International Cancer Benchmarking Partnership (ICBP) Module 4
The ICBP is a partnership between England, Australia, Canada, Denmark, Northern Ireland, Norway, Sweden and Wales co-ordinated by the Department of Health (DH) in England with support from Cancer Research UK.
Module 4 of the ICBP is an international survey on time intervals from onset of symptoms to commencement of treatment in newly diagnosed patients with lung, colorectal, breast, or ovarian cancer. It aims to explore whether variation in cancer survival between the participating countries may be partly rooted in differences in time interval from first symptom until diagnosis and treatment.
Patient information sheet for England (pdf) - Download
Prospective postal questionnaire survey
Module 4 seeks to explore whether variation in cancer survival between the
participating countries may be partly rooted in differences in time interval
from first symptom until diagnosis and treatment.
Patients diagnosed with breast, colorectal, lung and ovarian cancer during the
specified period of the survey.
Identification of potential participants
Patients will be identified via participating Cancer Registries using Cancer
Waiting Times, Multidisciplinary Team and pathology data feeds.
- Aged 40 and over
- Aware of their diagnosis of cance
- Male breast cancer
- Patient questionnaire completed >6 months following diagnosis
- Patients who have previously had a separate cancer of the same organ (e.g. consecutive breast cancers)
- Patient questionnaire
- Primary health care professional questionnaire
- Secondary care questionnaire
Sample size per jurisdiction
Pilot study – 50 confirmed patients per primary cancer
Main study – 200 confirmed patients per primary cancer
For 15 years via the cancer registries
Module 4 consists of a feasibility pilot and the main study.
The pilot study
will cover patients diagnosed up to 5 months prior to the pilot study start in
October 2012 and run for 3 months.
The main Module 4 data collection period
will start April-June 2013 and run up until June 2014. It will include all
patients newly diagnosed during that period.
The study in England is coordinated at University College London The
patient identification process is led by the Trent Cancer Registry (TrCR)
working in partnership with the West Midlands Cancer Intelligence Unit and the
Eastern Cancer Registration and Information Centre. The team at TrCR will
contact GPs of identified patients who will then forward the invitation to
participate in this study to the individual patient. The GP will send the
signed information pack to the selected patients and return a pre-stamped
acknowledgment slip to TrCR informing them whether the patient pack was sent on.
There will be no contact between patients and cancer registries.
Patients willing to take part in the study will return their signed
consent form and completed questionnaire to the academic Module 4 study team at
University College London. The academic team will not have access to any patient
level information unless the patient has consented to take part in this study.
After obtaining consent from the patients the primary and specialist care
questionnaire will be sent to GP and consultants to obtain information on
diagnosis and treatment.
Prof Usha Menon (Co-chair module 4 and Lead England)
Dr Evangelia-Ourania Fourkala (Co-ordinator)
Mr Robert Liston
Mr Rakshit Desai
Trent Cancer Registry
Mr Hales Jack
Ms Thackeray Alexandra
Mr David Meechan
Mike Richards – England
Todd Harper, Nicola Quin, Bob Thomas - Australia (Victoria)
David Currow - Australia (New South Wales)
Heather Bryant, Michael Sherar, Linda Rabeneck - Canada
Søren Brostrøm, Ole Andersen - Denmark
Anna Gavin - Northern Ireland
Stein Kaasa - Norway
Aileen Keel (Scotland)
Gunilla Gunnarsson - Sweden
Jane Hanson – Wales
A mixture of government boies and cancer charities in the participating countries are funding the study. CR UK is overseeing study management. The England arm of module 4 is funded by the Department of Health for England with the UCL team receiving additional support from the charity Eve Appeal.
Prof Peter Vedsted (co-chair Module 4) (Denmark)
Prof David Weller (co-chair Module 4), Chantelle Anandan (Scotland)
Dr Vicky White - Australia (Victoria)
Dr Jane Young - Australia (New South Wales)
Ms Susan Fekete – Canada (Canadian Partnership against Cancer)
Dr Juanita Hatcher, Dr Peter Craighead - Canada (Alberta)
Dr Andy Coldman, Dr Mark Elwood, Dr Ivo Olivotto, Coleen McGahan- Canada (British Columbia)
Prof Dhali Dhaliwal, Dr Donna Turner, Dr Sue Bates, Breann Hawryluk- Canada (Manitoba)
Prof Eva Grunfeld, Dr Andriana Barisic - Canada (Ontario)
Dr Jackie Boylan, Mr Conan Donnelly - Northern Ireland
Dr Anne Kari Knudsen, Dr Sigrun Saur Almberg – Norway
Prof Mats Lambe, Dr Annette Wigertz, Dr Martin Malmberg - Sweden
Prof Richard Neal – Wales
CRUK Management team
Dr Martine Bomb
Page last modified on 09 jun 13 21:18