Literature DB >> 32505447

Eltrombopag olamine for refractory immune-related thrombocytopenia induced by pembrolizumab in a non-small cell lung cancer patient.

Munehiro Ito1, Shintaro Kanda2, Tatsuya Yoshida1, Yusuke Okuma1, Hitomi Jo1, Suguru Fukuhara3, Akiko Miyagi Maeshima4, Yuichiro Ohe1.   

Abstract

OBJECTIVES: Immune checkpoint inhibitors (ICIs) have shown antitumor activity against a wide variety of malignancies. ICI-induced immune-related thrombocytopenia is a rare immune-related adverse event (irAE). Little is known about the treatment of refractory immune-related thrombocytopenia in non-small cell lung cancer (NSCLC) patients treated with pembrolizumab.
RESULTS: We report the case of a patient with advanced NSCLC complicated by pembrolizumab-induced refractory immune-related thrombocytopenia who showed remarkable improvement in the thrombocytopenia in response to eltrombopag olamine treatment.
CONCLUSION: Eltrombopag olamine can be a viable treatment option for refractory pembrolizumab-induced immune-related thrombocytopenia in an NSCLC patient.
Copyright © 2020 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  eltrombopag olamine; immune-related thrombocytopenia; non-small cell lung cancer; pembrolizumab; rituximab

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Year:  2020        PMID: 32505447     DOI: 10.1016/j.lungcan.2020.05.015

Source DB:  PubMed          Journal:  Lung Cancer        ISSN: 0169-5002            Impact factor:   5.705


  2 in total

1.  Efficacy and Immunomodulating Properties of Eltrombopag in Aplastic Anemia following Autologous Stem Cell Transplant: Case Report and Review of the Literature.

Authors:  Marta Bortolotti; Loredana Pettine; Anna Zaninoni; Giorgio Alberto Croci; Wilma Barcellini; Bruno Fattizzo
Journal:  Pharmaceuticals (Basel)       Date:  2022-03-30

Review 2.  Immune Thrombocytopenia Induced by Immune Checkpoint Inhibitrs in Lung Cancer: Case Report and Literature Review.

Authors:  Wang Xie; NaNa Hu; LeJie Cao
Journal:  Front Immunol       Date:  2021-12-09       Impact factor: 7.561

  2 in total

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