Naidoo Jarushka, Wang Xuan, Woo Kaitlin M, Iyriboz Tunc, Halpenny Darragh, Cunningham Jane, Chaft Jamie E, Segal Neil H, Callahan Margaret K, Lesokhin Alexander M, Rosenberg Jonathan, Voss Martin H, Rudin Charles M, Rizvi Hira, Hou Xue, Rodriguez Katherine, Albano Melanie, Gordon Ruth-Ann, Leduc Charles, Rekhtman Natasha, Harris Bianca, Menzies Alexander M, Guminski Alexander D, Carlino Matteo S, Kong Benjamin Y, Wolchok Jedd D, Postow Michael A, Long Georgina V, Hellmann Matthew D
Jarushka Naidoo, Kaitlin M. Woo, Tunc Iyriboz, Darragh Halpenny, Jane Cunningham, Jamie E. Chaft, Neil H. Segal, Margaret K. Callahan, Alexander M. Lesokhin, Jonathan Rosenberg, Martin H. Voss, Charles M. Rudin, Hira Rizvi, Xue Hou, Katherine Rodriguez, Melanie Albano, Ruth-Ann Gordon, Charles Leduc, Natasha Rekhtman, Bianca Harris, Jedd D. Wolchok, Michael A. Postow, and Matthew D. Hellmann, Memorial Sloan Kettering Cancer Center; Jamie E. Chaft, Neil H. Segal, Margaret K. Callahan, Alexander M. Lesokhin, Jonathan Rosenberg, Martin H. Voss, Charles M. Rudin, Jedd D. Wolchok, Michael A. Postow, and Matthew D. Hellmann, Weill Cornell Medical College, New York, NY; Jarushka Naidoo, Sidney Kimmel Cancer Center at Johns Hopkins University, Baltimore, MD; Xuan Wang, Peking University Cancer Hospital and Institute, Beijing; Xue Hou, Sun Yat-sen University Cancer Center, Guangdong Province, People's Republic of China; Xuan Wang, Matteo S. Carlino, Benjamin Y. Kong, and Georgina V. Long, The University of Sydney; Alexander M. Menzies and Alexander D. Guminski, Royal North Shore and Mater Hospital; and Matteo S. Carlino and Benjamin Y. Kong, Westmead and Blacktown Hospitals, Sydney, Australia.
J Clin Oncol. 2017 Mar;35(7):709-717. doi: 10.1200/JCO.2016.68.2005. Epub 2016 Sep 30.
Purpose Pneumonitis is an uncommon but potentially fatal toxicity of anti-programmed death-1 (PD-1)/programmed death ligand 1 (PD-L1) monoclonal antibodies (mAbs). Clinical, radiologic, and pathologic features are poorly described. Methods Patients who received anti-PD-1/PD-L1 monotherapy or in combination with anti-cytotoxic T-cell lymphocyte-4 mAb were identified at two institutions (Memorial Sloan Kettering Cancer Center: advanced solid cancers, 2009 to 2014, and Melanoma Institute of Australia: melanomas only, 2013 to 2015). Pneumonitis was diagnosed by the treating investigator; cases with confirmed malignant lung infiltration or infection were excluded. Clinical, radiologic, and pathologic features of pneumonitis were collected. Associations among pneumonitis incidence, therapy received, and underlying malignancy were examined with Fisher's exact test as were associations between pneumonitis features and outcomes. Results Of 915 patients who received anti-PD-1/PD-L1 mAbs, pneumonitis developed in 43 (5%; 95% CI, 3% to 6%; Memorial Sloan Kettering Cancer Center, 27 of 578 [5%]; Melanoma Institute of Australia, 16 of 337 [5%]). Time to onset of pneumonitis ranged from 9 days to 19.2 months. The incidence of pneumonitis was higher with combination immunotherapy versus monotherapy (19 of 199 [10%] v 24 of 716 [3%]; P < .01). Incidence was similar in patients with melanoma and non-small-cell lung cancer (overall, 26 of 532 [5%] v nine of 209 [4%]; monotherapy, 15 of 417 v five of 152 [ P = 1.0]; combination, 11 of 115 v four of 57 [ P = .78]). Seventy-two percent (31 of 43) of cases were grade 1 to 2, and 86% (37 of 43) improved/resolved with drug holding/immunosuppression. Five patients worsened clinically and died during the course of pneumonitis treatment; proximal cause of death was pneumonitis (n = 1), infection related to immunosuppression (n = 3), or progressive cancer (n = 1). Radiologic and pathologic features of pneumonitis were diverse. Conclusion Pneumonitis associated with anti-PD-1/PD-L1 mAbs is a toxicity of variable onset and clinical, radiologic, and pathologic appearances. It is more common when anti-PD-1/PD-L1 mAbs are combined with anti-cytotoxic T-cell lymphocyte-4 mAb. Most events are low grade and improve/resolve with drug holding/immunosuppression. Rarely, pneumonitis worsens despite immunosuppression, and may result in infection and/or death.
目的 肺炎是抗程序性死亡蛋白1(PD-1)/程序性死亡配体1(PD-L1)单克隆抗体(mAb)一种不常见但可能致命的毒性反应。临床、放射学及病理学特征的描述较少。方法 在两家机构(纪念斯隆凯特琳癌症中心:2009年至2014年的晚期实体癌患者,以及澳大利亚黑色素瘤研究所:2013年至2015年的仅黑色素瘤患者)中确定接受抗PD-1/PD-L1单药治疗或联合抗细胞毒性T淋巴细胞相关抗原4 mAb治疗的患者。肺炎由主治研究人员诊断;排除确诊为恶性肺浸润或感染的病例。收集肺炎的临床、放射学及病理学特征。采用Fisher精确检验分析肺炎发生率、所接受治疗及潜在恶性肿瘤之间的关联,以及肺炎特征与结局之间的关联。结果 在915例接受抗PD-1/PD-L1 mAb治疗的患者中,43例(5%;95%可信区间,3%至6%)发生肺炎(纪念斯隆凯特琳癌症中心,578例中的27例[5%];澳大利亚黑色素瘤研究所,337例中的16例[5%])。肺炎发病时间为9天至19.2个月。联合免疫治疗组肺炎发生率高于单药治疗组(199例中的19例[10%]对716例中的24例[3%];P<0.01)。黑色素瘤和非小细胞肺癌患者的发生率相似(总体而言,532例中的26例[5%]对209例中的9例[4%];单药治疗,417例中的15例对152例中的5例[P=1.0];联合治疗,115例中的11例对57例中的4例[P=0.78])。72%(43例中的31例)的病例为1至2级,86%(43例中的37例)通过停药/免疫抑制得到改善/缓解。5例患者在肺炎治疗过程中临床症状恶化并死亡;死亡的直接原因是肺炎(n=1)、免疫抑制相关感染(n=3)或癌症进展(n=1)。肺炎的放射学和病理学特征多样。结论 抗PD-1/PD-L1 mAb相关肺炎是一种起病时间、临床、放射学及病理学表现各异的毒性反应。当抗PD-1/PD-L1 mAb与抗细胞毒性T淋巴细胞相关抗原4 mAb联合使用时更为常见。大多数事件为低级别,通过停药/免疫抑制可改善/缓解。尽管进行了免疫抑制,肺炎仍很少恶化,并可能导致感染和/或死亡。