Literature DB >> 23448772

Dose reduction or intermittent administration of erlotinib: which is better for patients suffering from intolerable toxicities?

Akito Hata1, Shiro Fujita, Reiko Kaji, Shigeki Nanjo, Nobuyuki Katakami.   

Abstract

Erlotinib is an epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitor that is widely used in the treatment of non-small cell lung cancer. Skin rashes and diarrhea are frequent side effects of erlotinib therapy. When these toxicities become intolerable, dose reduction is commonly performed. However, dose reduction may not maintain the effective dose levels in some specific situations, such as in cases of wild-type EGFR tumors or central nervous system metastases. We speculate that intermittent administration is better than dose reduction to simultaneously maintain the effective dose levels and reduce toxicities in such situations. We herein present four cases of patients who successfully received intermittent administration of erlotinib.

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Year:  2013        PMID: 23448772     DOI: 10.2169/internalmedicine.52.8543

Source DB:  PubMed          Journal:  Intern Med        ISSN: 0918-2918            Impact factor:   1.271


  3 in total

1.  A phase I, dose-escalation trial of continuous- and pulsed-dose afatinib combined with pemetrexed in patients with advanced solid tumors.

Authors:  Quincy S Chu; Randeep Sangha; Sebastien J Hotte; Gwen Sergenson; David Schnell; Vikram K Chand; Hal W Hirte
Journal:  Invest New Drugs       Date:  2014-07-19       Impact factor: 3.850

2.  A systematic review of non-standard dosing of oral anticancer therapies.

Authors:  Faouzi Djebbari; Nicola Stoner; Verna Teresa Lavender
Journal:  BMC Cancer       Date:  2018-11-22       Impact factor: 4.430

3.  A case report of metastatic lung adenocarcinoma with long-term survival for over 11 years.

Authors:  Tatsu Matsuzaki; Eri Iwami; Kotaro Sasahara; Aoi Kuroda; Takahiro Nakajima; Takeshi Terashima
Journal:  Medicine (Baltimore)       Date:  2019-01       Impact factor: 1.817

  3 in total

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