Major pathological response obtained after neoadjuvant chemotherapy combined with dual immunotherapy for malignant pleural mesothelioma: a case report.

IF 4 2区 医学 Q2 ONCOLOGY Translational lung cancer research Pub Date : 2024-06-30 Epub Date: 2024-06-21 DOI:10.21037/tlcr-24-195
Yuchen Zhang, Guangyin Zhao, Chen Xu, Jie Gu, Di Ge
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Abstract

Background: Malignant pleural mesothelioma (MPM) is a rare thoracic malignancy with high morbidity and mortality. A combination of systemic therapy and surgery may be a promising modality for the treatment of MPM, but evidence-based medicine is still lacking.

Case description: Here we report a case of MPM. The patient presented to hospital with cough and sputum. After ineffective symptomatic treatment, computed tomography (CT) examination suggested a malignant tumor of pleural origin. Positron emission tomography/computed tomography (PET/CT) examination suggested no lymph node metastasis or distant metastasis. The pathologic diagnosis of MPM was confirmed after CT-guided puncture biopsy. Next, she underwent 3 courses of neoadjuvant chemotherapy combined with dual immunotherapy (carboplatin and pemetrexed combined with anti-CTLA4 and anti-PD-1), resulting in significant tumor shrinkage. After obtaining the patient's consent and completing a preoperative evaluation, we modified the extrapleural pneumonectomy (EPP) and pleurectomy/decortication (P/D) by performing a lower lobe resection and partial pleurectomy of the left lung. Intraoperative rapid frozen pathology suggested that the margins of the tumor were negative and complete resection was achieved. The postoperative pathology report showed 10% residual viable tumor, so the major pathological response (MPR) was achieved after treatment.

Conclusions: MPM might respond well to neoadjuvant chemotherapy and dual immunotherapy, improving the probability of complete surgical resection and attaining an encouraging pathologic response.

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恶性胸膜间皮瘤新辅助化疗联合双重免疫疗法后获得重大病理反应:病例报告。
背景:恶性胸膜间皮瘤(MPM)是一种罕见的胸部恶性肿瘤,发病率和死亡率都很高。系统治疗与手术相结合可能是治疗 MPM 的一种有前途的方式,但目前仍缺乏循证医学证据:我们在此报告一例肺间质瘤。患者因咳嗽、咳痰入院。对症治疗无效后,计算机断层扫描(CT)检查提示为胸膜源性恶性肿瘤。正电子发射断层扫描/计算机断层扫描(PET/CT)检查显示没有淋巴结转移或远处转移。CT 引导下的穿刺活检证实了 MPM 的病理诊断。接下来,她接受了3个疗程的新辅助化疗和双免疫疗法(卡铂和培美曲塞联合抗CTLA4和抗PD-1),结果肿瘤明显缩小。在征得患者同意并完成术前评估后,我们对胸膜外气胸切除术(EPP)和胸膜切除/去皮层术(P/D)进行了改良,实施了左肺下叶切除和部分胸膜切除术。术中快速冰冻病理显示肿瘤边缘阴性,实现了完全切除。术后病理报告显示有10%的肿瘤残留,因此治疗后获得了主要病理反应(MPR):结论:MPM可能对新辅助化疗和双重免疫疗法反应良好,提高了手术完全切除的概率,并获得了令人鼓舞的病理反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.20
自引率
2.50%
发文量
137
期刊介绍: Translational Lung Cancer Research(TLCR, Transl Lung Cancer Res, Print ISSN 2218-6751; Online ISSN 2226-4477) is an international, peer-reviewed, open-access journal, which was founded in March 2012. TLCR is indexed by PubMed/PubMed Central and the Chemical Abstracts Service (CAS) Databases. It is published quarterly the first year, and published bimonthly since February 2013. It provides practical up-to-date information on prevention, early detection, diagnosis, and treatment of lung cancer. Specific areas of its interest include, but not limited to, multimodality therapy, markers, imaging, tumor biology, pathology, chemoprevention, and technical advances related to lung cancer.
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