Wang Huan, Wu Zhenyan, Shi Guangqing, Zhou Jing, Xiao Zhenliang
Department of Respiratory and Critical Care Medicine, General Hospital of Western Theater Command, Chengdu, Sichuan 610083, P.R. China.
Oncol Lett. 2023 Oct 23;26(6):526. doi: 10.3892/ol.2023.14113. eCollection 2023 Dec.
Fusion of the anaplastic lymphoma kinase (ALK) gene is a rare driver in non-small cell lung cancer (NSCLC). Lorlatinib is a third-generation ALK inhibitor approved for the treatment of locally advanced or metastatic ALK NSCLC. The traditional administration method of lorlatinib is whole tablet ingestion, while the efficacy effect of gastric tube injection after water dissolution remains unclear. In the present report, a marked response to lorlatinib in a 49-year-old patient with ALK NSCLC who was administered lorlatinib through a gastric tube, was described. The patient had received chemotherapy combined with immune checkpoint inhibitors prior to targeted drug therapy and developed hyperprogression, which was mainly manifested as rapid enlargement of the primary lesion with multiple new systemic metastases, accompanied by poor performance status score, esophageal compression and difficulty eating. The patient was injected with pre-dissolved lorlatinib through the nasogastric tube. After 6 days, related symptoms, such as dyspnea and dysphagia, were relieved. After 18 days, the esophageal stenosis was significantly alleviated, and the gastric tube was removed. In conclusion, gastric tube injection be used as a means of lorlatinib administration in patients with ALK NSCLC with dysphagia, regardless of previous immunotherapy-associated hyperprogression.
间变性淋巴瘤激酶(ALK)基因融合是非小细胞肺癌(NSCLC)中一种罕见的驱动因素。洛拉替尼是一种第三代ALK抑制剂,被批准用于治疗局部晚期或转移性ALK NSCLC。洛拉替尼的传统给药方式是整片吞服,而水溶后经胃管注入的疗效尚不清楚。在本报告中,描述了一名49岁的ALK NSCLC患者通过胃管给予洛拉替尼后对该药有显著反应。该患者在靶向药物治疗前接受过化疗联合免疫检查点抑制剂治疗,并出现了超进展,主要表现为原发灶迅速增大并伴有多处新的全身转移,同时患者体能状态评分较差,食管受压且进食困难。通过鼻胃管给该患者注入水溶后的洛拉替尼。6天后,呼吸困难和吞咽困难等相关症状得到缓解。18天后,食管狭窄明显减轻,胃管拔除。总之,对于有吞咽困难的ALK NSCLC患者,无论之前是否有免疫治疗相关的超进展,均可将胃管注入作为洛拉替尼的给药方式。