲唑与他莫昔芬的相对益处。结果:总体而言,基线时 BMI 较高(BMI > 35 kg/m(2))的女性比 BMI 较低(BMI < 23 kg/m(2))的女性复发更多(调整后的危险比[HR],1.39;95%置信区间,1.06 至 1.82;P(异质性) =.03),远处复发也更多(调整后的 HR,1.46;95%置信区间,1.07 至 1.61;P(异质性) =.01)。总体而言,与超重女性相比,阿那曲唑与他莫昔芬相比,瘦弱女性的相对益处无显著差异。
这些结果证实了肥胖早期乳腺癌妇女预后较差。对于所有 BMI 五分位组,阿那曲唑的复发率均低于他莫昔芬。我们的结果表明,与他莫昔芬相比,阿那曲唑在瘦弱绝经后女性中的相对疗效更大,而较高剂量或更完全的抑制剂可能对超重女性更有效,但这需要独立证实。