Bioequivalence of Biosimilar Tumor Necrosis Factor-α Inhibitors Compared With Their Reference Biologics A Systematic Review

被引:45
作者
Chingcuanco, Francine [1 ]
Segal, Jodi B. [2 ]
Kim, Seoyoung C. [3 ]
Alexander, G. Caleb [1 ]
机构
[1] Johns Hopkins Bloomberg Sch Publ Hlth, Dept Epidemiol, 615 North Wolfe St,W6035, Baltimore, MD USA
[2] Johns Hopkins Bloomberg Sch Publ Hlth, Hampton House,624 North Broadway,Room 644, Baltimore, MD 21205 USA
[3] Brigham & Womens Hosp, Div Pharmacoepidemiol & Pharmacoecon, 1620 Tremont St,Suite 3030, Boston, MA 02115 USA
关键词
INFLAMMATORY-BOWEL-DISEASE; PARALLEL-GROUP; DOUBLE-BLIND; COMPARATIVE PHARMACOKINETICS; ANKYLOSING-SPONDYLITIS; INNOVATOR INFLIXIMAB; CLINICAL-EXPERIENCE; SAFETY; CT-P13; EFFICACY;
D O I
10.7326/M16-0428
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Background: Biosimilars are of growing clinical, regulatory, and commercial importance. Purpose: To summarize evidence about the bioequivalence between biosimilar and reference tumor necrosis factor-alpha (TNF-alpha) inhibitors. Data Sources: PubMed, EMBASE, Cochrane Central Register of Controlled Trials, and LILACS from inception through 13 April 2016 and ClinicalTrials. gov, World Health Organization International Clinical Trials Registry Platform, EU Clinical Trials Register, U.S. Food and Drug Administration, and European Medicines Agency from inception through 30 April 2016. Study Selection: Published English-language studies of any size or design that compared the pharmacokinetics, clinical efficacy, adverse events, or immunogenicity of a biosimilar TNF-alpha inhibitor with a reference biologic in humans. Data Extraction: Two reviewers independently screened titles and abstracts, extracted data from selected studies, and assessed study quality. Data Synthesis: Of 19 eligible studies, 8 were phase 1 randomized trials, 5 were phase 3 randomized trials, and 6 were observational studies. Most phase 1 trials (n = 7) involved healthy vol-unteers, phase 3 trials involved patients with rheumatoid arthritis, and observational studies involved those with rheumatoid arthritis or inflammatory bowel disease. All phase 1 trials showed that pharmacokinetic parameters of the biosimilar and respective biologic were within the prespecified equivalence margin of 80% to 125%. Phase 3 trials suggested similar clinical responses and adverse events. Adverse events were usually of mild to moderate severity. Two cross-sectional observational studies showed cross-reactivity between products, whereas 4 cohort studies of patients switched from reference to biosimilar products suggested similar efficacy and safety outcomes. Limitation: Possible publication bias, small sample sizes of many studies, and lack of published studies for several biosimilars. Conclusion: Preliminary evidence supports the biosimilarity and interchangeability of biosimilar and reference TNF-alpha inhibitors.
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页码:565 / +
页数:21
相关论文
共 59 条
[1]
[Anonymous], REMS
[2]
[Anonymous], READ SIGNS ROADM ENG
[3]
[Anonymous], CHS 0214 ET BIOS
[4]
[Anonymous], PROSPERO INT PROSPEC
[5]
[Anonymous], The Newcastle-Ottawa Scale (NOS) for Assessing the Quality of Nonrandomized Studies in Meta- Analysis
[6]
[Anonymous], REP SER PROBL FDA
[7]
[Anonymous], EXTR IND BIOS INFL
[8]
[Anonymous], AD
[9]
[Anonymous], 2014, GUID SIM BIOL MED PR
[10]
[Anonymous], ANK SPOND REM INFL E