Evidence map›Paper›PMID 41488014›Full record

ReviewTherapeutic advances in hematology2026

Efficacy and safety of avatrombopag in aplastic anemia: a comprehensive review of clinical evidence.

Mostafa F Mohammed Saleh, Abdulrahman Nasiri, Ahmed Kotb Abdrabou, Alfadil Haroon, Hadeel Samarkandi, Hazza Alzahrani, Mahmoud Aljurf, Ali Alahmari

Abstract readReview
In one paragraph

Review in Therapeutic advances in hematology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Mostafa F Mohammed SalehDepartment of Hematology, Stem Cell Transplant & Cellular Therapy, Cancer Centre of Excellence, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Abdulrahman NasiriDepartment of Internal Medicine, College of Medicine, Imam Mohammad Ibn Saud Islamic University (IMSIU), PO Box 5701, Riyadh 11432, Saudi Arabia.ORCID https://orcid.org/0000-0002-9401-810X
Ahmed Kotb AbdrabouDepartment of Hematology, Stem Cell Transplant & Cellular Therapy, Cancer Centre of Excellence, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Alfadil HaroonDepartment of Hematology, Stem Cell Transplant & Cellular Therapy, Cancer Centre of Excellence, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Hadeel SamarkandiDepartment of Pharmacy, Cancer Centre of Excellence, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Hazza AlzahraniDepartment of Hematology, Stem Cell Transplant & Cellular Therapy, Cancer Centre of Excellence, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Mahmoud AljurfDepartment of Hematology, Stem Cell Transplant & Cellular Therapy, Cancer Centre of Excellence, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Ali AlahmariDepartment of Hematology, Stem Cell Transplant & Cellular Therapy, Cancer Centre of Excellence, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aplastic anemia is a bone marrow failure disorder marked by cytopenias that impair oxygen delivery, immune defense, and hemostasis. Standard therapy traditionally combines immunosuppression with or without hematopoietic stem cell transplantation, and more recently incorporates thrombopoietin receptor agonists to stimulate residual hematopoiesis. Eltrombopag improved outcomes when added to immunosuppressive therapy, but its association with hepatotoxicity limits its suitability for patients with underlying liver disease or elevated baseline liver enzymes. Avatrombopag is a newer oral thrombopoietin receptor agonist that does not require dietary restrictions and does not undergo significant hepatic metabolism, which offers a potential therapeutic advantage in settings where liver function is compromised. This review evaluated ten clinical studies published from 2023 to October 2025 that investigated avatrombopag in acquired aplastic anemia across varied patient populations, including treatment-naive, relapsed or refractory cases, older adults, and patients with secondary aplastic anemia related to chemoradiation. Across these studies, overall response rates ranged from 55% to 85%, and complete response rates reached up to one-third of treated patients. Response onset typically occurred within 1-2 months, which aligns with clinical decision timelines for assessing therapeutic benefit. Avatrombopag supported reductions in transfusion requirements and sustained hematologic improvement in both severe and non-severe disease. Patients previously intolerant or non-responsive to eltrombopag also demonstrated clinical improvement, which suggests pharmacologic differences translate into meaningful therapeutic effects. Importantly, avatrombopag demonstrated a favorable safety profile in all reviewed settings. Reports did not identify clinically relevant hepatotoxicity, clonal evolution, or treatment-limiting adverse effects. Its tolerability in patients with liver dysfunction distinguishes it from earlier agents in this drug class. Ongoing trials will clarify optimal dosing strategies and define its future role within first-line therapy and salvage treatment pathways for aplastic anemia.

Indexed as

aplastic anemiaavatrombopagthrombopoietin receptor agonist

Identifiers

PMID41488014
PMCPMC12759122

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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.