Tumor-Infiltrating Clonal Hematopoiesis

TI-CH increased the risk of disease recurrence or death among patients with NSCLC and the risk of death from any cause among patients with solid tumors. TI-CH remodeled the tumor immune microenvironment and accelerated tumor organoid growth, findings that support a role for an aging-related hematologic clonal proliferation in cancer evolution. (Funded by the Royal Society and others.).

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Publication Details

Journal
New England Journal of Medicine
Published
2025-04-23
DOI
https://doi.org/10.1056/nejmoa2413361
Citations
58
Primary Topic
Acute Myeloid Leukemia Research
Type
article
Field-Weighted Citation Impact
102.66

Funders

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article

Tumor-Infiltrating Clonal Hematopoiesis

Krijn K. Dijkstra, Jennifer O’Sullivan, Johanna A. Joyce, Julian Downward et al.
58 citations
New England Journal of Medicine
Acute Myeloid Leukemia Research
102.66
article

Tumor-Infiltrating Clonal Hematopoiesis

Krijn K. Dijkstra, Jennifer O’Sullivan, Johanna A. Joyce, Julian Downward, Panayiotis Anastasiou, Sergio A. Quezada, Jayant K. Rane, Simone Zaccaria, Dominique A. Bonnet, Elena Hoxha, Aaron James Stonestrom, Andreas Wack, Rachel Scott, Allan Hackshaw, Katey S.S. Enfield, Elsa Bernard, Mary Green, Charlotte Brierley, Oriol Pich, Sally‐Ann Clark, Adam J. Mead, Vittorio Barbè, David R. Pearce, Ángel F. Álvarez-Prado, C. Donovan Bailey, Alastair Magness, Hector Huerga Encabo, Robert E. Hynds, Maria Zagorulya, Supreet Kaur Bola, Charles M. Rudin, Rija Zaidi, Eva Grönroos, Kerstin Thol, Ilaria Malanchi, William Grey, Steve Harris, Cristina Lo Celso, Constandina Pospori, Elli Papaemmanuil, Despoina Papazoglou, Chrysante S. Iliakis, Michael F. Berger, Mariam Jamal-Hanjani, Charles Swanton, Ramy Slama, Karl S. Peggs, Andrew Rowan
article en
58 citations

Abstract

TI-CH increased the risk of disease recurrence or death among patients with NSCLC and the risk of death from any cause among patients with solid tumors. TI-CH remodeled the tumor immune microenvironment and accelerated tumor organoid growth, findings that support a role for an aging-related hematologic clonal proliferation in cancer evolution. (Funded by the Royal Society and others.).

New England Journal of MedicineVol. 392(16)
University of Maryland, Baltimore (US), Memorial Sloan Kettering Cancer Center (US), University College London Hospitals NHS Foundation Trust (GB), The Francis Crick Institute (GB), Royal London Hospital (GB), Cancer Research UK (GB), Cancer Institute (WIA) (IN), Institut Gustave Roussy (FR), Centre Hospitalier Universitaire Vaudois (CH), The Netherlands Cancer Institute (NL), University of Oxford (GB), London Cancer (GB), MRC Weatherall Institute of Molecular Medicine (GB), Oncode Institute (NL), Ludwig Cancer Research (CH), UCL Biomedical Research Centre (GB), Immune Regulation (United Kingdom) (GB), Oxford University Hospitals NHS Trust (GB), CRUK Lung Cancer Centre of Excellence (GB), Swiss Cancer Center Léman (CH), Protéomique, Réponse Inflammatoire et Spectrométrie de Masse (FR), University College London (GB), Imperial College London (GB), University of York (GB), Medical Research Council (GB), University of Lausanne (CH)
National Science Foundation, Damon Runyon Cancer Research Foundation, European Molecular Biology Organization, European Hematology Association, Edward P. Evans Foundation, Wellcome Trust, Francis Crick Institute, UK Research and Innovation, Leukaemia UK, Cancer Research UK, National Institute for Health and Care Research, Royal Society, Kay Kendall Leukaemia Fund, European Commission, Agence Nationale de la Recherche, Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung, University College London Hospitals NHS Foundation Trust, National Institutes of Health, Horizon 2020 Framework Programme, HORIZON EUROPE Framework Programme, Medical Research Council, European Research Council, Clarendon Fund, National Cancer Institute, HORIZON EUROPE European Innovation Council
Good health and well-being
Openalex Percentile: Top 0%
Acute Myeloid Leukemia Research
102.66
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