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新辅助化疗联合双重免疫疗法治疗恶性胸膜间皮瘤后获得的主要病理反应:一例病例报告

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

作者信息

Zhang Yuchen, Zhao Guangyin, Xu Chen, Gu Jie, Ge Di

机构信息

Department of Thoracic Surgery, Zhongshan Hospital, Fudan University, Shanghai, China.

Department of Pathology, Zhongshan Hospital, Fudan University, Shanghai, China.

出版信息

Transl Lung Cancer Res. 2024 Jun 30;13(6):1420-1425. doi: 10.21037/tlcr-24-195. Epub 2024 Jun 21.

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.

摘要

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。全身治疗与手术相结合可能是治疗MPM的一种有前景的方式,但循证医学证据仍然不足。

病例描述

在此,我们报告一例MPM病例。患者因咳嗽、咳痰入院。对症治疗无效后,计算机断层扫描(CT)检查提示为胸膜起源的恶性肿瘤。正电子发射断层扫描/计算机断层扫描(PET/CT)检查提示无淋巴结转移或远处转移。经CT引导下穿刺活检确诊为MPM。接下来,她接受了3个疗程的新辅助化疗联合双重免疫治疗(卡铂和培美曲塞联合抗CTLA4和抗PD-1),肿瘤明显缩小。在获得患者同意并完成术前评估后,我们对胸膜外全肺切除术(EPP)和胸膜剥脱术/纤维板剥脱术(P/D)进行了改良,行左肺下叶切除及部分胸膜切除术。术中快速冰冻病理提示肿瘤切缘阴性,实现了完整切除。术后病理报告显示有10%的残余存活肿瘤,因此治疗后达到了主要病理缓解(MPR)。

结论

MPM可能对新辅助化疗和双重免疫治疗反应良好,提高了完整手术切除的概率,并获得了令人鼓舞的病理反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f9a/11225053/b0a550c761a4/tlcr-13-06-1420-f1.jpg

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