Evidence map›Paper›PMID 27638773›Full record

ArticleJournal of cancer research and clinical oncology2017

Cancer incidence in patients with hereditary hemorrhagic telangiectasia.

Christine W Duarte, Adam W Black, F Lee Lucas, Calvin P H Vary

Abstract read
In one paragraph

Article in Journal of cancer research and clinical oncology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.2field-weighted citation impact, top 20% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Cancer and hereditary haemorrhagic telangiectasia.Journal of cancer research and clinical oncology · 2017
    Article
  5. Article
  6. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 1 country.

Christine W DuarteCenter for Outcomes Research and Evaluation, Maine Medical Center Research Institute, 509 Forest Ave. Suite 200, Portland, ME, USA. duartc@mmc.org.
Adam W BlackCenter for Outcomes Research and Evaluation, Maine Medical Center Research Institute, 509 Forest Ave. Suite 200, Portland, ME, USA.
F Lee LucasCenter for Outcomes Research and Evaluation, Maine Medical Center Research Institute, 509 Forest Ave. Suite 200, Portland, ME, USA.
Calvin P H VaryCenter for Molecular Medicine, Maine Medical Center Research Institute, Scarborough, ME, USA.
Maine Medical Center · USMaine Medical Center · US

Funding

WNT SIGNALING IN PREIMPLANTATION EMBRYOP20RR018789 · NCRR · MAINE MEDICAL CENTER · PI WOJCHOWSKI, DON MICHAEL · 2003 to 2011
$18.9M
Progenitor Cell Analysis CoreP30GM106391 · NIGMS · MAINEHEALTH · PI WOJCHOWSKI, DON MICHAEL · 2013 to 2017
$5.7M
Phase III COBRE in Vascular BiologyP30GM103392 · NIGMS · MAINEHEALTH · PI ST. GERMAIN, DONALD L. · 2012 to 2016
$4.7M
Regulation of TGF-beta Receptor-dependent Vascular DiseaseR01HL083151 · NHLBI · MAINEHEALTH · PI VARY, CALVIN PARDEE HULL · 2007 to 2011
$2.0M
COBRE in Stem Cell Biology and Regenerative MedicineP20GM103465 · NIGMS · MAINEHEALTH · PI WOJCHOWSKI, DON MICHAEL · 2012 to 2012
$2.0M
PHASE III COBRE IN VASCULAR BIOLOGYP30RR030927 · NCRR · MAINEHEALTH · PI FRIESEL, ROBERT E · 2011 to 2011
$1.2M
NCRR NIH HHS P20 RR018789NCRR NIH HHS P30 RR030927NHLBI NIH HHS R01 HL083151NIGMS NIH HHS P20 GM103465NIGMS NIH HHS P30 GM103392NIGMS NIH HHS P30 GM106391
6 · The paper itself

Abstract

purposeHereditary hemorrhagic telangiectasia (HHT) is a genetic disorder characterized by deficiency in endoglin, an angiogenic protein. We previously showed that HHT, in which systemic endoglin expression is reduced, was associated with better survival outcomes in cancer patients (Duarte et al. in Cancer Epidemiol Biomarkers Prev 23:117-125, 2014). Here, we evaluated whether HHT was associated with reduced cancer incidence.

methodsA matched case-control analysis using SEER Medicare was conducted to evaluate the effect of HHT on diagnosis with breast, colorectal, lung, or prostate cancer between 2000 and 2007 (n = 633,162). Cancer and non-cancer patients were matched on age, sex, SEER registry region, and length of the ascertainment period for HHT. We assessed crude association using a McNemar's test and then adjusted for demographic variables, cancer type, cancer stage, comorbidities, and ascertainment period with a conditional logistic regression model for cancer incidence.

resultsThe McNemar's test showed no significant association between HHT and cancer incidence (p = 0.74). Adjusting for covariates with the conditional logistic regression model did not change the result [HHT odds ratio 0.978; 95 % CI (0.795, 1.204)]. The lack of association between HHT and cancer incidence is unexpected given the previously discovered significant association between HHT and improved survival outcomes (Duarte et al. in Cancer Epidemiol Biomarkers Prev 23:117-125, 2014).

conclusionsWe conclude that the protective effect of reduced systemic endoglin expression in cancer is specific to cancer progression through its effect on vascularization and other stromal effects but does not extend to cancer initiation.

Indexed as

AgedAged, 80 and overBreast NeoplasmsColorectal NeoplasmsFemaleHumansIncidenceLung NeoplasmsMaleMiddle AgedProstatic NeoplasmsProtective FactorsSEER ProgramTelangiectasia, Hereditary HemorrhagicCancer incidenceCase–controlEndoglinHHTSEER Medicare

Identifiers

PMID27638773
PMCPMC5263109
OpenAlexW2520659774

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.