Cited by 83Chemotherapy-induced cardiotoxicity and mitigationChronic Myeloid Leukemia TreatmentsChronic Lymphocytic Leukemia Research

Cancer-Drug Discovery and Cardiovascular Surveillance

Groarke, John D., Cheng, Susan, Moslehi, Javid·2013·New England Journal of Medicine

Abstract

The story of impressive evolution in treatment for chronic myeloid leukemia has taken an unexpected turn, as serious adverse cardiovascular events have occurred in patients treated with the tyrosine kinase inhibitors ponatinib and nilotinib.

Integrity signals

Registry

Crossref · 10.1056/nejmp1313140

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  • ICI targeting PD-1 and CTLA-4 is clinically effective in enhancing T-cell-mediated antitumor responses.

    “Although proving to be clinically effective in enhancing T-cell-mediated antitumor responses”

    From Autoimmune Myocarditis, Old Dogs and New Tricks. (2024) · cites this paper as [171]

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Authors
Groarke, J. D., Cheng, S., & Moslehi, J.
Affiliations
Brigham and Women's Hospital (US)
Venue
New England Journal of Medicine
Published
2013-11-07
Volume
369
Issue
19
Pages
1779-1781
ISSN
  • 0028-4793 (ISSN-L)
  • 1533-4406
OpenAlex
W2061613118
Cited by
83
References
0
Citations by year
2026: 1 · 2025: 5 · 2024: 5 · 2023: 7 · 2022: 5 · 2021: 5 · 2020: 5 · 2019: 3 · 2018: 6 · 2017: 6 · 2016: 11 · 2015: 12 · 2014: 12
FWCI
7.94
Type
journal article
Language
en
Open access
closed
Locations
  • New England Journal of Medicine (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Chemotherapy-induced cardiotoxicity and mitigation
  • Health Sciences › Medicine › Hematology › Chronic Myeloid Leukemia Treatments
  • Health Sciences › Medicine › Genetics › Chronic Lymphocytic Leukemia Research
Keywords
chronic myeloid leukemia, tyrosine kinase inhibitors, ponatinib, nilotinib, cardiovascular adverse events, drug safety, cardiovascular surveillance, anticancer drug discovery
MeSH terms
Antineoplastic Agents, Cardiovascular System, Humans, Imidazoles, Protein-Tyrosine Kinases, Pyridazines, Pyrimidines, Vascular Diseases, Leukemia, Myelogenous, Chronic, BCR-ABL Positive, Fusion Proteins, bcr-abl, Protein Kinase Inhibitors, Drug Discovery

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