Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/91363
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Type: Conference item
Title: The inherited cancer connect (iccon) mutation-carrier database
Author: James, P.A.
Petelin, L.
Campbell, I.
Dawkins, H.
Fox, S.
Hiller, J.
Kirk, J.
Lindeman, G.
Macrae, F.
Mascarenhas, L.
McGaughran, J.
Meiser, B.
Morrow, A.
Nichols, C.
Pachter, N.
Saunders, C.
Scott, C.
Poplawski, N.
Thrupp, L.
Trainer, A.
Ward, R.
Young, M.A.
Mitchell, G.
Citation: Asia-Pacific Journal Of Clinical Oncology, 2014 / vol.10, iss.Suppl. 8, pp.167-168
Publisher: Wiley
Issue Date: 2014
ISSN: 1743-7555
1743-7563
Conference Name: COSA's 41st Annual Scientific Meeting. Joining Forces - Accelerating Progress (02 Dec 2014 - 04 Dec 2014 : Melbourne, Vic.)
Statement of
Responsibility: 
Paul A James, Lara Petelin, Ian Campbell, Hugh Dawkins, Stephen Fox, Janet Hiller, Judy Kirk, Geoffrey Lindeman, Finlay Macrae, Lyon Mascarenhas, Julie McGaughran, Bettina Meiser, April Morrow, Cassandra Nichols, Nicholas Pachter, Christobel Saunders, Clare Scott, Nicola Poplawski, Letitia Thrupp, Alison Trainer, Robyn Ward, Mary-Anne Young, Gillian Mitchell
Abstract: The ICCon Partnership was formed in 2013 through the support of a CCNSW STREP grant. A principal goal of this collaboration is to build a national database of individuals with germline mutations causing hereditary cancer syndromes to promote translational research and improve the health of people with a hereditary predisposition to cancer. The ICCon database is currently in development and will comprise of de-identified clinical data that can be extracted for the purposes of linking families across Australia, providing supportive data for health policy applications, responding to feasibility enquiries for clinical trials, or to identify those patients who are eligible to participate in specific trials, or who may benefit from new advances in therapeutic interventions. The ICCon database will include all known carriers of pathogenic mutations in a cancer predisposition gene who have attended a familial cancer clinic (FCC). It will cover the range of hereditary cancer syndromes and include data collected as part of routine clinical care within the FCC. Data that is planned to be stored include mutation type, cancer diagnosis (if appropriate), cancer treatment (if known), family pedigree (de-identified) and cancer risk management information (if known). FCC patients will have the opportunity to provide additional consent for their treatment information to be linked to ICCon through the CART-WHEEL rare cancer registry. In addition to enabling HREC-approved projects and providing data to inform national policy in the hereditary cancer arena, data from the ICCon database will be able to contribute to both clinical and translational research activities. In the translational research arena the ICCon database will be able to contribute data to the international initiatives aiming to amalgamate mutation data, such as BIC (the Breast Cancer Information Core http://research.nhgri.nih.gov/bic/) and InSiGHT (the International Society for Gastrointestinal Hereditary Tumours http://www.insight-group.org/).
Rights: © 2014 The Authors. Asia-Pacific Journal of Clinical Oncology © 2014 Wiley Publishing Asia Pty Ltd
RMID: 0030028788
DOI: 10.1111/ajco.12305
Appears in Collections:Paediatrics publications

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