Zhou Shengyu, Sun Guanxing, Wang Jianwei, Zhang Hongtu
Department of Medical Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences (CAMS) and Peking Union Medical College (PUMC), Beijing, China.
Department of Medical Oncology, Zaozhuang Municipal Hospital, Zaozhuang, China.
Transl Androl Urol. 2020 Dec;9(6):2855-2861. doi: 10.21037/tau-20-1343.
Renal cell carcinoma (RCC) with anaplastic lymphoma kinase (ALK) rearrangement is rare, and the genetic profiles of the tumor have not been elucidated. Here, we report a case with recurrent papillary RCC and lung metastasis after nephrectomy for nearly 7 years. The patient first received sunitinib, whereas the drug toxicity was intolerable. Combined Immunohistology (IHC) and fluorescence in situ hybridization (FISH) revealed the patient has an ALK rearrangement, and the patient then was treated with crizotinib. The patient had good tolerance, and a partial response in the target lesions was achieved. In order to further understand the benefit of crizotinib in ALK-rearranged RCC, the patient was detected with whole exome sequencing (WES) to study her genetic profiles. Compared those of RCC cases without ALK rearrangement (nALK-RCC), the patient and nine RCC cases with ALK rearrangement (ALK-RCC) revealed unique genetic characteristics: 1) The common mutations that occurred in RCC were not found in ALK-RCC.; 2) A total of 11 co-existing mutations in ALK-RCC were found, and they occurred in nALK-RCC at a relatively low frequency. DNMT3A mutations were concurrent with ALK fusions in our case. These findings indicated a different genetic alteration pattern of ALK-RCC from nALK-RCC. Our case demonstrated the efficacy of crizotinib in an RCC patient with ALK rearrangement.
伴有间变性淋巴瘤激酶(ALK)重排的肾细胞癌(RCC)较为罕见,其肿瘤的基因特征尚未阐明。在此,我们报告1例肾切除术后近7年出现复发性乳头状RCC并肺转移的病例。患者最初接受舒尼替尼治疗,但药物毒性难以耐受。联合免疫组织化学(IHC)和荧光原位杂交(FISH)检测发现患者存在ALK重排,随后患者接受克唑替尼治疗。患者耐受性良好,靶病灶获得部分缓解。为进一步了解克唑替尼对ALK重排RCC的疗效,对该患者进行全外显子测序(WES)以研究其基因特征。与无ALK重排的RCC病例(nALK-RCC)相比,该患者及9例ALK重排的RCC病例(ALK-RCC)呈现出独特的基因特征:1)RCC中常见的突变在ALK-RCC中未发现;2)在ALK-RCC中共发现11种共存突变,这些突变在nALK-RCC中出现频率相对较低。在我们的病例中,DNMT3A突变与ALK融合同时存在。这些发现表明ALK-RCC与nALK-RCC的基因改变模式不同。我们的病例证明了克唑替尼对1例ALK重排的RCC患者有效。