Evidence map›Paper›PMID 40645690›Full record

ArticleJACC. Case reports2025

Permissive Cardiotoxicity and Determination of Anthracycline Risk With Previous Anthracycline Exposure.

Richard J Travers, Nicholas Camarda, Iris Z Jaffe, Raphael A Lizcano, Jenica N Upshaw

Abstract readCase Reports
In one paragraph

Article in JACC. Case reports, 2025. 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

5 authors.

Richard J TraversDivision of Hematology/Oncology, Tufts Medical Center, Boston, Massachusetts, USA; Molecular Cardiology Research Institute, Tufts Medical Center, Boston, Massachusetts, USA.
Nicholas CamardaMolecular Cardiology Research Institute, Tufts Medical Center, Boston, Massachusetts, USA.
Iris Z JaffeMolecular Cardiology Research Institute, Tufts Medical Center, Boston, Massachusetts, USA.
Raphael A LizcanoTransplant and Cellular Therapy Program, Dartmouth Cancer Center, Dartmouth-Hitchcock Medical Center, Lebanon, New Hampshire, USA.
Jenica N UpshawRichard A. and Susan F. Smith Center for Outcomes Research, Division of Cardiology, Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA. Electronic address: jupshaw@bidmc.harvard.edu.

Funding

Credentialing a Cross-Species Platform to Investigate Cancer Therapy-Associated Cardiovascular ToxicityR01CA243542 · NCI · TUFTS MEDICAL CENTER · PI JAFFE, IRIS Z, LONDON, CHERYL A · 2019 to 2023
$3.1M
Novel strategies to understand, predict, and prevent vascular toxicity of targeted CML therapiesR01HL155078 · NHLBI · TUFTS MEDICAL CENTER · PI JAFFE, IRIS Z · 2021 to 2024
$2.6M
Medical Scientist Training Program at Tufts UniversityT32GM146621 · NIGMS · TUFTS UNIVERSITY BOSTON · PI MICHAEL T CHIN · 2023 to 2026
$2.1M
Prevention of Anthracycline Chemotherapy CardiotoxicityK08HL146959 · NHLBI · TUFTS MEDICAL CENTER · PI UPSHAW, JENICA · 2020 to 2024
$885k
Endothelium as a mediator of BCR-ABL tyrosine kinase inhibitor vascular toxicityF32HL165838 · NHLBI · TUFTS MEDICAL CENTER · PI TRAVERS, RICHARD · 2022 to 2023
$138k
NCI NIH HHS R01 CA243542NHLBI NIH HHS F32 HL165838NHLBI NIH HHS K08 HL146959NHLBI NIH HHS R01 HL155078NIGMS NIH HHS T32 GM146621
6 · The paper itself

Abstract

Anthracyclines are an effective treatment for hematologic malignancies but have significant risk of cardiotoxicity that increases with lifetime dose, best characterized for doxorubicin. However, patients may receive different anthracycline formulations, and cardiotoxic dose equivalency for nondoxorubicin anthracyclines is uncertain, making it challenging to calculate a patient's lifetime dose to make decisions about safety of additional anthracycline treatment and risk stratification for monitoring and cardioprotective strategies. In addition, dexrazoxane reduces the risk of cardiovascular toxicity with anthracyclines but how to incorporate previous dexrazoxane treatment into risk stratification is unclear. Here, a young woman previously treated with anthracyclines as induction therapy for acute myeloid leukemia and concern for previous anthracycline cardiotoxicity presented with disease relapse. Because optimal therapy included retreatment with anthracyclines, this case demonstrates the multidisciplinary discussion for her case, reviewing the risks and benefits of repeat anthracycline exposure and detailing the evidence for strategies to monitor and prevent worsening cardiotoxicity.

Indexed as

acute myeloid leukemiaanthracyclinecardiotoxicitypermissive toxicitysurvivorship

Identifiers

PMID40645690
PMCPMC12441384

What OpenQuestion holds

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Registered trials

None linked

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.