宫颈透明细胞癌;一种不寻常的不依赖hpv的肿瘤:16例临床病理特征、PD-L1表达和错配修复蛋白缺乏状态。

IF 1 Q4 OBSTETRICS & GYNECOLOGY
Pınar Bulutay, Özgür Can Eren, Özlem Özen, Asuman Nihan Haberal, Nilgün Kapucuoğlu
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引用次数: 0

摘要

目的:宫颈内透明细胞癌(c-CCC)是一种罕见的宫颈腺癌,与hpv无关。通常对常规化疗有抵抗力。最近,免疫治疗作为程序性细胞死亡配体1 (PD-L1)阳性或错配修复(MMR)缺陷宫颈癌的首选二线治疗方案。本研究探讨了c-CCCs的临床病理特征、PD-L1表达和MMR缺乏状态。材料与方法:本研究纳入16例c-CCC确诊病例。使用两个不同的PD-L1克隆(22C3和SP263)评估PD-L1的表达。使用四种MMR蛋白(MLH1、PMS2、MSH2和MSH6)评估病例的MMR缺乏状态。结果:大多数c-CCC病例表现为FIGO I期(68.75%)。在22C3和SP263克隆中,分别有62.5%(10/16)和69%(11/16)的肿瘤或肿瘤浸润性免疫细胞(til)表达PD-L1。大部分TIL密度高的病例PD-L1阳性。大多数病例的PD-L1表达率低于50%,12.5%的病例具有广泛的PD-L1染色。总体而言,31.25%的病例存在MMR缺乏症。大多数mmr缺陷病例(80%)为PD-L1阳性。结论:虽然我们的研究队列有限,但我们已经表明,在不同程度的c-CCCs中可以发现PD-L1表达和MMR缺乏。这些发现表明,伴随的TIL密度和MMR缺乏可以作为预测c-CCCs PD-L1阳性的候选指标。然而,为了表明这些发现的临床重要性,应该看到免疫治疗病例的客观治疗结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Clear cell carcinoma of the uterine cervix; an unusual HPV-independent tumor: Clinicopathological features, PD-L1 expression, and mismatch repair protein deficiency status of 16 cases.

Clear cell carcinoma of the uterine cervix; an unusual HPV-independent tumor: Clinicopathological features, PD-L1 expression, and mismatch repair protein deficiency status of 16 cases.

Clear cell carcinoma of the uterine cervix; an unusual HPV-independent tumor: Clinicopathological features, PD-L1 expression, and mismatch repair protein deficiency status of 16 cases.

Clear cell carcinoma of the uterine cervix; an unusual HPV-independent tumor: Clinicopathological features, PD-L1 expression, and mismatch repair protein deficiency status of 16 cases.

Objective: Endocervical clear cell carcinoma (c-CCC) is a rare and HPV-independent adenocarcinoma type of cervix. Being usually resistant to conventional chemotherapy. Immunotherapy has recently been added as a preferred regimen as a second-line treatment option for programed cell death-ligand 1 (PD-L1)-positive or mismatch repair (MMR) deficient cervical carcinomas. In this study, clinicopathological features, PD-L1 expression, and MMR deficiency status of c-CCCs were investigated.

Materials and methods: Sixteen c-CCC diagnosed cases were included in this study. PD-L1 expression was evaluated using two different PD-L1 clones (22C3 and SP263). MMR deficiency status of the cases was evaluated using four MMR proteins (MLH1, PMS2, MSH2, and MSH6).

Results: Most of the c-CCC cases were presented as FIGO Stage I (68.75%). PD-L1 expression in either tumoral or tumor-infiltrating immune cells (TILs) was present in 62.5% (10/16) and 69% (11/16) of the 22C3 and SP263 clones, respectively. Most of the cases with high TIL density were also positive for PD-L1. The PD-L1 expression rate was less than 50% in most of the cases and 12.5% of the cases shared extensive PD-L1 staining. Overall, MMR deficiency was observed in 31.25% of the cases. Most of the MMR-deficient cases (80%) were PD-L1 positive.

Conclusion: Although our study cohort is limited, we have shown that PD-L1 expression and MMR deficiency can be found in c-CCCs in variable degrees. These findings suggest that accompanying TIL density and MMR deficiency could be used as candidates for predicting PD-L1 positivity for c-CCCs. However, to indicate the clinical importance of these findings, objective treatment outcomes of cases treated with immunotherapy should be seen.

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