37 episodes

The Collaborative Group of the Americas on Inherited Gastrointestinal Cancer (CGA-IGC) was established in 1995 to improve understanding of the basic science of inherited colorectal cancer and the clinical management of affected families, with an emphasis on the particular aspects of caring for families living in the Americas. The Expert Approach to Hereditary Gastrointestinal Cancers podcast series (seasons 1 and 2), and more recently, the Journal Club podcast series (season 3, 4, 5), are presented by the CGA-IGC Education Committee.

CGA-IGC Podcast Series CGA-IGC

    • Education
    • 5.0 • 11 Ratings

The Collaborative Group of the Americas on Inherited Gastrointestinal Cancer (CGA-IGC) was established in 1995 to improve understanding of the basic science of inherited colorectal cancer and the clinical management of affected families, with an emphasis on the particular aspects of caring for families living in the Americas. The Expert Approach to Hereditary Gastrointestinal Cancers podcast series (seasons 1 and 2), and more recently, the Journal Club podcast series (season 3, 4, 5), are presented by the CGA-IGC Education Committee.

    Season 7 - Episode 1: Constitutional MLH1 hypermethylation

    Season 7 - Episode 1: Constitutional MLH1 hypermethylation

    This episode is hosted by Emma Keel, MS, CGC, and features Megan Hoenig, MS, MPH, CGC a certified genetic counselor at the Mayo Clinic. Together, they discuss the contribution of MLH1 constitutional methylation to Lynch syndrome diagnosis. They also explore disease definitions and mechanisms and current genetic testing guidelines while discussing the open questions in the field. This podcast was released on #LynchSyndromeAwarenessDay.  Read our blog post "MLH1 hypermethylation during #LynchSyndromeAwarenessDay" here https://tinyurl.com/3zkurynf

    • 10 min
    Episode 5: S.6 Ep.5 Position statement of the International Society for Gastrointestinal Hereditary Tumours (InSiGHT) on APC I1307K and Cancer Risk

    Episode 5: S.6 Ep.5 Position statement of the International Society for Gastrointestinal Hereditary Tumours (InSiGHT) on APC I1307K and Cancer Risk

    This episode is hosted by Thomas Slavin, MD, FACMG, DABMD, a Chief Scientific Officer at HALO Precision Diagnostics  and features Laura Valle, PhD, a Principal Investigator, at the Catalan Institute of Oncology, IDIBELL. They discuss the position statement on the APC I1307K allele and its association with cancer predisposition which was generated by a multidisciplinary international expert group endorsed by the International Society for Gastrointestinal Hereditary Tumours (InSiGHT). Read our blog post "Evidence based guidance for APC I1307K and Cancer Risk" hereStay tuned for more podcasts in 2024! If you missed any of our earlier 2023 podcasts, you can find them here

    • 17 min
    Episode 4: S.6 Ep.4 Fight CRC Advocate Danielle Ripley-Burgess: "Life After Total Proctocolectomy in Lynch Syndrome”

    Episode 4: S.6 Ep.4 Fight CRC Advocate Danielle Ripley-Burgess: "Life After Total Proctocolectomy in Lynch Syndrome”

    This episode is hosted by Thomas Slavin, MD, FACMG, DABMD, a Chief Scientific Officer, and Emma Keel, MS, CGC, a genetic counselor, who have the privilege of speaking with Danielle Ripley-Burgess as she shares her story and experience on "Life After Total Proctocolectomy in Lynch Syndrome.”We're incredibly grateful that she took the time to share her story with us, and we hope it will give our members and the broader #HereditaryGICancer community greater insight into the patient's perspective. 

    • 23 min
    Episode 3: S.6 Ep.3 Clinical characteristics of pancreatic and biliary tract cancers in Lynch syndrome: A retrospective analysis from the Finnish National Lynch Syndrome Research Registry

    Episode 3: S.6 Ep.3 Clinical characteristics of pancreatic and biliary tract cancers in Lynch syndrome: A retrospective analysis from the Finnish National Lynch Syndrome Research Registry

    This episode is hosted by Julie Yang, MD, a gastroenterologist at the Icann School of Medicine at Mount Sinai, New York, USA and features Toni T. Seppälä, M.D., PhD, a GI surgeon and Professor of Cancer Research at Tampere University, Helsinki, Finland. They discuss the results from a retrospective analysis published this year, “Clinical characteristics of pancreatic and biliary tract cancers in Lynch syndrome: A retrospective analysis from the Finnish National Lynch Syndrome Research Registry,"  which can be found here. Read our blog post "Insights gained from the largest cohort of patients with pancreaticobiliary cancer and Lynch Syndrome" here

    • 17 min
    Episode 2: S.6 Ep.2 Considerations for individuals with Hereditary Diffuse Gastric Cancer Syndrome when considering a prophylactic gastrectomy

    Episode 2: S.6 Ep.2 Considerations for individuals with Hereditary Diffuse Gastric Cancer Syndrome when considering a prophylactic gastrectomy

    This episode is hosted by Josie Baker, MS, CGC, a genetic counselor at The Ohio State University, and features Rachael Lopez, MPH, RD, CSO, a clinical research dietitian at the National Institutes of Health. Together they discuss the considerations for individuals with Hereditary Diffuse Gastric Cancer Syndrome when considering a prophylactic gastrectomy. This episode highlights the professional experience when working with these individuals before and after surgery, as well as the challenges individuals may face during this process. 

    • 20 min
    Previous CGA-IGC Grant recipients - Dr. Allison Burton-Chase

    Previous CGA-IGC Grant recipients - Dr. Allison Burton-Chase

    The CGA-IGC Research Committee will host a new podcast series highlighting the work of the CGA-IGC Research Grant recipients. The first episode will feature the 2014 grant recipient, Dr. Allison Burton-Chase, and explore her research into Lynch syndrome patient-provider relationships, communication, and transition.The papers in the order they were referenced:  Hennig K, DeCoster B, Chu R, Parker W, Campo-Engelstein L, Burton-Chase AM. Patients educating health care providers on Lynch syndrome. Patient Experience Journal. 2018; 5(3):91-96. doi: 10.35680/ 2372-0247.1319.  https://pxjournal.org/cgi/viewcontent.cgi?article=1319&context=journal  Burton-Chase AM, Parker WM, Hennig K, Sisson F, Bruzzone LL. The Use of Social Media to Recruit Participants With Rare Conditions: Lynch Syndrome as an Example. JMIR Res Protoc. 2017 Jan 23;6(1):e12. doi: 10.2196/resprot.6066. PMID: 28115298; PMCID: PMC5294367. https://pubmed.ncbi.nlm.nih.gov/28115298/

    • 23 min

Customer Reviews

5.0 out of 5
11 Ratings

11 Ratings

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