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器官移植后新发胃肠道肿瘤的前沿与争议:当前进展与未来方向

Frontiers and Controversies in De Novo Gastrointestinal Tumors After Organ Transplantation: Current Progress and Future Directions.

作者信息

Xu Ximo, Zhang Shaopeng, Luo Zai, Zheng Yan, Kong Tingting, Huang Chen, Qiu Zhengjun

机构信息

Department of General Surgery, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

Shanghai Key Laboratory of Pancreatic Disease, Institute of Pancreatic Disease, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

出版信息

Ann Surg Oncol. 2025 May;32(5):3392-3405. doi: 10.1245/s10434-025-16975-w. Epub 2025 Mar 4.

DOI:10.1245/s10434-025-16975-w
PMID:40035907
Abstract

The increasing success of organ transplantation has significantly improved survival for patients with end-stage diseases, yet it introduces a complex dilemma: the elevated risk for the development of de novo gastrointestinal (GI) tumors. The sustained immunosuppression required to maintain graft function paradoxically undermines the body's natural defenses against cancer, leading to a higher incidence, aggressive progression, and atypical presentations of GI tumors among transplant recipients compared with the general population. This presents a pressing challenge: balancing the dual imperatives of preventing graft rejection and effectively managing malignancies. Current treatment paradigms, including surgical approaches, chemotherapy, radiation therapy, and the emerging role of immunotherapy, are fraught with complexities due to the altered immune landscape in these patients. This review underscores the critical need to understand the multifaceted relationship between post-transplantation immunosuppression and tumorigenesis, providing a comprehensive exploration of epidemiologic shifts, pathophysiologic insights, and the intricacies of the tumor microenvironment in this unique patient population. Understanding and managing GI tumors in transplant recipients is not only a clinical challenge, but also a necessary frontier in transplant oncology, promising to refine therapeutic strategies and improve the longevity and quality of life for this growing patient cohort.

摘要

器官移植越来越高的成功率显著提高了终末期疾病患者的生存率,但也带来了一个复杂的困境:新发胃肠道(GI)肿瘤的发生风险升高。维持移植物功能所需的持续免疫抑制反而削弱了机体对癌症的天然防御能力,导致与普通人群相比,移植受者中胃肠道肿瘤的发病率更高、进展更具侵袭性且表现不典型。这带来了一个紧迫的挑战:如何平衡预防移植物排斥和有效管理恶性肿瘤这两个相互矛盾的需求。由于这些患者的免疫格局发生了变化,目前的治疗模式,包括手术方法、化疗、放疗以及免疫疗法的新兴作用,都充满了复杂性。这篇综述强调了理解移植后免疫抑制与肿瘤发生之间多方面关系的迫切需求,全面探讨了这一独特患者群体中的流行病学变化、病理生理学见解以及肿瘤微环境的复杂性。了解和管理移植受者的胃肠道肿瘤不仅是一项临床挑战,也是移植肿瘤学的一个必要前沿领域,有望优化治疗策略,提高这一不断增长的患者群体的寿命和生活质量。

相似文献

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Frontiers and Controversies in De Novo Gastrointestinal Tumors After Organ Transplantation: Current Progress and Future Directions.器官移植后新发胃肠道肿瘤的前沿与争议:当前进展与未来方向
Ann Surg Oncol. 2025 May;32(5):3392-3405. doi: 10.1245/s10434-025-16975-w. Epub 2025 Mar 4.
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[Occurrence, diagnosis and treatment of de novo gastrointestinal malignancies after organ transplantation].[器官移植后新发胃肠道恶性肿瘤的发生、诊断与治疗]
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本文引用的文献

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FOXP3 regulatory T cell perturbation mediated by the IFNγ-STAT1-IFITM3 feedback loop is essential for anti-tumor immunity.干扰素 γ-STAT1-IFITM3 反馈回路介导的 FOXP3 调节性 T 细胞扰动对于抗肿瘤免疫至关重要。
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Acquisition of suppressive function by conventional T cells limits antitumor immunity upon T depletion.常规 T 细胞获得抑制功能会限制 T 细胞耗竭后抗肿瘤免疫。
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Targeting TREM1 augments antitumor T cell immunity by inhibiting myeloid-derived suppressor cells and restraining anti-PD-1 resistance.
靶向 TREM1 通过抑制髓系来源的抑制细胞并抑制抗 PD-1 耐药性来增强抗肿瘤 T 细胞免疫。
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Modulating Treg stability to improve cancer immunotherapy.调节调节性T细胞稳定性以改善癌症免疫疗法。
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The Akt/mTOR and MNK/eIF4E pathways rewire the prostate cancer translatome to secrete HGF, SPP1 and BGN and recruit suppressive myeloid cells.Akt/mTOR 和 MNK/eIF4E 通路重塑前列腺癌翻译组以分泌 HGF、SPP1 和 BGN 并募集抑制性髓样细胞。
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TIGIT Expression Delineates T-cell Populations with Distinct Functional and Prognostic Impact in Pancreatic Cancer.TIGIT 表达可区分胰腺癌中具有不同功能和预后影响的 T 细胞群体。
Clin Cancer Res. 2023 Jul 14;29(14):2638-2650. doi: 10.1158/1078-0432.CCR-23-0258.
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Conserved transcriptional connectivity of regulatory T cells in the tumor microenvironment informs new combination cancer therapy strategies.肿瘤微环境中调节性 T 细胞的保守转录连通性为新的联合癌症治疗策略提供信息。
Nat Immunol. 2023 Jun;24(6):1020-1035. doi: 10.1038/s41590-023-01504-2. Epub 2023 May 1.
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Therapeutic targeting of tumour myeloid cells.肿瘤髓样细胞的治疗靶点
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10
Solid Organ Transplantation Is Associated with an Increased Rate of Mismatch Repair Deficiency and PIK3CA Mutations in Colorectal Cancer.实体器官移植与结直肠癌中错配修复缺陷和 PIK3CA 突变的发生率增加有关。
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