PMID- 32831120 OWN - NLM STAT- MEDLINE DCOM- 20210621 LR - 20210621 IS - 1748-717X (Electronic) IS - 1748-717X (Linking) VI - 15 IP - 1 DP - 2020 Aug 24 TI - Efficacy and safety of recombinant human endostatin combined with radiotherapy or chemoradiotherapy in patients with locally advanced non-small cell lung cancer: a pooled analysis. PG - 205 LID - 10.1186/s13014-020-01646-9 [doi] LID - 205 AB - PURPOSE: To assess the efficacy and safety of recombinant human endostatin in combination with radiotherapy (RT) or concurrent chemoradiotherapy (CCRT) in patients with locally advanced non-small cell lung cancer (LA-NSCLC). METHODS: We searched eligible literature in available databases using combinations of the following search terms: lung cancer, endostatin or endostar, radiotherapy or radiation therapy or chemoradiotherapy. The inclusion criteria were: prospective or retrospective (including single-arm) studies that evaluated the efficacy and safety of endostatin plus radiotherapy (ERT) or concurrent chemoradiotherapy (ECRT) in patients with LA-NSCLC. Primary outcomes included the following: objective response rate (ORR), local control rates (LCR), overall survival (OS), progression-free survival (PFS), and adverse events (AEs). Tests of heterogeneity, sensitivity, and publication bias were performed. RESULTS: A total of 271 patients with LA-NSCLC from 7 studies were enrolled, including six prospective trials and one retrospective study. The pooled median PFS was 11.3 months overall, 11.2 months in the ECRT group, and 11.8 months in the ERT group. Pooled median OS and ORR were 18.9 months and 77.2% overall, 18.4 months and 77.5% in the ECRT group, and 19.6 months and 76.1% in the ERT group, respectively. The incidences of major grade >/= 3 AEs for all patients, subgroups of ECRT and ERT were 10.9% vs 11.9% vs 9.4% for radiation pneumonitis, 11.6% vs 12.2% vs 9.4% for radiation esophagitis, 35.5% vs 43.4% vs 0 for leukopenia, 27.8% vs 40.7% vs 2.1% for neutropenia, and 10.5% vs 12.3% vs 2.1% for anemia. CONCLUSIONS: Combined endostatin with RT or CCRT is effective and well tolerated in treating LA-NSCLC, and less toxicities occur. Further validation through prospective randomized control trials is required. FAU - Zhang, Shu-Ling AU - Zhang SL AD - Department of Oncology, Shengjing Hospital of China Medical University, Shenyang, 110004, China. FAU - Han, Cheng-Bo AU - Han CB AD - Department of Oncology, Shengjing Hospital of China Medical University, Shenyang, 110004, China. FAU - Sun, Li AU - Sun L AD - Department of Oncology, Shengjing Hospital of China Medical University, Shenyang, 110004, China. FAU - Huang, Le-Tian AU - Huang LT AD - Department of Oncology, Shengjing Hospital of China Medical University, Shenyang, 110004, China. FAU - Ma, Jie-Tao AU - Ma JT AD - Department of Oncology, Shengjing Hospital of China Medical University, Shenyang, 110004, China. ma_jt@126.com. LA - eng GR - 81501990/National Natural Science Foundation of China/ PT - Journal Article PT - Meta-Analysis DEP - 20200824 PL - England TA - Radiat Oncol JT - Radiation oncology (London, England) JID - 101265111 RN - 0 (Endostatins) RN - 0 (Recombinant Proteins) SB - IM MH - Carcinoma, Non-Small-Cell Lung/pathology/*therapy MH - Chemoradiotherapy/*methods MH - Combined Modality Therapy MH - Endostatins/*administration & dosage MH - Humans MH - Lung Neoplasms/pathology/*therapy MH - Prognosis MH - Recombinant Proteins/*administration & dosage PMC - PMC7446219 OTO - NOTNLM OT - Chemoradiotherapy OT - Endostatin OT - Non-small cell lung cancer OT - Radiotherapy COIS- The authors declare that they have no competing interests. EDAT- 2020/08/25 06:00 MHDA- 2021/06/22 06:00 PMCR- 2020/08/24 CRDT- 2020/08/25 06:00 PHST- 2019/11/14 00:00 [received] PHST- 2020/08/19 00:00 [accepted] PHST- 2020/08/25 06:00 [entrez] PHST- 2020/08/25 06:00 [pubmed] PHST- 2021/06/22 06:00 [medline] PHST- 2020/08/24 00:00 [pmc-release] AID - 10.1186/s13014-020-01646-9 [pii] AID - 1646 [pii] AID - 10.1186/s13014-020-01646-9 [doi] PST - epublish SO - Radiat Oncol. 2020 Aug 24;15(1):205. doi: 10.1186/s13014-020-01646-9.