Anirudh Pabba, Gitte Zels, Maxim De Schepper, Tatjana Geukens, Karen Van Baelen, Marion Maetens, Sophia Leduc, Ha Linh Nguyen, Amena Mahdami, Josephine Van Cauwenberge, Kristien Borremans, Hava Izci, Sigrid Hatse, Patrick Neven, Hans Wildiers, Elia Biganzoli, Wouter Van Den Bogaert, François Richard, Giuseppe Floris, Christine Desmedt
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In this study, we explored stromal tumor-infiltrating lymphocytes (sTIL) in metastatic samples collected through our post-mortem tissue donation program UPTIDER (NCT04531696). sTIL were scored as a continuous parameter according to international guidelines on 427 metastases and 38 primary untreated tumors acquired from 20 patients with HR+/HER2- mBC. ER-status was evaluated on 362 metastases with a cut-off for positivity set at 1% according to ASCO/CAP guidelines. Our analyses show that 54% and 15% of metastases had sTIL levels >1% and >5% respectively. sTIL levels tended to be lower in metastases as compared to their respective primary tumor (Estimate: -2.83, 95%CI: -5.77-0.11, p:0.07). sTIL levels were lower in metastases from invasive lobular carcinoma than in metastases from invasive breast carcinoma of no special type (Estimate: -1.67, 95%CI: -2.35--0.98, p:<0.001). 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引用次数: 0
摘要
激素受体阳性、HER2 阴性的转移性乳腺癌(HR+/HER2- mBC)是最常见的乳腺癌亚型,其免疫状况仍未得到充分研究。这主要是因为与原发肿瘤相比,从转移灶获取样本的机会较少。在这项研究中,我们探讨了通过死后组织捐献计划 UPTIDER(NCT04531696)收集的转移瘤样本中的基质肿瘤浸润淋巴细胞(sTIL)。根据国际指南,我们对从 20 位 HR+/HER2- mBC 患者身上采集的 427 例转移瘤和 38 例未经治疗的原发肿瘤的 sTIL 进行了连续参数评分。根据 ASCO/CAP 指南,对 362 例转移瘤进行了ER状态评估,阳性临界值定为 1%。我们的分析表明,分别有 54% 和 15% 的转移灶的 sTIL 水平大于 1% 和大于 5%。与各自的原发肿瘤相比,转移灶的 sTIL 水平往往较低(估计值:-2.浸润性小叶癌转移灶的 sTIL 水平低于无特殊类型的浸润性乳腺癌转移灶(估计值:-1.67,95%CI:-2.35--0.98,P:0.07):
Stromal tumor infiltrating lymphocytes in hormone receptor positive/HER2 negative metastatic breast cancer.
The immune landscape of hormone receptor positive, HER2-negative metastatic breast cancer (HR+/HER2- mBC), the most common subtype of BC, remains understudied. This is mainly due to reduced sample acquisition opportunities from metastases as compared to primary tumors. In this study, we explored stromal tumor-infiltrating lymphocytes (sTIL) in metastatic samples collected through our post-mortem tissue donation program UPTIDER (NCT04531696). sTIL were scored as a continuous parameter according to international guidelines on 427 metastases and 38 primary untreated tumors acquired from 20 patients with HR+/HER2- mBC. ER-status was evaluated on 362 metastases with a cut-off for positivity set at 1% according to ASCO/CAP guidelines. Our analyses show that 54% and 15% of metastases had sTIL levels >1% and >5% respectively. sTIL levels tended to be lower in metastases as compared to their respective primary tumor (Estimate: -2.83, 95%CI: -5.77-0.11, p:0.07). sTIL levels were lower in metastases from invasive lobular carcinoma than in metastases from invasive breast carcinoma of no special type (Estimate: -1.67, 95%CI: -2.35--0.98, p:<0.001). A loss of ER expression was observed in 14% of all metastases, yet a negative ER-status was not significantly associated with increased sTIL levels. Finally, sTIL levels were significantly higher in lung and axillary lymph node metastases compared to all metastases. While these analyses were conducted on multiple metastases obtained at the end of life after several lines of treatment, the data provides novel and valuable insights into the state of immune infiltration in patients with metastatic HR+/HER2- BC.
期刊介绍:
Modern Pathology, an international journal under the ownership of The United States & Canadian Academy of Pathology (USCAP), serves as an authoritative platform for publishing top-tier clinical and translational research studies in pathology.
Original manuscripts are the primary focus of Modern Pathology, complemented by impactful editorials, reviews, and practice guidelines covering all facets of precision diagnostics in human pathology. The journal's scope includes advancements in molecular diagnostics and genomic classifications of diseases, breakthroughs in immune-oncology, computational science, applied bioinformatics, and digital pathology.