用免疫检查点抑制剂治疗原发性肺癌合并肺泡蛋白沉着症病例报告

IF 0.8 Q4 RESPIRATORY SYSTEM
Mika Horie, Kazuhisa Nakashima, Yoshihiro Amano, Yohei Shiratsuki, Kotaro Murakami, Takeshi Isobe, Yukari Tsubata
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引用次数: 0

摘要

原发性肺癌合并肺泡蛋白增生症(PAP)是一种罕见病。我们介绍了一例使用免疫检查点抑制剂(ICI)治疗原发性肺癌合并肺泡蛋白沉着症的患者。一名 62 岁的男性患者在入院 8 年前被诊断出患有自身免疫性肺泡蛋白增生症。他的右肺发现了肺腺癌,接受了铂类化疗,随后又接受了阿特珠单抗治疗。阿特珠单抗治疗后,他的病情出现进展,而 ICI 引发的肺炎或 PAP 恶化并未发生。这表明,ICI 可以安全地用于伴有 PAP 的原发性肺癌患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Primary lung cancer with pulmonary alveolar proteinosis treated with immune checkpoint inhibitor: A case report

Primary lung cancer with pulmonary alveolar proteinosis (PAP) is a rare condition. We present a case of a patient with primary lung cancer with PAP treated with an immune checkpoint inhibitor (ICI). A 62-year-old man was diagnosed with autoimmune PAP 8 years prior to current admission. Lung adenocarcinoma was found in his right lung, and platinum-based chemotherapy was administered, followed by atezolizumab. He experienced disease progression after atezolizumab treatment, whereas ICI-induced pneumonia or exacerbation of PAP did not occur. This indicates that ICI may be safely used in patients with primary lung cancer with PAP.

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来源期刊
Respiratory Medicine Case Reports
Respiratory Medicine Case Reports RESPIRATORY SYSTEM-
CiteScore
2.10
自引率
0.00%
发文量
213
审稿时长
87 days
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