Taniwaki Masaya, Yamasaki Masahiro, Kawata Koto, Kawamoto Kazuma, Funaishi Kunihiko, Matsumoto Yu, Matsumoto Naoko, Ohashi Nobuyuki, Hattori Noboru
Department of Respiratory Disease, Hiroshima Red Cross Hospital and Atomic-bomb Survivors Hospital, Naka-ku, Hiroshima, Japan.
Ohashi Clinic, Naka-ku, Hiroshima, Japan.
Oncotarget. 2018 Oct 16;9(81):35278-35282. doi: 10.18632/oncotarget.26233.
Carcinoma of unknown primary site (CUP) is diagnosed only in 2-9% of all cancer cases. Adenocarcinomas account for approximately 60% of CUP, and some of these are putative lung adenocarcinomas. The frequency of driver oncogene positivity in the putative lung adenocarcinomas is unknown, and the efficacy of targeting therapies for the driver oncogene is also unknown. This is the first case report of C-ros oncogene 1 (ROS1)-rearranged putative lung adenocarcinoma presenting as CUP showing a good response to ROS1 inhibitor therapy. A 55-year-old woman presented with neck lymphadenopathy. Computed tomography and [18F]-fluorodeoxyglucose (FDG) positron emission tomography (PET) showed swelling of the bilateral supraclavicular, left accessory, mediastinal, and abdominal lymph nodes. The pathological analysis of the lymph node specimen biopsy indicated adenocarcinoma with cytokeratin 7 and thyroid transcription factor-1 positivity. Thus, this case was identified as ROS1- rearranged putative lung adenocarcinoma presenting as CUP. Oral crizotinib, an ROS1 inhibitor, was administered at a dose of 250 mg twice daily. Four weeks later, several swollen nodes showed marked improvement, and eight weeks later, FDG PET showed almost no uptake. In conclusion, putative lung adenocarcinoma presenting as CUP may involve ROS1 rearrangement, and ROS1 inhibitor therapy may be effective.
原发部位不明的癌(CUP)仅在所有癌症病例的2%-9%中被诊断出来。腺癌约占CUP的60%,其中一些是推定的肺腺癌。推定的肺腺癌中驱动癌基因阳性的频率尚不清楚,针对驱动癌基因的靶向治疗的疗效也不清楚。这是首例C-ros癌基因1(ROS1)重排的推定肺腺癌表现为CUP且对ROS1抑制剂治疗显示出良好反应的病例报告。一名55岁女性因颈部淋巴结病就诊。计算机断层扫描和[18F] - 氟脱氧葡萄糖(FDG)正电子发射断层扫描(PET)显示双侧锁骨上、左侧副、纵隔和腹部淋巴结肿大。淋巴结标本活检的病理分析表明为细胞角蛋白7和甲状腺转录因子-1阳性的腺癌。因此,该病例被确定为表现为CUP的ROS1重排的推定肺腺癌。口服ROS1抑制剂克唑替尼,剂量为每日两次,每次250mg。四周后,几个肿大的淋巴结显示出明显改善,八周后,FDG PET显示几乎无摄取。总之,表现为CUP的推定肺腺癌可能涉及ROS1重排,且ROS1抑制剂治疗可能有效。