Brigatinib combined with cetuximab in the fifth-line treatment of non-small cell lung cancer with EGFR p.C797S mutation in critically ill patients: a report of two cases and literature review

被引:0
|
作者
Liu, Juanjuan [1 ]
Lei, Hongtao [2 ]
Zhang, Ding [3 ]
Zhang, Ning [1 ]
机构
[1] Fudan Univ, Minhang Branch Hosp, Shanghai Canc Ctr, Dept Med Oncol, Shanghai, Peoples R China
[2] Shanghai Jiao Tong Univ, Affiliated Peoples Hosp 6, Dept Cardiol, South Campus, Shanghai, Peoples R China
[3] 3D Med Inc, Med Dept, Shanghai, Peoples R China
关键词
acquired resistance; brigatinib; case report; cetuximab; critically ill patients; epidermal growth factor receptor; lung adenocarcinoma; OSIMERTINIB; RESISTANCE; T790M; GEFITINIB; SURVIVAL; TKI;
D O I
10.1097/CAD.0000000000001598
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
For critically ill patients with non-small cell lung cancer (NSCLC) in need of life-saving treatment, there is currently no reported evidence regarding the use of medication specifically targeting epidermal growth factor receptor (EGFR) p.C797S mutation, which is known to cause resistance to third-generation tyrosine kinase inhibitors (TKIs). Our report aims to investigate and explore treatment strategies to overcome resistance associated with EGFR p.C797S mutation in order to provide potential therapeutic options for these patients. Here, we reported two cases with NSCLC who initially harbored an EGFR-sensitive mutation and were both treated with osimertinib, a third-generation TKI. Next-generation sequencing tests conducted prior to the initiation of fifth-line therapy in critically ill patients revealed the presence of EGFR p.C797S mutations in both patients, suggesting acquired resistance. In the course of fifth-line therapy, the administration of a combination of brigatinib and cetuximab proved vital in saving critically ill patients, moderately extending their overall survival period. Our findings suggested that a combined regimen of brigatinib and cetuximab could serve as a potentially life-saving therapeutic strategy for critically ill patients with NSCLC, particularly those demonstrating EGFR p.C797S-mediated resistance. Further studies, however, are required to validate and expand upon these promising findings.
引用
收藏
页码:569 / 575
页数:7
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