Burdette-Radoux Susan, Muss Hyman B
Hematology/Oncology Unit, University of Vermont and Vermont Cancer Center, Burlington, VT 05405, USA.
Clin Breast Cancer. 2009 Jun;9 Suppl 1:S37-41. doi: 10.3816/CBC.2009.s.004.
Women with hormone receptor-positive breast cancer continue to be at risk for recurrence and mortality for many years after diagnosis. Previous clinical trials established 5 years of endocrine therapy as a standard of care for both premenopausal and postmenopausal women, resulting in long-lasting benefit over shorter durations of treatment. Until recently, trials testing durations of tamoxifen longer than 5 years have not shown additional benefit, but the ATLAS (Adjuvant Tamoxifen, Longer Against Shorter) trial, reported in 2007, showed a small but significant reduction in risk of recurrence with 10 compared with 5 years of tamoxifen therapy. Aromatase inhibitors (AIs) improve relapse-free survival (RFS) in postmenopausal women when they are used sequentially with, or replace, tamoxifen for a total of 5 years of therapy. Extension of endocrine therapy to 10 years in the National Cancer Institute of Canada Clinical Trials Group MA.17 trial demonstrated that 5 years of letrozole therapy following 5 years of tamoxifen therapy results in an improvement in RFS, but not overall survival, in postmenopausal women. Trials testing durations of AI therapy for longer than 5 years are ongoing. Selection of candidates for extended endocrine therapy should balance recurrence risk, toxicity of treatment, and comorbidities that might impact life expectancy and risk of side effects.
激素受体阳性乳腺癌女性在确诊后的许多年里仍有复发和死亡风险。以往的临床试验确定,5年内分泌治疗是绝经前和绝经后女性的标准治疗方案,与较短疗程的治疗相比,能带来持久益处。直到最近,测试他莫昔芬疗程超过5年的试验并未显示出额外益处,但2007年报道的ATLAS(辅助他莫昔芬,长疗程优于短疗程)试验表明,与5年他莫昔芬治疗相比,10年治疗可使复发风险有小幅但显著的降低。芳香化酶抑制剂(AIs)在与他莫昔芬序贯使用或替代他莫昔芬进行总共5年的治疗时,可提高绝经后女性的无复发生存期(RFS)。加拿大国家癌症研究所临床试验组MA.17试验将内分泌治疗延长至10年,结果表明,绝经后女性在接受5年他莫昔芬治疗后再接受5年来曲唑治疗,可改善RFS,但不能改善总生存期。测试AI治疗疗程超过5年的试验正在进行中。选择延长内分泌治疗的患者应权衡复发风险、治疗毒性以及可能影响预期寿命和副作用风险的合并症。