ArticleCureus2025
Premature Pembrolizumab-Induced Pulmonary Problems: A Case of Atypical Early-Onset Checkpoint Inhibitor Pneumonitis.
Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
2 citing papers in PubMed.
- Bronchoalveolar lavage fluid in immune checkpoint inhibitor-related pneumonitis: from pathophysiological window to a precision diagnostic tool.Frontiers in immunology · 2026Review
- Fatal early-onset checkpoint inhibitor pneumonitis in a patient with advanced squamous-cell lung cancer with underlying pulmonary fibrosis: a case report and review of the literature.Frontiers in oncology · 2025Article
Corrections and comments
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Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Checkpoint inhibitor pneumonitis (CIP) is a rare but potentially devastating complication of immune checkpoint inhibitor therapy. Due to its nonspecific and variable clinical appearance, CIP can be misdiagnosed or recognized late, resulting in delayed treatment and poor clinical outcomes. We report the case of a 65-year-old female patient with chronic obstructive pulmonary disease (COPD), a significant smoking history, and non-small cell lung carcinoma (NSCLC) who had an atypical early, moderate-to-severe CIP after just two infusions of pembrolizumab. During hospitalization, she demonstrated minimal improvement on empiric treatment for COPD, congestive heart failure (CHF) exacerbation, and pneumonia. On day 9 of hospitalization, computed tomography identified ground-glass opacities in the right posterior lung, prompting escalation of steroid treatment to 2 mg/kg/day to treat CIP. The patient subsequently improved, returned to her baseline oxygen requirements, and was discharged with plans to discontinue pembrolizumab therapy. This case report highlights the atypically early and rapid development of pembrolizumab-induced CIP, demonstrating the need for timely diagnosis and medical intervention. It also raises important questions regarding the continuation of immunotherapy following CIP.
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Registered trials
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