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Efficacy of cisplatin/pemetrexed with bevacizumab to treat advanced lung adenocarcinoma with different drive genes: case report and literature review

机译:顺铂/培美曲塞联合贝伐单抗治疗具有不同驱动基因的晚期肺腺癌的疗效:病例报告和文献复习

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Background: Bevacizumab combined with chemotherapy has become the first-line therapy in advanced nonsquamous non-small-cell lung cancer (NSCLC). However, few studies have focused on cisplatin/pemetrexed with bevacizumab as the first-line therapy to treat advanced nonsquamous NSCLC. Importantly, whether the epidermal growth factor receptor (EGFR) mutations or anaplastic lymphoma kinase (ALK) rearrangements can influence the efficacy of bevacizumab in combination with chemotherapy is very interesting. Herein, we report three cases with different types of gene drives in advanced nonsquamous NSCLC. Case presentation: In the first case, a patient presented with wild-type EGFR and negative ALK rearrangement. In the second case, a patient presented with wild-type EGFR and positive ALK rearrangement. In the third case, a patient presented with negative ALK rearrangement and mutated EGFR in exon 19. Conclusion: We speculate that bevacizumab in combination with cisplatin/pemetrexed as the first-line therapy is well tolerated and results in a clinically meaningful treatment benefit, irrespective of the gene drive type in advanced nonsquamous NSCLC. However, more data are needed to confirm the relationship.
机译:背景:贝伐单抗联合化疗已成为晚期非鳞状非小细胞肺癌(NSCLC)的一线治疗。但是,很少有研究集中于顺铂/培美曲塞联合贝伐单抗作为治疗晚期非鳞状非小细胞肺癌的一线治疗。重要的是,表皮生长因子受体(EGFR)突变或间变性淋巴瘤激酶(ALK)重排是否会影响贝伐单抗联合化疗的疗效非常有趣。在本文中,我们报告了晚期非鳞状非小细胞肺癌中三种不同基因驱动类型的病例。病例介绍:在第一个病例中,一名患者表现出野生型EGFR和ALK重排阴性。在第二种情况下,患者表现出野生型EGFR和ALK重排阳性。在第三例中,一名患者的外显子19出现ALK重排阴性且EGFR突变。结论:我们推测贝伐单抗联合顺铂/培美曲塞作为一线治疗的耐受性良好,并且无论在临床上均具有临床意义晚期非鳞状非小细胞肺癌中基因驱动类型的差异。但是,需要更多数据来确认关系。

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