派姆单抗治疗非v600e BRAF突变肺腺癌的疗效:1例报告

G. D. Di Fazio, F. Citarella, E. Dell'Aquila, M. Russano, A. Galletti, V. Santo, B. Vincenzi, G. Tonini, D. Santini
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摘要

一小部分非小细胞肺癌(NSCLC)患者(2-4%)存在BRAF突变,其分类很容易被认为是V600E/非V600E变体。BRAF突变的不同功能类别,包括I类突变(V600E突变)、II类突变(激酶激活的非V600E突变)和III类突变(激酶受损的非V600E突变,增加ERK信号或RAS活性),在非V600E突变的NSCLC中具有更强的侵袭性行为。V600E阳性突变患者易接受靶向治疗,如达非尼和曲美替尼联合用于一线和二线治疗;其余临床意义不明,无治疗标准。较高水平的程序性死亡配体1 (PD-L1)表达与BRAF突变的存在相关。此外,很少有证据表明免疫检查点抑制剂(ICIs)的疗效:与EGFR突变或ALK重排的肿瘤相比,ICIs在V600E中都比非V600E突变的BRAF变体具有更有利的活性。我们确定了在携带罕见BRAF突变的患者中使用免疫疗法的生物学原理。我们报告一例使用派姆单抗成功治疗的G466E braf突变肺腺癌。此外,我们的病例增加了关于携带BRAF突变的NSCLC的有限文献,表明在开始治疗之前分析特定BRAF突变的生物学意义的重要性。
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Efficacy of pembrolizumab in lung adenocarcinoma harboring non-V600E BRAF mutation: a case report
: Small percentage of non-small cell lung cancer (NSCLC) patients, ranging 2–4% present BRAF mutations whom classification is easily accounted as V600E/non-V600E variant. There is a growing interest linked to different functional classes of BRAF mutations, which include class I (V600E mutations), class II mutations (kinase-activating non-V600E mutations), and class III mutations (kinase-impaired non-V600E mutations that increase ERK signaling or RAS activity), with a more aggressive behavior in non-V600E mutant NSCLC. V600E positive mutation patients are susceptible to target therapies, as the combination dabrafenib and trametinib in first- and second-line setting; meanwhile the others have an unknown clinical significance and there is no standard of therapy. Higher levels of programmed death-ligand 1 (PD-L1) expression are associated with presence of BRAF mutation. Furthermore, there is little evidence on the efficacy of immune checkpoint inhibitors (ICIs): in contrast to EGFR mutated or ALK rearranged tumors, ICIs have favorable activity both in V600E than non-V600E mutated BRAF variant. We identified a biological rationale for the use of immunotherapy in patients harboring uncommon BRAF mutations. We report a case of a G466E BRAF-mutated lung adenocarcinoma successfully treated with pembrolizumab. Besides, our case adds to the limited literature on NSCLC harboring BRAF mutations, showing the importance of analyze the biological significance of specific BRAF mutation before starting a treatment.
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