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. 2014 Jul 16;9(7):e102309. doi: 10.1371/journal.pone.0102309

Table 1. Summary of the proportion of patients gaining ≥10 letters (BCVA) from baseline to month 12 by study and treatment group.

Treatment group
Study Outcome measured at Ranibizumab 0.5 mg PRN, n/N (%) Aflibercept 2.0 mg bi-monthly, n/N (%) Laser, n/N (%) Sham, n/N (%) Ranibizumab 0.5 mg PRN + laser, n/N (%)
DA VINCI [66] 12 months 19/42 (45.2) 13/44 (29.5)
VISTA[72] 12 months 88/151 (58.3) 30/154 (19.5)
VIVID[72] 12 months 72/135 (53.3) 34/132 (25.8)
DRCR.net Protocol I [67] 12 months 81/293 (27.6) 95/187 (50.8)
READ-2[69] * 6 months 17/42 (40.5) 2/42 (4.8) 12/42 (28.6)
RESOLVE [68] 12 months 62/102 (60.8) 9/49 (18.4)
RESPOND [73] 12 months 37/75 (49.3) 10/72 (13.9) 24/73 (32.9)
RESTORE [48] 12 months 43/115 (37.4) 17/110 (15.5) 51/118 (43.2)
Total 159/334 (47.6) 179/328 (54.6) 187/847 (22.1) 9/49 (18.4) 182/420 (43.3)

Not all treatment groups included in the network meta-analysis are presented. Analysis is based on the intention-to-treat population of each study.

*Data for READ-2 are proportion of patients who gained ≥10 letters (BCVA) from baseline to month 6. After 6 months, patients in the laser treatment arm could receive ranibizumab, preventing meaningful comparisons between treatment arms at 12 months.

BCVA, best-corrected visual acuity; bimonthly, every 2 months; n, number of patients in treatment arm with ≥10 letter increase in BCVA; N, total number of patients in study treatment arm; PRN, pro re nata (as needed).