Immunotherapy in GI Cancers: Lessons from Key Trials and Future Clinical Applications.

IF 2.7 Q3 IMMUNOLOGY
Antibodies Pub Date : 2025-07-11 DOI:10.3390/antib14030058
Supriya Peshin, Faizan Bashir, Naga Anvesh Kodali, Adit Dharia, Sajida Zaiter, Sakshi Singal, Nagaishwarya Moka
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引用次数: 0

Abstract

Immunotherapy has emerged as a transformative approach in gastrointestinal (GI) cancers, addressing historically poor survival rates in advanced-stage disease. Immune checkpoint inhibitors (ICIs) targeting the PD-1/PD-L1 axis demonstrate remarkable efficacy in colorectal cancer with deficient mismatch repair (dMMR) or high microsatellite instability (MSI-H), exemplified by trials like NICHE-2 achieving exceptional pathological response rates. However, significant limitations persist, including resistance in some dMMR/MSI-H tumors, minimal efficacy in proficient mismatch repair (pMMR) tumors, and low overall response rates across most GI malignancies due to tumor heterogeneity and immune evasion mechanisms. Predictive biomarkers such as tumor mutational burden (TMB) and PD-L1 expression are crucial for optimizing patient selection, while hypermutated pMMR tumors with POLE mutations represent emerging therapeutic opportunities. In pancreatic adenocarcinoma, where survival remains dismal, combination strategies with chemotherapy and novel approaches like cancer vaccines show promise but lack transformative breakthroughs. Esophagogastric cancers benefit from ICIs combined with chemotherapy, particularly in MSI-H and HER2-positive tumors, while hepatocellular carcinoma has achieved significant progress with combinations like atezolizumab-bevacizumab and durvalumab-tremelimumab surpassing traditional therapies. Biliary tract cancers show modest improvements with durvalumab-chemotherapy combinations. Despite these advances, immunotherapy faces substantial challenges including immune-related adverse events, acquired resistance through cancer immunoediting, and the need for biomarker-driven approaches to overcome tumor microenvironment barriers. This review discusses key clinical trials, therapeutic progress, and emerging modalities including CAR T-cell therapies and combination strategies, emphasizing the critical need to address resistance mechanisms and refine precision medicine approaches to fully realize immunotherapy's potential in GI malignancies.

免疫治疗在胃肠道肿瘤:从关键试验和未来临床应用的教训。
免疫疗法已成为胃肠道(GI)癌症的一种变革性方法,解决了历史上晚期疾病的低生存率。靶向PD-1/PD-L1轴的免疫检查点抑制剂(ICIs)在具有缺陷错配修复(dMMR)或高微卫星不稳定性(MSI-H)的结直肠癌中显示出显着的疗效,例如NICHE-2试验获得了异常的病理反应率。然而,显著的局限性仍然存在,包括在一些dMMR/MSI-H肿瘤中的耐药性,在精通错配修复(pMMR)肿瘤中的最低疗效,以及由于肿瘤异质性和免疫逃避机制,大多数胃肠道恶性肿瘤的总体应答率较低。预测性生物标志物如肿瘤突变负荷(TMB)和PD-L1表达对于优化患者选择至关重要,而极突变的pMMR肿瘤代表了新兴的治疗机会。在生存率仍然很低的胰腺腺癌中,化疗和癌症疫苗等新方法的联合策略显示出希望,但缺乏变革性的突破。食管胃癌从ICIs联合化疗中获益,特别是在MSI-H和her2阳性肿瘤中,而肝细胞癌在atezolizumab-bevacizumab和durvalumab-tremelimumab等联合治疗中取得了显着进展,超过了传统疗法。胆道肿瘤在杜伐单抗联合化疗中表现出适度的改善。尽管取得了这些进展,但免疫治疗面临着巨大的挑战,包括免疫相关的不良事件,通过癌症免疫编辑获得的耐药性,以及需要生物标志物驱动的方法来克服肿瘤微环境障碍。本文讨论了关键的临床试验、治疗进展和包括CAR - t细胞治疗和联合策略在内的新兴模式,强调了解决耐药机制和完善精准医学方法的关键必要性,以充分发挥免疫治疗在胃肠道恶性肿瘤中的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Antibodies
Antibodies IMMUNOLOGY-
CiteScore
7.10
自引率
6.40%
发文量
68
审稿时长
11 weeks
期刊介绍: Antibodies (ISSN 2073-4468), an international, peer-reviewed open access journal which provides an advanced forum for studies related to antibodies and antigens. It publishes reviews, research articles, communications and short notes. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. There is no restriction on the length of the papers. Full experimental and/or methodical details must be provided. Electronic files or software regarding the full details of the calculation and experimental procedure - if unable to be published in a normal way - can be deposited as supplementary material. This journal covers all topics related to antibodies and antigens, topics of interest include (but are not limited to): antibody-producing cells (including B cells), antibody structure and function, antibody-antigen interactions, Fc receptors, antibody manufacturing antibody engineering, antibody therapy, immunoassays, antibody diagnosis, tissue antigens, exogenous antigens, endogenous antigens, autoantigens, monoclonal antibodies, natural antibodies, humoral immune responses, immunoregulatory molecules.
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