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抗 PD-1 抗体的尾部效应导致不可切除的多发性原发性肺癌呈磨玻璃样混浊完全消退:一例报告。

Tailing effect of PD-1 antibody results in the eradication of unresectable multiple primary lung cancer presenting as ground-glass opacities: a case report.

机构信息

Department of Respiratory Medicine, Lihuili Hospital, Ningbo Medical Center, Ningbo, China.

Department of Cardiology, The Second Hospital of Yinzhou, Ningbo, China.

出版信息

Ann Palliat Med. 2021 Jan;10(1):778-784. doi: 10.21037/apm-20-2132.

DOI:10.21037/apm-20-2132
PMID:33545799
Abstract

There is currently no standard treatment for multiple primary lung cancer (MPLC). We report a case of synchronous MPLC presenting as one ground-glass opacity (GGO) with predominant consolidation accompanied by at least parietal pleura involvement, and another with >30 GGOs distributed across bilateral lungs, which was ineligible for complete resection. CT-guided percutaneous biopsy of the nearly pure-solid mass showed invasive lung adenocarcinoma mainly composed of acinar type. Capture-based, ultra-deep targeted sequencing (Burning Rock, Guangzhou, China) was performed on the tumor tissue biopsy. The result revealed no druggable mutations according to the guideline and a high TMB of 34.1 Mb. Immunohistochemical staining (22C3; Dako, Denmark) was positive for PD-L1 expression with a tumor expression level of 30%. Based on the clinical information and patient's decision, he received 3 cycles of pemetrexed plus pembrolizumab and was subsequently forced to withdraw due to acquired immune-related pneumonitis. After discontinuation of corticosteroids, he was subjected to wedge resection for the nearly pure-solid lesion, and then refused further treatment for the other tumors. After a follow-up of 12 months from termination of immunotherapy, almost all GGOs achieved radiographically complete remission, attributed to the tailing effect of the programmed cell death protein 1 (PD-1) antibody of pembrolizumab. Through the case study we found that unresectable synchronous MPLC presenting as GGOs may respond well to immunotherapy.

摘要

目前,多原发性肺癌(MPLC)尚无标准治疗方法。我们报告了一例同时性 MPLC 病例,表现为一个主要为实变伴至少壁层胸膜受累的磨玻璃影(GGO),另一个则表现为分布于双肺的 >30 个 GGO,无法进行完全切除。对几乎纯实性肿块进行 CT 引导下经皮穿刺活检显示为主要由腺泡型组成的浸润性肺腺癌。对肿瘤组织活检进行基于捕获的超深度靶向测序(广州燃石医学检验所有限公司)。结果根据指南显示没有可用药的突变,并且 TMB 很高,为 34.1 Mb。免疫组织化学染色(22C3;Dako,丹麦)显示 PD-L1 表达阳性,肿瘤表达水平为 30%。根据临床信息和患者的决定,他接受了 3 个周期的培美曲塞加帕博利珠单抗治疗,随后由于获得性免疫相关肺炎而被迫停药。停用皮质类固醇后,他接受了楔形切除术治疗几乎纯实性病变,然后拒绝进一步治疗其他肿瘤。免疫治疗结束后 12 个月的随访显示,几乎所有的 GGO 均在影像学上完全缓解,这归因于帕博利珠单抗程序性细胞死亡蛋白 1(PD-1)抗体的拖尾效应。通过该病例研究,我们发现无法切除的同时性 MPLC 表现为 GGOs 可能对免疫治疗有良好的反应。

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