Johnson Douglas B, Balko Justin M, Compton Margaret L, Chalkias Spyridon, Gorham Joshua, Xu Yaomin, Hicks Mellissa, Puzanov Igor, Alexander Matthew R, Bloomer Tyler L, Becker Jason R, Slosky David A, Phillips Elizabeth J, Pilkinton Mark A, Craig-Owens Laura, Kola Nina, Plautz Gregory, Reshef Daniel S, Deutsch Jonathan S, Deering Raquel P, Olenchock Benjamin A, Lichtman Andrew H, Roden Dan M, Seidman Christine E, Koralnik Igor J, Seidman Jonathan G, Hoffman Robert D, Taube Janis M, Diaz Luis A, Anders Robert A, Sosman Jeffrey A, Moslehi Javid J
From the Departments of Medicine (D.B.J., J.M.B., M.H., I.P., M.R.A., T.L.B., J.R.B., D.A.S., E.J.P., M.A.P., D.M.R., J.A.S., J.J.M.), Cancer Biology (J.M.B., J.J.M.), Pathology, Microbiology, and Immunology (M.L.C., L.C.-O., R.D.H.), Biostatistics (Y.X.), Pharmacology (D.M.R.), and Biomedical Informatics (Y.X., D.M.R.), the Cardio-oncology Program (D.A.S., J.J.M.), the Breast Cancer Research Program (J.M.B.), and the Center for Quantitative Sciences (Y.X.), Vanderbilt University Medical Center, Nashville; the Department of Medicine (S.C.) and the Division of Neuroimmunology (S.C., I.J.K.), Beth Israel Deaconess Medical Center, the Departments of Medicine (B.A.O., C.E.S., J.G.S.) and Pathology (A.H.L.), Brigham and Women's Hospital, the Department of Genetics, Harvard Medical School (J.G., C.E.S., J.G.S.) - all in Boston; Howard Hughes Medical Institute, Chevy Chase, MD (C.E.S.); Bristol-Myers Squibb, New York (N.K., G.P., D.S.R., J.S.D.); Neon Therapeutics, Cambridge, MA (R.P.D.); and the Departments of Pathology (J.M.T., R.A.A.), Dermatology (J.M.T.), and Oncology (L.A.D.), Johns Hopkins University, Baltimore.
N Engl J Med. 2016 Nov 3;375(18):1749-1755. doi: 10.1056/NEJMoa1609214.
Immune checkpoint inhibitors have improved clinical outcomes associated with numerous cancers, but high-grade, immune-related adverse events can occur, particularly with combination immunotherapy. We report the cases of two patients with melanoma in whom fatal myocarditis developed after treatment with ipilimumab and nivolumab. In both patients, there was development of myositis with rhabdomyolysis, early progressive and refractory cardiac electrical instability, and myocarditis with a robust presence of T-cell and macrophage infiltrates. Selective clonal T-cell populations infiltrating the myocardium were identical to those present in tumors and skeletal muscle. Pharmacovigilance studies show that myocarditis occurred in 0.27% of patients treated with a combination of ipilimumab and nivolumab, which suggests that our patients were having a rare, potentially fatal, T-cell-driven drug reaction. (Funded by Vanderbilt-Ingram Cancer Center Ambassadors and others.).
免疫检查点抑制剂改善了多种癌症的临床疗效,但可能会发生高级别、免疫相关不良事件,联合免疫治疗时尤其如此。我们报告了两例黑色素瘤患者的病例,他们在接受伊匹单抗和纳武单抗治疗后发生了致命性心肌炎。在这两名患者中,均出现了伴有横纹肌溶解的肌炎、早期进行性和难治性心脏电不稳定,以及有大量T细胞和巨噬细胞浸润的心肌炎。浸润心肌的选择性克隆T细胞群体与肿瘤和骨骼肌中的相同。药物警戒研究表明,接受伊匹单抗和纳武单抗联合治疗的患者中,心肌炎发生率为0.27%,这表明我们的患者发生了一种罕见的、可能致命的、T细胞驱动的药物反应。(由范德比尔特-英格拉姆癌症中心大使及其他机构资助。)