Real-world evidence in the use of Bevacizumab in age-related macular degeneration (ArMD): a scoping review

被引:5
作者
Gomez-Lumbreras, Ainhoa [1 ]
Ghule, Priyanka [1 ]
Panchal, Rupesh [1 ,2 ,3 ]
Giannouchos, Theodoros [1 ,4 ]
Lockhart, Catherine M. [5 ]
Brixner, Diana [1 ]
机构
[1] Univ Utah, Coll Pharm, Dept Pharmacotherapy, 30S 2000E, Salt Lake City, UT 84112 USA
[2] Univ Utah Hlth Plans, Murray, UT USA
[3] ZS, 2535 West Hillcrest Dr,Suite 100, Thousand Oaks, CA 91320 USA
[4] Univ Alabama Birmingham, Sch Publ Hlth, Dept Hlth Policy & Org, Birmingham, AL 35233 USA
[5] Biol & Biosimilars Collect Intelligence Consortium, Alexandria, VA USA
关键词
Macular degeneration; Bevacizumab; Biosimilar pharmaceuticals; Drug utilization review; Systematic review; Treatment outcome; Patient-reported outcome measures; Observational studies as topic; ENDOTHELIAL GROWTH-FACTOR; ANTI-VEGF AGENTS; INTRAVITREAL INJECTION; BIOSIMILARS; OPHTHALMOLOGY; OUTCOMES; THERAPY; VISION; TRENDS; TREAT;
D O I
10.1007/s10792-023-02853-5
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
PurposePharmacological treatments for age-related macular degeneration (ArMD) include anti-vascular endothelial growth factor therapies. Bevacizumab is used off-label, as it has no indication for ArMD. This study aims to identify and describe literature on real-world evidence of bevacizumab (originator or biosimilars) use in ArMD.MethodsA scoping review was conducted in Medline, CINAHL and Embase databases. Studies published in English after September 2017, conducted in USA, including adults (& GE; 18 years old) with ArMD who received treatment with bevacizumab for ArMD were included. The review was further limited to peer-reviewed observational studies that quantitatively analyze either clinical or patient-reported outcomes among patients treated with bevacizumab for ArMD.ResultsThe search strategy retrieved 543 studies. After title and abstract screening, a total of 142 studies were selected for full-text review leading to a total of 12 studies qualifying for data charting. All were retrospective studies. Five (41.6%) of the studies had less than 500 eyes included in the analysis, and the rest had over a thousand eyes. All except one study reported clinical outcomes (visual acuity was the main outcome in 8 (66.6%) studies). There were 3 (25%) studies reporting adverse events of bevacizumab intravitreal injections. None of the studies specified using biosimilars for bevacizumab and none mentioned patient-reported outcomes.ConclusionThe lack of studies aiming to study the patient-reported outcomes as well as the use of biosimilars of bevacizumab in ArMD makes this field a potential for future research. The different exposures and times to follow-up make it difficult to compare results among the selected studies.
引用
收藏
页码:4527 / 4539
页数:13
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