Study summary: | This study aims to assess the feasibility of implementing surveillance protocols among high-risk individuals with a familial and/or genetic predisposition to pancreatic cancer. |
Status: | OPEN - Recruiting |
Sponsor: | Epworth HealthCare |
Diagnosis or condition: | Individuals considered at high-risk of developing pancreatic cancer |
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Key inclusion criteria
- Aged ≥ 18 and ≤ 90 years old
- Without medical history of pancreatic cancer
- Meet ANY of the following criteria:
- Familial Pancreatic Cancer Group 1
- ≥2 relatives with pancreatic cancer, on same side of family, where the 2 affected are first degree related to each other
AND - ≥ 1 affected is first degree related to participant
AND - ≥50 years of age, or 10 years younger than earliest pancreatic cancer in family at time of diagnosis.
- ≥2 relatives with pancreatic cancer, on same side of family, where the 2 affected are first degree related to each other
- Familial Pancreatic Cancer Group 2
- ≥2 affected first degree relatives with pancreatic cancer
AND - ≥50 years of age, or 10 years younger than earliest pancreatic cancer in family.
- ≥2 affected first degree relatives with pancreatic cancer
- Pathogenic Variants
- BRCA1, BRCA2, PALB2, ATM, MLH1, MSH2, MSH6, PMS2, or EPCAM pathogenic or likely pathogenic variant
AND - 1 first or second degree relative with pancreatic cancer
AND - ≥50 years of age, or 10 years younger than earliest pancreatic cancer in family.
- BRCA1, BRCA2, PALB2, ATM, MLH1, MSH2, MSH6, PMS2, or EPCAM pathogenic or likely pathogenic variant
- Familial Atypical Multiple Mole Melanoma Syndrome (FAMMM)
- Familial Atypical Multiple Mole Melanoma (FAMMM) with pathogenic or likely pathogenic CDKN2A variant
AND - ≥40 years of age.
- Familial Atypical Multiple Mole Melanoma (FAMMM) with pathogenic or likely pathogenic CDKN2A variant
- Peutz-Jeghers Syndrome
- Peutz-Jeghers syndrome with STK11 pathogenic or likely pathogenic variant
AND - ≥35 years of age.
- Peutz-Jeghers syndrome with STK11 pathogenic or likely pathogenic variant
- Hereditary Pancreatitis
- Hereditary pancreatitis with PRSS1 pathogenic or likely pathogenic variant
AND - History of pancreatitis
AND - ≥40 years of age, or 20 years after onset of pancreatitis (whichever is earlier).
- Hereditary pancreatitis with PRSS1 pathogenic or likely pathogenic variant
- Familial Pancreatic Cancer Group 1
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Key exclusion criteria
- Individuals who are considered clinically unfit to undergo surveillance by EUS or MRI.
- Individuals who have been previously diagnosed with or treated for pancreatic cancer.
APRISE
Locations: Epworth Richmond
Epworth PI: A/Prof Andrew Metz
Jreissati Pancreatic Centre at Epworth
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General enquiries
Please contact us for more information on 03 9426 8880 or email [email protected]