Evidence map›Paper›PMID 38684821›Full record

ArticleLeukemia2024

Clonal hematopoiesis-derived therapy-related myeloid neoplasms after autologous hematopoietic stem cell transplant for lymphoid and non-lymphoid disorders.

Hussein Awada, Carmelo Gurnari, Valeria Visconte, Arda Durmaz, Teodora Kuzmanovic, Hassan Awada, Zheng Jin Tu, James R Cook, Brian J Bolwell, Ronald Sobecks and 3 more

Abstract read
In one paragraph

Article in Leukemia, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

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  7. Influence ofBiomedicines · 2026
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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

13 authors.

Hussein Awada *Translational Hematology and Oncology Research Department of Cleveland Clinic, Cleveland, NY, USA.ORCID 0000-0002-1445-7947
Carmelo Gurnari *Translational Hematology and Oncology Research Department of Cleveland Clinic, Cleveland, NY, USA.
Valeria VisconteTranslational Hematology and Oncology Research Department of Cleveland Clinic, Cleveland, NY, USA.ORCID 0000-0002-2993-1509
Arda DurmazTranslational Hematology and Oncology Research Department of Cleveland Clinic, Cleveland, NY, USA.
Teodora KuzmanovicTranslational Hematology and Oncology Research Department of Cleveland Clinic, Cleveland, NY, USA.
Hassan AwadaRoswell Park Comprehensive Cancer Center, Buffalo, NY, USA.ORCID 0000-0003-4268-0756
Zheng Jin TuDepartment of Laboratory Medicine, Cleveland Clinic, Cleveland, OH, USA.
James R CookDepartment of Laboratory Medicine, Cleveland Clinic, Cleveland, OH, USA.ORCID 0000-0003-0456-8085
Brian J BolwellDepartment of Hematology and Oncology, Taussig Cancer Institute, Cleveland Clinic, Cleveland, OH, USA.
Ronald SobecksDepartment of Hematology and Oncology, Taussig Cancer Institute, Cleveland Clinic, Cleveland, OH, USA.
Matt KalaycioDepartment of Hematology and Oncology, Taussig Cancer Institute, Cleveland Clinic, Cleveland, OH, USA.
David BoslerDepartment of Laboratory Medicine, Cleveland Clinic, Cleveland, OH, USA.
Jaroslaw P MaciejewskiTranslational Hematology and Oncology Research Department of Cleveland Clinic, Cleveland, NY, USA. maciejj@ccf.org.ORCID 0000-0002-6837-4346

Funding

Therapeutic Implications of Molecular Defects in Bone Marrow FailureR35HL135795 · NHLBI · CLEVELAND CLINIC LERNER COM-CWRU · PI MACIEJEWSKI, JAROSLAW P. · 2017 to 2023
$5.7M
Leukemia and Lymphoma Society (Leukemia & Lymphoma Society) TRP Award 6645-22NHLBI NIH HHS R35 HL135795U.S. Department of Health & Human Services | NIH | National Heart, Lung, and Blood Institute (NHLBI) R35HL135795
6 · The paper itself

Abstract

Therapy-related myeloid neoplasms (tMN) are complications of cytotoxic therapies. Risk of tMN is high in recipients of autologous hematopoietic stem cell transplantation (aHSCT). Acquisition of genomic mutations represents a key pathogenic driver but the origins, timing and dynamics, particularly in the context of preexisting or emergent clonal hematopoiesis (CH), have not been sufficiently clarified. We studied a cohort of 1507 patients undergoing aHSCT and a cohort of 263 patients who developed tMN without aHSCT to determine clinico-molecular features unique to post-aHSCT tMN. We show that tMN occurs in up to 2.3% of patients at median of 2.6 years post-AHSCT. Age ≥ 60 years, male sex, radiotherapy, high treatment burden ( ≥ 3 lines of chemotherapy), and graft cellularity increased the risk of tMN. Time to evolution and overall survival were shorter in post-aHSCT tMN vs. other tMN, and the earlier group's mutational pattern was enriched in PPM1D and TP53 lesions. Preexisting CH increased the risk of adverse outcomes including post-aHSCT tMN. Particularly, antecedent lesions affecting PPM1D and TP53 predicted tMN evolution post-transplant. Notably, CH-derived tMN had worse outcomes than non CH-derived tMN. As such, screening for CH before aHSCT may inform individual patients' prognostic outcomes and influence their prospective treatment plans. Presented in part as an oral abstract at the 2022 American Society of Hematology Annual Meeting, New Orleans, LA, 2022.

Indexed as

Clonal HematopoiesisHematopoietic Stem Cell TransplantationMutationNeoplasms, Second PrimaryTransplantation, AutologousAdolescentAdultAgedFemaleFollow-Up StudiesHumansLymphomaMaleMiddle AgedMyeloproliferative DisordersPrognosisPPM1D protein, humanProtein Phosphatase 2CTumor Suppressor Protein p53

Identifiers

PMID38684821
PMCPMC11147764

What OpenQuestion holds

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Registered trials

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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.