Dieci Maria Vittoria, Bisagni Giancarlo, Bartolini Stefania, Frassoldati Antonio, Vicini Roberto, Balduzzi Sara, D'amico Roberto, Conte Pierfranco, Guarneri Valentina
Department of Surgery, Oncology and Gastroenterology, University of Padova, via Giustiniani 2, 35128, Padova, Italy.
Oncology 2, Veneto Institute of Oncology IOV-IRCCS, via Gattamelata 64, 35128, Padova, Italy.
NPJ Breast Cancer. 2023 Feb 4;9(1):6. doi: 10.1038/s41523-023-00509-2.
The optimal adjuvant endocrine therapy for HR-positive/HER2-positive breast cancer patients is unknown. We included in this analysis 784 patients with HR-positive/HER2-positive BC from the randomized ShortHER trial of adjuvant trastuzumab (1 year vs 9 weeks) + chemotherapy. At a median follow-up of 8.7 years, patients who received AI had a significantly better DFS vs patients who received TAM or TAM-AI: 8-yr DFS 86.4 vs 79.7%, log-rank P = 0.013 (HR 1.52, 95% CI 1.09-2.11). In multivariate analysis, the type of endocrine therapy maintained a significant association with DFS (HR 1.64, 95% CI 1.07-2.52, p = 0.025 for TAM/TAM-AI vs AI). Among premenopausal patients aged ≤45 years, the use of GnRHa was associated with longer DFS: 8-yr DFS rate 85.2 vs 62.6% (log-rank p = 0.019, HR 0.41, 95% CI 0.19-0.88). In this post-hoc analysis of the ShortHER trial adjuvant treatment with AI was independently associated with improved DFS. Subgroup analysis in premenopausal patients suggests benefits with ovarian suppression.Trial registration: NCI ClinicalTrials.gov number: NCT00629278.
激素受体(HR)阳性/人表皮生长因子受体2(HER2)阳性乳腺癌患者的最佳辅助内分泌治疗方案尚不清楚。我们纳入了784例HR阳性/HER2阳性乳腺癌患者,这些患者来自辅助曲妥珠单抗(1年与9周)联合化疗的随机ShortHER试验。在中位随访8.7年时,接受芳香化酶抑制剂(AI)的患者的无病生存期(DFS)显著优于接受他莫昔芬(TAM)或TAM-AI的患者:8年DFS分别为86.4%和79.7%,对数秩检验P = 0.013(风险比[HR] 1.52,95%置信区间[CI] 1.09 - 2.11)。在多变量分析中,内分泌治疗类型与DFS仍保持显著关联(TAM/TAM-AI与AI相比,HR 1.64,95% CI 1.07 - 2.52,P = 0.025)。在年龄≤45岁的绝经前患者中,使用促性腺激素释放激素激动剂(GnRHa)与更长的DFS相关:8年DFS率分别为85.2%和62.6%(对数秩检验P = 0.019,HR 0.41,95% CI 0.19 - 0.88)。在ShortHER试验的这项事后分析中,AI辅助治疗与DFS改善独立相关。绝经前患者的亚组分析提示卵巢抑制有益。试验注册:美国国立癌症研究所(NCI)临床试验.gov编号:NCT00629278。