Table 1.
Outcome | No of studies* (references) | Total No of participants | Vaccine group (events per total n/N (%)) |
Non-vaccine group (events per total n/N (%)) |
Risk ratio (95% CI) random effects model (inverse variance method) |
I2 | τ2 | PI |
---|---|---|---|---|---|---|---|---|
CIN2+† | 11 (18, 19, 21, 22, 42, 44-49) | 19 909 | 141/3472 (4%) | 926/16437 (5.6%) | 0.43 (0.30 to 0.60) | 58% | 0.14 | 0.16 to 1.12 |
CIN1+ | 5 (21, 22, 44, 47, 48) | 1045 | 89/587 (15.1%) | 116/458 (25.3%) | 0.55 (0.31 to 0.96) | 63% | 0.15 | 0.13 to 2.26 |
CIN3 | 3 (18, 19, 47) | 17 757 | 45/2428 (1.4%) | 420/15329 (2.7%) | 0.28 (0.01 to 6.37) | 71% | 1.23 | N/A |
CIN2 | 3 (18, 19, 47) | 17 757 | 15/2428 (0.6%) | 365/15329 (2.3%) | 0.23 (0.11 to 0.48) | 0% | 0 | 0.03 to 1.99 |
CIN1 | 4 (21, 22, 47, 48) | 970 | 55/562 (9.7%) | 44/408 (10.7%) | 0.86 (0.31 to 2.33) | 62% | 0.27 | 0.06 to 11.88 |
CIN2+ related to HPV16 or HPV18 | 6 (18, 21, 42, 45, 46, 48) | 1879 | 12/953 (1.2%) | 53/926 (5.7%) | 0.26 (0.16 to 0.43) | 0% | 0 | 0.16 to 0.45 |
CIN1+ related to HPV16 or HPV18 | 1 (21) | 178 | 2/89 (2.2%) | 8/89 (8.9%) | 0.25 (0.05 to 1.14) | N/A | N/A | N/A |
Abnormal cytology | 1 (21) | 178 | 7/89 (7.8%) | 23/89 (25.8%) | 0.30 (0.14 to 0.67) | N/A | N/A | N/A |
VIN1+ or VaIN1+ | 1 (21) | 178 | 0/89 (0%) | 3/89 (3.3%) | 0.14 (0.01 to 2.73) | N/A | N/A | N/A |
VIN2+ or VaIN2+ | 2 (21, 50) | 296 | 8/131 (6.1%) | 27/165 (16.3%) | 0.56 (0.01 to 35.16) | 0% | 0 | N/A |
Genital warts | 1 (41) | 171 | 45/91 (49.4%) | 35/80 (43.7%) | 0.14 (0.01 to 2.73) | N/A | N/A | N/A |
High grade AIN | 1 (43) | 152 | 12/38 (31.5%) | 35/114 (40.7%) | 1.03 (0.60 to 1.77) | N/A | N/A | N/A |
Persistent HPV infection‡ | 1 (18) | 344 | 26/166 (15.6%) | 32/178 (17.9%) | 0.87 (0.54 to 1.40) | N/A | N/A | N/A |
AIN=anal intraepithelial neoplasia; CIN=cervical intraepithelial neoplasia, grade 1 (CIN1), grade 1 or higher (CIN1+), grade 2 (CIN2), grade 2 or higher (CIN2+), grade 3 (CIN3); N/A=not applicable; PI=prediction interval; VIN1+ or VaIN1+=vulvar or vaginal intraepithelial neoplasia grade 1 or higher, grade 2 or higher (VIN2+ or VaIN2+).
All studies included an intervention (vaccine) and a control (non-vaccine) group.
Adjusted data were used when available
HPV type detected at baseline and six months after local surgical treatment.