CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:The Value of Tumor Infiltrating Lymphocytes (TIL) for Predicting the Response to Neoadjuvant Chemotherapy (NAC) in Breast Cancer according to the Molecular Subtypes.
The Value of Tumor Infiltrating Lymphocytes (TIL) for Predicting the Response to Neoadjuvant Chemotherapy (NAC) in Breast Cancer according to the Molecular Subtypes.
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本研究揭示了 TIL 作为乳腺癌预测性生物标志物的作用,不仅适用于已确立的 TNBC(三阴性乳腺癌)和 HER2+(Her2 过表达)亚型,也适用于 Luminal A 和 B 分子亚型。
我们评估了2020至2022年在克卢日-纳波卡“I. Chiricuta教授”肿瘤研究所肿瘤外科第一诊所接受NAC后手术切除的334例乳腺癌病例。其中122例同时有NAC前活检和NAC后切除组织可供组织学评估。采用苏木精-伊红(H&E)染色评估活检及切除标本中的TIL,并遵循国际TIL工作组(ITILWG)建议。
NAC前TIL水平升高与治疗反应之间存在强相关。同时,间质TIL与肿瘤分级、淋巴结转移数、分子亚型及有丝分裂数显著相关(p<0.005)。瘤内TIL与肿瘤大小、远处转移、分子亚型、有丝分裂数、分期及淋巴结转移也显著相关(p<0.005)。我们还证明,NAC前间质TIL(sTIL)高水平是pCR的有力预测标志。
本研究揭示TIL不仅可作为已广泛研究的三阴性乳腺癌(TNBC)和HER2阳性亚型的预测生物标志物,也适用于Luminal A和B型。由此,sTIL评估作为一种新型预测及治疗应答指标,应纳入常规分析,帮助临床医师选择最合适的疗法。
We evaluated 334 cases of BC treated with NAC followed by surgical resection from 2020-2022 at the Ist Clinic of Oncological Surgery, Oncological Institute "Prof Dr I Chiricuta" Cluj Napoca. Of the above, 122 cases were available for histological evaluation both in pre-NAC biopsy and post-NAC resection tissue. Evaluation of biopsy fragments and resection parts were performed using hematoxylin eosin (H&E). The TIL evaluation took place according to the recommendations of the International TIL Working Group (ITILWG).
There was a strong association between elevated levels of pre-NAC TIL. At the same time, there is a statistically significant correlation between stromal TIL and tumor grade, the number of lymph node metastases, the molecular subtype and the number of mitoses ( p < 0.005). Intratumoral TIL showed a significant correlation with tumor size, distant metastasis, molecular subtype, number of mitosis, stage and lymph node metastasis ( p < 0.005). We also demonstrated that high pre-NAC STIL represents a strong predictive marker for pCR.
This study reveals the role of TIL as a predictive biomarker in breast cancer not only for the well-established TNBC (triple negative breast cancer) and HER2+ (Her2 overexpressed) subtypes but also in Luminal A and B molecular subtypes. In this scenario, the evaluation of sTIL as a novel predictive and therapy-predicting factor should become a routinely performed analysis that could guide clinicians when choosing the most appropriate therapy.
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