The benefit of pancreatic cancer surveillance in carriers of germline BRCA1/2 pathogenic variants.

BRCA carrier pancreatic cancer surveillance

Journal

Cancer
ISSN: 1097-0142
Titre abrégé: Cancer
Pays: United States
ID NLM: 0374236

Informations de publication

Date de publication:
20 Oct 2023
Historique:
revised: 22 07 2023
received: 08 04 2023
accepted: 03 08 2023
medline: 20 10 2023
pubmed: 20 10 2023
entrez: 20 10 2023
Statut: aheadofprint

Résumé

Surveillance of high-risk individuals for pancreatic ductal adenocarcinoma (PDAC) is recommended. This study aimed to determine the prevalence and outcomes of PDAC and its precursor lesions in BRCA1/2 pathogenic variants (PVs) carriers undergoing pancreatic surveillance. A retrospective multicenter cohort study of pancreatic surveillance outcomes in Israeli BRCA1/2 carriers preferably with a family history of PDAC. A total of 180 asymptomatic carriers participated in the screening programs, including 57 (31.7%) with BRCA1 PVs, 121 (67.2%) with BRCA2 PVs, and 12 (6.6%) with PVs in BRCA1/2 and other genes, for a median follow-up period of 4 years. Ninety-one individuals (50.5%) fulfilled the International Cancer of the Pancreas Screening (CAPS) criteria for surveillance whereas 116 (64.4%) fulfilled the American College of Gastroenterology (ACG) criteria. There were four cases of adenocarcinoma and four cases of grade 1-neuroendocrine tumor (G1-NET). All were BRCA2 carriers, and two had no family history of PDAC. Three cancer patients were at resectable stages (IA, IIA, IIB) whereas one had a stage IIIB tumor. Of the G1-NET cases, one had surgery and the others were only followed. Success rate for detection of confined pancreatic carcinoma was thus 1.6% (three of 180) in the whole cohort, 1.6% (two of 116) among individuals who fulfilled ACG criteria and 2.2% (two of 91) in those fulfilling CAPS criteria for surveillance. Despite the low detection rate of PDAC and its' high-risk neoplastic precursor lesions among BRCA1/2 carriers undergoing pancreatic surveillance, 75% of cancer cases were detected at a resectable stage.

Sections du résumé

BACKGROUND BACKGROUND
Surveillance of high-risk individuals for pancreatic ductal adenocarcinoma (PDAC) is recommended. This study aimed to determine the prevalence and outcomes of PDAC and its precursor lesions in BRCA1/2 pathogenic variants (PVs) carriers undergoing pancreatic surveillance.
METHODS METHODS
A retrospective multicenter cohort study of pancreatic surveillance outcomes in Israeli BRCA1/2 carriers preferably with a family history of PDAC.
RESULTS RESULTS
A total of 180 asymptomatic carriers participated in the screening programs, including 57 (31.7%) with BRCA1 PVs, 121 (67.2%) with BRCA2 PVs, and 12 (6.6%) with PVs in BRCA1/2 and other genes, for a median follow-up period of 4 years. Ninety-one individuals (50.5%) fulfilled the International Cancer of the Pancreas Screening (CAPS) criteria for surveillance whereas 116 (64.4%) fulfilled the American College of Gastroenterology (ACG) criteria. There were four cases of adenocarcinoma and four cases of grade 1-neuroendocrine tumor (G1-NET). All were BRCA2 carriers, and two had no family history of PDAC. Three cancer patients were at resectable stages (IA, IIA, IIB) whereas one had a stage IIIB tumor. Of the G1-NET cases, one had surgery and the others were only followed. Success rate for detection of confined pancreatic carcinoma was thus 1.6% (three of 180) in the whole cohort, 1.6% (two of 116) among individuals who fulfilled ACG criteria and 2.2% (two of 91) in those fulfilling CAPS criteria for surveillance.
CONCLUSIONS CONCLUSIONS
Despite the low detection rate of PDAC and its' high-risk neoplastic precursor lesions among BRCA1/2 carriers undergoing pancreatic surveillance, 75% of cancer cases were detected at a resectable stage.

Identifiants

pubmed: 37861363
doi: 10.1002/cncr.35052
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2023 American Cancer Society.

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Auteurs

Ido Laish (I)

Gastroenterology Institute, Chaim Sheba Medical Center, Tel Hashomer, Israel.
Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.

Menachem Schechter (M)

Gastroenterology Institute, Shaare Zedek Medical Center, Jerusalem, Israel.

Alain Dancour (A)

Gastroenterology Institute, Shaare Zedek Medical Center, Jerusalem, Israel.

Sari Lieberman (S)

Medical Genetics Institute, Shaare Zedek Medical Center, Jerusalem, Israel.

Zohar Levi (Z)

Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.
Gastroenterology Institute, Beilinson Hospital, Petah Tikva, Israel.

Yael Goldberg (Y)

Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.
Raphael Recanati Genetics Institute, Beilinson Hospital, Petah Tikva, Israel.

Inbal Kedar (I)

Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.
Raphael Recanati Genetics Institute, Beilinson Hospital, Petah Tikva, Israel.

Erez Hasnis (E)

Gastroenterology Institute, Rambam Health Care Campus, Haifa, Israel.

Elizabeth Half (E)

Gastroenterology Institute, Rambam Health Care Campus, Haifa, Israel.

Gili Reznick Levi (GR)

Genetic Institute, Rambam Health Care Campus, Haifa, Israel.

Lior Katz (L)

Section of Gastroenterology and Hepatology, Hadassah Medical Center, Jerusalem, Israel.
Faculty of Medicine, Hebrew University, Jerusalem, Israel.

Elez D Vainer (ED)

Section of Gastroenterology and Hepatology, Hadassah Medical Center, Jerusalem, Israel.
Faculty of Medicine, Hebrew University, Jerusalem, Israel.

Dor Genzel (D)

Section of Gastroenterology and Hepatology, Hadassah Medical Center, Jerusalem, Israel.
Faculty of Medicine, Hebrew University, Jerusalem, Israel.

Maya Aharoni (M)

Gastroenterology Institute, Kaplan Medical Center, Rehovot, Israel.

Rakefet Chen-Shtoyerman (R)

The Genetic Institute, Kaplan Medical Center, Rehovot, Israel.
The Adelson School of Medicine and the Molecular Biology Department, Ariel University, Ariel, Israel.

Naim Abu-Freha (N)

The Institute of Gastroenterology and Hepatology, Soroka University Medical Center, Beer-Sheva, Israel.

Maria Raitses-Gurevich (M)

Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.
Department of Oncology, Chaim Sheba Medical Center, Tel Hashomer, Israel.

Talia Golan (T)

Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.
Department of Oncology, Chaim Sheba Medical Center, Tel Hashomer, Israel.

Rinat Bernstein-Molho (R)

Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.
The Danek Gertner Institute of Human Genetics, Chaim Sheba Medical Center, Tel Hashomer, Israel.

Merav Ben Yehoyada (M)

Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.
Department of Gastroenterology and Liver Diseases, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.

Nathan Gluck (N)

Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.
Department of Gastroenterology and Liver Diseases, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.

Guy Rosner (G)

Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.
Department of Gastroenterology and Liver Diseases, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.

Classifications MeSH