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Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/ct2/show/NCT01393470




Registration number
NCT01393470
Ethics application status
Date submitted
5/07/2011
Date registered
13/07/2011
Date last updated
15/05/2014

Titles & IDs
Public title
Evaluation of Long-term HPV Vaccine Efficacy
Scientific title
A Long-term Follow-up Registry-based Cohort Study of HPV Vaccine Efficacy Against Cervical Pre-cancerous Lesions and Cervical Cancers in a Cohort of Females Previously Enrolled From Finland in Study HPV-008, as Compared to a Non-intervention Population -Based Reference Cohort of Females From Finland
Secondary ID [1] 0 0
115006 (HPV-027)
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Uterine Cervical Cancer 0 0
Condition category
Condition code
Cancer 0 0 0 0
Womb (Uterine or endometrial cancer)
Cancer 0 0 0 0
Cervical (cervix)

Intervention/exposure
Study type
Observational
Patient registry
Target follow-up duration
Target follow-up type
Description of intervention(s) / exposure
Treatment: Surgery - Screening for cervical cancer

Cohort A (Trial Cohort, Vaccinated during HPV-008) - Cohort A subjects were previously enrolled in the HPV-008 study, and have received at least 1 dose of the HPV vaccine.
Cohort A subjects have provided written informed consent prior to enrolment to allow retrieval of biospecimens for HPV DNA testing and confirmation of diagnosis.
Subjects who provided written informed consent prior to enrolment for the use of their personal identifier for linkage purposes to Finnish Registries.

Cohort B1 + B2 - Cohort B1 subjects were previously enrolled in the HPV-008 study and received at least 1 dose of HPV vaccine as cross-over vaccination at the end of the HPV-008 study.
Cohort B1 subjects have provided written informed consent prior to enrolment to allow retrieval of biospecimens for HPV DNA testing and confirmation of diagnosis.
Subjects who provided written informed consent prior to enrolment for the use of their personal identifier for linkage purposes to Finnish Registries.
Cohort B2 (Trial Cohort, Non-Vaccinated)

Cohort C (Referent Cohort, Non-Vaccinated) - Cohort C subjects have not participated in the HPV-008 study but have been enrolled in the Referent Cohort.
Cohort C subjects have not received any HPV vaccination (neither Cervarix, nor Gardasil, nor any experimental HPV vaccine).
Cohort C subjects are partially matched to HPV-008 in terms of the geographical recruitment area.
Subjects who provided written informed consent prior to enrolment for the use of their personal identifier for linkage purposes to Finnish Registries.


Treatment: Surgery: Screening for cervical cancer
Organized screening for cervical cancer start for all cohorts at the age of 25 years with 5 year interval.
Intervention code [1] 0 0
Treatment: Surgery
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
Occurrence of intraepithelial neoplasia grade 3 or worse (CIN3+). including CIN3, cervical cancer (squamous cell carcinoma or adenocarcinoma).
Timepoint [1] 0 0
The time frame is up to 15 years (for the interim analyses: 4, 7 and 10 years). (Start and end of passive follow-up, Cohorts A and B: 01.01.2010 - 31.12. 2024; Cohorts C1 and C2: 01.10.2007/01.10.2008 - 30.09.2021/30.09.2023.)
Secondary outcome [1] 0 0
Occurrence of potentially HPV related non-cervical cancers or pre cancerous lesions, including but not limited to the occurrence of vulvar intraepithelial neoplasia and vaginal intraepithelial neoplasia.
Timepoint [1] 0 0
The time frame for the objectives of the study is up to 15 years. (Start and end of passive follow-up, Cohorts A and B: 01.01.2010 - 31.12. 2024; Cohorts C1 and C2: 01.10.2007/01.10.2008 - 30.09.2021/30.09.2023.)

Eligibility
Key inclusion criteria
- Trial Cohort (16-17 years at baseline) - the cohort of Finnish subjects who
participated in the GSK Biologicals' HPV-008 trial (NCT00122681):

- Cohort A: subjects who received HPV-16/18 L1 VLP AS04 vaccine between May 2004 and May
2005.

- Cohort B: subjects who received the Hepatitis A control vaccine. All subjects were
offered the HPV-16/18 L1 VLP AS04 vaccine at the end of the study (age 21-22).

- Cohort B1: subjects who received the Hepatitis A control vaccine and then received
cross-over HPV vaccination at HPV-008 study end.

- Cohort B2: subjects who received the Hepatitis A control vaccine and who did not
receive cross-over HPV vaccination at HPV-008 study end.

- Referent cohort (18-19 years at baseline):

- Cohort C: A population-based reference cohort of female subjects from Finland who have
not been exposed to any HPV vaccine enrolled in this study in May 2005, immediately
after recruitment of the HPV-008 clinical trial subjects had been stopped
(approximately 9,000 subjects).
Minimum age
16 Years
Maximum age
19 Years
Sex
Females
Can healthy volunteers participate?
Yes
Key exclusion criteria
- Trial Cohort (Cohort A and B): Previous or planned administration of an HPV vaccine
not foreseen by the HPV-008 study protocol or any HPV-008 extension study protocol
(Gardasil or any experimental HPV vaccine).

