Xie Xiao-Hong, Zhan Ze-Jiang, Qin Yin-Yin, Jiang Ju-Hong, Yin Wei-Qiang, Zheng Rong-Hui, Li Shi-Yue, Zhou Cheng-Zhi
Department of Pulmonary and Critical Care Medicine, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou Institute of Respiratory Health, State Key Laboratory of Respiratory Disease, National Clinical Research Center for Respiratory Disease, Guangzhou, China.
Guangzhou Medical University, Guangzhou, China.
Front Oncol. 2021 Mar 17;11:655856. doi: 10.3389/fonc.2021.655856. eCollection 2021.
The treatment of anaplastic lymphoma kinase (ALK)-positive locally advanced non-small-cell lung cancer (NSCLC) is challenging because there is no randomized controlled trial has been reported. The value of neoadjuvant and adjuvant targeted therapy remains unclear. Herein, we show that systemic treatment with ALK inhibitor crizotinib before surgery can provide the potential to cure the initially inoperable tumor. A 27-year-old man was diagnosed with a stage IIIAcT3N2M0 (7UICC/AJCC) upper left lung adenocarcinoma harboring EML4-ALK fusion gene. Clinically, the patient had a large primary lesion adjacent to the pericardium and regional lymph node metastasis at the ipsilateral mediastinum. Poor tumor response was observed after 3 cycles of chemotherapy (gemcitabine plus cisplatin), and upon multidisciplinary discussion, the patient was started with 250 mg crizotinib twice daily. Successive clinical examinations showed a progressive reduction of the lesions. After 2 months of therapy, the patient was downstaged to cT2aN2M0, then video-assisted thoracic surgery was performed and the final histopathological stage was ypT2aN2M0. The treatment with crizotinib (250 mg, qd) was continued more than 30 months post surgery and stopped until intracranial oligometastasis. The patient's overall survival (OS) time is 68 months at last follow-up. This case presented here supports the use of neoadjuvant and adjuvant treatment with ALK inhibitors in ALK positive locally advanced NSCLC.
间变性淋巴瘤激酶(ALK)阳性的局部晚期非小细胞肺癌(NSCLC)的治疗具有挑战性,因为尚无随机对照试验的报道。新辅助和辅助靶向治疗的价值仍不明确。在此,我们表明术前使用ALK抑制剂克唑替尼进行全身治疗有可能治愈最初无法手术切除的肿瘤。一名27岁男性被诊断为III AcT3N2M0(第7版国际抗癌联盟/美国癌症联合委员会)左上肺腺癌,伴有EML4-ALK融合基因。临床上,患者有一个与心包相邻的大的原发灶,同侧纵隔有区域淋巴结转移。在3个周期的化疗(吉西他滨加顺铂)后观察到肿瘤反应不佳,经多学科讨论后,患者开始每日两次服用250mg克唑替尼。连续的临床检查显示病变逐渐缩小。治疗2个月后,患者分期降为cT2aN2M0,随后进行了电视辅助胸腔镜手术,最终组织病理学分期为ypT2aN2M0。术后继续使用克唑替尼(250mg,每日一次)治疗超过30个月,直至出现颅内寡转移才停药。最后一次随访时患者的总生存期(OS)为68个月。本文介绍的该病例支持在ALK阳性的局部晚期NSCLC中使用ALK抑制剂进行新辅助和辅助治疗。