Concomitant double-fusion of PLEKHA7-ALK and INPP5D-ALK reveals favorable alectinib sensitivity in lung adenocarcinoma: a case report and literature review

被引:0
|
作者
Li, Pei [1 ,2 ]
Ju, Xiao [2 ,3 ]
Yang, Guangjian [1 ,2 ]
机构
[1] Shandong First Med Univ, Shandong Canc Hosp & Inst, Dept Resp Med Oncol, 440 Jiyan Rd, Jinan 250117, Peoples R China
[2] Shandong Acad Med Sci, 440 Jiyan Rd, Jinan 250117, Peoples R China
[3] Shandong First Med Univ, Shandong Canc Hosp & Inst, Dept Radiat Oncol, 440 Jiyan Rd, Jinan 250117, Peoples R China
关键词
Double-fusion; PLEKHA7-ALK; INPP5D-ALK; Alectinib; Lung adenocarcinoma; ONE PATIENT; ALK; EML4-ALK; VARIANT; COEXISTENCE;
D O I
10.1007/s12672-024-00899-0
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Anaplastic lymphoma kinase (ALK) gene fusion is a classic driver mutation in non-small cell lung cancer (NSCLC); however, ALK double-fusion variants in NSCLC have rarely been reported. In this study, we reported a case with extremely uncommon ALK double-fusion variants. A 32-year-old female diagnosed with lung adenocarcinoma, who had developed multiple intrapulmonary and brain metastases, experienced worsening of her condition despite undergoing prior chemotherapy. Subsequent testing using next-generation sequencing (NGS) detected the presence of PLEKHA7-ALK and INPP5D-ALK double-fusion. The prescription of alectinib revealed potent efficacy and resulted in an increase in the survival rate. This case presented two uncommon and concomitant ALK fusion partners in NSCLC; more importantly, the INPP5D-ALK subtype has not been reported, therefore this study broadens the spectrum of ALK double-fusion variants and provides insight into the use of ALK inhibitors for the treatment of NSCLC in patients with double ALK fusions.
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页数:6
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