Efficacy and safety of oxaliplatin-based regimen versus cisplatin-based regimen in the treatment of gastric cancer: a meta-analysis of randomized controlled trials
Autor: | Binfeng Yang, Xin Wang, Gongchen Wang, Zhiming Zhang, Zhaoyuan Fu |
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Rok vydání: | 2019 |
Předmět: |
0301 basic medicine
Oncology medicine.medical_specialty medicine.medical_treatment Cochrane Library law.invention 03 medical and health sciences 0302 clinical medicine Randomized controlled trial Stomach Neoplasms law Internal medicine Antineoplastic Combined Chemotherapy Protocols Humans Medicine Randomized Controlled Trials as Topic Cisplatin Chemotherapy business.industry Cancer Hematology General Medicine medicine.disease Oxaliplatin Regimen 030104 developmental biology Tolerability 030220 oncology & carcinogenesis Surgery Safety business medicine.drug |
Zdroj: | International Journal of Clinical Oncology. 24:614-623 |
ISSN: | 1437-7772 1341-9625 |
DOI: | 10.1007/s10147-019-01425-x |
Popis: | Cisplatin played an important role in the treatment of gastric cancer (GC). Oxaliplatin has been shown to be at least as effective as cisplatin for GC, with less toxicity and a better tolerability profile. We performed a meta-analysis to compare the efficacy and safety of oxaliplatin-based regimen versus cisplatin-based regimen in the treatment of GC. Databases of CNKI, CBM, VIP, Wanfang, PubMed, Embase, Cochrane Library were searched for eligible literatures from their establishments to November 2018. Randomized controlled trials that compared the efficacy and safety of oxaliplatin-based regimen with that of cisplatin-based regimen in the treatment of GC were included. Statistical analyses were calculated using RevMan 5.3 software. Seven randomized controlled trials including 2297 patients were included. Compared with cisplatin-based regimen intervention in GC, oxaliplatin-based regimen treatment was able to significantly improve the partial response rate (OR = 1.26, 95% CI 1.07–1.49; p = 0.007), disease progression rate (OR = 0.41, 95% CI 0.25–0.66; p = 0.0002) and 1-year survival (OR = 1.25, 95% CI 1.00–1.56; p = 0.05). The toxicities of hematopoietic system were significantly higher in cisplatin-based regimen group (OR = 0.6, 95% CI 0.46–0.79; p = 0.0002), while oxaliplatin-based regimen group had higher neurosensory toxicity (OR = 2.21, 95% CI 1.52–3.21; p |
Databáze: | OpenAIRE |
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