Evidence map›Paper›PMID 36444235›Full record

ArticleJACC. CardioOncology2022

Prevalence, Treatment, and Prognosis of Tumor Thrombi in Renal Cell Carcinoma.

Fleur H J Kaptein, Tom van der Hulle, Sander J E Braken, Erik J van Gennep, Jeroen T Buijs, Mark C Burgmans, Suzanne C Cannegieter, Emma M E du Chatinier, Menno V Huisman, Els L van Persijn van Meerten and 3 more

Abstract read
In one paragraph

Article in JACC. CardioOncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed, 2 pooled it
–field-weighted citation impact
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

38 citing papers in PubMed, 2 syntheses or guidelines pooled it.

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  7. Renal Vein Thrombosis: A Narrative Review.Diagnostics (Basel, Switzerland) · 2026
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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

13 authors.

Fleur H J KapteinDepartment of Medicine-Thrombosis and Hemostasis, Leiden University Medical Center, Leiden, the Netherlands.
Tom van der HulleDepartment of Medicine-Oncology, Leiden University Medical Center, Leiden, the Netherlands.
Sander J E BrakenDepartment of Medicine-Thrombosis and Hemostasis, Leiden University Medical Center, Leiden, the Netherlands.
Erik J van GennepDepartment of Urology, Leiden University Medical Center, Leiden, the Netherlands.
Jeroen T BuijsDepartment of Medicine-Thrombosis and Hemostasis, Leiden University Medical Center, Leiden, the Netherlands.
Mark C BurgmansDepartment of Radiology, Leiden University Medical Center, Leiden, the Netherlands.
Suzanne C CannegieterDepartment of Medicine-Thrombosis and Hemostasis, Leiden University Medical Center, Leiden, the Netherlands.
Emma M E du ChatinierDepartment of Medicine-Thrombosis and Hemostasis, Leiden University Medical Center, Leiden, the Netherlands.
Menno V HuismanDepartment of Medicine-Thrombosis and Hemostasis, Leiden University Medical Center, Leiden, the Netherlands.
Els L van Persijn van MeertenDepartment of Radiology, Leiden University Medical Center, Leiden, the Netherlands.
Henri H VersteegDepartment of Medicine-Thrombosis and Hemostasis, Leiden University Medical Center, Leiden, the Netherlands.
Rob C M PelgerDepartment of Urology, Leiden University Medical Center, Leiden, the Netherlands.
Frederikus A KlokDepartment of Medicine-Thrombosis and Hemostasis, Leiden University Medical Center, Leiden, the Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Renal cell carcinoma (RCC) can be complicated by a venous tumor thrombus (TT), of which the optimal management is unknown. Objectives: This study sought to assess the prevalence of TT in RCC, its current management, and its association with venous thromboembolism (VTE), arterial thromboembolism (ATE), major bleeding (MB), and mortality. Methods: Patients diagnosed with RCC between 2010 and 2019 in our hospital were included and followed from RCC diagnosis until 2 years after, or until an outcome of interest (VTE, ATE, and MB) or death occurred, depending on the analysis. Cumulative incidences were estimated with death as a competing risk. Cause-specific hazard models were used to identify predictors and the prognostic impact. Results: Of the 647 patients, 86 had a TT (prevalence 13.3%) at RCC diagnosis, of which 34 were limited to the renal vein, 37 were limited to the inferior vena cava below the diaphragm, and 15 extended above the diaphragm; 20 patients started therapeutic anticoagulation and 45 underwent thrombectomy with/without anticoagulation. During follow-up (median 24.0 [IQR: 7.0-24.0] months), 17 TT patients developed a VTE, 0 developed an ATE, and 11 developed MB. TT patients were more often diagnosed with VTE (adjusted HR: 6.61; 95% CI: 3.18-13.73) than non-TT patients, with increasing VTE risks in more proximal TT levels. TT patients receiving anticoagulation still developed VTE (HR: 0.56; 95% CI: 0.13-2.48), at the cost of more MB events (HR: 3.44; 95% CI: 0.95-12.42) compared with those without anticoagulation. Conclusions: Patients with RCC-associated TT were at high risk of developing VTE. Future studies should establish which of these patients benefit from anticoagulation therapy.

Indexed as

aHR, adjusted HRanticoagulantsATE, arterial thromboembolismCT, computed tomographyDVT, deep vein thrombosishemorrhageinferior vena cavaIVC, inferior vena cavaLMWH, low-molecular-weight heparinMB, major bleedingPE, pulmonary embolismprognosisRCC, renal cell carcinomarenal cell carcinomaTT, tumor thrombusvenous thrombosisVKA, vitamin K antagonistVTE, venous thromboembolism

Identifiers

PMID36444235
PMCPMC9700252

What OpenQuestion holds

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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.