Evidence map›Paper›PMID 34409743›Full record

ArticleJournal of thrombosis and haemostasis : JTH2021

Evaluation of the Khorana, PROTECHT, and 5-SNP scores for prediction of venous thromboembolism in patients with cancer.

Noori A M Guman, Roos J van Geffen, Frits I Mulder, Thijs F van Haaps, Vahram Hovsepjan, Mariette Labots, Geert A Cirkel, Filip Y F L de Vos, Albert J Ten Tije, Laurens V Beerepoot and 12 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of thrombosis and haemostasis : JTH, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
4.1field-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, 31 citations in OpenAlex.

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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

22 authors at 13 institutions in 1 country.

Noori A M GumanDepartment of Vascular Medicine, Amsterdam Cardiovascular Science, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, the Netherlands.ORCID 0000-0003-1426-3170
Roos J van GeffenDepartment of Vascular Medicine, Amsterdam Cardiovascular Science, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, the Netherlands.ORCID 0000-0003-1818-3928
Frits I MulderDepartment of Vascular Medicine, Amsterdam Cardiovascular Science, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, the Netherlands.ORCID 0000-0002-6902-3425
Thijs F van HaapsDepartment of Vascular Medicine, Amsterdam Cardiovascular Science, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, the Netherlands.ORCID 0000-0002-8358-2426
Vahram HovsepjanDepartment of Vascular Medicine, Amsterdam Cardiovascular Science, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, the Netherlands.
Mariette LabotsDepartment of Medical Oncology, Cancer Center Amsterdam, Amsterdam University Medical Centers, Vrije Universiteit Amsterdam, Amsterdam, the Netherlands.
Geert A CirkelDepartment of Internal Medicine, Meander Medical Center, Amersfoort, the Netherlands.
Filip Y F L de VosDepartment of Medical Oncology, University Medical Center Utrecht, Utrecht, the Netherlands.
Albert J Ten TijeDepartment of Internal Medicine, Amphia Hospital, Breda, the Netherlands.
Laurens V BeerepootDepartment of Internal Medicine, Elisabeth-Tweesteden Hospital, Tilburg, the Netherlands.
Vivianne C G Tjan-HeijnenDepartment of Medical Oncology, Maastricht University Medical Center, Maastricht, the Netherlands.
Hanneke W M van LaarhovenDepartment of Medical Oncology, Cancer Center Amsterdam, Amsterdam University Medical Centers, Vrije Universiteit Amsterdam, Amsterdam, the Netherlands.
Paul HambergDepartment of Internal Medicine, Franciscus Gasthuis & Vlietland, Rotterdam-Schiedam, the Netherlands.
Annelie J E VulinkDepartment of Medical Oncology, Reinier de Graaf Hospital, Delft, the Netherlands.
Maartje LosDepartment of Internal Medicine, St Antonius Hospital, Nieuwegein, the Netherlands.
Aeilko H ZwindermanDepartment of Clinical Epidemiology, Biostatistics and Bioinformatics, Amsterdam University Medical Center, Amsterdam, the Netherlands.
Bart FerwerdaDepartment of Clinical Epidemiology, Biostatistics and Bioinformatics, Amsterdam University Medical Center, Amsterdam, the Netherlands.
Martijn P J K LolkemaDepartment of Medical Oncology, Erasmus Medical Center, Rotterdam, the Netherlands.
Neeltje SteeghsDepartment of Medical Oncology, Netherlands Cancer Institute, Amsterdam, the Netherlands.
Harry R BüllerDepartment of Vascular Medicine, Amsterdam Cardiovascular Science, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, the Netherlands.
Pieter W KamphuisenDepartment of Vascular Medicine, Amsterdam Cardiovascular Science, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, the Netherlands.
Nick van EsDepartment of Vascular Medicine, Amsterdam Cardiovascular Science, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, the Netherlands.
Amsterdam University Medical Centers · NLTergooi · NLUniversity of Amsterdam · NLAmphia Ziekenhuis · NLElisabeth-TweeSteden Ziekenhuis · NLErasmus MC · NLMaastricht University · NLMeander Medisch Centrum · NLReinier de Graaf Hospital · NLSint Franciscus Gasthuis · NLSt. Antonius Ziekenhuis · NLThe Netherlands Cancer Institute · NLUniversity Medical Center Utrecht · NL

Funding

Tergooi academy
6 · The paper itself

Abstract

backgroundThe Khorana score is a validated tool to identify cancer patients at higher risk of venous thromboembolism (VTE).

objectiveWe compared its predictive performance to that of the clinical PROTECHT and the polygenic 5-SNP scores in patients who participated in the Dutch CPCT-02 study. PATIENTS/

methodsData on VTE and its risk factors were retrospectively collected for 2729 patients with advanced stage solid tumors planned for systemic cancer treatment. Patients were followed for 6 months. Overall discriminatory performance of the scores was evaluated by time-dependent c-indices. The scores were additionally evaluated dichotomously in competing risk models.

resultsA total of 160 (5.9%) patients developed VTE during follow-up. Time-dependent c-indices at 6 months for the Khorana, PROTECHT, and 5-SNP scores were 0.57 (95% confidence interval [CI]: 0.55-0.60), 0.60 (95% CI: 0.57-0.62), and 0.54 (95% CI: 0.51-0.57), respectively. The dichotomous scores classified 9.6%, 16.8%, and 9.5% as high-risk, respectively. VTE risk was about 2-fold higher among high-risk patients than low-risk patients for the Khorana (subdistribution hazard ratio [SHR] 1.9, 95% CI: 1.3-3.0), PROTECHT (SHR 2.1, 95% CI: 1.5-3.0), and 5-SNP scores (SHR 1.7, 95% CI: 1.03-2.8). The sensitivity at 6 months was 16.6% (95% CI: 10.5-22.7), 28.9% (95% CI: 21.5-36.3), and 14.9% (95% CI: 8.5-21.2), respectively.

conclusionsPerformance of the PROTECHT or 5-SNP score was not superior to that of the Khorana score. The majority of cancer patients who developed VTE during 6-month follow-up were not identified by these scores. Future directions for studies on cancer-associated VTE prediction may include combined clinical-genetic scores.

Indexed as

NeoplasmsVenous ThromboembolismForecastingHumansRetrospective StudiesRisk AssessmentRisk Factorsneoplasmspolymorphismrisk assessmentsingle nucleotidethrombosisvenous thromboembolism

Identifiers

PMID34409743
PMCPMC9291564
OpenAlexW3195788761

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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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.