Yagami Yuri, Nakahara Yoshiro, Manabe Hideaki, Yamamoto Hiroki, Otani Sakiko, Sato Takashi, Igawa Satoshi, Kubota Masaru, Sasaki Jiichiro, Naoki Katsuhiko
Department of Respiratory Medicine, Kitasato University School of Medicine, Sagamihara, Kanagawa, 252-0374, Japan.
School of Allied Health Sciences, Kitasato University, Sagamihara, Kanagawa, 252-0374, Japan.
Onco Targets Ther. 2022 Nov 11;15:1369-1374. doi: 10.2147/OTT.S375246. eCollection 2022.
The prognosis of peritoneal carcinomatosis in patients with lung cancer is poor. However, some cases of peritoneal carcinomatosis from lung cancer harboring specific gene alterations have responded to molecular targeted drugs. B-Raf proto-oncogene (BRAF) mutations occur in about 2-4% of NSCLCs, with about half of these cases having the BRAF V600E mutation. Concomitant inhibition of BRAF with dabrafenib and inhibition of the downstream mitogen-activated protein kinase with trametinib showed efficacy in NSCLC patients with the BRAF V600E mutation. Herein, we report a patient with peritoneal carcinomatosis from lung cancer with the BRAF V600E mutation who responded to dabrafenib plus trametinib.
A 67-year-old Japanese male never-smoker was diagnosed with stage IA3 lung adenocarcinoma. He underwent thoracoscopic left lower lobectomy but developed recurrence of the cancer with peritoneal carcinomatosis 33 months after the operation. An Oncomine Dx target test of the resected specimen was positive for the V600E mutation. He was started on dabrafenib 150 mg twice per day and trametinib 2 mg once per day. He had a good clinical response to dabrafenib/trametinib therapy with resolution of abdominal distention. He continued dabrafenib/trametinib treatment without disease progression for 7 months, with no severe adverse effects.
This case highlights the importance of assessing genetic alterations in lung cancer patients with peritoneal carcinomatosis and treating them with appropriate molecular targeted drugs.
肺癌患者发生腹膜转移癌的预后较差。然而,一些具有特定基因改变的肺癌腹膜转移癌病例对分子靶向药物有反应。B-Raf原癌基因(BRAF)突变约发生于2%-4%的非小细胞肺癌(NSCLC)患者中,其中约一半病例存在BRAF V600E突变。达拉非尼对BRAF的抑制作用与曲美替尼对下游丝裂原活化蛋白激酶的抑制作用联合应用,在携带BRAF V600E突变的NSCLC患者中显示出疗效。在此,我们报告1例患有BRAF V600E突变的肺癌腹膜转移癌患者,其对达拉非尼联合曲美替尼治疗有反应。
一名67岁从不吸烟的日本男性被诊断为IA3期肺腺癌。他接受了胸腔镜下左肺下叶切除术,但术后33个月癌症复发并出现腹膜转移癌。对切除标本进行的Oncomine Dx靶向检测显示V600E突变呈阳性。他开始接受每日2次、每次150 mg的达拉非尼及每日1次、每次2 mg的曲美替尼治疗。他对达拉非尼/曲美替尼治疗有良好的临床反应,腹胀症状消失。他持续接受达拉非尼/曲美替尼治疗7个月,病情无进展,且无严重不良反应。
该病例突出了评估肺癌腹膜转移癌患者基因改变并使用适当分子靶向药物进行治疗的重要性。