Collaborating Institutions
Cancer Care Ontario, Toronto, Ontario; Hamilton Regional Cancer Centre, Hamilton; Kingston Regional Cancer Centre, Kingston, London Regional Cancer Centre, London; Mount Sinai Hospital, Toronto; Northeastern Ontario Regional Cancer Centre, Sudbury; Northwestern Ontario Regional Cancer Centre, Thunder Bay; Ottawa Regional Cancer Centre, Ottawa; Toronto-Sunnybrook Regional Cancer Centre, North York, Ontario; Windsor Regional Cancer Centre, Windsor, Ontario; University of Newfoundland, Newfoundland

Ellen McGannon 
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Collaborating Institutions
The University of Melbourne, Victoria, Australia; Queensland Institute of Medical Research, Brisbane, Queensland, Australia; Royal Melbourne Hospital, Victoria, Australia; King Edward Memorial Hospital, Perth, Western Australia, Australia; Westmead Hospital, Sydney, New South Wales, Australia; Prince of Wales Hospital, Sydney, New South Wales, Australia; Women's and Children's Hospital, Adelaide, South Australia, Australia; University of Auckland, New Zealand; Victorian Cancer Registry, Melbourne, Victoria, Australia

Mayo Clinic
Rochester, Minnesota 
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www.fredhutch.org/corestudies

Survival WG

[Meets quarterly] 3rd Thursday, alternating time:

• Thu, Nov 16, 2017 at 12:00pm ET
• Thu, Feb 15, 2018 at 5:00pm ET
• Thu, May 17,2018 at 12:00pm ET
• Thur, Aug 16, 2018 at 5:00pm ET
• Etc.

Phoenix, Arizona (details tbd)

The Colon Cancer Family Registry has served as an international resource for studies of the genetics and epidemiology of colorectal cancer (CRC) since 1997. It is the largest single family-based resource in the world for the study of CRC (and other cancers, such as endometrial cancer, that occur in these families).  The CCFR has supported and facilitated over 200 scientific projects, many including collaborations with other top CRC groups in the world, and has generated over 400 publications to date. This annual in-person meeting enhances the monthly one-hour Steering Committee and other working group conference calls.

These in-person meetings provide the opportunity for more in-depth discussions, break-out sessions, and concentrated impromptu meetings, all of which benefit the research agenda, scope of work, and the collaborative focus of the Colon Cancer Family Registry Cohort. Discussions focus on reviewing ongoing projects, updates on progress on the scope of work, brainstorming on novel scientific ideas and evaluation of opportunities for collaborating with other consortia as a group.  These meetings are also focused on the genesis and development of new grant proposals which complement and further the aims of the cohort.