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Coverage: 2020-01-01 onwards, with up to 300 results per query from PubMed and Europe PMC and separate limits on other sources. This is a selected index, not a complete literature search.
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Familial Adenomatous Polyposis: Research Summary
Printed from RareWays (rareways.org)
For general awareness only. Not medical advice. Discuss all care options with your healthcare team.
5 Most Recent Research Articles
- 1.
Top Tips for Endoscopic Management of Lynch Syndrome and Familial Adenomatous Polyposis.
Katona Bryson W, Gastrointestinal endoscopy (15 October 2026)
https://pubmed.ncbi.nlm.nih.gov/42880509/
- 2.
Psychosocial experiences of individuals living with familial adenomatous polyposis more than 10 years after diagnosis
もも子 荒木 et al., Hereditary Cancer in Clinical Practice (8 October 2026)
https://doi.org/10.1186/s13053-026-00354-x
- 3.
Dual-docking robotic total proctocolectomy for familial adenomatous polyposis with synchronous rectal and sigmoid carcinomas: a methodology of port placement and docking strategy
Songjie Li et al., Techniques in Coloproctology (7 October 2026)
https://doi.org/10.1007/s10151-026-03438-x
- 4.
When is the right time? Rethinking risk-reducing colorectal surgery in APC-associated familial adenomatous polyposis.
Vitellaro Marco et al., European journal of surgical oncology : the journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology (5 October 2026)
https://pubmed.ncbi.nlm.nih.gov/42868947/
- 5.
Identification of a novel dependency between PRMT5 and APC-LOF in preclinical models of FAP disease
Dana S. Gaffney et al., Communications Biology (3 October 2026)
https://doi.org/10.1038/s42003-026-11084-0
Clinical Trials : Currently Recruiting (Australia)
Ask your doctor whether you or your child may be eligible for any of these trials. Each has its ID and full eligibility criteria at the link shown.
- 1.
FOG-001 in Locally Advanced or Metastatic Solid Tumors
NCT05919264 · Recruiting · Phase 1 / Phase 2 · Parabilis Medicines, Inc.
Ages 18 and over
https://clinicaltrials.gov/study/NCT05919264
Source: RareWays research directory. Data from PubMed, Europe PMC, OpenAlex, ClinicalTrials.gov.
Always verify information with your healthcare team before making any decisions about your care.
Familial Adenomatous Polyposis
Familial adenomatous polyposis is an inherited condition, usually caused by changes in the APC gene, in which hundreds to thousands of polyps grow in the large bowel from the teenage years. Without treatment bowel cancer is almost certain, so regular colonoscopy and preventive surgery are standard care. Relatives can have genetic testing.
This overview is general information, not an individual medical assessment. Research is selected automatically and may include mismatches. How we select and explain research.
Most Recent Research
Common Questions
What is Familial Adenomatous Polyposis?
Familial adenomatous polyposis is an inherited condition, usually caused by changes in the APC gene, in which hundreds to thousands of polyps grow in the large bowel from the teenage years. Without treatment bowel cancer is almost certain, so regular colonoscopy and preventive surgery are standard care. Relatives can have genetic testing.
How many clinical trials are available for Familial Adenomatous Polyposis?
RareWays currently indexes 60 clinical trials for Familial Adenomatous Polyposis, of which 8 are actively recruiting. These counts cover indexed trials across countries, not just your country. An Australian site does not necessarily mean that site is recruiting. Check locations, eligibility and current availability with the study team.
Where does the research data for Familial Adenomatous Polyposis come from?
RareWays aggregates research from PubMed, Europe PMC, OpenAlex, and ClinicalTrials.gov. Data is refreshed automatically every day. All articles and trials link directly to their original sources.
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