Nagykálnai Tamás
Bajcsy-Zsilinszky Kórház és Rendelôintézet 1106 Budapest Maglódi u. 89-91.
Magy Onkol. 2008 Jun;52(2):133-43. doi: 10.1556/MOnkol.52.2008.2.1.
From the big randomized clinical trials there are evidences that adjuvant endocrine therapy for hormone-sensitive early breast cancer in postmenopausal women should include an aromatase inhibitor (AI). Anastrozole or letrozole should be used upfront for 5 years (ATAC and BIG 1-98), the sequential approach of tamoxifen for 2-3 years, followed by anastrozole or exemestane for 2-3 years is a reasonable alternative (ABCSG8, ARNO 95, IES, ITA), and mostly in patients with node-positive disease completing 5 years of tamoxifen should be offered letrozole up to 4-5 years (MA-17). In each of these trials incorporation of an AI resulted in significant improvement in study endpoints. Further results will be needed to establish the optimal beneficial effect, use, duration and safety of adjuvant AI therapies.
大型随机临床试验表明,绝经后激素敏感性早期乳腺癌的辅助内分泌治疗应包括一种芳香化酶抑制剂(AI)。阿那曲唑或来曲唑应 upfront 使用 5 年(ATAC 和 BIG 1-98),他莫昔芬序贯治疗 2 - 3 年,随后使用阿那曲唑或依西美坦 2 - 3 年是一种合理的替代方案(ABCSG8、ARNO 95、IES、ITA),并且主要是对于淋巴结阳性疾病患者,完成 5 年他莫昔芬治疗后应给予来曲唑治疗 4 - 5 年(MA - 17)。在这些试验中的每一项中,加入 AI 均导致研究终点有显著改善。需要进一步的结果来确定辅助 AI 治疗的最佳有益效果、使用方法、持续时间和安全性。