Lifestyle and outcomes after gastrointestinal cancer: A prospective cohort study (LOGIC).

Authors

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Marissa Barbara Savoie

Helen Diller Family Comprehensive Cancer Center, University of California San Francisco, San Francisco, CA

Marissa Barbara Savoie , Katherine Van Loon , Angela Laffan , Andrea Grace Bocobo , Li Zhang , Alan T Paciorek , Chloe Evelyn Atreya , Mekhail Anwar , Tami Rowen , James F Smith , Dianne Shumay , Stacey A. Kenfield , June M. Chan , Alan P. Venook , Erin Van Blarigan

Organizations

Helen Diller Family Comprehensive Cancer Center, University of California San Francisco, San Francisco, CA, University of California San Francisco, San Francisco, CA, UC San Francisco Helen Diller Family Comprehensive Cancer Center, San Francisco, CA

Research Funding

NIH

Background: The number of individuals living after a diagnosis of gastrointestinal (GI) cancer is increasing. Emerging data suggest modifiable lifestyle factors impact survival after colorectal cancer (CRC), however very little is known about survivorship in other GI cancers. Given the common thread of multimodality therapy among many GI cancer survivors, there is a paucity of data on sexual function, fertility, anxiety/depression, changes in comorbidities, and quality of life after cancer treatment. Additionally, existing cohort studies of GI survivors are primarily European, and further data are needed from survivor populations in the US . Methods: Patients of the University of California, San Francisco GI Oncology Survivorship Clinic who are designated disease-free are recruited by mail or in clinic. We send secure online questionnaires to participants every six months for five years and annually thereafter. At varying intervals, questionnaires solicit sociodemographics, diet, physical activity, fertility, medical and smoking history, fear of cancer recurrence, sexual health, quality of life, psychological well-being, and sleep quality. Pathoclinical disease characteristics, treatment, and recurrence status are abstracted from the medical record at baseline and updated annually. Results: Between February and August 2017, 111 patients were enrolled; 68% of participants completed ≥1 and 57% completed all baseline questionnaires. Most patients had a history of colon cancer (52%, n = 58) or rectal cancer (31%, n = 34). Other diseases include: anal cancer (12%, n = 13), gastrointestinal stromal tumor (3%, n = 3), and other GI cancers (3%, n = 3). Fifty-eight percent of patients were female, 76% identified as white and median age at diagnosis was 55 (range 20-81). Median time from initial GI cancer diagnosis to study entry was 27 months. Following the initial recruitment wave of established patients, the average rate of enrollment is ~3 patients/week. Conclusions: Results from this ongoing cohort study will improve our understanding of modifiable risk factors for GI cancer recurrence and key survivorship issues related to psychological well-being, sexual function, fertility management, and quality of life.

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Abstract Details

Meeting

2018 Cancer Survivorship Symposium

Session Type

Poster Session

Session Title

Poster Session B: Chronic Anticancer Therapy; Late- and Long-term Effects/Comorbitidities; Psychosocial Issues; Risk Assessment

Track

Care Coordination, Cost, and Education,Late- and Long-term Effects/Comorbidities,Health Promotion,Psychosocial Issues,Communication and Transitions,Risk Assessment,Chronic Anti-Cancer Therapy

Sub Track

Detection of Recurrence and Secondary Malignancies

Citation

J Clin Oncol 36, 2018 (suppl 7S; abstr 180)

DOI

10.1200/JCO.2018.36.7_suppl.180

Abstract #

180

Poster Bd #

D18

Abstract Disclosures

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