Evidence map›Paper›PMID 38142448›Full record

Observational studyBlood2024

Association between elevated white blood cell counts and thrombotic events in polycythemia vera: analysis from REVEAL.

Aaron T Gerds, Ruben Mesa, John M Burke, Michael R Grunwald, Brady L Stein, Peg Squier, Jingbo Yu, J E Hamer-Maansson, Stephen T Oh

Registry-linked trialAbstract readObservational Study
In one paragraph

Observational study in Blood, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02252159 (Prospective, Non-interventional Study of Disease Progression and Treatment of Patients With Polycythemia Vera in United States Academic or Community Clinical Practices), which is not on this map. Cited by 34 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 1 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.

NCT02252159 completednot on this map

Prospective, Non-interventional Study of Disease Progression and Treatment of Patients With Polycythemia Vera in United States Academic or Community Clinical Practices

TypeobservationalSponsorIncyte CorporationRan2014 to 2019Enrolled2,544ConditionsMPN (Myeloproliferative Neoplasms)
3 · Its place in the literature

Who cites it

34 citing papers in PubMed, 1 synthesis or guideline pooled it.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Aaron T GerdsCleveland Clinic Taussig Cancer Institute, Cleveland, OH.ORCID 0000-0002-3422-1309
Ruben MesaUT Health San Antonio MD Anderson Cancer Center, San Antonio, TX.
John M BurkeRocky Mountain Cancer Centers, Aurora, CO.ORCID 0000-0002-5144-6710
Michael R GrunwaldLevine Cancer Institute, Atrium Health, Charlotte, NC.
Brady L SteinNorthwestern University Feinberg School of Medicine, Chicago, IL.
Peg SquierIncyte Corporation, Wilmington, DE.
Jingbo YuIncyte Corporation, Wilmington, DE.ORCID 0000-0001-9819-0735
J E Hamer-MaanssonIncyte Corporation, Wilmington, DE.
Stephen T OhWashington University School of Medicine, St. Louis, MO.ORCID 0000-0002-8564-5400

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

abstractPolycythemia vera (PV) is a myeloproliferative neoplasm characterized by clonal proliferation of hematopoietic progenitor cells and is associated with an increased risk of thrombotic events (TEs). Established risk factors for TEs in patients with PV include advanced age, TE history, and elevated hematocrit. Although an association of TE with elevated white blood cell (WBC) counts has been suggested by retrospective studies, this relationship needs further validation. The prospective observational study of patients with polycythemia vera in US clinical practices (REVEAL) study collected prospective clinical data from 2510 patients with PV with a median follow-up of 44.7 months (range, 2-59 months) from enrollment. Using time-dependent covariate Cox proportional hazards models, blood counts were individually modeled with sex, age, disease duration, TE history at enrollment (baseline covariates), and treatment (time-dependent covariate). Analysis of 2271 participants identified 142 TEs in 106 patients. Significant associations with initial TE occurrence during the study period were observed for hematocrit level >45% (hazard ratio [HR], 1.84; 95% confidence interval [95% CI], 1.234-2.749; P = .0028) and WBCs >11 × 109/L (HR, 2.35; 95% CI, 1.598-3.465; P < .0001). Elevated WBC count was significantly associated with initial TE occurrence in both low-risk and high-risk PV. When hematocrit was controlled at ≤45%, WBC count >12 × 109/L was significantly associated with TE occurrence (HR, 1.95; 95% CI, 1.066-3.554; P = .0300). The results support incorporation of WBC count into PV risk stratification and studies of treatment strategies, and indicate the importance of controlling both hematocrit and WBC count in disease management. This trial was registered at www.clinicaltrials.gov as #NCT02252159.

Indexed as

Polycythemia VeraThrombosisHumansLeukocyte CountProspective StudiesRetrospective StudiesRisk Factors

Identifiers

PMID38142448
PMCPMC11103079

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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.