PMID- 33474947 OWN - NLM STAT- MEDLINE DCOM- 20210514 LR - 20220603 IS - 2224-5839 (Electronic) IS - 2224-5820 (Linking) VI - 10 IP - 2 DP - 2021 Feb TI - The efficacy and safety of Osimertinib in advanced non-small cell lung cancer patients with Thr790Met resistance mutations: a systematic review and meta-analysis. PG - 1851-1860 LID - 10.21037/apm-20-1357 [doi] AB - BACKGROUND: Osimertinib, a third-generation epidermal growth factor receptor-tyrosine kinase inhibitor (EGFR-TKI), has been approved by the U.S. Food and Drug Administration in treating T790M mutationpositive advanced non-small cell lung cancer (NSCLC). A systematic review and meta-analysis was conducted to assess the efficacy and safety of osimertinib in treating advanced NSCLC patients with acquired T790M mutation. METHODS: PubMed, EMBASE, Cochrane Library and Web of Science were searched to obtain the eligible studies following the "population, interventions, comparisons, outcomes, study design" (PICOS) criteria. The pooled analysis of objective response rate (ORR), disease controlled rate (DCR), progressionfree survival (PFS), overall survival (OS) and adverse events (AEs) were performed using STATA12.0 and RevMan5.0. RESULTS: A total of 1,050 patients were included in the meta-analysis. The combined osimertinib ORR was 0.64 (95% CI, 0.60-0.69), the ORR of central nervous system (CNS) was 0.54 (95% CI, 0.37-0.71), DCR was 0.89 (95% CI, 0.86-0.92), PFS at six months (PFS-6m) rate was 0.69 (95% CI, 0.58-0.79), PFS at one year (PFS-1y) rate was 0.33 (95% CI, 0.20-0.46), OS at one year (OS-1y) rate was 0.69 (95% CI, 0.55-0.84). The pooled incidence rate of the AEs of grade >/= III was 0.25 (95% CI, 0.09-0.40). The results from Begg's and Egger's tests presented no publication bias in the included studies. CONCLUSIONS: Osimertinib demonstrated a superior therapeutic benefit with high efficacy and low toxicity for T790M-positive advanced NSCLC patients who were treated with early-generation EGFR-TKIs. Meanwhile, osimertinib showed promising for the treatment of advanced patients with CNS metastases. FAU - Cui, Saijin AU - Cui S AD - Cancer Institute, The Fourth Hospital of Hebei Medical University, Shijiazhuang, China. FAU - Zhang, Yaling AU - Zhang Y AD - Cancer Institute, The Fourth Hospital of Hebei Medical University, Shijiazhuang, China. FAU - Liu, Lu AU - Liu L AD - Cancer Institute, The Fourth Hospital of Hebei Medical University, Shijiazhuang, China. FAU - Li, Yan AU - Li Y AD - Cancer Institute, The Fourth Hospital of Hebei Medical University, Shijiazhuang, China. FAU - Zhou, Rongmiao AU - Zhou R AD - Cancer Institute, The Fourth Hospital of Hebei Medical University, Shijiazhuang, China. FAU - Huang, Xi AU - Huang X AD - Cancer Institute, The Fourth Hospital of Hebei Medical University, Shijiazhuang, China. FAU - Cao, Shiru AU - Cao S AD - Cancer Institute, The Fourth Hospital of Hebei Medical University, Shijiazhuang, China. FAU - Huo, Xiangran AU - Huo X AD - Cancer Institute, The Fourth Hospital of Hebei Medical University, Shijiazhuang, China. FAU - Wang, Na AU - Wang N AD - Cancer Institute, The Fourth Hospital of Hebei Medical University, Shijiazhuang, China. hbykdxwn@163.com. LA - eng PT - Journal Article PT - Meta-Analysis PT - Systematic Review DEP - 20210114 PL - China TA - Ann Palliat Med JT - Annals of palliative medicine JID - 101585484 RN - 0 (Acrylamides) RN - 0 (Aniline Compounds) RN - 0 (Protein Kinase Inhibitors) RN - 3C06JJ0Z2O (osimertinib) RN - EC 2.7.10.1 (ErbB Receptors) SB - IM MH - Acrylamides MH - Aniline Compounds MH - *Carcinoma, Non-Small-Cell Lung/drug therapy/genetics MH - ErbB Receptors/genetics MH - Humans MH - *Lung Neoplasms/drug therapy/genetics MH - Mutation MH - Protein Kinase Inhibitors/therapeutic use OTO - NOTNLM OT - Osimertinib OT - T790M mutation OT - advanced non-small cell lung cancer (NSCLC) OT - central nervous system (CNS) OT - meta-analysis EDAT- 2021/01/22 06:00 MHDA- 2021/05/15 06:00 CRDT- 2021/01/21 08:37 PHST- 2020/07/03 00:00 [received] PHST- 2020/10/23 00:00 [accepted] PHST- 2021/01/22 06:00 [pubmed] PHST- 2021/05/15 06:00 [medline] PHST- 2021/01/21 08:37 [entrez] AID - apm-20-1357 [pii] AID - 10.21037/apm-20-1357 [doi] PST - ppublish SO - Ann Palliat Med. 2021 Feb;10(2):1851-1860. doi: 10.21037/apm-20-1357. Epub 2021 Jan 14.