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Erschienen in: Investigational New Drugs 5/2018

02.05.2018 | SHORT REPORT

Crizotinib-induced simultaneous multiple cardiac toxicities

verfasst von: Takuya Oyakawa, Nao Muraoka, Kei Iida, Masatoshi Kusuhara, Takahisa Kawamura, Tateaki Naito, Toshiaki Takahashi

Erschienen in: Investigational New Drugs | Ausgabe 5/2018

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Summary

Crizotinib is a receptor tyrosine kinase inhibitor that has several targets, including c-ros oncogene 1 and the MET proto-oncogene. Considering its known cardiac toxicity, bradycardia is often investigated following treatment with crizotinib. Our patients had bradycardia, QT prolongation, ventricular rhythm, ventricular fibrillation, and pericarditis simultaneously. The cardiotoxicity of crizotinib can sometimes be simultaneous; thus, intensive observation is needed.
Literatur
2.
Zurück zum Zitat Zamorano JL, Lancellotti P, Rodriguez Muñoz D et al (2016) ESC position paper on cancer treatments and cardiovascular toxicity developed under the auspices of the ESC Committee for practice guidelines:  the task force for cancer treatments and cardiovascular toxicity of the European Society of Cardiology (ESC). Eur Heart J 37:2768–2801CrossRefPubMed Zamorano JL, Lancellotti P, Rodriguez Muñoz D et al (2016) ESC position paper on cancer treatments and cardiovascular toxicity developed under the auspices of the ESC Committee for practice guidelines:  the task force for cancer treatments and cardiovascular toxicity of the European Society of Cardiology (ESC). Eur Heart J 37:2768–2801CrossRefPubMed
3.
Zurück zum Zitat Deshpande H, Marler V, Sosa JA (2011) Clinical utility of vandetanib in the treatment of patients with advanced medullary thyroid cancer. Onco Targets Ther 4:209–215CrossRefPubMedPubMedCentral Deshpande H, Marler V, Sosa JA (2011) Clinical utility of vandetanib in the treatment of patients with advanced medullary thyroid cancer. Onco Targets Ther 4:209–215CrossRefPubMedPubMedCentral
4.
Zurück zum Zitat Gallo S, Sala V, Gatti S, Crepaldi T (2015) Cellular and molecular mechanisms of HGF/met in the cardiovascular system. Clin Sci (Lond) 129:1173–1193CrossRef Gallo S, Sala V, Gatti S, Crepaldi T (2015) Cellular and molecular mechanisms of HGF/met in the cardiovascular system. Clin Sci (Lond) 129:1173–1193CrossRef
5.
Zurück zum Zitat Scagliotti G, von Pawel J, Novello S, Ramlau R, Favaretto A, Barlesi F, Akerley W, Orlov S, Santoro A, Spigel D, Hirsh V, Shepherd FA, Sequist LV, Sandler A, Ross JS, Wang Q, von Roemeling R, Shuster D, Schwartz B (2015) Phase III multinational, randomized, double-blind, placebo-controlled study of tivantinib (ARQ 197) plus erlotinib versus erlotinib alone in previously treated patients with locally advanced or metastatic nonsquamous non-small-cell lung cancer. J Clin Oncol 33:2667–2674CrossRefPubMed Scagliotti G, von Pawel J, Novello S, Ramlau R, Favaretto A, Barlesi F, Akerley W, Orlov S, Santoro A, Spigel D, Hirsh V, Shepherd FA, Sequist LV, Sandler A, Ross JS, Wang Q, von Roemeling R, Shuster D, Schwartz B (2015) Phase III multinational, randomized, double-blind, placebo-controlled study of tivantinib (ARQ 197) plus erlotinib versus erlotinib alone in previously treated patients with locally advanced or metastatic nonsquamous non-small-cell lung cancer. J Clin Oncol 33:2667–2674CrossRefPubMed
Metadaten
Titel
Crizotinib-induced simultaneous multiple cardiac toxicities
verfasst von
Takuya Oyakawa
Nao Muraoka
Kei Iida
Masatoshi Kusuhara
Takahisa Kawamura
Tateaki Naito
Toshiaki Takahashi
Publikationsdatum
02.05.2018
Verlag
Springer US
Erschienen in
Investigational New Drugs / Ausgabe 5/2018
Print ISSN: 0167-6997
Elektronische ISSN: 1573-0646
DOI
https://doi.org/10.1007/s10637-018-0605-x

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