CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Tumor-Infiltrating Lymphocytes and Survival Outcomes in Early ERBB2-Positive Breast Cancer: 10-Year Analysis of the ShortHER Randomized Clinical Trial.
Tumor-Infiltrating Lymphocytes and Survival Outcomes in Early ERBB2-Positive Breast Cancer: 10-Year Analysis of the ShortHER Randomized Clinical Trial.
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这项 ShortHER 随机临床试验的随访分析,据我们所知,是首次证明 TILs 在接受辅助化疗和抗 ERBB2 治疗的 ERBB2 阳性早期乳腺癌患者中对 OS 具有独立影响。TILs 为 20% 或更高且降低了 trastuzumab 疗程和化疗剂量的患者,并未面临远处复发或死亡的额外风险。
对于早期ERBB2(原HER2)阳性乳腺癌患者,需要识别生物标志物以指导治疗降阶梯。
评估TIL(肿瘤浸润淋巴细胞)(TILs)与ERBB2阳性早期乳腺癌患者远处无病生存期(DDFS)及总生存期(OS)的关联。设计、环境、
ShortHER 随机临床试验是一项在意大利开展的多中心试验,于 2007 年 12 月至 2013 年 10 月入组 ERBB2 阳性乳腺癌患者。患者接受 9 周或 1 年辅助 trastuzumab 联合化疗。对肿瘤样本进行了 TILs 评估。在此,患者在中位随访 9 年时接受评估,数据于 2023 年 2 月至 2024 年 8 月进行分析。4 周期以蒽环类为基础的化疗后接 4 疗程紫杉烷类联合 trastuzumab 治疗 1 年(长臂),或 3 疗程紫杉烷类联合 trastuzumab 治疗 9 周后接减量以蒽环类为基础的化疗 3 疗程(短臂)。采用 Cox 模型评估 TILs 与 DDFS 和 OS 的关联。
在ShortHER试验入组的1253例患者中,866例女性(中位[IQR]年龄,56[48-64]岁)的TILs可评估。在纳入相关因素的Cox模型中,TIL每增加5%与DDFS改善相关(风险比[HR],0.87;95% CI,0.80-0.95;P = .001)和OS改善相关(HR,0.89;95% CI,0.81-0.98;P = .01)。TILs为20%或更高的患者10年OS率为91.3%,TILs为30%或更高的患者为93.3%,TILs为50%或更高的患者为98.1%,均高于TILs较低的患者。TILs低于20%的患者接受长疗程 vs 短疗程治疗结局更好(10年DDFS,88.7% vs 81.0%),而TILs为20%或更高的患者则相反(10年DDFS,87.1% vs 92.2%;交互作用P = .01)。同样,TILs为20%或更高的患者中,长疗程组10年OS率为89.3%,短疗程组为93.1%(HR,0.36;95% CI,0.10-1.36);TILs低于20%的患者中,长疗程组10年OS率为91.3%,短疗程组为86.9%(HR,1.36;95% CI,0.82-2.23;交互作用P = .06)。
For patients with early ERBB2 (formerly HER2)-positive breast cancer, there is a need to identify biomarkers to guide treatment de-escalation.
To evaluate the association of tumor-infiltrating lymphocytes (TILs) with distant disease-free (DDFS) and overall survival (OS) for patients with ERBB2-positive early breast cancer. DESIGN, SETTING, AND PARTICIPANTS: The ShortHER randomized clinical trial was a multicentric trial in Italy that enrolled patients with ERBB2-positive breast cancer from December 2007 to October 2013. Patients received 9 weeks or 1 year of adjuvant trastuzumab combined with chemotherapy. Tumor samples were evaluated for TILs. Herein, patients were evaluated at a median follow-up of 9 years, and data were analyzed from February 2023 to August 2024. INTERVENTION: Four cycles of anthracycline-based chemotherapy followed by 4 courses of taxanes combined with trastuzumab for 1 year (long arm) or 3 courses of taxanes combined with trastuzumab for 9 weeks followed by reduced-dose anthracycline-based chemotherapy for 3 courses (short arm). MAIN OUTCOMES AND MEASURES: The association of TILs with DDFS and OS was assessed with Cox models.
Of 1253 patients enrolled in the ShortHER trial, 866 women (median [IQR] age, 56 [48-64] years) had evaluable TILs. In Cox models with relevant factors, each 5% TIL increment was associated with improved DDFS (hazard ratio [HR], 0.87; 95% CI, 0.80-0.95; P = .001) and OS (HR, 0.89; 95% CI, 0.81-0.98; P = .01). The 10-year OS rate was 91.3% for patients with TILs 20% or higher, 93.3% for patients with TILs 30% or higher, and 98.1% for patients with TILs 50% or higher, resulting higher vs lower TIL counterparts. Patients with TILs lower than 20% showed a better outcome with the long vs short treatment (10-year DDFS, 88.7% vs 81.0%), whereas patients with TILs 20% or higher showed the opposite (10-year DDFS, 87.1% vs 92.2%; P for interaction = .01). Similarly, patients with TILs 20% or higher had a 10-year OS rate of 89.3% in the long arm vs 93.1% in the short arm (HR, 0.36; 95% CI, 0.10-1.36); patients with TILs lower than 20% had a 10-year OS rate of 91.3% in the long arm vs 86.9% in the short arm (HR, 1.36; 95% CI, 0.82-2.23; P for interaction = .06).
This follow-up analysis of the ShortHER randomized clinical trial is, to our knowledge, the first demonstration of an independent effect of TILs in terms of OS for patients with ERBB2-positive early breast cancer treated with adjuvant chemotherapy and anti-ERBB2 therapy. Patients with TILs 20% or higher who de-escalated trastuzumab duration and chemotherapy dose were not exposed to an excess risk of distant relapse or death. TRIAL REGISTRATION: EudraCT: 2007-004326-25.
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