Qiu Ye, Li Bixun, Zhang Yihong, Guo Xiaoyun, Xiang Chunzhi, Wang Congshui, Lu Yang, Ren Shuang, Zhao Juan
Department of Integrated Medicine, Affiliated Tumor Hospital of Guangxi Medical University.
Respiratory and Critical Care Medicine, The First Affiliated Hospital of Guangxi Medical University, Nanning.
Medicine (Baltimore). 2019 Mar;98(11):e14826. doi: 10.1097/MD.0000000000014826.
The anaplastic lymphoma kinase (ALK) rearrangements represent a subtype of nonsmall-cell lung cancer (NSCLC), and targeting ALK has radically changed the treatment of NSCLC. Crizotinib, as an ALK inhibitor, has been used in the treatment of ALK-rearranged NSCLC for several years and some adverse effects should be given attention.
A 64-year-old woman with a no-smoking history visited hospital in November 2016 because of a persistent cough, expectoration, and progressive dysphagia for 2 months.
She was diagnosed with primary lung adenocarcinoma, accompanied by pleural and bone metastases. After receiving chemotherapy for nearly 1 year, she showed progressive disease. DNA-sequencing identified an intergenic ALK rearrangement. Surprisingly, RNA-sequencing revealed the EML4-ALK fusion transcript. Subsequently, this patient switched to crizotinib therapy.
The patient achieved partial response after 1-month treatment. However, this patient suffered a severe sinus bradycardia after 4 months of treatment. When reducing the dose of crizotinib, the side effect was alleviated and this patient showed stable disease until now.
Given that the severe sinus bradycardia was an unusual adverse effect, physicians should be aware of these side effects when using crizotinib. Moreover, it should be noted that this patient harbored an intergenic ALK rearrangement identified by DNA-sequencing, but EML4-ALK fusion transcript verified by RNA-sequencing. However, the mechanism remains unknown and requires further research.
间变性淋巴瘤激酶(ALK)重排是非小细胞肺癌(NSCLC)的一种亚型,靶向ALK已彻底改变了NSCLC的治疗方法。克唑替尼作为一种ALK抑制剂,已用于治疗ALK重排的NSCLC数年,一些不良反应应予以关注。
一名64岁无吸烟史的女性于2016年11月因持续咳嗽、咳痰及进行性吞咽困难2个月就诊。
她被诊断为原发性肺腺癌,伴有胸膜和骨转移。接受近1年化疗后,病情进展。DNA测序确定存在基因间ALK重排。令人惊讶的是,RNA测序显示有EML4-ALK融合转录本。随后,该患者改用克唑替尼治疗。
治疗1个月后患者达到部分缓解。然而,治疗4个月后该患者出现严重窦性心动过缓。降低克唑替尼剂量后,副作用减轻,该患者至今病情稳定。
鉴于严重窦性心动过缓是一种不常见的不良反应,医生在使用克唑替尼时应注意这些副作用。此外,应注意该患者通过DNA测序确定存在基因间ALK重排,但通过RNA测序验证有EML4-ALK融合转录本。然而,其机制仍不清楚,需要进一步研究。