Evidence map›Paper›PMID 30191360›Full record

Trial reportAngiogenesis2019

Pazopanib may reduce bleeding in hereditary hemorrhagic telangiectasia.

Marie E Faughnan, James R Gossage, Murali M Chakinala, S Paul Oh, Raj Kasthuri, Christopher C W Hughes, Justin P McWilliams, Joseph G Parambil, Nicholas Vozoris, Jill Donaldson and 3 more

Registry-linked trialOpen access · hybridAbstract readClinical TrialMulticenter Study
In one paragraph

Trial report in Angiogenesis, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03850964 (A Phase II/III Randomized, Placebo Controlled, Double Blind Study to Evaluate the Effects of up to 24 Weeks of Low Dose Pazopanib on Hereditary Hemorrhagic Telangiectasia Related Epistaxis and Anemia), which is not on this map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
6.7field-weighted citation impact, top 2% 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.

NCT03850964 phase2 / phase3active not recruitingnot on this mapstarted 2023, after this paper: background citation

A Phase II/III Randomized, Placebo Controlled, Double Blind Study to Evaluate the Effects of up to 24 Weeks of Low Dose Pazopanib on Hereditary Hemorrhagic Telangiectasia Related Epistaxis and Anemia

TypeinterventionalSponsorCure HHTRan2023 to 2026Enrolled70ConditionsHereditary Hemorrhagic Telangiectasia, Epistaxis, Anemia, NosebleedArmsPazopanib, Placebo oral capsule
3 · Its place in the literature

Who cites it

54 citing papers in PubMed, 100 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Trial
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Review
  11. Hereditary haemorrhagic telangiectasia.Nature reviews. Disease primers · 2025
    Review
  12. Review
  13. Article
  14. Potential and emerging therapeutics for HHT.Hematology. American Society of Hematology. Education Program · 2024
    Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Review
  20. 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

13 authors at 10 institutions in 2 countries.

Marie E FaughnanToronto HHT Program, Division of Respirology, Department of Medicine, St. Michael's Hospital, University of Toronto, Toronto, ON, Canada. faughnanm@smh.ca.
James R GossageDivision of Pulmonary and Critical Care Medicine, Augusta University, Augusta, GA, USA.
Murali M ChakinalaDivision of Pulmonary and Critical Care Medicine, Washington University, St. Louis, MO, USA.
S Paul OhBarrow Aneurysm & AVM Research Center, Barrow Neurological Institute/Dignity Health, Phoenix, AZ, USA.
Raj KasthuriDivision of Hematology and Oncology, Department of Medicine, UNC School of Medicine, Chapel Hill, NC, USA.
Christopher C W HughesDepartment of Molecular Biology & Biochemistry, and Department of Biomedical Engineering, University of California Irvine, Irvine, CA, USA.
Justin P McWilliamsDivision of Interventional Radiology, Department of Radiology, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.
Joseph G ParambilCleveland Clinic, Respiratory Institute, Cleveland, OH, USA.
Nicholas VozorisToronto HHT Program, Division of Respirology, Department of Medicine, St. Michael's Hospital, University of Toronto, Toronto, ON, Canada.
Jill DonaldsonGlaxoSmithKline, King of Prussia, PA, USA.
Gitanjali PaulGlaxoSmithKline, King of Prussia, PA, USA.
Pamela BerryPatient Reported Outcomes, Janssen Global Services, LLC, Horsham, PA, USA.
Dennis L SprecherGlaxoSmithKline, King of Prussia, PA, USA.
GlaxoSmithKline (United States) · USAugusta University · USCleveland Clinic · USDignity Health · USJanssen (United States) · USSt. Michael's Hospital · CAUniversity of California, Irvine · USUniversity of California, Los Angeles · USUniversity of Toronto · CAWashington University in St. Louis · US

Funding

MIcrophysiological systems to model vascular malformationsUH3HL141799 · NHLBI · UNIVERSITY OF CALIFORNIA-IRVINE · PI HUGHES, CHRISTOPHER C. W. · 2019 to 2021
$2.3M
NHLBI NIH HHS UH3 HL141799
6 · The paper itself

Abstract

Pazopanib (Votrient) is an orally administered tyrosine kinase inhibitor that blocks VEGF receptors potentially serving as anti-angiogenic treatment for hereditary hemorrhagic telangiectasia (HHT). We report a prospective, multi-center, open-label, dose-escalating study [50 mg, 100 mg, 200 mg, and 400 mg], designed as a proof-of-concept study to demonstrate efficacy of pazopanib on HHT-related bleeding, and to measure safety. Patients, recruited at 5 HHT Centers, required ≥ 2 Curacao criteria AND [anemia OR severe epistaxis with iron deficiency]. Co-primary outcomes, hemoglobin (Hgb) and epistaxis severity, were measured during and after treatment, and compared to baseline. Safety monitoring occurred every 1.5 weeks. Seven patients were treated with 50 mg pazopanib daily. Six/seven showed at least 50% decrease in epistaxis duration relative to baseline at some point during study; 3 showed at least 50% decrease in duration during Weeks 11 and 12. Six patients showed a decrease in ESS of > 0.71 (MID) relative to baseline at some point during study; 3/6 showed a sustained improvement. Four patients showed > 2 gm improvement in Hgb relative to baseline at one or more points during study. Health-related QOL scores improved on all SF-36 domains at Week 6 and/or Week 12, except general health (unchanged). There were 19 adverse events (AE) including one severe AE (elevated LFTs, withdrawn from dosing at 43 days); with no serious AE. In conclusion, we observed an improvement in Hgb and/or epistaxis in all treated patients. This occurred at a dose much lower than typically used for oncologic indications, with no serious AE. Further studies of pazopanib efficacy are warranted.

Indexed as

HemorrhagePyrimidinesSulfonamidesTelangiectasia, Hereditary HemorrhagicAdultFemaleHumansIndazolesMaleMiddle AgedIndazolespazopanibPyrimidinesSulfonamidesAnemiaEpistaxisHereditaryTelangiectasiaTyrosine kinase inhibitor

Identifiers

PMID30191360
PMCPMC6510884
OpenAlexW2889896836

What OpenQuestion holds

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LicenceCC BY
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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.