2016
DOI: 10.1097/cej.0000000000000199
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Cancer incidence predictions in the North of Portugal: keeping population-based cancer registration up to date

Abstract: Decision making towards cancer prevention and control requires monitoring of trends in cancer incidence and accurate estimation of its burden in different settings. We aimed to estimate the number of incident cases in northern Portugal for 2015 and 2020 (all cancers except nonmelanoma skin and for the 15 most frequent tumours). Cancer cases diagnosed in 1994-2009 were collected by the North Region Cancer Registry of Portugal (RORENO) and corresponding population figures were obtained from Statistics Portugal. … Show more

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Cited by 10 publications
(8 citation statements)
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“…Given the expected increase in population and in life expectancy (36), the burden of the disease is also expected to increase. At least for the North, this is in accordance with a previous study (37). In fact, if the drastic trend observed in this region upholds, it will not take long before women from the North present the highest risk for being diagnosed with breast cancer.…”
Section: Discussionsupporting
confidence: 94%
“…Given the expected increase in population and in life expectancy (36), the burden of the disease is also expected to increase. At least for the North, this is in accordance with a previous study (37). In fact, if the drastic trend observed in this region upholds, it will not take long before women from the North present the highest risk for being diagnosed with breast cancer.…”
Section: Discussionsupporting
confidence: 94%
“…In the present study, breast and prostate cancer were the most prevalent, and multiple myeloma the least prevalent. This is consistent with the reported prevalence of the population (5760). Furthermore, at diagnosis, 28% patients with solid tumors present with stage IV disease.…”
Section: Discussionsupporting
confidence: 93%
“…After confirming that CDH1 c.1901C>T is a bona fide splice-site variant, we used ACMG/AMP guidelines for its classification (12). A PVS1_strong criterium was attributed, as RNA analysis has been previously performed in a cancer cell line (18) supporting our current data. We also considered for classification clinical information from 13 families fulfilling HDGC criteria and carrying this variant (reported to us by different labs), as well as two families fulfilling HDGC criteria and reported in the literature (14,27).…”
Section: The Cdh1 C1901c>t Variant Generates Cryptic Splicing Within Exon 12 Leading To Premature Truncation and Decreased Cdh1 Rna Levelsupporting
confidence: 61%
“…However, if this hypothesis holds true, it is important to highlight that the recent population rise could have also promoted the spread and frequency increase of a previously rare and deleterious variant [16,17]. The high incidence of GC in Northern Portugal [18,19] and the privileged industrial and economic situation of this region, which allowed inhabitants to settle and succeed, further support a possible clustering of CDH1 germline variant carriers predisposed to early-onset DGC and/or LBC in this region [14,20].…”
Section: Introductionmentioning
confidence: 99%