The Effect of PD-1/PD-L1 Inhibitor and Statin Combination Therapy on Overall Survival and Gastrointestinal Toxicity.

IF 1.6 4区 医学 Q4 ONCOLOGY
Jay Shah, Andres Caleb Urias Rivera, Irene Jeong-Ah Lee, Kei Takigawa, Antony Mathew, Deanna Wu, Eric Lu, Malek Shatila, Anusha S Thomas, Hao Chi Zhang, Mehmet Altan, Dan Zhao, Qinghuan Xiao, Yinghong Wang
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引用次数: 0

Abstract

Objectives: Immune checkpoint inhibitors (ICIs), such as programmed cell death 1 (PD-1) and programmed cell death ligand 1 (PD-L1) inhibitors, have been approved to treat a variety of cancers. Recently, studies have suggested that ICIs and statins are synergistic. However, the addition of statins to ICI therapy may increase the risk of gastrointestinal immune-related adverse events (irAEs). We investigated the effect of combination therapy with PD-1 and/or L1 inhibitors and statins on overall survival and gastrointestinal irAEs.

Methods: We reviewed the charts of patients with select cancers who received PD-1 and/or PD-L1 inhibitors and statins. The incidence of gastrointestinal irAEs and overall survival were compared with that in a matched control group of patients who received PD-1 and/or PD-L1 inhibitors without statins.

Results: Of the 823 patients in the statin group, 707 received PD-1 inhibitors, 86 received PD-L1 inhibitors, and 30 received both. Patients taking any statins (10.8%) and those taking high-intensity statins (15.8%) had higher rates of gastrointestinal irAEs than patients not taking statins (8.7%; P=0.046 and 0.006, respectively). Compared with the nonstatin treatments, statin use was associated with improved overall survival for patients taking PD-1 inhibitors (P<0.001) and for patients with (P=0.021) and without (P<0.001) gastrointestinal irAEs.

Conclusions: Synergism of statins with PD-1 and PD-L1 inhibitors continues to be a developing field of interest. Our data demonstrate the survival benefit of combination therapy with PD-1 and/or PD-L1 inhibitors and statins, warranting further investigation.

PD-1/PD-L1抑制剂和他汀类药物联合疗法对总生存期和胃肠道毒性的影响
目的:免疫检查点抑制剂(ICIs),如程序性细胞死亡 1(PD-1)和程序性细胞死亡配体 1(PD-L1)抑制剂,已被批准用于治疗多种癌症。最近有研究表明,ICIs 和他汀类药物具有协同作用。然而,在 ICI 治疗中加入他汀类药物可能会增加胃肠道免疫相关不良事件(irAEs)的风险。我们研究了PD-1和/或L1抑制剂与他汀类药物联合治疗对总生存期和胃肠道IRAEs的影响:我们回顾了接受 PD-1 和/或 PD-L1 抑制剂和他汀类药物治疗的特定癌症患者的病历。结果:在接受 PD-1 和/或 PD-L1 抑制剂治疗但未服用他汀类药物的 823 名他汀类药物对照组患者中,有 823 人发生了胃肠道虹膜异位症:在他汀类药物组的823名患者中,707人接受了PD-1抑制剂治疗,86人接受了PD-L1抑制剂治疗,30人同时接受了两种治疗。与未服用他汀类药物的患者(8.7%;P=0.046 和 0.006)相比,服用任何他汀类药物的患者(10.8%)和服用高强度他汀类药物的患者(15.8%)的胃肠道irAEs发生率更高。与非他汀类药物治疗相比,他汀类药物的使用与服用 PD-1 抑制剂的患者总生存期的改善有关(PConclusions:他汀类药物与PD-1和PD-L1抑制剂的协同作用仍是一个备受关注的发展领域。我们的数据表明,PD-1和/或PD-L1抑制剂与他汀类药物联合治疗可提高生存率,值得进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
4.90
自引率
0.00%
发文量
130
审稿时长
4-8 weeks
期刊介绍: ​​​​​​​American Journal of Clinical Oncology is a multidisciplinary journal for cancer surgeons, radiation oncologists, medical oncologists, GYN oncologists, and pediatric oncologists. The emphasis of AJCO is on combined modality multidisciplinary loco-regional management of cancer. The journal also gives emphasis to translational research, outcome studies, and cost utility analyses, and includes opinion pieces and review articles. The editorial board includes a large number of distinguished surgeons, radiation oncologists, medical oncologists, GYN oncologists, pediatric oncologists, and others who are internationally recognized for expertise in their fields.
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