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多柔比星联合顺铂同期放化疗治疗肺多形性癌的长期疗效:1 例报告。

Long-term response with durvalumab after chemoradiotherapy for pulmonary pleomorphic carcinoma: A case report.

机构信息

Department of Respiratory Medicine, Wakamatsu, Otaru General Hospital, Otaru, Japan.

Department of Respiratory Medicine and Allergology, Sapporo Medical University School of Medicine, Sapporo, Japan.

出版信息

Thorac Cancer. 2020 Apr;11(4):1090-1093. doi: 10.1111/1759-7714.13331. Epub 2020 Feb 11.

Abstract

Pulmonary pleomorphic carcinoma (PPC) is a non-small-cell lung cancer, resistant to chemotherapy and no standard therapy has as yet been established. We herein report the case of a 59-year-old man with PPC who showed a long-term response with durvalumab after chemoradiotherapy. He was referred to our hospital with a mass shadow at the right upper lung. PPC clinical stage IIIB was diagnosed, and the tumor proportion score of programmed death-ligand 1 (PD-L1) was 100%. Six days after transbronchial biopsy, he had difficulty walking owing to sensory abnormalities. We found that the primary tumor had invaded the spinal cord and compressed the cord at T1-T4, resulting in the abnormalities. He underwent tumor resection and received chemotherapy involving cisplatin (CDDP) + S-1 and concurrent radiotherapy (66 Gy). Subsequently, durvalumab treatment as consolidation therapy was commenced. After one year of durvalumab treatment had been completed, he had no apparent signs of relapse or severe adverse events. This case suggests that a long-term response can be achieved with durvalumab after chemoradiotherapy for stage III inoperable PPC showing high PD-L1 expression. KEY POINTS: Significant findings of the report A long-term response might be achieved with durvalumab after chemoradiotherapy in patients with stage III inoperable pulmonary pleomorphic carcinoma showing high expression of programmed death-ligand What this study adds It is possible to continue durvalumab treatment for one year without any severe adverse events. Although pulmonary pleomorphic carcinoma is considered to have a poor prognosis, the combination therapy of immune checkpoint inhibitors and radiotherapy may be an effective treatment option.

摘要

肺多形性癌(PPC)是一种非小细胞肺癌,对化疗有耐药性,目前尚未确立标准治疗方法。我们在此报告 1 例 PPC 患者,该患者在放化疗后使用度伐利尤单抗治疗显示出长期缓解。患者因右上肺肿块阴影就诊,59 岁,男性。诊断为 PPC 临床 3B 期,程序性死亡配体 1(PD-L1)肿瘤比例评分 100%。经支气管活检后 6 天,因感觉异常出现行走困难。我们发现原发肿瘤已侵犯脊髓并压迫 T1-T4 段脊髓,导致异常。他接受了肿瘤切除术,并接受了含顺铂(CDDP)+S-1 的化疗和同步放疗(66 Gy)。随后,开始进行度伐利尤单抗巩固治疗。完成 1 年的度伐利尤单抗治疗后,他没有明显的复发迹象或严重不良事件。本病例提示,对于高 PD-L1 表达的不可手术的 III 期 PPC 患者,在放化疗后使用度伐利尤单抗可能获得长期缓解。关键点:本报告的重要发现对于高表达程序性死亡配体的不可手术的 III 期肺多形性癌患者,在放化疗后使用度伐利尤单抗可能实现长期缓解。本研究增加的内容可能在没有严重不良事件的情况下继续使用度伐利尤单抗治疗 1 年。虽然肺多形性癌被认为预后不良,但免疫检查点抑制剂联合放疗的联合治疗可能是一种有效的治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8c1/7113037/39caf4e24f5c/TCA-11-1090-g001.jpg

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