中国实用外科杂志 ›› 2025, Vol. 45 ›› Issue (06): 659-665.DOI: 10.19538/j.cjps.issn1005-2208.2025.06.11

• 专题笔谈 • 上一篇    下一篇

胰腺癌免疫治疗联合方案的应用价值与前景

浦    宁,刘    亮   

  1. 复旦大学附属中山医院胰腺外科,上海200032
  • 出版日期:2025-06-01 发布日期:2025-07-01

  • Online:2025-06-01 Published:2025-07-01

摘要: 胰腺癌因其高度免疫抑制性的肿瘤微环境,被认为是典型的免疫“冷肿瘤”,使免疫检查点抑制剂(ICIs)单药治疗疗效受限。近年来,多种联合治疗策略被提出以增强ICIs的疗效,包括与化疗、放疗、靶向治疗、溶瘤病毒、STING激动剂、个体化疫苗和嵌合抗原受体T细胞疗法(CAR-T)等手段的协同应用。这些联合方案通过诱导免疫原性细胞死亡、激活干扰素通路、重塑肿瘤微环境及增强T细胞活性,提升了胰腺癌对免疫治疗的敏感性。尽管初步研究显示联合治疗具有一定临床获益,但仍面临免疫毒性增加、个体异质性大、生物标记物缺乏和耐药机制复杂等挑战。未来应聚焦精准适应证识别、生物机制研究与高质量临床试验验证,推动胰腺癌免疫治疗从探索走向标准化,提升其在晚期与术后辅助等多阶段治疗中的转化潜力。

关键词: 胰腺癌, 免疫治疗, 肿瘤微环境, 联合治疗策略, 前景

Abstract: pancreatic cancer is characterized by a profoundly immunosuppressive tumor microenvironment, rendering it a prototypical“cold tumor”and limiting the efficacy of immune checkpoint inhibitors (ICIs) as monotherapy. In recent years, various combination strategies have been proposed to enhance the therapeutic response to ICIs, including their integration with chemotherapy, radiotherapy, targeted therapy, oncolytic viruses, STING agonists, personalized vaccines, and chimeric antigen receptor (CAR) T-cell therapies. These combinatorial approaches aim to induce immunogenic cell death, activate interferon signaling pathways, remodel the tumor microenvironment, and enhance T cell function, thereby increasing the immunogenicity of pancreatic cancer. Although preliminary studies have shown that such combinations can yield clinical benefits, challenges remain complex, including increased immune-related toxicity, high interpatient heterogeneity, the lack of predictive biomarkers, and complex mechanisms of resistance. Future efforts should focus on refining patient selection, elucidating underlying biological mechanisms, and conducting robust clinical trials to facilitate the transition of immunotherapy for pancreatic cancer from experimental exploration to standardized clinical application, particularly in advanced-stage and adjuvant treatment settings.

Key words: pancreatic cancer, immunotherapy, tumor microenvironment, combination therapeutic strategy, prospect