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病例报告:替雷利珠单抗胸腔内联合全身注射化疗治疗RET基因融合阳性肺腺癌并难治性恶性胸腔积液

Case report: Intrapleural plus systemic Tislelizumab injection combined chemotherapy in RET gene fusion-positive lung adenocarcinoma presenting refractory malignant pleural effusion.

作者信息

Qiu Dong, Zhang Xiao-Hui, Wang Yang, Chen Cheng

机构信息

Department of Respiratory and Critical Medicine, The First Affiliated Hospital of Soochow University, Suzhou, China.

出版信息

Front Oncol. 2024 Sep 20;14:1404173. doi: 10.3389/fonc.2024.1404173. eCollection 2024.

DOI:10.3389/fonc.2024.1404173
PMID:39372862
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11449677/
Abstract

RET fusions were discovered in non-small cell lung cancer (NSCLC), and the efficacy of RET-targeted treatment in these patients has been previously established. However, patients with required resistance to RET-TKIs have limited treatment options. Herein, we describe a case of critical and advanced lung adenocarcinoma harboring RET fusion. Despite a significant response to Prasetinib previously, the patient developed refractory malignant pleural effusion after 24 months of treatment. He was treated simultaneously with intrapleural plus systemic Tislelizumab injection combined chemotherapy, thereby achieving an excellent clinical benefit maintaining control of pleural effusion for over 6 months. Hence, we would like to discuss intrapleural immunotherapy as an additional treatment method in refractory malignant pleural effusion while demonstrating good treatment tolerance.

摘要

在非小细胞肺癌(NSCLC)中发现了RET融合,并且先前已经确定了RET靶向治疗在这些患者中的疗效。然而,对RET-TKIs产生耐药性的患者治疗选择有限。在此,我们描述了一例患有RET融合的晚期肺腺癌病例。尽管患者先前对普拉替尼有显著反应,但在治疗24个月后出现了难治性恶性胸腔积液。他接受了胸腔内联合全身注射替雷利珠单抗联合化疗,从而获得了良好的临床疗效,胸腔积液得到控制超过6个月。因此,我们想讨论胸腔内免疫疗法作为难治性恶性胸腔积液的一种额外治疗方法,同时证明其具有良好的治疗耐受性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d563/11449677/8bd170247333/fonc-14-1404173-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d563/11449677/8bd170247333/fonc-14-1404173-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d563/11449677/8bd170247333/fonc-14-1404173-g001.jpg

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本文引用的文献

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Intrapleural Anticancer Therapy for Malignant Pleural Diseases: Facts or Fiction?胸膜内抗癌治疗恶性胸膜疾病:事实还是虚构?
Semin Respir Crit Care Med. 2023 Aug;44(4):462-467. doi: 10.1055/s-0043-1769094. Epub 2023 Jun 12.
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Current status of and progress in the treatment of malignant pleural effusion of lung cancer.肺癌恶性胸腔积液的治疗现状与进展
Front Oncol. 2023 Jan 20;12:961440. doi: 10.3389/fonc.2022.961440. eCollection 2022.
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Safety and efficacy of pralsetinib in RET fusion-positive non-small-cell lung cancer including as first-line therapy: update from the ARROW trial.
普拉替尼治疗 RET 融合阳性非小细胞肺癌(包括一线治疗)的安全性和疗效:ARROW 试验的更新结果。
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Phenotypic and functional characterizations of CD8 T cell populations in malignant pleural effusion.恶性胸腔积液中 CD8 T 细胞群体的表型和功能特征。
Exp Cell Res. 2022 Aug 1;417(1):113212. doi: 10.1016/j.yexcr.2022.113212. Epub 2022 May 17.
5
Intrapleural Injection of Anti-PD1 Antibody: A Novel Management of Malignant Pleural Effusion.胸腔内注射抗 PD1 抗体:恶性胸腔积液的一种新的治疗方法。
Front Immunol. 2021 Dec 13;12:760683. doi: 10.3389/fimmu.2021.760683. eCollection 2021.
6
Clinical efficacy of bevacizumab combined with cisplatin in the treatment of malignant pleural effusion and ascites caused by lung cancer: a randomized trial.贝伐珠单抗联合顺铂治疗肺癌所致恶性胸腔积液和腹水的临床疗效:一项随机试验。
Ann Palliat Med. 2021 Oct;10(10):10575-10583. doi: 10.21037/apm-21-2623.
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Pralsetinib for RET fusion-positive non-small-cell lung cancer (ARROW): a multi-cohort, open-label, phase 1/2 study.普拉替尼治疗 RET 融合阳性非小细胞肺癌(ARROW):多队列、开放标签、1/2 期研究。
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Development of RECLS score to predict survival in lung cancer patients with malignant pleural effusion.用于预测恶性胸腔积液肺癌患者生存情况的RECLS评分的开发。
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