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一例肺硬化性肺细胞瘤患者使用伊匹单抗和纳武单抗免疫治疗成功。

Successful immunotherapy with ipilimumab and nivolumab in a patient with pulmonary sclerosing pneumocytoma.

作者信息

Inukai-Motokura Yumi, Ninomiya Kiichiro, Baba Takahiro, Omori Hiroki, Takeguchi Tetsuya, Uno Mari, Ayada Yoshiyuki, Tanaka Takehiro, Maeda Yoshinobu, Ohashi Kadoaki

机构信息

Department of Allergy and Respiratory Medicine, Okayama University Hospital, Okayama, Japan.

Center for Comprehensive Genomic Medicine, Okayama University Hospital, 2-5-1 Shikata-cho Kita-ku, Okayama, 700-8558 Japan.

出版信息

Int Cancer Conf J. 2024 Nov 29;14(1):60-63. doi: 10.1007/s13691-024-00737-8. eCollection 2025 Jan.

DOI:10.1007/s13691-024-00737-8
PMID:39758787
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11695534/
Abstract

Pulmonary sclerosing pneumocytoma (PSP) is a rare form of lung cancer that occasionally presents with lymph node and extrapulmonary metastases, and multiple lesions. The treatment of metastatic PSP remains undefined. This study reports the case of a 48-year-old female patient diagnosed with PSP following surgical intervention for a solitary nodule in the left lower lobe. Four years later, recurrence occurred in the left hilar and mediastinal lymph nodes, necessitating an additional resection. Concurrently, sacral metastases developed and required palliative radiotherapy. Genetic analysis identified an E17K mutation, characteristic of PSP, and absence of programmed cell death ligand 1 (PD-L1) expression in the tumor. Two years post-recurrence, the tumor recurred in the left mammary gland and mediastinal lymph nodes. Combination immunotherapy with ipilimumab and nivolumab yielded a significantly positive response in this metastatic PSP case. This is the first reported case of successful treatment of multiple distant metastatic PSP with ipilimumab and nivolumab, following the failure of various local treatments. Further case series are warranted to validate the efficacy of immunotherapy in metastatic PSP.

摘要

肺硬化性细胞瘤(PSP)是一种罕见的肺癌形式,偶尔会出现淋巴结和肺外转移以及多发病灶。转移性PSP的治疗方法尚不明确。本研究报告了一例48岁女性患者的病例,该患者因左下叶孤立性结节接受手术干预后被诊断为PSP。四年后,左肺门和纵隔淋巴结出现复发,需要再次进行切除。同时,出现了骶骨转移,需要进行姑息性放疗。基因分析发现了PSP特有的E17K突变,且肿瘤中无程序性细胞死亡配体1(PD-L1)表达。复发两年后,肿瘤在左乳腺和纵隔淋巴结再次出现。在这个转移性PSP病例中,伊匹单抗和纳武单抗联合免疫治疗产生了显著的阳性反应。这是首例在各种局部治疗失败后,使用伊匹单抗和纳武单抗成功治疗多发远处转移性PSP的病例报告。需要进一步的病例系列研究来验证免疫治疗在转移性PSP中的疗效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4740/11695534/19276da07b0f/13691_2024_737_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4740/11695534/341e9b291457/13691_2024_737_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4740/11695534/19276da07b0f/13691_2024_737_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4740/11695534/341e9b291457/13691_2024_737_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4740/11695534/19276da07b0f/13691_2024_737_Fig2_HTML.jpg

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本文引用的文献

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J Clin Oncol. 2023 Feb 20;41(6):1200-1212. doi: 10.1200/JCO.22.01503. Epub 2022 Oct 12.
2
Case Report and Literature Review: Pulmonary Sclerosing Pneumocytoma With Multiple Metastases Harboring E17K Somatic Mutation and C176Y Germline Mutation.病例报告与文献综述:伴有E17K体细胞突变和C176Y胚系突变且发生多处转移的肺硬化性肺细胞瘤
Front Med (Lausanne). 2021 Sep 8;8:655574. doi: 10.3389/fmed.2021.655574. eCollection 2021.
3
Case Report: Rare Pulmonary Sclerosing Pneumocytoma: Large, Multiple, Metastatic, and Fatal.
病例报告:罕见的肺硬化性肺细胞瘤:巨大、多发、转移且致命。
Front Med (Lausanne). 2021 Aug 16;8:661032. doi: 10.3389/fmed.2021.661032. eCollection 2021.
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Effect of Capivasertib in Patients With an AKT1 E17K-Mutated Tumor: NCI-MATCH Subprotocol EAY131-Y Nonrandomized Trial.AKT1 E17K 突变肿瘤患者中 Capivasertib 的疗效:NCI-MATCH 子方案 EAY131-Y 非随机试验。
JAMA Oncol. 2021 Feb 1;7(2):271-278. doi: 10.1001/jamaoncol.2020.6741.
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The 2015 World Health Organization Classification of Lung Tumors: Impact of Genetic, Clinical and Radiologic Advances Since the 2004 Classification.2015 年世界卫生组织肺肿瘤分类:自 2004 年分类以来遗传、临床和放射学进展的影响。
J Thorac Oncol. 2015 Sep;10(9):1243-1260. doi: 10.1097/JTO.0000000000000630.
6
Treatment of 28 patients with sclerosing hemangioma (SH) of the lung.28例肺硬化性血管瘤(SH)患者的治疗。
J Cardiothorac Surg. 2012 Jun 18;7:34. doi: 10.1186/1749-8090-7-34.
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Arch Pathol Lab Med. 2003 Mar;127(3):321-5. doi: 10.5858/2003-127-0321-PSHWLN.
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