- Referent cohort (Cohort C): Previous or planned administration of an HPV vaccine
(Cervarix, Gardasil or any experimental HPV vaccine).

Study design
Purpose
Duration
Selection
Timing
Prospective
Statistical methods / analysis

Recruitment
Recruitment status
Recruiting
Data analysis
Reason for early stopping/withdrawal
Other reasons
Date of first participant enrolment
Anticipated
Actual
1/05/2011
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
1/12/2024
Actual
Sample size
Target
10000
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)
Recruitment outside Australia
Country [1] 0 0
Finland
State/province [1] 0 0
Helsinki
Country [2] 0 0
Finland
State/province [2] 0 0
Jyväskylä
Country [3] 0 0
Finland
State/province [3] 0 0
Kotka
Country [4] 0 0
Finland
State/province [4] 0 0
Kouvola
Country [5] 0 0
Finland
State/province [5] 0 0
Kuopio
Country [6] 0 0
Finland
State/province [6] 0 0
Lahti
Country [7] 0 0
Finland
State/province [7] 0 0
Lappeenranta
Country [8] 0 0
Finland
State/province [8] 0 0
Mikkeli
Country [9] 0 0
Finland
State/province [9] 0 0
Oulu
Country [10] 0 0
Finland
State/province [10] 0 0
Pori
Country [11] 0 0
Finland
State/province [11] 0 0
Rauma
Country [12] 0 0
Finland
State/province [12] 0 0
Seinäjoki
Country [13] 0 0
Finland
State/province [13] 0 0
Tampere
Country [14] 0 0
Finland
State/province [14] 0 0
Turku
Country [15] 0 0
Finland
State/province [15] 0 0
Vaasa

Funding & Sponsors
Primary sponsor type
Other
Name
Tampere University
Address
Country
Other collaborator category [1] 0 0
Commercial sector/Industry
Name [1] 0 0
FinnMedi Oy
Address [1] 0 0
Country [1] 0 0
Other collaborator category [2] 0 0
Commercial sector/Industry
Name [2] 0 0
GlaxoSmithKline
Address [2] 0 0
Country [2] 0 0

Ethics approval
Ethics application status

Summary
Brief summary
Summary

For ethical and practical reasons pre-licensure clinical efficacy phase III trials for GSK
Biologicals' HPV-16/18 LI VLP AS04 vaccine used cervical intraepithelial grade 2 and above
(CIN2+) lesions as surrogate efficacy endpoint for cervical cancer. The long-term impact of
HPV vaccination on cervical cancer as well as other HPV-related non- cervical cancers is,
however, an area warranting further exploration in the post-licensure setting. Results of the
multinational phase III trial demonstrated high vaccine efficacy against CIN2+ associated
with HPV-16 and/or HPV-18, significant vaccine efficacy against CIN2+ and CIN3+ irrespective
of HPV type in the lesion as well as evidence of protection against CIN2+ associated with HPV
types 31 and 45 [Paavonen, et al. 2009]. Over time, vaccinated cohorts should benefit from a
substantial reduction in the incidence of cervical cancer considering impact on oncogenic
non-vaccine HPV types. This long-term study is conducted to evaluate the long-term impact of
GSK Biologicals' HPV-16/18 vaccine on the occurrence of cervical pre-cancerous lesions and
cervical cancer with the following objectives:

- To assess the long-term efficacy of the HPV-16/18 L1 VLP AS04 vaccine on the occurrence
of cervical cancer including its immediate precursors (CIN3+): cervical intraepithelial
neoplasia grade 3 (CIN3) and adenocarcinoma in situ (AIS) by comparing cohorts A and C
(see below).

- To assess the efficacy of HPV-16/18 L1 VLP AS04 vaccine on the occurrence of the
following potentially HPV related non-cervical cancers such as vulvar intraepithelial
neoplasia, vaginal intraepithelial neoplasia, anogenital neoplasia and oropharyngeal
neoplasia by comparing cohorts A and C (see below)

- To assess as an explanatory objective the occurrence of CIN3+ breakthrough cases
associated with HPV-16 or HPV-18 infection in subjects vaccinated with HPV-16/18 L1 VLP
AS04 vaccine by close surveillance of cohorts and cross vaccinated cohort B (see below)

This prospective, observational cohort study is undertaken in originally 16-17 year-old
Finnish females who have participated in the GSK Biologicals' HPV-008 trial (NCT00122681)
with regular clinical follow-up, and can be divided in Cohort A: Female subjects from Finland
who received HPV-16/18 L1 VLP AS04 vaccine in the HPV-008 study between May 2004 and May 2005
(N=2409), and Cohort B: Female subjects from Finland who received the Hepatitis A control
vaccine in the HPV-008 study (N=2399). All subjects were offered the HPV-16/18 L1 VLP AS04
vaccine or screening for cervical cancer at the end of the study (age 21-22): 50% of the
subjects, chose not to take cross-over HPV vaccination at HPV-008 study end. Referent Cohort
C: A population-based reference cohort of female subjects from Finland who have not been
exposed to any HPV vaccine (either during a HPV vaccine trial, or commercially available
vaccine; i.e. Cervarix or Gardasil), enrolled in this study in May - September 2003 or May -
September 2005, altogether 15536 subjects).

