Pleuritis Induced by Brigatinib During the Treatment of Non‐Small Cell Lung Cancer

This report describes the first documented case of brigatinib-induced pleuritis in a patient with ALK-positive non-small cell lung cancer. A 77-year-old woman developed dyspnoea, fever, elevated inflammatory markers, and bilateral pleural effusion shortly after starting brigatinib as third-line therapy. Pleural fluid analysis showed lymphocyte-predominant exudative effusion without evidence of malignancy or infection, suggesting drug-induced pleuritis. Discontinuation of brigatinib led to rapid clinical and radiographic improvement. Although disease progression later occurred, pleuritis did not recur. Re-administration of brigatinib at a reduced dose of 30 mg/day achieved tumour shrinkage without pleuritis recurrence, and subsequent dose escalation to 60 mg/day was also tolerated. This case highlights that clinicians should consider drug-induced pleuritis when pleural effusion develops during brigatinib therapy, particularly when it is inconsistent with the disease progression. Dose reduction to as low as 30 mg/day may be a safe and effective therapeutic option for selected patients.

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Journal
Respirology Case Reports
Published
2026-05-01
DOI
https://doi.org/10.1002/rcr2.70598
Primary Topic
Lung Cancer Treatments and Mutations
Type
article
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article

Pleuritis Induced by Brigatinib During the Treatment of Non‐Small Cell Lung Cancer

Tomoko Harima, Nao Yoshida, Yuki Yoshida, Shohei Yano et al.
Respirology Case Reports
Lung Cancer Treatments and Mutations
article

Pleuritis Induced by Brigatinib During the Treatment of Non‐Small Cell Lung Cancer

Tomoko Harima, Nao Yoshida, Yuki Yoshida, Shohei Yano, Takumi Yamada, Shota Takahashi, Moon Hee Hwang, Atsushi Hirai
article en

Abstract

This report describes the first documented case of brigatinib-induced pleuritis in a patient with ALK-positive non-small cell lung cancer. A 77-year-old woman developed dyspnoea, fever, elevated inflammatory markers, and bilateral pleural effusion shortly after starting brigatinib as third-line therapy. Pleural fluid analysis showed lymphocyte-predominant exudative effusion without evidence of malignancy or infection, suggesting drug-induced pleuritis. Discontinuation of brigatinib led to rapid clinical and radiographic improvement. Although disease progression later occurred, pleuritis did not recur. Re-administration of brigatinib at a reduced dose of 30 mg/day achieved tumour shrinkage without pleuritis recurrence, and subsequent dose escalation to 60 mg/day was also tolerated. This case highlights that clinicians should consider drug-induced pleuritis when pleural effusion develops during brigatinib therapy, particularly when it is inconsistent with the disease progression. Dose reduction to as low as 30 mg/day may be a safe and effective therapeutic option for selected patients.

Respirology Case ReportsVol. 14(5)
Osaka Red Cross Hospital (JP)
Good health and well-being
Openalex Percentile: Top 9%
Lung Cancer Treatments and Mutations
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Pleuritis Induced by Brigatinib During the Treatment of Non‐Small Cell Lung Cancer — Tomoko Harima, Nao Yoshida, et al. · Respirology Case Reports (2026) | TGRS Research Map | TGRS