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肿瘤细胞密度和浸润淋巴细胞可作为 HER2 阳性乳腺癌的生存替代标志物。

Tumor Cellularity and Infiltrating Lymphocytes as a Survival Surrogate in HER2-Positive Breast Cancer.

机构信息

Department of Medical Oncology, Hospital Clinic of Barcelona, Barcelona, Spain.

Translational Genomics and Targeted Therapies in Solid Tumors, August Pi i Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain.

出版信息

J Natl Cancer Inst. 2022 Mar 8;114(3):467-470. doi: 10.1093/jnci/djab057.

Abstract

In early-stage HER2-positive breast cancer, biomarkers that guide deescalation and/or escalation of systemic therapy are needed. CelTIL score is a novel, combined biomarker based on stromal tumor-infiltrating lymphocytes and tumor cellularity and is determined in tumor biopsies at week 2 of anti-HER2 therapy only. We evaluated the prognostic value of CelTIL in 196 patients with early-stage HER2-positive disease treated with standard trastuzumab-based chemotherapy in the NeoALTTO phase III trial. Using a prespecified CelTIL cutoff, a better 5-year event-free survival and overall survival was observed between CelTIL-high and CelTIL-low score with a 76.4% (95% confidence interval [CI] = 68.0% to 85.0%) vs 59.7% (95% CI = 50.0% to 72.0%) (hazard ratio = 0.40, 95% CI = 0.17 to 0.94) and 86.4% (95% CI = 80.0% to 94.0%) vs 73.5% (95% CI = 64.0% to 84.0%) (hazard ratio = 0.43, 95% CI = 0.20 to 0.92), respectively. Statistical significance was maintained after adjusting for baseline tumor-infiltrating lymphocytes, hormone receptor status, pretreatment tumor size and nodal status, type of surgery, treatment arm, and pathological complete response. Further studies to support CelTIL as an early readout biomarker to help deescalate or escalate systemic therapy in HER2-positive breast cancer seem warranted.

摘要

在早期 HER2 阳性乳腺癌中,需要有指导系统治疗降级和/或升级的生物标志物。CelTIL 评分是一种新的、基于间质肿瘤浸润淋巴细胞和肿瘤细胞密度的联合生物标志物,仅在抗 HER2 治疗的第 2 周通过肿瘤活检确定。我们在 NeoALTTO 三期临床试验中评估了 CelTIL 在 196 例早期 HER2 阳性疾病患者中的预后价值,这些患者接受了标准的曲妥珠单抗为基础的化疗。使用预设的 CelTIL 截止值,CelTIL 高评分和 CelTIL 低评分之间观察到更好的 5 年无事件生存率和总生存率,分别为 76.4%(95%置信区间[CI] = 68.0%至 85.0%)和 59.7%(95% CI = 50.0%至 72.0%)(风险比= 0.40,95% CI = 0.17 至 0.94)和 86.4%(95% CI = 80.0%至 94.0%)和 73.5%(95% CI = 64.0%至 84.0%)(风险比= 0.43,95% CI = 0.20 至 0.92)。在调整了基线肿瘤浸润淋巴细胞、激素受体状态、预处理肿瘤大小和淋巴结状态、手术类型、治疗臂和病理完全缓解等因素后,统计学意义仍然保持。进一步的研究似乎支持 CelTIL 作为一种早期读出生物标志物,以帮助降低或升级 HER2 阳性乳腺癌的系统治疗。

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