Hiroki Watanabe, Yuihci Murai, Asumi Suzuki, Ikumi Yamagishi, E. Ogata, T. Miyabayashi, Akira Youkou, Masatoshi Watanabe, T. Abe
{"title":"Successful Treatment of Sarcomatoid Carcinoma Using Nivolumab Plus Ipilimumab Combination Immunotherapy: a Case Report","authors":"Hiroki Watanabe, Yuihci Murai, Asumi Suzuki, Ikumi Yamagishi, E. Ogata, T. Miyabayashi, Akira Youkou, Masatoshi Watanabe, T. Abe","doi":"10.2482/haigan.62.996","DOIUrl":null,"url":null,"abstract":". ABSTRACT ━━ Background. Pulmonary pleomorphic carcinoma, a subtype of sarcomatoid carcinoma, is a rare lung malignancy. This cancer is usually resistant to chemo- and radiotherapy, and no standard treatment proto-cols are currently available. We herein report a case of sarcomatoid carcinoma in a patient who responded to combination therapy using nivolumab plus ipilimumab. Case. A 62-year-old man who was a current smoker was re-ferred to our hospital with right lower extremity paresis. Computed tomography revealed a mass in the right upper lung, and magnetic resonance imaging showed multiple brain metastases. Endobronchial ultrasound-guided transbronchial needle aspiration of the mass revealed sarcomatoid carcinoma with a low expression of programmed cell death ligand-1 (PD-L1), and the tumor proportion score was 10%, being classified as clinical stage IVB (cT3N0M1c [BRA]). Following stereotactic radiotherapy to the brain lesions, he was administered combination immunotherapy using nivolumab (360 mg/kg every 3 weeks) and ipilimumab (1 mg/kg every 6 weeks). We observed shrinkage of both lung and brain lesions, which was considered a partial response, and he showed only mild immunotherapy-induced toxicity. Conclusion. Immune checkpoint inhibitors may serve as an effective therapeutic option in patients with sarcomatoid carcinoma; combination therapy using these agents may provide an improved therapeutic benefit in such cases. (","PeriodicalId":35081,"journal":{"name":"Japanese Journal of Lung Cancer","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-12-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Japanese Journal of Lung Cancer","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2482/haigan.62.996","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0
Abstract
. ABSTRACT ━━ Background. Pulmonary pleomorphic carcinoma, a subtype of sarcomatoid carcinoma, is a rare lung malignancy. This cancer is usually resistant to chemo- and radiotherapy, and no standard treatment proto-cols are currently available. We herein report a case of sarcomatoid carcinoma in a patient who responded to combination therapy using nivolumab plus ipilimumab. Case. A 62-year-old man who was a current smoker was re-ferred to our hospital with right lower extremity paresis. Computed tomography revealed a mass in the right upper lung, and magnetic resonance imaging showed multiple brain metastases. Endobronchial ultrasound-guided transbronchial needle aspiration of the mass revealed sarcomatoid carcinoma with a low expression of programmed cell death ligand-1 (PD-L1), and the tumor proportion score was 10%, being classified as clinical stage IVB (cT3N0M1c [BRA]). Following stereotactic radiotherapy to the brain lesions, he was administered combination immunotherapy using nivolumab (360 mg/kg every 3 weeks) and ipilimumab (1 mg/kg every 6 weeks). We observed shrinkage of both lung and brain lesions, which was considered a partial response, and he showed only mild immunotherapy-induced toxicity. Conclusion. Immune checkpoint inhibitors may serve as an effective therapeutic option in patients with sarcomatoid carcinoma; combination therapy using these agents may provide an improved therapeutic benefit in such cases. (