Retrospektiv populasjonsbasert HPV-studie basert på unike data fra Kreftregisteret i Norge:

Retrospektiv populasjonsbasert HPV-studie
basert på unike data fra Kreftregisteret i
Norge:
HPV-data og celleforandringer hos kvinner
som er konisert en gang og som må
gjennomgå ny konisering
Steinar Ø Thoresen
Klinisk forskningssjef GSK
Professor dr med UiB
Oslo 25. mai 2010
Out-line of presentation

Background: HPV and development of cervical neoplasi

Rationale for study

Why Norway and Why The Cancer Registry of Norway?

Current study: objectives and study design

Conclusion
Out-line of presentation
Background:
HPV and development of cervical
neoplasi

Natural History
From Infection to Cervical Cancer
Time
Normal
epithelium
Months
HPV infection;
koilocytosis
CIN I
Low grade squamous
intraepithelial lesion
(ASCUS/LSIL)
Years
CIN II
High grade squamous
intraepithelial lesion (HSIL)
From incident to persistent HPV infection
Spontaneous regression
Screening
Treatment
CIN III
Invasive
Carcinoma
Conization and later pregnancy out-come
Distribution of HPV-types in CC
16
18
17,2
45
6,7
31
2,9
33
2,6
52
HPV genotype
53.5%
70.7%
77.4%
80.3%
82.9%
85.2%
87.4%
88.8%
53,5
2,3
58
2,2
35
1,4
59
1,3
56
1,2
51
1,0
39
0,7
68
0,6
73
0,5
82
0,3
Other
1,2
4,4
X
0
10
20
30
40
50
60
70
80
90
Cervical cancer cases attributed to the most frequent HPV genotypes (%)
Munoz N et al. Int J Cancer 2004; 111: 278–85.
100
Oncogenic HPV distribution in CIN2/3 Norway
HPV Type
% AHUS (n=643)
16
51.2
18
10.8
31
16.3
33
15.2
35
3.4
39
9.3
52
11.2
AHUS: Sjøborg et al, Gyn Oncol 2010
HUMAN PAPILLOMAVIRUS TYPE DISTRIBUTION IN CERVICAL NEOPLASIA:
RESULTS FROM TWO PARALLEL EPIDEMIOLOGICAL STUDIES IN WOMEN WITH
HIGH-GRADE CERVICAL INTRAEPITHELIAL NEOPLASIA AND INVASIVE
CERVICAL CANCER IN EUROPE
W. Tjalma on behalf of the HERACLES/SCALE study group (Montreal IPV Congress
July 2010)
Cervarix® efficacy in TVC-naïve: final analysis of
Phase III trial (39.4 months)
Primary analysis (TVC-naïve)
Vaccine Efficacy (96.1%CI)
Endpoint
CIN2+
HPV 16/18
Group
N
n
HPV
5,449
1
Control
5,436
63
%
LL
UL
p-value
98.4
90.4
100
< 0.0001
Vaccine Efficacy (96.1%CI)
Endpoint
CIN3+
HPV 16/18
Group
N
n
HPV
5,449
0
Control
5,436
13
%
LL
UL
p-value
100
64.7
100
< 0.0001
The TVC-naïve cohort approximates adolescent girls pre-exposure
Paavonen J, et al. Lancet 2009; 374:301–314.
Results CIN2+ (CERVARIX)
Vaccine efficacy associated with the most frequent non-vaccine oncogenic
HPV types and 14 oncogenic types (TVC naive)
HPV type
N
n
HPV 31/45
Vaccine
2 most frequent nonControl
vaccine types
5449
0
5436
24
HPV 31/33/45/52/58 Vaccine
5 most frequent nonControl
vaccine types
5449
15
HPV 31/33/35/
39/45/51/52/56/58/
59/66/68
any oncogenic types
except 16/18
Group
Vaccine
Control
HPV 16/18/31/33/35/
Vaccine
39/45/51/52/56/58/
59/66/68
14 oncogenic types
Control
including 16/18
5436
47
5449
20
5436
63
5449
22
5436
Vaccine
Efficacy %
96.1% CI
p-value
100
(82.2; 100)
< 0.0001
68,2
(40.5; 84.1)
< 0.0001
68.4
(45.7; 82.4)
< 0.0001
77.7
(63.5; 87.0)
< 0.0001
98
N = number of evaluable women in each group; n = number of evaluable women reporting at least one event in each group
Paavonen J, et al. Lancet 2009; 374:301–314;
Adapted from Skinner SR et al. IPvC 2009:Abstract
Out-line of presentation
The
scientific challenge and
rationale for study
Will Cervarix show efficacy in women treated for
CIN2+ lesions? ( about 3 000 women/year)
•
Oncogenic HPV-infections
High-grade lesions
Surgery on cervical uterus (conization)
HPV-persistent after surgery?
New HPV-infections?
High risk of recurrence of CIN and ICC
•
HPV-vaccination or not?
•
•
•
•
•
Cervarix-vaccination in women submitted to
conization?
As a first step to fill this gap of knowledge,
GSK will implement a register-based
retrospective study of natural history of HPV
infections and cervical lesion (CIN2+)
recurrences in women submitted to a
conization, in Norway.
Out-line of presentation
Why
Norway and why The Cancer
Registry of Norway?
The Cancer Registry of Norway, established 1951
Nationwide - population-based
Compulsory reporting on all cancers
Complete on all solid cancers
Includes:
ID of patients and all specimens
Sites, histology (grading), staging
ID of labs and all parafin blocks (stored)
Copy and ID of reports
Treatment
Survival, time and cause of death
The Cancer Registry of Norway, established 1951
Nationwide - population-based
National cervical cancer screening program since 1995:






One cytology form
One national cytology database (1992)
One national cervical biopsy database (2002)
National CIN-treatment database (1997)
CIN 2+ registration
ICC registration
The Cancer Registry of Norway, established 1951
Completeness of records and blocks (in the hospitals):
Bilet et al: Acta Oncol 2009:
Completeness estimate of CC in CRN was 98.8% in 1985 and 100% in 1999.
Availability of blocks in hospitals: 97.9 % in both years.
Out-line of presentation
Current
study: objectives and
study design
A retrospective, register-based, epidemiological study
of natural history of HPV infections in women aged 18
years and above with recurrent conization following a
primary conization for high grade lesion diagnosis/
microinvasive cervical carcinomas, in Norway.
Utprøvere: Professor Ole Erik Iversen og professor Olav Vintermyr UiB, Haukeland
Universitetsykehus
Tor Molden GSK Bio
Ann-Kirst Johansen GSK Norway
Steinar Thoresen GSK Norway
Primary objetives
To assess the distribution of oncogenic HPVtypes in recurrent conization considered as:
New infections or
Probably recurrent infections
Study design
The Cancer Registry to identify 550 women with the first conization 19982003 and the second conization 2003-2008; including all biopsies
between conizations. 100 % follow-up of all patients
Retrieve all parafin blocks from Norwegian pat labs
Review of all blocks/slides in one dedicated lab
HPV-testing in one dedicated lab
Approved by EC/SLV and based on informed consent
Decision tree for sample selection and
testing
Conclusion

The infrastructure of The Norwegian Cancer Registry is unique for
retrospective population-based epidemiological research on HPV and
cervival neoplasi, including the retrieval of parafin blocks and complete
follow-up of all participants

The current post-conization study could not be performed out-side
Norway ( Scandinavia)

We expect the current study to provide new knowledge about HPVinfections after primary conization and be an important step before a
Cervarix vaccination phase lll study in women submitted for conization