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TANDEM TRIAL: a factorial randomised controlled trial of dose and review schedule of bevacizumab (Avastin) for neovascular macular degeneration in the East Midlands

Foss, Alexander J E; Haydock, Rebecca; Childs, Margaret; Duley, Lelia; Empeslidis, Theo; Dhar-Munshi, Sushma; Montgomery, Alan; Ogollah, Reuben; Ozolins, Mara; Tesha, Paul; Mitchell, Eleanor

TANDEM TRIAL: a factorial randomised controlled trial of dose and review schedule of bevacizumab (Avastin) for neovascular macular degeneration in the East Midlands Thumbnail


Authors

Alexander J E Foss

Margaret Childs

Lelia Duley

Theo Empeslidis

Sushma Dhar-Munshi

ALAN MONTGOMERY ALAN.MONTGOMERY@NOTTINGHAM.AC.UK
Director Nottingham Clinical Trials Unit

REUBEN OGOLLAH REUBEN.OGOLLAH@NOTTINGHAM.AC.UK
Associate Professor of Medical Statistics and Clinical Trials

Mara Ozolins

Paul Tesha



Abstract

Objective: Neovascular age-related macular degeneration (nAMD) causes damage to the macula and severe vision loss. Bevacizumab is the most cost-effective nAMD treatment. The TANDEM trial was designed to determine whether, in patients with nAMD, low-dose bevacizumab is non-inferior to the standard dose in terms of visual deterioration and whether a bimonthly regimen is non-inferior to monthly, treatment as required, regimens.

Methods: This was a multicentre, 2×2 factorial, double-masked, non-inferiority randomised trial with patients considered eligible if they met the National Institute for Health and Care Excellence criteria for nAMD treatment with ranibizumab. Participants were randomly assigned to standard (1.25 mg) or low (0.625 mg) dose bevacizumab and either monthly or bimonthly review regimen. The primary outcome was time to vision deterioration, defined as reduction of ≥15 letters (three lines) during the loading phase (visual acuity scores at visits B and C compared with the initial visit A), or ≥6 letters (one line) during the maintenance phase (visual acuity scores at subsequent visits compared with mean vision at visits A–C).

Results: In total 812 participants (918 eyes) were randomised into the trial. The low dose showed some evidence of being non-inferior to standard dose (HR 1.07; 95% CI 0.80 to 1.42), however, there was no strong evidence of bimonthly review being non-inferior to monthly review (HR 1.45; 95% CI 1.09 to 1.94). There was no difference in visual acuity when assessed at 9 months and no major differences in the frequency of serious adverse events or reactions between the groups.

Conclusion: The standard dose of bevacizumab can be halved without compromising efficacy. Bimonthly review cannot be considered to be no worse than monthly review.

Citation

Foss, A. J. E., Haydock, R., Childs, M., Duley, L., Empeslidis, T., Dhar-Munshi, S., …Mitchell, E. (2020). TANDEM TRIAL: a factorial randomised controlled trial of dose and review schedule of bevacizumab (Avastin) for neovascular macular degeneration in the East Midlands. BMJ Open Ophthalmology, 5(1), Article e000588. https://doi.org/10.1136/bmjophth-2020-000588

Journal Article Type Article
Acceptance Date Nov 10, 2020
Online Publication Date Dec 8, 2020
Publication Date 2020-12
Deposit Date Dec 10, 2020
Publicly Available Date Dec 11, 2020
Journal BMJ Open Ophthalmology
Print ISSN 2397-3269
Publisher BMJ Publishing Group
Peer Reviewed Peer Reviewed
Volume 5
Issue 1
Article Number e000588
DOI https://doi.org/10.1136/bmjophth-2020-000588
Keywords Ophthalmology
Public URL https://nottingham-repository.worktribe.com/output/5053447
Publisher URL https://bmjophth.bmj.com/content/5/1/e000588

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