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. Author manuscript; available in PMC: 2015 Nov 7.
Published in final edited form as: Vaccine. 2012 Nov 20;30(0 5):F123–F138. doi: 10.1016/j.vaccine.2012.04.108

Table 7.

Cross-type protection against 6-month persistent infection

Efficacy (95% CI)

Trial: FutureI/II PATRICIA CVT
Vacccine: Gardasil® Cervarix® Cervarix®
Cohort: ITT-Naive TVC-Naive ATP
Mean 3.6 yrs 3.3 yrs 4 yrs
Follow-up:
HPV31 46.2 (15.3–66.4) 77.1 (67.2–84.4) 64.7 (42.6–78.9)
HPV33 28.7 (45.1–65.4) 43.1 (19.3–60.2) 32.1 (41.1–68.2)
HPV35 17.8 (77.1–62.5) 21.8 (102.5–26.2) 25.0 (40.6–60.6)
HPV52 18.4 (−20–45.0) 18.9 (3.2–32.2) 19.6 (8.1–40.4)
HPV58 5.5 (54.3–42.2) 6.2 (44.0–21.6) 2.8 (48.0–36.2)
Non-Vaccine A9 21.9 (0.6–38.8) 27.6 (17.6–36.5) NR
HPV39 NRa 20.9 (2.3–39.9) 30.8 (109.2–17.6)
HPV45 7.8 (67.0–49.3) 79.0 (61.3–89.4) 73.0 (45.3–87.8)
HPV59 18.7 (22.8–46.4) 3.9 (61.7–33.1) 30.3 (130.3–25.6)
HPV68 NR 8.9 (18.8–30.1) NR
Non-vaccine A7 14.8 (19.9–39.6)b 22.3 (8.4–34.2) NR
HPV51 NR 25.5 (12.0–37.0) 56.1 (114.3–14.2)
HPV56 NR 1.4 (24.8–22.0) 25.8 (12.7–51.4)
HPV66 NR 1.5 (29.3–20.3) 1.6 (41.0–31.3)
a

NR = not reported

b

HPV45 and 59 only

CVT: Costa Rica HPV Trial; CI: Confidence interval; HPV: Human papillomavirus.

Data from references [26,29,30].