Kciuk Mateusz, Wanke Katarzyna, Kruczkowska Weronika, Marciniak Beata, Kontek Renata
Department of Molecular Biotechnology and Genetics, Faculty of Biology and Environmental Protection, University of Lodz, Banacha Street 12/16, 90-237 Lodz, Poland.
Department of Functional Genomics, Medical University of Lodz, 90-752 Lodz, Poland.
Molecules. 2025 Jun 21;30(13):2686. doi: 10.3390/molecules30132686.
The PD-1/PD-L1 pathway has emerged as a critical target in colorectal cancer (CRC) immunotherapy, with pembrolizumab, nivolumab, and dostarlimab demonstrating significant clinical efficacy, particularly in microsatellite instability-high (MSI-H) and mismatch repair-deficient (dMMR) tumors. However, a growing number of additional PD-1/PD-L1 inhibitors, including AMP-224, atezolizumab, avelumab, camrelizumab, durvalumab, envafolimab, sintilimab, spartalizumab, tislelizumab, and toripalimab, are currently under investigation, offering new possibilities for the expansion of treatment options. This review evaluates the therapeutic potential of these emerging agents, assessing their clinical development, mechanisms of action, and potential advantages over established therapies. Additionally, it explores key challenges such as primary and acquired resistance, limited efficacy in microsatellite-stable (MSS) CRC, and the complexities of combination strategies aimed at enhancing immunotherapeutic responses. By addressing these obstacles and highlighting prospects, this review provides insights into the evolving landscape of PD-1/PD-L1-targeted therapies in CRC and their potential to improve patient outcomes.
PD-1/PD-L1通路已成为结直肠癌(CRC)免疫治疗的关键靶点,派姆单抗、纳武单抗和多斯塔利单抗已显示出显著的临床疗效,尤其是在微卫星高度不稳定(MSI-H)和错配修复缺陷(dMMR)肿瘤中。然而,越来越多的其他PD-1/PD-L1抑制剂,包括AMP-224、阿替利珠单抗、阿维鲁单抗、卡瑞利珠单抗、度伐利尤单抗、恩沃利单抗、信迪利单抗、斯帕妥珠单抗、替雷利珠单抗和托瑞帕利单抗,目前正在研究中,为扩大治疗选择提供了新的可能性。本综述评估了这些新兴药物的治疗潜力,评估了它们的临床开发、作用机制以及相对于现有疗法的潜在优势。此外,它还探讨了关键挑战,如原发性和获得性耐药、微卫星稳定(MSS)CRC中疗效有限,以及旨在增强免疫治疗反应的联合策略的复杂性。通过解决这些障碍并突出前景,本综述深入探讨了CRC中以PD-1/PD-L1为靶点的治疗方法的不断演变格局及其改善患者预后的潜力。