Gao Peng, Tang Kangning, Hao Yuqiu, Li Wei, Lv Xuejiao, Li Dapeng, Jia Yuxi
Department of Respiratory and Critical Care Medicine, Second Hospital of Jilin University, Changchun, China.
Department of Respiratory and Critical Care Medicine, The Affiliated Hospital of Jilin Medical College, Jilin, China.
Front Oncol. 2022 Feb 25;12:762338. doi: 10.3389/fonc.2022.762338. eCollection 2022.
The anaplastic lymphoma kinase (ALK) gene rearrangement is a driving mutation that underlies about 5-6% of non-small cell lung cancer (NSCLC) cases. Lung cancers that are ALK gene rearrangement-positive can be effectively treated with ALK inhibitors. However, the response of patients with rarer ALK gene rearrangements to ALK inhibitors remains unknown. Herein, we described a case of lung adenocarcinoma carrying ALK-HLA-DRB1 fusion in a 48-year-old nonsmoking woman. A similar case of ALK-HLA-DRB1 rearrangement in NSCLC has not been described previously neither in NSCLC nor in other disease. The patient achieved a progression-free survival of 18 months after sequential therapy consisting of crizotinib and then ceritinib during the follow-up. These findings provide basis for the application of ALK inhibitors in patients carrying the rare ALK-HLA-DRB1 fusion.
间变性淋巴瘤激酶(ALK)基因重排是一种驱动突变,约占非小细胞肺癌(NSCLC)病例的5%-6%。ALK基因重排阳性的肺癌可用ALK抑制剂有效治疗。然而,携带罕见ALK基因重排的患者对ALK抑制剂的反应仍不清楚。在此,我们描述了一例48岁不吸烟女性肺腺癌患者携带ALK-HLA-DRB1融合基因的病例。此前,无论是在NSCLC还是其他疾病中,均未描述过NSCLC中类似的ALK-HLA-DRB1重排病例。在随访期间,该患者在接受克唑替尼序贯色瑞替尼治疗后,实现了18个月的无进展生存期。这些发现为ALK抑制剂在携带罕见ALK-HLA-DRB1融合基因的患者中的应用提供了依据。