Literature DB >> 23602600

Erlotinib-related skin toxicities: treatment strategies in patients with metastatic non-small cell lung cancer.

Yoshio Kiyohara1, Naoya Yamazaki, Akiko Kishi.   

Abstract

Skin toxicities are the most common side effects associated with the epidermal growth factor receptor inhibitor erlotinib, occurring in most patients receiving the drug. Clinical trials evaluating erlotinib for the treatment of non-small cell lung cancer have reported a range of skin disorders, the most common being acneiform rash, xeroderma (dry skin), pruritus, and paronychia. Although in the majority of cases these effects are mild and transient, they can have a considerable impact on a patient's quality of life and, if particularly severe and persistent, may necessitate treatment interruption or cessation and compromise treatment outcome. This coupled with recent evidence to suggest a positive correlation between the incidence and severity of rash and clinical outcome among erlotinib-treated patients with advanced or metastatic non-small cell lung cancer highlights the importance of adequately managing epidermal growth factor receptor inhibitor--related skin disorders. Clear treatment strategies are therefore necessary to ensure the prevention and optimal management of erlotinib-related skin toxicities thereby enabling patients to continue erlotinib treatment. In this review we present a practical approach for the treatment of erlotinib-related cutaneous side effects in Japanese patients with advanced non-small cell lung cancer providing details of specific treatment interventions, according to symptom severity, for each of the common skin disorders. In addition, the importance of preventive skin care measures--namely maintaining cleanliness, moisturization, and protection from external stimuli--in preventing the development of serious skin disorders is discussed and guidelines for the practice of proper skin care are presented.
Copyright © 2013 American Academy of Dermatology, Inc. Published by Mosby, Inc. All rights reserved.

Entities:  

Keywords:  ADL; AEs; BSA; CI; CRC; EGFR; FTUs; HR; Japanese patients; NSCLC; OS; STEPP; Skin Toxicity Evaluation Protocol with Panitumumab; UV; acneiform rash; activities of daily living; adverse events; body surface area; colorectal cancer; confidence interval; cutaneous side effects; epidermal growth factor receptor; epidermal growth factor receptor inhibitor; erlotinib; fingertip units; hazard ratio; non-small cell lung cancer; overall survival; prevention; skin toxicities; ultraviolet

Mesh:

Substances:

Year:  2013        PMID: 23602600     DOI: 10.1016/j.jaad.2013.02.025

Source DB:  PubMed          Journal:  J Am Acad Dermatol        ISSN: 0190-9622            Impact factor:   11.527


  24 in total

1.  Substance P receptor blocker, aprepitant, inhibited cutaneous and other neurogenic inflammation side effects of the EGFR1-TKI, erlotinib.

Authors:  Joanna J Chmielinska; Jay H Kramer; I-Tong Mak; Christopher F Spurney; William B Weglicki
Journal:  Mol Cell Biochem       Date:  2019-12-18       Impact factor: 3.396

2.  Targeting the Trafficking of Kidney Water Channels for Therapeutic Benefit.

Authors:  Pui W Cheung; Richard Bouley; Dennis Brown
Journal:  Annu Rev Pharmacol Toxicol       Date:  2019-09-27       Impact factor: 13.820

3.  Treatment strategies of epidermal growth factor receptor inhibitor-induced skin toxicities: pre-emptive or reactive?

Authors:  Yung-Tsu Cho; Kai-Lung Chen; Chia-Yu Chu
Journal:  Ann Transl Med       Date:  2016-08

4.  Purpuric Drug Eruptions Caused by Epidermal Growth Factor Receptor Inhibitors for Non-Small Cell Lung Cancer: A Clinicopathologic Study of 32 Cases.

Authors:  Yung-Tsu Cho; Kai-Lung Chen; Yi-Shuan Sheen; Che-Wen Yang; Jau-Yu Liau; Yu-Pin Cheng; Chia-Yu Chu
Journal:  JAMA Dermatol       Date:  2017-09-01       Impact factor: 10.282

5.  The Use of Ziziphus spina-christi Extract in Treating Erlotinib (Tarceva®) Associated Rash: A Case Report.

Authors:  Ali M Alzahrani; Asma A Alzahrani; Abdullah A Alsharm
Journal:  Case Rep Oncol       Date:  2019-12-06

6.  Nimotuzumab in combination with radiotherapy in high grade glioma patients: a single institution experience.

Authors:  Maria Teresa Solomon; Nederlay Miranda; Eugenia Jorrín; Ivonne Chon; Jorge Juan Marinello; José Alert; Patricia Lorenzo-Luaces; Tania Crombet
Journal:  Cancer Biol Ther       Date:  2014-02-12       Impact factor: 4.742

7.  Structures of human cytochrome P450 1A1 with bergamottin and erlotinib reveal active-site modifications for binding of diverse ligands.

Authors:  Aaron G Bart; Emily E Scott
Journal:  J Biol Chem       Date:  2018-09-25       Impact factor: 5.157

8.  Results of the non-small cell lung cancer part of a phase III, open-label, randomized trial evaluating topical corticosteroid therapy for facial acneiform dermatitis induced by EGFR inhibitors: stepwise rank down from potent corticosteroid (FAEISS study, NCCH-1512).

Authors:  Kazumi Nishino; Yutaka Fujiwara; Yuichiro Ohe; Ryota Saito; Eisaku Miyauchi; Tetsu Kobayashi; Yasuo Nakai; Toshiaki Takahashi; Taro Shibata; Tetsuya Hamaguchi; Katsuko Kikuchi; Naoya Yamazaki; Haruhiko Fukuda; Keiko Nozawa; Yoshio Kiyohara
Journal:  Support Care Cancer       Date:  2020-09-11       Impact factor: 3.603

9.  Optimal strength and timing of steroids in the management of erlotinib-related skin toxicities in a post-marketing surveillance study (POLARSTAR) of 9909 non-small-cell lung cancer patients.

Authors:  Naoya Yamazaki; Yoshio Kiyohara; Shoji Kudoh; Akihiro Seki; Masahiro Fukuoka
Journal:  Int J Clin Oncol       Date:  2015-10-26       Impact factor: 3.402

10.  Erlotinib augmentation with dapsone for rash mitigation and increased anti-cancer effectiveness.

Authors:  R E Kast
Journal:  Springerplus       Date:  2015-10-23
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.