Goss Paul E
Massachusetts General Hospital Cancer Center and Harvard Medical School, Boston, MA 02114, USA.
Semin Oncol. 2006 Apr;33(2 Suppl 7):S8-12. doi: 10.1053/j.seminoncol.2006.03.025.
For patients with hormone-receptor-positive breast cancer, the risk of relapse remains significant even after successfully completing 5 years of adjuvant tamoxifen. The use of tamoxifen beyond 5 years is not recommended, but the need to protect against relapse following tamoxifen is clear. The third-generation aromatase inhibitors offer a new approach to treating postmenopausal women with receptor-positive early stage breast cancer through the potent and specific systemic inhibition of estrogen synthesis. MA.17, a large, randomized, double-blind, placebo-controlled phase III study, investigated whether extended adjuvant therapy with letrozole following completion of around 5 years of standard tamoxifen therapy could prolong disease-free survival in postmenopausal women with hormone-receptor-positive or receptor-unknown early stage breast cancer. The updated analyses of the trial results (median follow-up, 2.5 years) confirm that letrozole significantly reduced the risk of recurrent breast cancer (42%) regardless of the patient's nodal status or receipt of prior chemotherapy, and significantly reduced the risk of distant metastasis (40%). Importantly, letrozole as extended adjuvant therapy achieved a significant improvement in overall survival in women with node-positive disease. Mortality was reduced by 39% among the approximately 2,500 women with node-positive disease randomized in the study. Letrozole showed minimal side effects compared with placebo; adverse effects on bone metabolism of uncertain clinical significance were the most noteworthy side effect. Thus, the updated results from the MA.17 trial support the previous findings and show extended adjuvant therapy with letrozole to be a well-tolerated protection against the continuing risk of breast cancer recurrence for thousands of women currently receiving standard adjuvant tamoxifen. The re-randomization of MA.17 patients to an additional 5 years of letrozole or to no treatment will provide further insights into the benefits and side effects of long-term treatment.
对于激素受体阳性的乳腺癌患者,即使成功完成5年的辅助他莫昔芬治疗后,复发风险仍然很高。不建议使用他莫昔芬超过5年,但预防他莫昔芬治疗后复发的需求是明确的。第三代芳香化酶抑制剂通过对雌激素合成的强效和特异性全身抑制,为治疗绝经后受体阳性早期乳腺癌女性提供了一种新方法。MA.17是一项大型、随机、双盲、安慰剂对照的III期研究,调查了在完成约5年的标准他莫昔芬治疗后,来曲唑延长辅助治疗是否能延长激素受体阳性或受体未知的绝经后早期乳腺癌女性的无病生存期。试验结果的更新分析(中位随访2.5年)证实,无论患者的淋巴结状态或是否接受过先前的化疗,来曲唑均显著降低了乳腺癌复发风险(42%),并显著降低了远处转移风险(40%)。重要的是,来曲唑作为延长辅助治疗,在淋巴结阳性疾病的女性中显著提高了总生存期。在该研究中随机分组的约2500名淋巴结阳性疾病女性中,死亡率降低了39%。与安慰剂相比,来曲唑的副作用最小;对骨代谢有不确定临床意义的不良反应是最值得注意的副作用。因此,MA.17试验的更新结果支持了先前的发现,并表明来曲唑延长辅助治疗对目前正在接受标准辅助他莫昔芬治疗的数千名女性来说,是一种耐受性良好的预防乳腺癌复发持续风险的方法。将MA.17研究的患者重新随机分组,接受额外5年来曲唑治疗或不接受治疗,将进一步深入了解长期治疗的益处和副作用。