Send to

Choose Destination
Lancet Oncol. 2012 Jan;13(1):100-10. doi: 10.1016/S1470-2045(11)70287-X. Epub 2011 Nov 8.

Cross-protective efficacy of HPV-16/18 AS04-adjuvanted vaccine against cervical infection and precancer caused by non-vaccine oncogenic HPV types: 4-year end-of-study analysis of the randomised, double-blind PATRICIA trial.

Collaborators (159)

Denham I, Garland SM, Mindel A, O'Sullivan M, Skinner SR, Waddell R, De Sutter P, Poppe WA, Tjalma W, De Carvalho NS, Naud P, Teixeira JC, Aoki FY, Diaz-Mitoma F, Dionne M, Ferguson L, Miller M, Papp K, Ramjattan B, Romanowski B, Somani R, Apter D, Karppa T, Kudjoi N, Kyha-österlund L, Lehtinen M, Levanen H, Lönnberg K, Lunnas T, Niemi L, Paavonen J, Palmroth J, Petaja T, Rekonen S, Siitari-Mattila M, Tuomivaara L, Vilkki M, Belling KH, Gent T, Gieseking F, Grubert T, Harlfinger W, Höpker WD, Kohoutek U, Jensen-El Tobgui S, Merder G, Peters K, Schoenian S, Schulze K, Schwarz TF, Wackernagel C, Boselli F, Liverani CA, Salmerón J, Del Rosario-Raymundo R, Germar MJ, Limson G, Villanueva G, Villanueva S, Zamora JD, Bajo J, Bayas J, Campins M, Castellsagué X, Castro M, Rodríguez L, Chow SN, Yu MH, Yuan CC, Angsuwathana S, Jaisamrarn U, Cruickshank M, Hakim E, Kitchener H, Lewis D, Szarewski A, Ackerman R, Caldwell M, Chambers C, Chatterjee A, Civitarese L, Demars L, Ferris D, Fine P, Gall S, Hedrick J, Herzig W, Huh W, Klein T, Koltun W, Lalezari J, Lee P, Luber S, Martens M, Nebel W, Peterson C, Pitts K, Rosen J, Rosenfeld W, Scutella M, Seidman L, Sperling M, Sperling R, Stager M, Stapleton J, Swenson K, Thoming C, Twiggs L, Waldbaum A, Wheeler CM, Zbella E, Camier A, Colau B, Xhenseval V, Genevrois S, Issaka Z, Marius P, Martens N, Ouammou T, Peeters P, Rahier M, Smoes N, Spiessens B, Meurée A, Houard N, Dessy F, Poncelet S, Tonglet A, Van Hoof C, Vilain AS, Zahaf T, Zima J, Alt E, Iskaros B, Limaye A, Liu-Jarin X, Luff RD, McNeeley M, Provenzano C, Winkler B, Molijn A, Quint W, Struijk L, Van de Sandt M, Van Doorn LJ, Catteau G, David MP, Zahaf T, Declerck L, Dupin J, Maroye JL, Kiviat N, Klugman KP, Nieminen P, Bergeron C, Eisenstein E, Marks R, Nolan T, Tay SK.

Author information

Department of Pathology, University of New Mexico Health Sciences Center, Albuquerque, NM, USA.

Erratum in

  • Lancet Oncol. 2012 Jan;13(1):e1.



We evaluated the efficacy of the human papillomavirus HPV-16/18 AS04-adjuvanted vaccine against non-vaccine oncogenic HPV types in the end-of-study analysis after 4 years of follow-up in PATRICIA (PApilloma TRIal against Cancer In young Adults).


Healthy women aged 15-25 years with no more than six lifetime sexual partners were included in PATRICIA irrespective of their baseline HPV DNA status, HPV-16 or HPV-18 serostatus, or cytology. Women were randomly assigned (1:1) to HPV-16/18 vaccine or a control hepatitis A vaccine, via an internet-based central randomisation system using a minimisation algorithm to account for age ranges and study sites. The study was double-blind. The primary endpoint of PATRICIA has been reported previously; the present analysis evaluates cross-protective vaccine efficacy against non-vaccine oncogenic HPV types in the end-of-study analysis. Analyses were done for three cohorts: the according-to-protocol cohort for efficacy (ATP-E; vaccine n=8067, control n=8047), total vaccinated HPV-naive cohort (TVC-naive; no evidence of infection with 14 oncogenic HPV types at baseline, approximating young adolescents before sexual debut; vaccine n=5824, control n=5820), and the total vaccinated cohort (TVC; all women who received at least one vaccine dose, approximating catch-up populations that include sexually active women; vaccine n=9319, control=9325). Vaccine efficacy was evaluated against 6-month persistent infection, cervical intraepithelial neoplasia grade 2 or greater (CIN2+) associated with 12 non-vaccine HPV types (individually or as composite endpoints), and CIN3+ associated with the composite of 12 non-vaccine HPV types. This study is registered with, number NCT00122681.


Consistent vaccine efficacy against persistent infection and CIN2+ (with or without HPV-16/18 co-infection) was seen across cohorts for HPV-33, HPV-31, HPV-45, and HPV-51. In the most conservative analysis of vaccine efficacy against CIN2+, where all cases co-infected with HPV-16/18 were removed, vaccine efficacy was noted for HPV-33 in all cohorts, and for HPV-31 in the ATP-E and TVC-naive. Vaccine efficacy against CIN2+ associated with the composite of 12 non-vaccine HPV types (31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66, and 68), with or without HPV-16/18 co-infection, was 46·8% (95% CI 30·7-59·4) in the ATP-E, 56·2% (37·2-69·9) in the TVC-naive, and 34·2% (20·4-45·8) in the TVC. Corresponding values for CIN3+ were 73·8% (48·3-87·9), 91·4% (65·0-99·0), and 47·5% (22·8-64·8).


Data from the end-of-study analysis of PATRICIA show cross-protective efficacy of the HPV-16/18 vaccine against four oncogenic non-vaccine HPV types-HPV-33, HPV-31, HPV-45, and HPV-51-in different trial cohorts representing diverse groups of women.


GlaxoSmithKline Biologicals.

[Indexed for MEDLINE]

Publication types, MeSH terms, Substances, Secondary source ID

Supplemental Content

Full text links

Icon for Elsevier Science
Loading ...
Support Center