Evidence map›Paper›PMID 36637474›Full record

Observational studyAnnals of hematology2023

Real-world treatments and thrombotic events in polycythemia vera patients in the USA.

Srdan Verstovsek, Naveen Pemmaraju, Nancy L Reaven, Susan E Funk, Tracy Woody, Frank Valone, Suneel Gupta

Open access · hybridAbstract readObservational Study
In one paragraph

Observational study in Annals of hematology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
5.8field-weighted citation impact, top 4% 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

13 citing papers in PubMed, 20 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Cytoreduction for ET and PV: who, what, when, and how?Hematology. American Society of Hematology. Education Program · 2023
    Review
  13. 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

7 authors at 3 institutions in 2 countries.

Srdan VerstovsekMD Anderson Cancer Center, Houston, TX, USA.
Naveen PemmarajuMD Anderson Cancer Center, Houston, TX, USA.
Nancy L ReavenStrategic Health Resources, La Canada, CA, USA. nancy.reaven@strathealth.com.ORCID http://orcid.org/0000-0002-1636-0735
Susan E FunkStrategic Health Resources, La Canada, CA, USA.
Tracy WoodyProtagonist Therapeutics, Newark, CA, USA.
Frank ValoneProtagonist Therapeutics, Newark, CA, USA.
Suneel GuptaProtagonist Therapeutics, Newark, CA, USA.
Protagonist Therapeutics (United States) · USThe University of Texas MD Anderson Cancer Center · USHealth Strat (Kenya) · KE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Polycythemia vera (PV) is a myeloproliferative neoplasm associated with increased risk of thrombotic events (TE) and death. Therapeutic interventions, phlebotomy and cytoreductive medications, are targeted to maintain hematocrit levels < 45% to prevent adverse outcomes. This retrospective observational study examined medical and pharmacy claims of 28,306 PV patients initiating treatment for PV in a data period inclusive of 2011 to 2019. Study inclusion required ≥ 2 PV diagnosis codes in the full data period, at least 1 year of PV treatment history, and ≥ 1 prescription claim and medical claim in both 2018 and 2019. Patients having ≥ 2 hematocrit (HCT) test results in linked outpatient laboratory data (2018-2019) were designated as the HCT subgroup (N = 4246). Patients were characterized as high- or low-risk at treatment initiation based on age and prior thrombotic history. The majority of patients in both risk groups (60% of high-risk and 83% of low-risk) initiated treatment with phlebotomy monotherapy, and during a median follow-up period of 808 days, the vast majority (81% low-risk, 74% high-risk) maintained their original therapy during the follow-up period. Hematocrit control was suboptimal in both risk groups; 54% of high-risk patients initiating with phlebotomy monotherapy sometimes/always had HCT levels > 50%; among low-risk patients, 64% sometimes/always had HCT levels above 50%. Overall, 16% of individuals experienced at least 1 TE subsequent to treatment initiation, 20% (n = 3920) among high-risk and 8% (n = 629) among low-risk patients. This real-world study suggests that currently available PV treatments may not be used to full advantage.

Indexed as

Myeloproliferative DisordersPolycythemia VeraThrombosisHumansPhlebotomyRisk FactorsCytoreductive medicationHematocrit controlMyeloproliferative neoplasmPolycythemia veraTherapeutic phlebotomyThrombotic events

Identifiers

PMID36637474
PMCPMC9977710
OpenAlexW4315928109

What OpenQuestion holds

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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.