Evidence map›Paper›PMID 42662888›Full record

ArticleResearch and practice in thrombosis and haemostasis2026

Avatrombopag in thrombopoietin receptor agonist-naïve patients with immune thrombocytopenia: real-world treatment patterns and clinical outcomes from the REAL-AVA 3.0 study.

Sandhya Panch, Abiola Oladapo, Scott Kolodny, Michael Vredenburg, Sarah Lucht, Emily Bland, Prathamesh Pathak, Bruce Feinberg, Debbie Jiang

Abstract read
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Article in Research and practice in thrombosis and haemostasis, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

9 authors.

Sandhya PanchDivision of Hematology and Oncology, University of Washington, Seattle, Washington, USA.
Abiola OladapoHematology Medical Affairs, Sobi, Inc, Waltham, Massachusetts, USA.
Scott KolodnyHematology Medical Affairs, Sobi, Inc, Waltham, Massachusetts, USA.
Michael VredenburgHematology Medical Affairs, Sobi, Inc, Waltham, Massachusetts, USA.
Sarah LuchtSpecialty Networks Solutions, Cardinal Health, Dublin, Ohio, USA.
Emily BlandSpecialty Networks Solutions, Cardinal Health, Dublin, Ohio, USA.
Prathamesh PathakSpecialty Networks Solutions, Cardinal Health, Dublin, Ohio, USA.
Bruce FeinbergSpecialty Networks Solutions, Cardinal Health, Dublin, Ohio, USA.
Debbie JiangHematology Division, Massachussetts General Hospital, Boston, Massachusetts, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Avatrombopag (AVA) is a thrombopoietin receptor agonist (TPO-RA) approved for patients with immune thrombocytopenia (ITP), but real-world data is limited in TPO-RA-naïve patients. Objectives: To describe treatment patterns and outcomes in TPO-RA-naïve adult patients with primary ITP treated with AVA. Methods: This retrospective chart review study included TPO-RA-naïve adults with primary ITP who initiated AVA on or after July 1, 2019, with ≥ 6 months of follow-up. Patients were followed from AVA initiation until the earliest of either last contact, death, or study end (January 20, 2025). Response was defined as achieving a platelet count (PC) ≥ 30, ≥ 50, or ≥ 100 × 10 Results: Among 200 patients, 84.0% initiated AVA with baseline PCs < 30 × 10 Conclusion: AVA is an effective treatment option for TPO-RA-naïve patients with ITP, demonstrating a high real-world rate of sustained PC response.

Indexed as

HydrazinesPurpura, Thrombocytopenic, IdiopathicReceptors, ThrombopoietinThiazolesThiophenesAdultAgedFemaleHumansMaleMiddle AgedPlatelet CountPyrazolesRetrospective StudiesTreatment OutcomeavatrombopagHydrazinesPyrazolesReceptors, ThrombopoietinThiazolesThiophenesavatrombopagplatelet countpurpura, thrombocytopenic, idiopathicretrospective studiestreatment outcome

Identifiers

PMID42662888
PMCPMC13520991

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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.