Treatment beyond progression in non-small cell lung cancer: A systematic review and meta-analysis

被引:2
|
作者
Kuo, Wei-Ke [1 ]
Weng, Ching-Fu [2 ,3 ]
Lien, Yin-Ju [4 ]
机构
[1] Sijhih Cathay Gen Hosp, Div Resp Therapy & Chest Med, Taipei, Taiwan
[2] Hsinchu Cathay Gen Hosp, Div Pulm Med, Dept Internal Med, Hsinchu, Taiwan
[3] Natl Tsing Hua Univ, Sch Med, Hsinchu, Taiwan
[4] Natl Taiwan Normal Univ, Dept Hlth Promot & Hlth Educ, Taipei, Taiwan
来源
FRONTIERS IN ONCOLOGY | 2022年 / 12卷
关键词
treatment beyond progression; NSCLC; meta-analysis; systemic review; survival; TYROSINE KINASE INHIBITOR; GEFITINIB PLUS CHEMOTHERAPY; DISEASE PROGRESSION; ACQUIRED-RESISTANCE; OPEN-LABEL; SURVIVAL; BEVACIZUMAB; OUTCOMES; OSIMERTINIB; ERLOTINIB;
D O I
10.3389/fonc.2022.1023894
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objectives Treatment beyond progression (TBP) is defined as treatment continuing in spite of disease progression, according to the Response Evaluation Criteria In Solid Tumors. We performed a systematic review and meta-analysis to provide evidence for the effects of TBP on lung cancer survival. Materials and methods This study has been conducted following the PRISMA guidelines. A systematic review of PubMed, MEDLINE, Embase, and Cochrane Collaboration Central Register of Controlled Clinical Trials from the inception of each database to December 2021 was conducted. Two authors independently reviewed articles for inclusion and extract data from all the retrieved articles. Random-effects meta-analysis was performed using Comprehensive Meta-Analysis software, version 3 (Biostat, Englewood, NJ, USA). Hazard ratios (HRs) with the corresponding 95% confidence intervals (CI) were used for survival outcomes. Results We identified five (15.6%) prospective randomized trials and twenty-seven (84.4%) retrospective observational studies of a total of 9,631 patients for the meta-analysis. 3,941 patients (40.9%) were in a TBP group and 5,690 patients (59.1%) were in a non-TBP group. There is a statistically significant advantage for patients who received TBP compared with those who did not in post progression progression-free survival (ppPFS), post progression overall survival (ppOS), and overall survival (OS) from initiation of drugs (ppPFS: HR, 0.746; 95% CI, 0.644-0.865; P<0.001; ppOS: HR, 0.689; 95% CI, 0.596-0.797; P<0.001; OS from initiation of drugs: HR, 0.515; 95% CI, 0.387-0.685; P<0.001) Conclusion This study provides further evidence in support of TBP for NSCLC, however, these results require cautious interpretation. Large, randomized, controlled trials investigating the efficacy of TBP in lung cancer treatment are warranted. Systemic Review Registration https://www.crd.york.ac.uk/PROSPERO/ identifier CRD42021285147
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页数:13
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