Evidence map›Paper›PMID 21802118›Full record

ArticleThrombosis research2012

A pilot study utilizing whole body 18 F-FDG-PET/CT as a comprehensive screening strategy for occult malignancy in patients with unprovoked venous thromboembolism.

Matthew T Rondina, Nathan Wanner, Robert C Pendleton, Larry W Kraiss, Russell Vinik, Guy A Zimmerman, Marta Heilbrun, John M Hoffman, Kathryn A Morton

Abstract read
In one paragraph

Article in Thrombosis research, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

8 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Observational
  6. Article
  7. The role of molecular imaging in diagnosis of deep vein thrombosis.American journal of nuclear medicine and molecular imaging · 2014
    Review
  8. Thrombosis and cancer.Nature reviews. Clinical oncology · 2012
    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

9 authors at 1 institution in 1 country.

Matthew T RondinaDivision of General Internal Medicine, University of Utah, Salt Lake City, Utah 84132, USA. matthew.rondina@hsc.utah.edu
Nathan Wanner
Robert C Pendleton
Larry W Kraiss
Russell Vinik
Guy A Zimmerman
Marta Heilbrun
John M Hoffman
Kathryn A Morton
University of Utah · US

Funding

UNIVERSITY OF UTAH CENTER FOR CLINICAL AND TRANSLATIONAL SCIENCE-UL1: BPCAUL1RR025764 · NCRR · UNIVERSITY OF UTAH · PI MCCLAIN, DONALD A. · 2008 to 2011
$19.4M
Molecular Interactions of Myeloid Cells with EndotheliumR37HL044525 · NHLBI · UNIVERSITY OF UTAH · PI ZIMMERMAN, GUY A. · 2004 to 2013
$3.5M
Novel Thrombotic & Inflammatory Mechanisms of Venous Thromboembolism in ElderlyR01HL092746 · NHLBI · UNIVERSITY OF UTAH · PI WEYRICH, ANDREW S · 2007 to 2010
$2.0M
FDG PET in cancer-associated venothromboembolic diseaseR01CA121003 · NCI · UNIVERSITY OF UTAH · PI MORTON, KATHRYN ANN · 2006 to 2009
$1.9M
Novel Activities of Platelets in Acute Lung InjuryR01HL091754 · NHLBI · UNIVERSITY OF UTAH · PI WEYRICH, ANDREW S · 2008 to 2011
$1.5M
Novel Platelet Functions in Sepsis and Venous ThromboembolismK23HL092161 · NHLBI · UNIVERSITY OF UTAH · PI RONDINA, MATTHEW THOMAS · 2009 to 2013
$775k
NCI NIH HHS CA121003NCI NIH HHS R01 CA121003NCRR NIH HHS UL1 RR025764NCRR NIH HHS UL1RR025764NHLBI NIH HHS 1K23HL092161NHLBI NIH HHS 5R01HL091754NHLBI NIH HHS 5R01HL092746NHLBI NIH HHS K23 HL092161NHLBI NIH HHS R01 HL091754NHLBI NIH HHS R01 HL092746NHLBI NIH HHS R37 HL044525
6 · The paper itself

Abstract

backgroundApproximately 7-10% of patients with unprovoked VTE will be diagnosed with cancer within 12 months. Although cancer screening has been proposed in these patients, the optimal strategy remains unclear. In a pilot study, we prospectively investigated the use of FDG-PET/CT to screen for occult malignancy in 40 patients with unprovoked VTE. MATERIALS/

methodsPatients were initially screened for occult malignancy with a focused history, physical, and laboratory evaluation. Patients underwent whole body FDG-PET/CT and were followed for up to two years for a new diagnosis of cancer. The total costs of using FDG-PET/CT as a comprehensive screening strategy were determined using 2010 Medicare reimbursement rates.

resultsCompletion of FDG-PET/CT imaging was feasible and identified abnormal findings requiring additional evaluations in 62.5% of patients. Occult malignancy was evident in only one patient (cancer incidence 2.5%) and FDG-PET/CT imaging excluded malignancy in the remainder of patients. No patients with a negative FDG-PET/CT were diagnosed with malignancy during an average (±SD) follow-up of 449 (±311) days. The use of FDG-PET/CT to screen for occult malignancy added $59,151 in total costs ($1,479 per patient). The majority of these costs were due to the cost of the FDG-PET/CT ($1,162 per patient or 78.5% of total per-patient costs).

conclusionsFDG-PET/CT may have utility for excluding occult malignancy in patients with unprovoked VTE. The costs of this comprehensive screening strategy were comparable to other screening approaches. Larger studies are needed to further evaluate the utility and cost-effectiveness of FDG-PET/CT as a cancer screening strategy in patients with unprovoked VTE.

Indexed as

Fluorodeoxyglucose F18Multimodal ImagingPositron-Emission TomographyRadiopharmaceuticalsTomography, X-Ray ComputedWhole Body ImagingAdultAgedCost-Benefit AnalysisEarly Detection of CancerFeasibility StudiesFemaleHealth Care CostsHumansInsurance, Health, ReimbursementMaleFluorodeoxyglucose F18Radiopharmaceuticals

Identifiers

PMID21802118
PMCPMC3277867
OpenAlexW2022029942

What OpenQuestion holds

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LicenceTDM
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.