In-depth exploration of the focus issues of TKI combined with radiotherapy for EGFR-mutant lung adenocarcinoma patients with brain metastasis: a systematic analysis based on literature metrology, meta-analysis, and real-world observational data.

IF 3.4 2区 医学 Q2 ONCOLOGY
Yalan Tong, Xiaosha Wan, Chang Yin, Ting Lei, Shan Gao, Yinghua Li, Xiaojing Du
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引用次数: 0

Abstract

Background: There is a growing interest in utilizing a combination of brain radiotherapy (RT) and tyrosine kinase inhibitors (TKIs) for patients diagnosed with brain metastases (BM) in epidermal growth factor receptor (EGFR) mutation-positive lung adenocarcinoma (LAC). The current status of this treatment strategy remains a subject of debate.

Methods: We initiated our study by conducting a comprehensive literature search using the SCI-expanded database of Web of Science Core Collection (WoSCC). We utilized the VOSPviewer software to analyze various aspects of the research, including the year of publication, authorship, keywords, and country.Subsequently, we performed an extensive and systematic literature search on popular online databases. Our primary outcome measures were overall survival (OS) and intracranial progression-free survival (iPFS), both quantified by hazard ratios (HRs). Additionally, for data verification, we included data from patients in non-small cell lung cancer with brain metastasis who underwent therapeutic intervention at the Cancer Prevention and Treatment Center of Sun Yat-sen University and the Radiotherapy Department of Hanzhong Central Hospital between August 2012 and November 2021.

Results: The bibliometric analysis revealed an increasing trend in research focused on the combination of RT and TKIs for the management of lung cancer brain metastases over the previous decade. Then, nine studies consistent with the research direction were included for meta-analysis. The meta-analysis showed that the OS (HR = 0.81, 95% confidence interval: 0.69-0.94; P = 0.007) and iPFS (HR = 0.71, 95% confidence interval: 0.61-0.82; P < 0.001) of the combination therapy were significantly prolonged. Finally, 168 EGFR-mutated BM advanced LAC patients in the real world were verified, and the median iPFS of the combination therapy (n = 88 and EGFR-TKIs alone (n = 80) were 16.0 and 9.0 months, respectively, (P < 0.001). The median OS was 29.0 and 27.0 months, respectively, with no dramatic difference (P = 0.188).

Conclusions: Research on EGFR-mutant LAC brain metastasis has turned towards exploring optimal treatment strategies for this condition. Our meta-analysis and real-world data analysis consistently demonstrate that combination therapy offers a substantial improvement in patient survival compared to EGFR-TKI monotherapy. Notably, among patients undergoing salvage radiotherapy (RT), our subgroup analysis reveals that those initially treated with third-generation TKIs experience more significant benefits than those treated with first- or second-generation TKIs.

深入探讨TKI联合放疗治疗脑转移的表皮生长因子受体突变肺腺癌患者的焦点问题:基于文献计量学、荟萃分析和真实世界观察数据的系统分析。
背景:对于表皮生长因子受体(EGFR)突变阳性的肺腺癌(LAC)脑转移患者,采用脑放疗(RT)和酪氨酸激酶抑制剂(TKIs)联合治疗的兴趣日益浓厚。这一治疗策略的现状仍存在争议:我们利用科学网核心数据库(Web of Science Core Collection,WoSCC)的 SCI 扩展数据库进行了全面的文献检索,从而开始了我们的研究。随后,我们在流行的在线数据库中进行了广泛而系统的文献检索。我们的主要结果指标是总生存期(OS)和颅内无进展生存期(iPFS),两者均以危险比(HRs)进行量化。此外,为了核实数据,我们还纳入了2012年8月至2021年11月期间在中山大学肿瘤防治中心和汉中市中心医院放疗科接受治疗干预的非小细胞肺癌脑转移患者的数据:文献计量学分析显示,在过去十年中,关于RT和TKIs联合治疗肺癌脑转移的研究呈上升趋势。随后,纳入了9项与研究方向一致的研究进行荟萃分析。荟萃分析结果显示,OS(HR = 0.81,95% 置信区间:0.69-0.94;P = 0.007)和 iPFS(HR = 0.71,95% 置信区间:0.61-0.82;P 结论:TKIs 是治疗肺癌脑转移的最佳选择:有关表皮生长因子受体突变 LAC 脑转移的研究已转向探索该病症的最佳治疗策略。我们的荟萃分析和实际数据分析一致表明,与 EGFR-TKI 单药治疗相比,联合治疗可大幅提高患者的生存率。值得注意的是,在接受挽救性放疗(RT)的患者中,我们的亚组分析显示,最初接受第三代 TKIs 治疗的患者比接受第一代或第二代 TKIs 治疗的患者获益更多。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BMC Cancer
BMC Cancer 医学-肿瘤学
CiteScore
6.00
自引率
2.60%
发文量
1204
审稿时长
6.8 months
期刊介绍: BMC Cancer is an open access, peer-reviewed journal that considers articles on all aspects of cancer research, including the pathophysiology, prevention, diagnosis and treatment of cancers. The journal welcomes submissions concerning molecular and cellular biology, genetics, epidemiology, and clinical trials.
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