为肝细胞癌武装 GPC3 CAR-T 细胞:多少才足够,下一步是什么?
Armouring GPC3 CAR T cells for hepatocellular carcinoma: how much is enough and what comes next?
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Pathologic assessment of hepatocellular carcinoma in the era of immunotherapy: a narrative review.
Pathologic assessment of hepatocellular carcinoma in the era of immunotherapy: a narrative review.
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免疫治疗时代 HCC 的管理带来了全新的病理学挑战,即提供免疫治疗相关的诊断报告。尽管许多相关研究尚处于临床前阶段或证据不足,但它们可能在未来极大地改变 HCC 的免疫治疗策略。
基于免疫检查点抑制剂(ICI)的治疗已在多种癌症类型中取得了令人瞩目的成功。近十年来,多种 ICI 首次被批准作为晚期肝细胞癌(HCC)的治疗方案。与此同时,大量临床试验正在开展,以探索更多 ICI 用于初始不可切除 HCC 和术后 HCC,分别期望诱导充分的肿瘤降期以进一步切除,或实施辅助治疗以实现无复发生存。在本综述中,我们旨在总结一些实用的组织形态学、免疫组织化学和分子病理学参数,这些参数有望指示新辅助/转化 ICI 相关治疗的应答,并预测辅助/治疗性 ICI 相关治疗对 HCC 的疗效。
我们使用肝细胞癌、免疫治疗、免疫检查点抑制剂、免疫检查点阻断、转化治疗、新辅助治疗、辅助治疗、生物标志物、病理学评估、病理学评价等术语在PubMed中检索了截至2023年2月的文献。关键内容与发现:尽管关于相关HCC标本的病理学评估尚无共识,但令人鼓舞的是,已有少数研究集中于该领域,此外,其他癌种中所述的方法和参数也值得参考。对于接受免疫治疗的HCC标本的病理学评估,应强调合适的采样方案、识别免疫治疗相关病理学反应以及病理学缓解率的量化。对于计划接受免疫治疗的HCC患者,TIL(肿瘤浸润淋巴细胞)、瘤内三级淋巴结构、程序性细胞死亡配体1、Wnt/β-catenin、微卫星不稳定和错配修复、肿瘤突变负荷和肿瘤新抗原,以及一些其他信号通路是ICI治疗反应的潜在预测生物标志物。
Immune checkpoint inhibitor (ICI)-based therapy has achieved impressive success in various cancer types. Several ICIs have been unprecedentedly approved as the treatment regimens for advanced hepatocellular carcinoma (HCC) in recent decade. Meanwhile, numerous clinical trials are being performed to exploit more ICIs into initially unresectable HCC and postoperative HCC to expectantly induce adequate tumor downstaging for further resection or implement adjuvant treatment for relapse-free survival, respectively. In this review, we aim to summarize some pragmatic histomorphologic, immunohistochemical, and molecular pathologic parameters which promisingly indicate the response of neoadjuvant/conversion ICI-related therapy and predict the efficacy of adjuvant/therapeutic ICI-related therapy for HCC.
We searched PubMed using the terms hepatocellular carcinoma, immunotherapy, immune checkpoint inhibitor, immune checkpoint blockade, conversion therapy, neoadjuvant therapy, adjuvant therapy, biomarker, pathologic evaluation, pathologic assessment till February 2023. KEY CONTENT AND FINDINGS: Although there is no consensus regarding the pathologic evaluation of relevant HCC specimens, it is encouraging that a few of studies have concentrated on this field, and moreover, the methods and parameters noted on other cancer types are also worthy of reference. For the pathologic assessment of HCC specimens underwent immunotherapy, a suitable sampling scheme, identifying immunotherapy-related pathologic response, and quantification of pathologic response rate should be emphasized. For the patients of HCC who are scheduled to receive immunotherapy, tumor-infiltrating lymphocyte, intratumoral tertiary lymphoid structure, programmed cell death ligand 1, Wnt/β-catenin , microsatellite instability and mismatch repair, tumor mutational burden and tumor neoantigen, as well as some other signaling pathways are the potential predictive biomarkers of treatment response of ICI.
The management of HCC in the era of immunotherapy arises a brand-new pathological challenge that is to provide an immunotherapy-related diagnostic report. Albeit many related researches are preclinical or insufficient, they may tremendously alter the immunotherapy strategy of HCC in future.
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