a School of Medicine and Health , Aalborg University , Aalborg , Denmark.
b Department of Oncology , Rigshospitalet , Copenhagen , Denmark.
Acta Oncol. 2018 Feb;57(2):176-186. doi: 10.1080/0284186X.2017.1404634. Epub 2017 Nov 25.
advanced-stage non-small cell lung cancer (NSCLC) is characterized by having limited treatment options and thus a poor prognosis. However, new treatment options, in the form of targeted agents (TA), have emerged during recent years. This systematic review aims to provide an overview of the accessible literature in PubMed evaluating TA used on NSCLC patients, and the resulting survival outcomes.
this systematic literature review was conducted by reviewing all relevant literature in PubMed. Six separate searches were performed: Three searches where controlled entry terms were used and three free text searches. Furthermore, other relevant publications were included manually. A total of seventy-two studies met the search criteria and were thus further analyzed and evaluated.
In the included studies, various TAs and their effect on different molecular targets have been evaluated. Clinical responses vary considerably among the different genetic aberrations. The majority of studies evaluated TA for epidermal growth factor receptor (EGFR) mutations and TA for echinoderm microtubule-associated protein-like 4-anaplastic lymphoma kinase (EML4-ALK) rearrangements. Studies regarding the use of TA for Rat sarcoma (RAS), rapidly accelerated fibrosarcoma (RAF), ROS proto-oncogene 1 (ROS1) rearrangement, Receptor tyrosine-protein kinase erbB-2 (ERBB2), Phosphatidylinositol 3-kinase (PIK3CA)/v-akt murine thymoma viral oncogene homolog; protein kinase B(AKT)/Phosphatase and tensin homolog deleted on chromosome 10(PTEN), The mammalian target of rapamycin (mTOR), and Mesenchymal-epithelial transition factor (MET) were included as well. In general, studies comparing treatment outcomes in EGFR-mutated patients and EML4-ALK (ALK) rearranged patients after use of either TA or standard chemotherapy, present significant better results after TA.
This systematic review provides an overview of available literature in PubMed regarding NSCLC and TA. Included studies point toward that TA appears to be a promising therapeutic tool in treating NSCLC patients and use of TA is expected to result in improved treatment outcomes.
晚期非小细胞肺癌(NSCLC)的特点是治疗选择有限,因此预后较差。然而,近年来出现了新的治疗选择,即靶向药物(TA)。本系统评价旨在提供 PubMed 中评估 NSCLC 患者使用 TA 的可获得文献的概述,并评估其生存结果。
本系统文献复习通过检索 PubMed 中的所有相关文献进行。进行了六次独立搜索:三次使用控制词进行搜索,三次自由文本搜索。此外,还手动纳入了其他相关出版物。共有 72 项研究符合搜索标准,因此进一步进行了分析和评估。
在纳入的研究中,评估了各种 TA 及其对不同分子靶标的影响。不同遗传异常的临床反应差异很大。大多数研究评估了表皮生长因子受体(EGFR)突变的 TA 和棘皮动物微管相关蛋白样 4-间变性淋巴瘤激酶(EML4-ALK)重排的 TA。关于 TA 用于 Rat sarcoma(RAS)、rapidly accelerated fibrosarcoma(RAF)、ROS proto-oncogene 1(ROS1)重排、Receptor tyrosine-protein kinase erbB-2(ERBB2)、Phosphatidylinositol 3-kinase(PIK3CA)/v-akt murine thymoma viral oncogene homolog;protein kinase B(AKT)/Phosphatase and tensin homolog deleted on chromosome 10(PTEN)、The mammalian target of rapamycin(mTOR)和 Mesenchymal-epithelial transition factor(MET)的使用的研究也包括在内。一般来说,比较 EGFR 突变患者和 EML4-ALK(ALK)重排患者使用 TA 或标准化疗后的治疗结果的研究表明,TA 后结果显著更好。
本系统评价提供了 PubMed 中 NSCLC 和 TA 可用文献的概述。纳入的研究表明,TA 似乎是治疗 NSCLC 患者的一种有前途的治疗工具,预计使用 TA 将改善治疗结果。