PMID- 31096438 OWN - NLM STAT- MEDLINE DCOM- 20190528 LR - 20221005 IS - 1536-5964 (Electronic) IS - 0025-7974 (Print) IS - 0025-7974 (Linking) VI - 98 IP - 20 DP - 2019 May TI - Efficacy and safety of perioperative appliance of sunitinib in patients with metastatic or advanced renal cell carcinoma: A systematic review and meta-analysis. PG - e15424 LID - 10.1097/MD.0000000000015424 [doi] LID - e15424 AB - BACKGROUND: The aim of this systematic review and meta-analysis is to comprehensively evaluate the efficacy and safety of the perioperative use of sunitinib in patients with metastatic and advanced renal cell carcinoma (RCC). MATERIALS AND METHODS: We searched authenticated databases for related clinical studies. The baseline characteristics, parameters concerning the efficacy and safety of the perioperative use of sunitinib were extracted for subsequent comprehensive analysis. The parameters which reflected the efficacy and safety as overall survival (OS), progression-free survival (PFS), occurrence rate of all-grade and grade >/=3 adverse effects (AEs) were carefully pooled using comprehensive meta-analysis. RESULTS: We finally recruited 411 patients from 14 eligible studies. We found proteinuria (75.0%, 95% CI 62.1%-84.6%), anemia (71.6%, 95% CI 60.9%-80.3%), athesia (60.0%, 95% CI 40.3%-77.0%), pause symptoms (59.2%, 95% CI 49.2%-68.4%), arterial hypertension (53.1%, 95% CI 43.2%-62.7%), and thrombocytopenia (52.5%, 95% CI 44.8%-60.0%) to be the most common all-grade AEs. And arterial hypertension, athesia, cutaneous toxicity, hypophosphatemia, leukopenia, pain, pause syndrome, renal dysfunction, and thrombocytopenia were the most common types of grade >/=3 AEs. In addition, objective response rate (ORR) of sunitinib to both the original and metastatic tumor sites increased with the use of sunitinib, so did the OS and PFS. CONCLUSION: Common all-grade and grade >/=3 AEs were carefully monitored. The perioperative use of sunitinib showed superior ORR, OS, and PFS rates. Nevertheless, more studies are required to further verify these findings. FAU - Jin, Hongyu AU - Jin H AD - Department of Biotherapy and Cancer Center, State Key Laboratory of Biotherapy, West China Hospital. AD - West China School of Medicine. AD - Department of Liver Surgery, Liver Transplantation Center, West China Hospital, Sichuan University, Chengdu 610041, China. FAU - Zhang, Jing AU - Zhang J AD - Department of Biotherapy and Cancer Center, State Key Laboratory of Biotherapy, West China Hospital. AD - West China School of Medicine. FAU - Shen, Kai AU - Shen K AD - Department of Biotherapy and Cancer Center, State Key Laboratory of Biotherapy, West China Hospital. AD - West China School of Medicine. FAU - Hao, Jianqi AU - Hao J AD - West China School of Medicine. FAU - Feng, Yuying AU - Feng Y AD - West China School of Medicine. FAU - Yuan, Chi AU - Yuan C AD - West China School of Medicine. FAU - Zhu, Yuqi AU - Zhu Y AD - West China School of Medicine. FAU - Ma, Xuelei AU - Ma X AD - Department of Biotherapy and Cancer Center, State Key Laboratory of Biotherapy, West China Hospital. AD - West China School of Medicine. LA - eng PT - Journal Article PT - Meta-Analysis PT - Systematic Review PL - United States TA - Medicine (Baltimore) JT - Medicine JID - 2985248R RN - 0 (Protein Kinase Inhibitors) RN - V99T50803M (Sunitinib) SB - IM MH - Adult MH - Aged MH - Aged, 80 and over MH - Anemia/chemically induced MH - Carcinoma, Renal Cell/*drug therapy/mortality/pathology/secondary MH - Disease-Free Survival MH - Female MH - Humans MH - Hypertension/chemically induced MH - Kidney Neoplasms/drug therapy/pathology/secondary MH - Male MH - Middle Aged MH - Perioperative Care/*standards MH - Progression-Free Survival MH - Protein Kinase Inhibitors/administration & dosage/adverse effects/therapeutic use MH - Proteinuria/chemically induced MH - Sunitinib/administration & dosage/*adverse effects/*therapeutic use MH - Thrombocytopenia/chemically induced PMC - PMC6531174 COIS- The authors declare no interest of conflict. EDAT- 2019/05/18 06:00 MHDA- 2019/05/29 06:00 PMCR- 2019/05/17 CRDT- 2019/05/18 06:00 PHST- 2019/05/18 06:00 [entrez] PHST- 2019/05/18 06:00 [pubmed] PHST- 2019/05/29 06:00 [medline] PHST- 2019/05/17 00:00 [pmc-release] AID - 00005792-201905170-00009 [pii] AID - MD-D-18-09282 [pii] AID - 10.1097/MD.0000000000015424 [doi] PST - ppublish SO - Medicine (Baltimore). 2019 May;98(20):e15424. doi: 10.1097/MD.0000000000015424.