Prospective data collection will start at the HPV screening invitation for each subject in
2013. Several analyses are planned including an analysis at 8 years post-completion of the
HPV-008 study (by 2020) and will provide a total evaluation time of approximately 15 years
since first vaccination in the Cohort A.

The study is self-contained for the primary and secondary endpoints. Data from the HPV-008
trial will be used to address exploratory objectives mentioned above. Data collection will be
performed using the databases from the University of Tampere.
Trial website
https://clinicaltrials.gov/ct2/show/NCT01393470
Trial related presentations / publications
Paavonen J, Naud P, Salmeron J, Wheeler CM, Chow SN, Apter D, Kitchener H, Castellsague X, Teixeira JC, Skinner SR, Hedrick J, Jaisamrarn U, Limson G, Garland S, Szarewski A, Romanowski B, Aoki FY, Schwarz TF, Poppe WA, Bosch FX, Jenkins D, Hardt K, Zahaf T, Descamps D, Struyf F, Lehtinen M, Dubin G; HPV PATRICIA Study Group. Efficacy of human papillomavirus (HPV)-16/18 AS04-adjuvanted vaccine against cervical infection and precancer caused by oncogenic HPV types (PATRICIA): final analysis of a double-blind, randomised study in young women. Lancet. 2009 Jul 25;374(9686):301-14. doi: 10.1016/S0140-6736(09)61248-4. Epub 2009 Jul 6. Erratum In: Lancet. 2010 Sep 25;376(9746):1054.
Paavonen J, Jenkins D, Bosch FX, Naud P, Salmeron J, Wheeler CM, Chow SN, Apter DL, Kitchener HC, Castellsague X, de Carvalho NS, Skinner SR, Harper DM, Hedrick JA, Jaisamrarn U, Limson GA, Dionne M, Quint W, Spiessens B, Peeters P, Struyf F, Wieting SL, Lehtinen MO, Dubin G; HPV PATRICIA study group. Efficacy of a prophylactic adjuvanted bivalent L1 virus-like-particle vaccine against infection with human papillomavirus types 16 and 18 in young women: an interim analysis of a phase III double-blind, randomised controlled trial. Lancet. 2007 Jun 30;369(9580):2161-2170. doi: 10.1016/S0140-6736(07)60946-5. Erratum In: Lancet. 2007 Oct 20;370(9596):1414.
Lehtinen M, Idanpaan-Heikkila I, Lunnas T, Palmroth J, Barr E, Cacciatore R, Isaksson R, Kekki M, Koskela P, Kosunen E, Kuortti M, Lahti L, Liljamo T, Luostarinen T, Apter D, Pukkala E, Paavonen J. Population-based enrolment of adolescents in a long-term follow-up trial of human papillomavirus vaccine efficacy. Int J STD AIDS. 2006 Apr;17(4):237-46. doi: 10.1258/095646206776253453.
Lehtinen M, Paavonen J. Effectiveness of preventive human papillomavirus vaccination. Int J STD AIDS. 2003 Dec;14(12):787-92. doi: 10.1258/095646203322556084.
Lehtinen M, Apter D, Dubin G, Kosunen E, Isaksson R, Korpivaara EL, Kyha-Osterlund L, Lunnas T, Luostarinen T, Niemi L, Palmroth J, Petaja T, Rekonen S, Salmivesi S, Siitari-Mattila M, Svartsjo S, Tuomivaara L, Vilkki M, Pukkala E, Paavonen J. Enrolment of 22,000 adolescent women to cancer registry follow-up for long-term human papillomavirus vaccine efficacy: guarding against guessing. Int J STD AIDS. 2006 Aug;17(8):517-21. doi: 10.1258/095646206778145550.
Public notes
This record is viewable in the ANZCTR as it had previously listed Australia and/or New Zealand as a recruitment site, however these sites have since been removed

Contacts
Principal investigator
Name 0 0
Matti Lehtinen, M.D., Ph.D.
Address 0 0
Tampere University
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for public queries
Name 0 0
Address 0 0
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for scientific queries



Summary Results

For IPD and results data, please see https://clinicaltrials.gov/ct2/show/NCT01393470