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Conbercept for patients with age-related macular degeneration: a systematic review.
Zhang, Jiaxing; Liang, Yi; Xie, Juan; Li, Dong; Hu, Qian; Li, Xiaosi; Zheng, Wenyi; He, Rui.
Afiliação
  • Zhang J; Department of Pharmacy, Guizhou provincial people's hospital, No.83 Zhongshandong Road, Nanming District, Guiyang, Guizhou Province, China.
  • Liang Y; Health Outcomes and Pharmacy Practice, College of Pharmacy, the University of Texas at Austin, Austin, Texas, USA.
  • Xie J; Department of Pharmacy, Guizhou provincial people's hospital, No.83 Zhongshandong Road, Nanming District, Guiyang, Guizhou Province, China.
  • Li D; Department of Ophthalmology, Guizhou provincial people's hospital, Guiyang, Guizhou Province, China.
  • Hu Q; Department of Ophthalmology, Guizhou provincial people's hospital, Guiyang, Guizhou Province, China.
  • Li X; Department of Pharmacy, Hospital of Chengdu Office of People's Government of Tibetan Autonomous Region, No.20 Ximianqiaoheng Street, Wuhou District, Chengdu, Sichuan Province, China. lixiaosiyyy@126.com.
  • Zheng W; Department of Laboratory Medicine, Experimental Cancer Medicine, Clinical Research Center, Karolinska Institute, 14186, Huddinge, Stockholm, Sweden.
  • He R; Department of Laboratory Medicine, Experimental Cancer Medicine, Clinical Research Center, Karolinska Institute, 14186, Huddinge, Stockholm, Sweden.
BMC Ophthalmol ; 18(1): 142, 2018 Jun 15.
Article em En | MEDLINE | ID: mdl-29902977
ABSTRACT

BACKGROUND:

Conbercept is a novel vascular endothelial growth factor (VEGF) inhibitor for the treatment of wet age-related macular degeneration (AMD). This systematic review aims to assess the efficacy and safety of conbercept in the treatment of wet AMD.

METHODS:

PubMed, Embase, Cochrane Library, China National Knowledge Infrastructure, VIP database, and Wanfang database were searched from their earliest records to June 2017. We included randomized controlled trials (RCTs) evaluating the efficacy and safety of conbercept in wet AMD patients. Outcomes included the mean changes from baseline in best-corrected visual acuity (BCVA) score (primary outcome), central retinal thickness (CRT), plasma level of vascular endothelial growth factor (VEGF) over time, and the incidence of adverse events (AEs).

RESULTS:

Eighteen RCTs (1285 participants) were included in this systematic review. Conbercept might improve BCVA compared to triamcinolone acetonide [MD = 0.11, 95% CI (0.08, 0.15)], and reduce CRT compared to the other four therapies (conservative treatment, ranibizumab, transpupillary thermotherapy, and triamcinolone acetonide). The incidence of AEs in patients receiving conbercept was significantly lower than those receiving triamcinolone acetonide [RR = 0.25, 95% CI (0.09-0.72)], but was similar to the other therapies. Conbercept seemed to be more effective than ranibizumab in lowering the plasma level of VEGF [MD = - 15.86, 95% CI (- 23.17, - 8.55)].

CONCLUSIONS:

Current evidence shows that conbercept is a promising option for the treatment of wet AMD. Nevertheless, further studies are required to compare the efficacy, long-term safety and cost-effectiveness between conbercept and other anti-VEGF agents in different populations.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas Recombinantes de Fusão / Acuidade Visual / Degeneração Macular Exsudativa Tipo de estudo: Clinical_trials / Systematic_reviews Limite: Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas Recombinantes de Fusão / Acuidade Visual / Degeneração Macular Exsudativa Tipo de estudo: Clinical_trials / Systematic_reviews Limite: Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article