Evidence map›Paper›PMID 42805147›Full record

ArticleJACC. Advances2026

Cardio-Oncological Sequelae of Autologous Stem Cell Transplantation: Role of Clonal Hematopoiesis in Cardiovascular Risk.

Zsófia Sándor, Zoltán V Varga, Tamás G Gergely, Laura Horváth, Tamás Masszi, Zsófia D Drobni, José J Fuster, Zoltán Pozsonyi

Abstract read
In one paragraph

Article in JACC. Advances, 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.

Zsófia SándorDepartment of Internal Medicine and Haematology, Semmelweis University, Budapest, Hungary; Department of Cardiology, Heart and Vascular Center, Semmelweis University, Budapest, Hungary. Electronic address: sandor.zsofia@stud.semmelweis.hu.
Zoltán V VargaDepartment of Pharmacology and Pharmacotherapy, Semmelweis University, Budapest, Hungary; Center for Pharmacology and Drug Research & Development, Semmelweis University, Budapest, Hungary; MTA-SE Momentum Cardio-Oncology and Cardioimmunology Research Group, Semmelweis University, Budapest, Hungary.
Tamás G GergelyDepartment of Pharmacology and Pharmacotherapy, Semmelweis University, Budapest, Hungary; Center for Pharmacology and Drug Research & Development, Semmelweis University, Budapest, Hungary; MTA-SE Momentum Cardio-Oncology and Cardioimmunology Research Group, Semmelweis University, Budapest, Hungary.
Laura HorváthDepartment of Internal Medicine and Haematology, Semmelweis University, Budapest, Hungary.
Tamás MassziDepartment of Internal Medicine and Haematology, Semmelweis University, Budapest, Hungary.
Zsófia D DrobniDepartment of Cardiology, Heart and Vascular Center, Semmelweis University, Budapest, Hungary.
José J FusterCentro Nacional de Investigaciones Cardiovasculares (CNIC), Madrid, Spain; CIBER en Enfermedades Cardiovasculares (CIBER-CV), Madrid, Spain.
Zoltán PozsonyiDepartment of Internal Medicine and Haematology, Semmelweis University, Budapest, Hungary.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autologous hematopoietic stem cell transplantation is a major milestone in modern oncohematological therapies; however, both in the peritransplant and post-transplant phase, the incidence of cardiovascular (CV) events is markedly higher than in the general population. The pathomechanism of CV complications is multifactorial, determined by complex interactions between patient-specific, transplant-related, and oncological risk factors. In recent years, clonal hematopoiesis has emerged as a clinically relevant determinant of adverse CV outcomes. Patients undergoing autologous hematopoietic stem cell transplantation represent a high-risk CV population due to cumulative cytotoxic exposure, treatment-driven clonal selection, and increasing long-term survival. These factors highlight the need for future development of clonal hematopoiesis-based risk stratification models that combine gene-specific alterations, clonal expansion magnitude, and mutational burden with conventional CV risk factors. Novel risk stratification approaches may enable tailored patient follow-up, individualized preventive interventions, and the early detection and prevention of CV complications in this sensitive patient population.

Indexed as

autologous hematopoietic stem cell transplantationcardiovascular eventsclonal hematopoiesisonco-hematologypreventionrisk stratification

Identifiers

PMID42805147
PMCPMC13653288

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.