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布加替尼联合西妥昔单抗治疗重症 EGFR p.C797S 突变非小细胞肺癌患者的五线治疗:两例报告及文献复习。

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.

机构信息

Department of Medical Oncology, Fudan University Shanghai Cancer Center, Minhang Branch Hospital.

Department of Cardiology, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, South Campus.

出版信息

Anticancer Drugs. 2024 Jul 1;35(6):569-575. doi: 10.1097/CAD.0000000000001598. Epub 2024 Mar 15.

Abstract

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.

摘要

对于需要救生治疗的非小细胞肺癌 (NSCLC) 重症患者,目前尚无针对表皮生长因子受体 (EGFR) p.C797S 突变的药物使用的报告证据,该突变已知会导致第三代酪氨酸激酶抑制剂 (TKI) 耐药。我们的报告旨在研究和探索克服与 EGFR p.C797S 突变相关的耐药性的治疗策略,以为这些患者提供潜在的治疗选择。在这里,我们报告了两例最初携带 EGFR 敏感突变并接受第三代 TKI 奥希替尼治疗的 NSCLC 患者。在第五线治疗开始前对重症患者进行的下一代测序测试显示,两名患者均存在 EGFR p.C797S 突变,提示获得性耐药。在第五线治疗过程中,布加替尼和西妥昔单抗联合治疗对拯救重症患者至关重要,适度延长了他们的总生存期。我们的研究结果表明,布加替尼和西妥昔单抗联合方案可能是一种潜在的、有救生命的治疗策略,适用于表现出 EGFR p.C797S 介导的耐药性的 NSCLC 重症患者。然而,需要进一步的研究来验证和扩展这些有希望的发现。

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