Immune Checkpoint Inhibitors Suppress Hepatitis C Virus Replication in Infected Patients With Solid Tumors

被引:3
|
作者
Yibirin, Marcel [1 ]
Mustafayev, Khalis [1 ]
Hosry, Jeff [1 ]
Pundhir, Pooja [1 ]
Klingen, Joseph [1 ]
Guevara, Eduardo Yepez [1 ]
Granwehr, Bruno P. [1 ]
Kaseb, Ahmed [2 ]
Naing, Aung [3 ]
Patel, Sapna [4 ]
Shah, Amishi Y. [5 ]
Skoulidis, Ferdinandos [6 ]
Tawbi, Hussein A. [4 ]
Wang, Lan [7 ]
Miller, Ethan [7 ]
Zhang, Hao Chi [7 ]
Zurita-Saavedra, Amado [5 ]
Torres, Harrys A. [1 ,7 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Infect Dis Infect Control & Employee Hlth, Houston, TX 77030 USA
[2] Univ Texas MD Anderson Canc Ctr, Dept Gastrointestinal Med Oncol, Houston, TX USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Invest Canc Therapeut, Houston, TX USA
[4] Univ Texas MD Anderson Canc Ctr, Dept Melanoma Med Oncol, Houston, TX USA
[5] Univ Texas MD Anderson Canc Ctr, Dept Genitourinary Med Oncol, Houston, TX USA
[6] Univ Texas MD Anderson Canc Ctr, Dept Thorac & Head & Neck Med Oncol, Houston, TX USA
[7] Univ Texas MD Anderson Canc Ctr, Gastroenterol Hepatol & Nutr, Houston, TX 77030 USA
来源
AMERICAN JOURNAL OF GASTROENTEROLOGY | 2023年 / 118卷 / 09期
关键词
immunotherapy; cancer; hepatitis C virus; inhibition; reactivation; CANCER; SAFETY; ANTI-PD-1; BLOCKADE; CHEMOTHERAPY; REACTIVATION; IPILIMUMAB; ANTIBODY;
D O I
10.14309/ajg.0000000000002361
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
INTRODUCTION:Data are scarce regarding the virologic impact and safety of immune checkpoint inhibitors (ICI) in patients with chronic hepatitis C virus (HCV) infection. We examined the virologic impact of ICI in HCV-infected patients with solid tumors and their safety.METHODS:HCV-infected patients with solid tumor treated with ICI at our institution between April 26, 2016, and January 5, 2022, were enrolled in a prospective observational study. The primary outcomes were ICI-induced changes in HCV viremia (HCV inhibition and HCV reactivation) and safety of ICI.RESULTS:We enrolled 52 consecutive patients with solid tumors treated with ICI. Most were men (41; 79%), White (31; 59%), without cirrhosis (34; 65%), and with HCV genotype 1 (40; 77%). Four patients (7.7%) experienced HCV inhibition while receiving ICI including 1 patient who developed undetectable viremia for 6 months in the absence of direct-acting antivirals (DAA). Two patients (4%) developed HCV reactivation, both while receiving immunosuppressive therapy for ICI-related toxic effects. Adverse events occurred in 36 patients (69%), and 39 of the 47 adverse events (83%) were grade 1-2. Grade 3-4 adverse events occurred in 8 patients (15%), and in all cases, they were related to ICI, not to HCV. No HCV-associated liver failure or death occurred.DISCUSSION:Inhibition of HCV replication with virologic cure can develop in patients receiving ICI without DAA. HCV reactivation occurs primarily in patients receiving immunosuppressants for ICI-related toxic effects. ICI are safe in HCV-infected patients with solid tumors. Chronic HCV infection should not be considered a contraindication for ICI therapy.
引用
收藏
页码:1609 / 1617
页数:9
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