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Pneumonitis in Patients Treated With Anti-Programmed Death-1/Programmed Death Ligand 1 Therapy
Jarushka Naidoo1, Xuan Wang1, Kaitlin M Woo1
1Jarushka 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.
Abstract:
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.
Insights
Pneumonitis is a rare but serious side effect of immune checkpoint inhibitors like anti-PD-1/PD-L1 monoclonal antibodies. Combination therapy increases pneumonitis risk, though most cases resolve with treatment.
Area of Science:
- Oncology
- Immunology
- Pulmonology
Background:
- Pneumonitis is an uncommon but potentially fatal toxicity associated with anti-programmed death-1 (PD-1)/programmed death ligand 1 (PD-L1) monoclonal antibodies (mAbs).
- The clinical, radiologic, and pathologic features of this toxicity are not well-described.
- Understanding these features is crucial for managing patients receiving these novel immunotherapies.
Purpose of the Study:
- To describe the clinical, radiologic, and pathologic features of pneumonitis associated with anti-PD-1/PD-L1 mAb therapy.
- To determine the incidence of pneumonitis in patients receiving monotherapy versus combination therapy.
- To examine the outcomes of pneumonitis in patients treated with these agents.
Main Methods:
- Retrospective review of patients who received anti-PD-1/PD-L1 mAbs at two institutions.
- Pneumonitis diagnosis by treating investigator, excluding malignant lung infiltration or infection.
- Analysis of clinical, radiologic, and pathologic features, and associations with therapy and outcomes.
Main Results:
- Pneumonitis occurred in 5% of 915 patients, with similar incidence in melanoma and non-small cell lung cancer.
- Incidence was significantly higher with combination immunotherapy (10%) versus monotherapy (3%) (P < .01).
- Most cases (72%) were low grade and improved with treatment; however, 5 patients died due to pneumonitis or related complications.
Conclusions:
- Pneumonitis from anti-PD-1/PD-L1 mAbs is a toxicity with variable presentation and onset.
- Combination immunotherapy with anti-cytotoxic T-cell lymphocyte-4 mAb increases pneumonitis risk.
- While most cases are manageable, severe outcomes including death can occur, necessitating careful monitoring and management.
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