Evidence map›Paper›PMID 40047384›Full record

ArticleAmerican journal of hematology2025

Clinical Outcomes and Treatment Strategies of Adult Transplant-Associated Thrombotic Microangiopathy: External Validation of Harmonizing Definitions and High-Risk Criteria.

Aldo A Acosta-Medina, Meera Sridharan, Ronald S Go, Ann M Moyer, Nelson Leung, Maria Alice V Willrich, Robert Wolf, Rabee Kassis, Almothana Manasrah, Mira A Kohorst and 10 more

Abstract readValidation Study
In one paragraph

Article in American journal of hematology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

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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

20 authors.

Aldo A Acosta-MedinaDivision of Hematology, Mayo Clinic, Rochester, Minnesota, USA.ORCID 0000-0001-9414-9153
Meera SridharanDivision of Hematology, Mayo Clinic, Rochester, Minnesota, USA.ORCID 0000-0001-7225-8228
Ronald S GoDivision of Hematology, Mayo Clinic, Rochester, Minnesota, USA.
Ann M MoyerDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, USA.
Nelson LeungDivision of Hematology, Mayo Clinic, Rochester, Minnesota, USA.ORCID 0000-0002-5651-1411
Maria Alice V WillrichDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, USA.ORCID 0000-0002-9318-7091
Robert WolfDivision of Hematology, Mayo Clinic, Rochester, Minnesota, USA.
Rabee KassisDivision of Hematology, Mayo Clinic, Rochester, Minnesota, USA.
Almothana ManasrahDivision of Hematology, Mayo Clinic, Rochester, Minnesota, USA.
Mira A KohorstDepartment of Pediatric and Adolescent Medicine, Mayo Clinic, Rochester, Minnesota, USA.
Urshila DuraniDivision of Hematology, Mayo Clinic, Rochester, Minnesota, USA.ORCID 0000-0003-1860-2424
Aasiya MatinDivision of Hematology, Mayo Clinic, Rochester, Minnesota, USA.
Mehrdad HefaziDivision of Hematology, Mayo Clinic, Rochester, Minnesota, USA.ORCID 0000-0001-8860-3380
Saad J KenderianDivision of Hematology, Mayo Clinic, Rochester, Minnesota, USA.ORCID 0000-0003-2767-3830
Abhishek A MangaonkarDivision of Hematology, Mayo Clinic, Rochester, Minnesota, USA.ORCID 0000-0003-2458-9887
Mithun V ShahDivision of Hematology, Mayo Clinic, Rochester, Minnesota, USA.ORCID 0000-0002-5359-336X
Mark R LitzowDivision of Hematology, Mayo Clinic, Rochester, Minnesota, USA.ORCID 0000-0002-9816-6302
William J HoganDivision of Hematology, Mayo Clinic, Rochester, Minnesota, USA.
David DingliDivision of Hematology, Mayo Clinic, Rochester, Minnesota, USA.
Hassan B AlkhateebDivision of Hematology, Mayo Clinic, Rochester, Minnesota, USA.

Funding

ASH Foundation HONORS (Hematology Opportunities for the Next Gene
6 · The paper itself

Abstract

Transplant-associated thrombotic microangiopathy (TA-TMA) is an endothelial dysfunction syndrome observed after allogeneic hematopoietic cell transplant (alloHCT). Our aim was to externally validate the impact of high-risk features on the clinical outcomes of adult patients meeting the updated TA-TMA harmonizing criteria. Between 2005 and 2022, 99 patients were diagnosed with TA-TMA at Mayo Clinic Rochester (incidence 6.2%) after a median of 137 days post alloHCT (IQR: 34-283 days). The development of TA-TMA was associated with an inferior overall survival posttransplant (HR: 3.8, 95% CI: 2.97-4.72). High-risk features, including concomitant infection, acute graft-versus-host disease (GVHD), and organ dysfunction, were associated with poor survival, while LDH elevation was not associated with inferior outcomes. The most common treatment strategy for TA-TMA was discontinuation of calcineurin or mTOR inhibitors in 80 (81%) patients. Thirty (37.5%) patients experienced worsening of GVHD with this strategy, of which 26 (86.7%) patients had died at last follow-up. The most common cause of death among these patients was worsening GVHD (69%; n = 18), followed by infection (11%; n = 3), disease relapse (8%; n = 2), other/unknown causes (8%; n = 2), or TA-TMA (4%; n = 1). Objective response rate (ORR) to initial treatment for the cohort was 56.6%. Eculizumab was used in 11 patients with an observed ORR of 70%, including 5 complete responses. In conclusion, TA-TMA remains a significant contributor to non-relapse mortality and is associated with worse survival following alloHCT. Not all high-risk features, particularly LDH elevation, have consistently demonstrated a negative impact in adult cohorts. Patients with TA-TMA may benefit from immune suppression dose adjustment, rather than a discontinuation, and the addition of complement-directed therapy, particularly among high-risk patients.

Indexed as

Hematopoietic Stem Cell TransplantationThrombotic MicroangiopathiesAdultAgedAntibodies, Monoclonal, HumanizedFemaleGraft vs Host DiseaseHumansMaleMiddle AgedRetrospective StudiesRisk FactorsTreatment OutcomeAntibodies, Monoclonal, Humanizedallogeneic transplantationcomplement inhibitorrisk assessmentthrombotic microangiopathy

Identifiers

PMID40047384
PMCPMC11966343

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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.