Evidence map›Paper›PMID 42262879›Full record

ArticleThe Journal of clinical investigation2026

Evolution of clonal hematopoiesis during cancer treatment and its impact on outcomes.

Mona Arabzadeh, Yi-Han Tang, Christelle Colin-Leitzinger, Sadegh Marzban, Daniel Walgenbach, Stefania Morganti, Vaidhyanathan Mahaganapathy, Erika Harper, Mingxiang Teng, Jacob K Kresovich and 7 more

Abstract read
In one paragraph

Article in The Journal of clinical investigation, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors.

Mona ArabzadehCenter for Systems and Computational Biology, and.
Yi-Han TangDepartment of Cancer Epidemiology.
Christelle Colin-LeitzingerDepartment of Cancer Epidemiology.
Sadegh MarzbanDepartment of Integrated Mathematical Oncology, Moffitt Cancer Center and Research Institute, Tampa, Florida, USA.
Daniel WalgenbachDepartment of Internal Medicine, University of South Florida, Tampa, Florida, USA.
Stefania MorgantiDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts, USA.
Vaidhyanathan MahaganapathyCenter for Systems and Computational Biology, and.
Erika HarperDepartment of Pathology, and.
Mingxiang TengDepartment of Biostatistics and Bioinformatics, and.
Jacob K KresovichDepartment of Cancer Epidemiology.
Iman WashingtonDepartment of Radiation Oncology, Moffitt Cancer Center and Research Institute, Tampa, Florida, USA.
Heather A ParsonsDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts, USA.
Judy E GarberDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts, USA.
Jeffrey WestDepartment of Integrated Mathematical Oncology, Moffitt Cancer Center and Research Institute, Tampa, Florida, USA.
Shridar GanesanCenter for Systems and Computational Biology, and.
Hossein KhiabanianCenter for Systems and Computational Biology, and.
Nancy GillisDepartment of Cancer Epidemiology.

Funding

TRANSLATIONAL RESEARCHP30CA076292 · NCI · UNIVERSITY OF SOUTH FLORIDA · PI John L. Cleveland · 1998 to 2026
$93.5M
Evolution and clinical impact of clonal hematopoiesis of indeterminate potential in breast tumor microenvironmentR01CA233662 · NCI · RUTGERS BIOMEDICAL AND HEALTH SCIENCES · PI GANESAN, SHRIDAR · 2019 to 2023
$3.2M
NCI NIH HHS P30 CA076292NCI NIH HHS R01 CA233662
6 · The paper itself

Abstract

Clonal hematopoiesis (CH) is the age-related expansion of mutated hematopoietic stem cells without hematologic abnormalities. In patients with solid tumors, CH is associated with higher mortality and may evolve to therapy-related myeloid neoplasms; however, the mechanisms by which cancer treatments promote CH dynamics remain largely unknown. Here, we analyzed 392 serial samples from a prospective cohort of patients with breast cancer and show that cytotoxic treatments led to strong therapeutic bottlenecks, resulting in significant reductions in hematopoietic allelic populations and differential clonal selection. Positively selected CH that expanded through dose-dependent therapeutic bottlenecks harbored mutations in TP53, PPM1D, SRCAP, DNMT3A, and YLPM1. Patients with positively selected CH during treatment had the shortest progression-free and overall survival compared with patients with unchanging or negatively selected CH across all therapies. These findings, validated in independent breast cancer and pan-cancer cohorts, provide strong evidence for the clinical relevance of monitoring CH during cancer treatment.

Indexed as

Breast NeoplasmsClonal HematopoiesisHematopoietic Stem CellsMutationNeoplasm ProteinsFemaleHumansNeoplasm ProteinsBreast cancerClinical ResearchClonal selectionGeneticsHematopoietic stem cellsOncology

Identifiers

PMID42262879
PMCPMC13367969

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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.