CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Evaluation of PD-L1 and tumor infiltrating lymphocytes in paired pretreatment biopsies and post neoadjuvant chemotherapy surgical specimens of breast carcinoma.
Evaluation of PD-L1 and tumor infiltrating lymphocytes in paired pretreatment biopsies and post neoadjuvant chemotherapy surgical specimens of breast carcinoma.
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本文评估了治疗前空芯针活检中PD-L1免疫组化表达及间质TIL(肿瘤浸润淋巴细胞)(sTIL)计数对乳腺癌(BC)患者新辅助化疗(NACT)反应的影响。在127对NACT前后BC标本中,评估了间质和肿瘤细胞中PD-L1的免疫组化表达。在同一批样本中,对肿瘤间质中的sTIL进行了半定量。NACT后标本经组织学评定为存在残余肿瘤负荷(RCB,任何程度),或达到完全病理缓解(pCR)。PD-L1表达和较高的sTIL计数与组织学分级3级BC相关。PD-L1表达还与BC的非luminal-HER2+和三阴性免疫组化分型相关。病理完全缓解与组织学分级3级肿瘤以及非luminal-HER2+和三阴性分型相关。
此外,我们的结果支持PD-L1表达与NACT后pCR之间的关联。还观察到,在达到pCR的患者NACT后标本中,sTIL计数有减少趋势。
值得注意的是,PD-L1在半数激素受体阳性病例中表达,这一发现可能扩大免疫检查点抑制剂在BC患者中的潜在应用。
Herein it was evaluated the impact of PD-L1 immunohistochemical expression and stromal tumor-infiltrating lymphocyte (sTIL) counts in pretreatment needle core biopsy on response to neoadjuvant chemotherapy (NACT) for patients with breast carcinomas (BC). In 127 paired pre- and post-NACT BC specimens, immunohistochemical expression of PD-L1 was evaluated in stroma and in neoplastic cells. In the same samples sTILs were semi-quantified in tumor stroma.
Post-NACT specimens were histologically rated as having residual cancer burden (RCB of any degree), or with complete pathological response (pCR). PD-L1 expression and higher sTIL counts were associated with histological grade 3 BC. PD-L1 expression was also associated with the non-luminal-HER2+ and triple negative immunohistochemical profiles of BC. Pathological complete response was associated with histological grade 3 tumors, and with the non-luminal-HER2+ and triple negative profiles.
Additionally, our results support an association between PD-L1 expression and pCR to NACT. It was also observed that there is a trend to reduction of sTIL counts in the post-NACT specimens of patients with pCR. Of note, PD-L1 was expressed in half of the hormone receptor positive cases, a finding that might expand the potential use of immune checkpoint inhibitors for BC patients.
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