domingo, 17 de junio de 2018

Results of surveillance in individuals at high-risk of pancreatic cancer: A systematic review and meta-analysis. - PubMed - NCBI

Results of surveillance in individuals at high-risk of pancreatic cancer: A systematic review and meta-analysis. - PubMed - NCBI



 2018 May;6(4):489-499. doi: 10.1177/2050640617752182. Epub 2018 Jan 8.

Results of surveillance in individuals at high-risk of pancreatic cancer: A systematic review and meta-analysis.

Abstract

BACKGROUND:

Data on surveillance for pancreatic ductal adenocarcinoma (PDAC) in high-risk individuals (HRIs) with "familial pancreatic cancer" (FPC) and specific syndromes are limited and heterogeneous.

OBJECTIVE:

We conducted a systematic review and meta-analysis of PDAC surveillance studies in HRIs.

METHODS:

Prevalence of solid/cystic pancreatic lesions and of lesions considered a successful target of surveillance (proven resectable PDAC and high-grade precursors) was pooled across studies. The rate of lesions diagnosed by endoscopic ultrasonography (EUS)/magnetic resonance imaging (MRI) and across different HRI groups was calculated.

RESULTS:

Sixteen studies incorporating 1588 HRIs were included. The pooled prevalence of pancreatic solid and cystic lesions was 5.8% and 20.2%, respectively. The pooled prevalence of patients with lesions considered a successful target of surveillance was 3.3%, being similar to EUS or MRI and varying across subgroups, being 3% in FPC, 4% in hereditary pancreatitis, 5% in familial melanoma, 6.3% in hereditary breast/ovarian cancer, and 12.2% in Peutz-Jeghers syndrome. The pooled estimated rate of lesions considered a successful target of surveillance during follow-up was 5/1000 person-years.

CONCLUSION:

Surveillance programs identify successful target lesions in 3.3% of HRIs with a similar yield of EUS and MRI and an annual risk of 0.5%. A higher rate of target lesions was reported in HRIs with specific DNA mutations.

KEYWORDS:

Pancreatic cancer; family history; meta-analysis; screening

PMID:
 
29881603
 
PMCID:
 
PMC5987280
 
DOI:
 
10.1177/2050640617752182

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