CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Interaction between tumor-infiltrating lymphocytes and BMI in early HER2-positive breast cancer: analysis of the ShortHER trial.
Interaction between tumor-infiltrating lymphocytes and BMI in early HER2-positive breast cancer: analysis of the ShortHER trial.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
我们认为,对于接受辅助化疗 + 曲妥珠单抗治疗的超重或肥胖 HER2 阳性早期乳腺癌患者,BMI 可能损害 TILs 的局部保护作用,但不影响其远处保护作用。
我们此前在ShortHER试验中证实,TIL(肿瘤浸润淋巴细胞)对早期人表皮生长因子受体2(HER2)阳性乳腺癌(eBC)患者具有预后作用。本研究分析体重指数(BMI)如何调节TIL的预后作用。
ShortHER研究将1,253例HER2阳性eBC患者随机分配至9周或1年的辅助曲妥珠单抗联合化疗。评估诊断时BMI(1,213例有数据,排除34例体重过轻患者)。生存终点包括无病生存期(DFS)、无复发生存期(RFS)、远处无病生存期(DDFS)和总生存期(OS)。通过竞争风险分析计算首次事件类型的累积发生率。
583例(48%)患者体型偏瘦,360例(29.7%)超重,236例(19.5%)肥胖。偏瘦患者与超重或肥胖患者的DFS、RFS、DDFS和OS相近。在包含TIL和BMI资料的队列(n=819)中,偏瘦患者的TIL(每增加5%)独立关联DFS(P=.003)、RFS(P=.001)和DDFS(P=.018);超重或肥胖患者中,TIL仅独立关联DDFS(P=.044)。偏瘦患者中,TIL≥20%与DFS(P=.007)、RFS(P=.002)及DDFS(P=.027)改善相关;超重或肥胖患者中,TIL≥20%与<20%患者的DFS、RFS、DDFS和OS差异均不显著。偏瘦患者中,TIL<20%组局部区域复发(P=.001)和远处复发(P=.07)的累积发生率较高;超重或肥胖患者中,TIL<20%组远处复发累积发生率较高(P=.005)。
研究提示,在接受辅助化疗联合曲妥珠单抗的HER2阳性eBC患者中,超重或肥胖可能削弱TIL的局部保护作用,但不影响其远处保护作用。
We demonstrated the prognostic role of tumor-infiltrating lymphocytes (TILs) in patients with early human epidermal growth factor receptor 2 (HER2)-positive breast cancer (eBC) enrolled in the ShortHER trial. Here, we analyze how body mass index (BMI) modulates the prognostic role of TILs.
The ShortHER study randomized 1253 patients with HER2-positive eBC to 9 weeks versus 1 year of adjuvant trastuzumab + chemotherapy. We assessed BMI at diagnosis (available for n = 1213, n = 34 underweight were excluded). Survival endpoints were disease-free survival (DFS), recurrence-free survival (RFS), distant DFS (DDFS) and overall survival (OS). We calculated the cumulative incidence of first event types by competing risk analysis.
A total of 583 (48%) patients were lean, 360 (29.7%) overweight and 236 (19.5%) obese. Lean patients versus those with overweight or obesity had similar DFS, RFS, DDFS and OS. Within the TIL + BMI cohort (n = 819), TILs (5% increase) were independently associated with DFS (P = 0.003), RFS (P = 0.001) and DDFS (P = 0.018) in lean patients. In patients with overweight or obesity, TILs were independently associated only with DDFS (P = 0.044). In lean patients, TILs 20% were associated with improved DFS (P = 0.007), RFS (P = 0.002) and DDFS (P = 0.027) compared with TILs <20%. In patients with overweight or obesity, DFS, RFS, DDFS and OS did not significantly differ between TILs 20% and TILs <20%. In lean patients, there was a higher cumulative incidence of locoregional relapse (P = 0.001) and distant relapse (P = 0.07) in patients with TILs <20% versus TILs 20%. In patients with overweight or obesity, there was a higher cumulative incidence of distant relapse (P = 0.005) in patients with TILs <20% versus TILs 20%.
We suggest that BMI may impair the local, but not distant, protective effect of TILs in patients with overweight or obesity with HER2-positive eBC treated with adjuvant chemotherapy + trastuzumab.
在 PubMed 查看 → 出版商原文(DOI) 全文 PDF(PMC)· 可下载 治疗专题与资料阅读指南 资料来源与翻译说明 报告译文或资料问题 →
MEMBER ACCOUNT
登录成功会直接打开下一页。