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Active, Not Recruiting

NCT Number: NCT01983410

A Registry for BRCA Mutation Carriers With Pancreatic Ductal Adenocarcinoma

The purpose of this study is to better understand why pancreatic cancer develops in some people who are known carriers of the gene mutation (an abnormality) called BRCA, or its close relative PALB2. The investigators hope to do this by establishing a BRCA/PALB2 mutation carriers Pancreatic Ductal Adenocarcinoma (the common form of pancreatic cancer) Registry. A registry is a database of information.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

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Key information

Age range

21 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Shaare Zedek Medical Center, Jerusalem, Israel

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Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • BRCA mutation carrier is defined as a person with any mutation of the BRCA gene, including BRCA1, or BRCA2. PALB2mut patients are also eligible.
  • Relative of a BRCA PDAC patient is defined as a first-degree relative, which includes, parents, siblings or children.

BRCAmut PDAC Group: Study Group A: Ashkenazi Jewish descent

  • Known BRCA mutation carrier.
  • Ashkenazi Jewish Descent (at least one parent of Ashkenazi Jewish origin).
  • Histologic proof of primary pancreatic ductal adenocarcinoma.
  • May have either potentially curable (resectable) primary PDAC, localized but unresectable primary PDAC, or metastatic (stage IV) PDAC.
  • Prior personal history of other malignancy; either prior or currently active, including breast , ovarian or prostate cancer is allowed.
  • Both previously treated and previously untreated patients are eligible. Previous treatment may include surgical resection, regional radiation therapy, or systemic therapy. Patient may be receiving active therapy.
  • Willing to provide blood specimens for correlative studies.
  • Willing to provide permission to obtain banked tumor tissue for analysis (previous biopsies or surgical material). New tumor biopsies are not required for entrance into the Registry.

BRCAmut PDAC Group: Study Group B: non-Ashkenazi Jewish descent

  • Know n BRCA mutation carrier.
  • Histologic proof of primary pancreatic ductal adenocarcinoma.
  • May have either potentially curable (resectable) primary PDAC, localized but unresectable primary PDAC, or metastatic (stage IV) PDAC.
  • Prior personal history of other malignancy; either prior or currently active, including breast, ovarian, or prostate cancer is allowed.
  • Both previously treated and previously untreated patients are eligible. Previous treatment may include surgical resection, regional radiation therapy, or systemic therapy. Patient may be receiving active therapy.
  • Willing to provide blood specimens for correlative studies.
  • Willing to provide permission to obtain banked tumor tissue for analysis (previous biopsies or surgical material). New tumor biopsies are not required for entrance into the Registry.

BRCA mutation carrier, relative of a BRCA PDAC patients, without PDAC or other BRCAmut related malignancy: (Control Cohort 1A): Ashkenazi Jewish descent

  • Known BRCA mutation carrier.
  • Ashkenazi Jewish Descent (at least one parent of Ashkenazi Jewish origin).
  • No current or prior history of PDAC.
  • Relative of a BRCAmut PDAC patient; no prior or active personal history of breast, ovarian, or prostate cancer
  • Willing to provide blood specimens for correlative studies.

BRCA mutation carrier, relative of a BRCA PDAC patients, without PDAC or other BRCAmut related malignancy: (Control Cohort 1B): non-Ashkenazi Jewish descent

  • Know n BRCA mutation carrier.
  • No current or prior history of PDAC.
  • First or second degree relative of a BRCAmut PDAC patient; no prior or active personal history of breast, ovarian, or prostate cancer.
  • Willing to provide blood specimens for correlative studies.

BRCAmut Carrier relative of a BRCAmut PDAC patient who themselves have prior or active BRCAmut related malignancy (Control Cohort 2A):Ashkenazi Jewish descent

  • Known BRCA mutation carrier.
  • Ashkenazi Jewish Descent (at least one parent of Ashkenazi Jewish origin).
  • No current or prior history of PDAC.
  • Relative of a BRCAmut PDAC patient.
  • Prior or active personal history of any BRCA-related cancer.
  • Willing to provide blood specimens for correlative studies.

BRCAmut Carrier relative of a BRCAmut PDAC patient who themselves have prior or active BRCAmut related malignancy (Control Cohort 2B): non-Ashkenazi Jewish descent

  • Know n BRCA mutation carrier.
  • No current or prior history of PDAC.
  • First or second degree relative of a BRCAmut PDAC patient.
  • Prior or active personal history of any BRCA-related cancer.
  • Willing to provide blood specimens for correlative studies.

BRCAmut carrier who is not related to a BRCAmut PDAC patient: (Control cohort 3A) Ashkenazi Jewish descent

  • Known BRCAmut carrier.
  • Ashkenazi Jewish decent (at least one parent of Ashkenazi Jewish origin).
  • No current or prior personal history of PDAC.
  • Prior personal history of other malignancy including breast, ovarian or prostate cancer is allowed.
  • Willing to provide blood specimens for correlative studies.

BRCAmut carrier who is not related to a BRCAmut PDAC patient: (Control cohort 3B) non-Ashkenazi Jewish descent

  • Know n BRCAmut carrier.
  • No current or prior personal history of PDAC.
  • Prior personal history of other malignancy including breast, ovarian, or prostate cancer is allowed.
  • Willing to provide blood specimens for correlative studies.

Non-BRCAmut carriers with histologically proven PDAC: (Control cohort 4) Tested for and negative for the BRCA founder mutations.

  • Ashkenazi Jewish Descent (at least one parent of Ashkenazi Jewish origin).
  • Not related to known BRCAmut carrier.
  • Histologic proof of primary pancreatic ductal adenocarcinoma. May have either potentially curable (resectable) primary PDAC, localized but unresectable primary PDAC, or metastatic (stage IV) PDAC.
  • Both previously treated and previously untreated patients are eligible. Previous treatment may include surgical resection, regional radiation therapy, or systemic therapy. Patient may be receiving active therapy.
  • Willing to provide blood specimens for correlative studies.
  • Willing to provide permission to obtain banked tumor tissue for analysis (previous biopsies or surgical material). New tumor biopsies are not required for entrance into the Registry

Exclusion criteria

  • Individuals will be excluded from the Registry if they:
  • Are unable to sign informed consent for medical or other reasons. Do not speak English (MSK and UPenn) or do not speak English or Hebrew (BCGC Sites).
  • Are under 21 years of age.
  • Not willing to provide blood samples for correlative studies.

Treatment and study plan

The risk assessment questionnaire

Behavioral

Blood specimens

Other

tumor tissue samples will be requested

Other

Primary outcomes

  1. prospective Registry

    Time frame: 3 years

    Establishment of a BRCA mutation carriers PDAC Registry with appropriate control groups, and collection and storage of biological material for future studies.

Sponsors and collaborators

Lead sponsor

Memorial Sloan Kettering Cancer Center

Other

Collaborators

  • Abramson Cancer Center at Penn Medicine
  • Dana-Farber Cancer Institute
  • Johns Hopkins University
  • Shaare Zedek Medical Center
  • Sheba Medical Center

Registry information

Important dates

Study start
2013
Primary completion
2026
Study completion
2026
First posted
Nov 14, 2013
Registry last updated
Dec 30, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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