Department of Surgical Oncology, The University of Texas M.D. Anderson Cancer Center, Houston, TX, USA.
Department of Hematology and Medical Oncology, Winship Cancer Institute of Emory University, Atlanta, GA, USA.
Curr Oncol Rep. 2024 Nov;26(11):1530-1542. doi: 10.1007/s11912-024-01610-w. Epub 2024 Oct 28.
This study aims to present the current landscape of immunotherapy in the management of small bowel neuroendocrine tumors and identify ongoing and future targets for improved response.
Somatostatin analogs and mTOR inhibitors remain cornerstones of non-surgical treatment, and applications of PRRT in SBNET are promising. Several efforts to replicate the success of immunotherapies in other solid tumors have been attempted in SBNET, with limited responses observed with current immune targets, such as PD-1/PD-L1 and CTLA-4. Epigenetic analyses have suggested a potential role for methylation and histone acetylation in SBNET tumorigenesis that warrant greater exploration. While the incidence of SBNET continues to increase, the number of effective therapies is few. Further elucidation of targetable components of the SBNET immune microenvironment with greater modulatory effects is necessary to improve outcomes in this growing patient population.
本研究旨在介绍免疫疗法在小肠神经内分泌肿瘤治疗中的现状,并确定当前和未来的潜在靶点,以提高治疗反应。
生长抑素类似物和 mTOR 抑制剂仍然是非手术治疗的基石,PRRT 在 SBNET 中的应用具有广阔前景。人们尝试在 SBNET 中复制免疫疗法在其他实体肿瘤中的成功经验,但是当前免疫靶点(如 PD-1/PD-L1 和 CTLA-4)的反应有限。表观遗传学分析表明,甲基化和组蛋白乙酰化在 SBNET 肿瘤发生中可能具有潜在作用,值得进一步研究。虽然 SBNET 的发病率持续上升,但有效的治疗方法却寥寥无几。需要进一步阐明 SBNET 免疫微环境中具有更大调节作用的靶向成分,以改善这一不断增长的患者群体的治疗效果。