Evidence map›Paper›PMID 18792787›Full record

ArticleJournal of cancer survivorship : research and practice2008

Predicted cardiovascular mortality and reported cardiovascular morbidity in testicular cancer survivors.

H S Haugnes, N Aass, S D Fosså, O Dahl, O Klepp, E A Wist, T Wilsgaard, R M Bremnes

Abstract read
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In one paragraph

Article in Journal of cancer survivorship : research and practice, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 2 pooled it
4.6field-weighted citation impact, top 5% 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

14 citing papers in PubMed, 2 syntheses or guidelines pooled it, 41 citations in OpenAlex.

  1. Pooled it
  2. Guideline
  3. Review
  4. Vascular toxic effects of cancer therapies.Nature reviews. Cardiology · 2020
    Review
  5. Article
  6. Article
  7. Erratum to: Dendritic cells as therapeutic targets in neuroinflammation.Cellular and molecular life sciences : CMLS · 2016
    Article
  8. [Follow-up of urological tumor treatment].Der Urologe. Ausg. A · 2015
    Review
  9. Article
  10. Article
  11. Pure seminoma: a review and update.Radiation oncology (London, England) · 2011
    Review
  12. Interdisciplinary evidence-based recommendations for the follow-up of early stage seminomatous testicular germ cell cancer patients.Strahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft ... [et al] · 2011
    Article
  13. Article
  14. Article
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

8 authors at 6 institutions in 1 country.

H S HaugnesDepartment of Oncology, Institute of Clinical Medicine, University of Tromsø, Tromsø, Norway. hegesa@fagmed.uit.no
N Aass
S D Fosså
O Dahl
O Klepp
E A Wist
T Wilsgaard
R M Bremnes
UiT The Arctic University of Norway · NOHaukeland University Hospital · NOMed-Storm Innovation (Norway) · NOOslo University Hospital · NOSt Olav's University Hospital · NOUniversity of Oslo · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionWe examined if testicular cancer (TC) treatment is associated with any risk for cardiovascular morbidity or predicted mortality according to the SCORE model, in which a 10-year future risk of >or=5% for developing a fatal cardiovascular event qualify for high-risk status.

methodsOne thousand one hundred thirty-four TC survivors treated 1980-1994 participated in this study (1998-2002). Patients were categorised in four treatment groups: surgery (n = 225), radiotherapy (n = 445), and two chemotherapy groups: cumulative cisplatin dose <or=850 mg (n = 375) and >850 mg (cis>850, n = 89). Patients with cardiovascular disease, diabetes or SCORE >or=5% constituted a high-risk group, and those with SCORE >1% an intermediate/high risk group.

resultsAge-adjusted mean SCORE was 0.93% for the surgery group. In comparison, chemotherapy treated patients had significantly higher SCORE (1.07%, p = 0.01). Only 15% of patients were scored to be at high-risk, while 53% qualified for the intermediate/high risk group. Patients in the cis>850 group had increased odds for having intermediate/high risk, compared with the surgery group (OR 3.4, 95% CI 1.3-8.7). Only 23 cardiovascular events had occurred since the testicular cancer diagnosis.

conclusionThe SCORE model indicates that patients treated with cisplatin-based chemotherapy have a significantly increased future risk of a fatal cardiovascular event. IMPLICATIONS FOR CANCER SURVIVORS: TC survivors should be followed regularly with respect to cardiovascular risk profile beyond the routine 10-year clinical follow-up.

Indexed as

AdolescentAdultAntineoplastic Combined Chemotherapy ProtocolsCarcinomaCardiovascular DiseasesCisplatinCohort StudiesComorbidityCross-Sectional StudiesFollow-Up StudiesHumansMaleMiddle AgedPrognosisResearch DesignRisk AssessmentCisplatin

Identifiers

PMID18792787
OpenAlexW2142546501

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.