Enteral lorlatinib after immune hyperprogression as a treatment option for anaplastic lymphoma kinase-positive non-small cell lung cancer: A case report

被引:0
|
作者
Wang, Huan [1 ]
Wu, Zhenyan [1 ]
Shi, Guangqing [1 ]
Zhou, Jing [1 ,2 ]
Xiao, Zhenliang [1 ]
机构
[1] Gen Hosp Western Theater Command, Dept Resp & Crit Care Med, Chengdu 610083, Sichuan, Peoples R China
[2] Gen Hosp Western Theater Command, Dept Resp & Crit Care Med, 270 Tianhui Rd,Rongdu Ave, Chengdu 610083, Sichuan, Peoples R China
关键词
dysphagia; lorlatinib; ALK; immune hyperprogression; ALK; PF-06463922; INHIBITOR; ROS1;
D O I
10.3892/ol.2023.14113
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
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页数:5
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