尽管EGFR G719S突变,但camrelizumab对PD-L1高表达的转移性肺鳞状细胞癌的长期反应:一个病例报告

IF 0.6 4区 医学 Q4 PHARMACOLOGY & PHARMACY Tropical Journal of Pharmaceutical Research Pub Date : 2023-08-19 DOI:10.4314/tjpr.v22i7.24
Yuhua Wang, Ke Fang
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引用次数: 0

摘要

免疫检查点抑制剂(ICIs)已广泛应用于具有野生型EGFR/ALK基因的非小细胞肺癌。然而,ICIs对EGFR基因敏感突变的晚期NSCLC的影响一直存在争议。目前还没有关于ICIs单药治疗是否可以用于EGFR敏感突变的NSCLC的报道。1例EGFR G719s突变、PD-L1评分高、有结核病史的转移性肺鳞状细胞癌患者,于2020年2月24日至2023年1月给予阿法替尼、camrelizumab单抗一线治疗(200mg,静脉注射,每3周1次)。患者在camrelizumab治疗后获得部分缓解(PR)。camrelizumab单药治疗的无进展生存期(PFS)超过34个月。综上所述,camrelizumab作为EGFR G719突变和高PD-L1评分的肺鳞状细胞癌的治疗选择具有良好的潜在有效性。
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Long response to camrelizumab in metastatic lung squamous cell carcinoma with high PD-L1 expression despite EGFR G719S mutation: A case report
Immune checkpoint inhibitors (ICIs) have been widely used in non-small cell lung cancer with wildtype EGFR/ALK genes. However, the effect of ICIs on advanced NSCLC with EGFR genes sensitive mutations has been controversial. There are no reports on whether ICIs monotherapy can be used in the treatment of NSCLC with EGFR sensitive mutations. A patient with metastatic lung squamous cell carcinoma with EGFR G719s mutations, high PD-L1 score and a tuberculosis history was given first-line treatment of afatinib, camrelizumab monotherapy (200 mg, intravenous, once every three weeks) from February 24,2020 to January 2023. The patient achieved partial response (PR) after treatment with camrelizumab. The progress-free survival (PFS) due to camrelizumab monotherapy was more than 34 months.It is concluded that camrelizumab has promising potential effectiveness as a treatment option for lung squamous cell cancer with EGFR G719 mutations and high PD-L1 score. 
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来源期刊
CiteScore
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自引率
33.30%
发文量
490
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4-8 weeks
期刊介绍: We seek to encourage pharmaceutical and allied research of tropical and international relevance and to foster multidisciplinary research and collaboration among scientists, the pharmaceutical industry and the healthcare professionals. We publish articles in pharmaceutical sciences and related disciplines (including biotechnology, cell and molecular biology, drug utilization including adverse drug events, medical and other life sciences, and related engineering fields). Although primarily devoted to original research papers, we welcome reviews on current topics of special interest and relevance.
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