Sahin Irem, Turen Sevda, Santapuram Pranav, Sahin Ibrahim Halil
Baskent University School of Medicine, Department of Medicine Ankara, Ankara 06810, Turkey.
TC Istanbul Kültür University, Faculty of Health Sciences, Department of Nursing, Istanbul 34158, Turkey.
Cancer Drug Resist. 2020 Sep 4;3(4):699-709. doi: 10.20517/cdr.2020.48. eCollection 2020.
Pancreatic cancer is one of the most aggressive cancers with a high mortality rate even among patients with early-stage disease. Although recent studies with novel therapeutic approaches have led to modest improvement in survival outcomes, limited progress is achieved for the use of immunotherapeutics in this challenging cancer. Immune checkpoint inhibitors, thus far, single-agent or in combination, have not yielded significant improvement in survival outcomes except in mismatch repair-deficient pancreatic cancer. The tumor microenvironment of pancreatic cancer has been considered as an attractive target for over a decade based on preclinical studies that suggested it may adversely affect drug delivery and antitumor immunity. In this review article, we elaborate on the biology of pancreatic cancer microenvironment, its highly complicated interaction with cancer cells, and the immune system. We also discuss plausible explanations that led to the failure of immune checkpoint inhibitors as therapeutic agents and the potential impacts of pancreatic cancer stroma on these negative studies.
胰腺癌是侵袭性最强的癌症之一,即便在早期疾病患者中死亡率也很高。尽管近期采用新型治疗方法的研究已使生存结果有了一定改善,但在这种具有挑战性的癌症中,免疫疗法的应用进展有限。迄今为止,免疫检查点抑制剂无论是单药治疗还是联合治疗,除了错配修复缺陷型胰腺癌外,均未在生存结果方面取得显著改善。基于临床前研究表明胰腺癌的肿瘤微环境可能会对药物递送和抗肿瘤免疫产生不利影响,十多年来它一直被视为一个有吸引力的靶点。在这篇综述文章中,我们详细阐述了胰腺癌微环境的生物学特性、它与癌细胞以及免疫系统之间极其复杂的相互作用。我们还讨论了导致免疫检查点抑制剂作为治疗药物失败的合理原因,以及胰腺癌基质对这些阴性研究的潜在影响。