医学
曲妥珠单抗
肿瘤科
内科学
危险系数
乳腺癌
肿瘤浸润淋巴细胞
三阴性乳腺癌
比例危险模型
队列
置信区间
阶段(地层学)
癌症
免疫疗法
生物
古生物学
作者
Sherene Loi,Stefan Michiels,Roberto Salgado,Nicolas Sirtaine,Vinu José,Debora Fumagalli,Pirkko‐Liisa Kellokumpu‐Lehtinen,Petri Bono,Vesa Kataja,Christine Desmedt,Martine Piccart,Sibylle Loibl,Carsten Denkert,Mark J. Smyth,Heikki Joensuu,Christos Sotiriou
标识
DOI:10.1093/annonc/mdu112
摘要
We have previously shown the prognostic importance of tumor-infiltrating lymphocytes (TILs) in newly diagnosed triple-negative breast cancer (TNBC) using tumor samples from a large clinical trial cohort. In this study, we aimed to validate these findings and also investigate associations with trastuzumab benefit in HER2-overexpressing disease (HER2+).A prospective-retrospective study was conducted using samples from the FinHER adjuvant, phase III trial that enrolled 1010 early-stage BC patients, 778 of whom were HER2-nonamplified. Those with HER2+ disease (n = 232) were randomized to 9 weeks of trastuzumab or no trastuzumab in addition to chemotherapy. Two pathologists independently quantified stromal TILs in 935 (92.6%) available slides. The primary end point of distant disease-free survival (DDFS) and interactions with trastuzumab were studied in Cox regression models.Confirming our previous findings, in TNBC (n = 134) each 10% increase in TILs was significantly associated with decreased distant recurrence in TNBC; for DDFS the hazard ratio adjusted for clinicopathological factors: 0.77; 95% confidence interval (CI) 0.61-0.98, P = 0.02. In HER2+ BC (n = 209), each 10% increase in lymphocytic infiltration was significantly associated with decreased distant recurrence in patients randomized to the trastuzumab arm (DDFS P interaction = 0.025).Higher levels of TILs present at diagnosis were significantly associated with decreased distant recurrence rates in primary TNBC. These results confirm our previous data and further support that TILs should be considered as a robust prognostic factor in this BC subtype. We also report for the first time an association between higher levels of TILs and increased trastuzumab benefit in HER2+ disease. Further research into why some TN and HER2+ BCs can or cannot generate a host antitumor immune response and how trastuzumab can favorably alter the immune microenvironment is warranted.
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