Literature DB >> 21655159

Managing treatment-related adverse events associated with egfr tyrosine kinase inhibitors in advanced non-small-cell lung cancer.

V Hirsh1.   

Abstract

Non-small-cell lung cancer (nsclc) has the highest prevalence of all types of lung cancer, which is the second most common cancer and the leading cause of cancer-related mortality in Canada. The need for more effective and less toxic treatment options for nsclc has led to the development of agents targeting the epidermal growth factor receptor (egfr)-mediated signalling pathway, such as egfr tyrosine kinase inhibitors (egfr-tkis). Although egfr-tkis are less toxic than traditional anti-neoplastic agents, they are commonly associated with acneiform-like rash and diarrhea. This review summarizes the clinical presentation and causes of egfr-tki-induced rash and diarrhea, and presents strategies for effective assessment, monitoring, and treatment of these adverse effects. Strategies to improve the management of egfr-tki-related adverse events should improve clinical outcomes, compliance, and quality of life in patients with advanced nsclc.

Entities:  

Keywords:  Epidermal growth factor receptor; adverse drug event; adverse drug reaction; diarrhea; skin rash

Year:  2011        PMID: 21655159      PMCID: PMC3108866          DOI: 10.3747/co.v18i3.877

Source DB:  PubMed          Journal:  Curr Oncol        ISSN: 1198-0052            Impact factor:   3.677


  39 in total

1.  Randomized phase 2b study of pralatrexate versus erlotinib in patients with stage IIIB/IV non-small-cell lung cancer (NSCLC) after failure of prior platinum-based therapy.

Authors:  Karen Kelly; Christopher G Azzoli; Petr Zatloukal; István Albert; Peter Y Z Jiang; David Bodkin; José Rodrigues Pereira; Erzsébet Juhász; Nicholas O Iannotti; Garry Weems; Tony Koutsoukos; Jyoti D Patel
Journal:  J Thorac Oncol       Date:  2012-06       Impact factor: 15.609

2.  Gefitinib plus best supportive care in previously treated patients with refractory advanced non-small-cell lung cancer: results from a randomised, placebo-controlled, multicentre study (Iressa Survival Evaluation in Lung Cancer).

Authors:  Nick Thatcher; Alex Chang; Purvish Parikh; José Rodrigues Pereira; Tudor Ciuleanu; Joachim von Pawel; Sumitra Thongprasert; Eng Huat Tan; Kristine Pemberton; Venice Archer; Kevin Carroll
Journal:  Lancet       Date:  2005 Oct 29-Nov 4       Impact factor: 79.321

Review 3.  Understanding and managing chemotherapy-induced diarrhea.

Authors:  Leonard B Saltz
Journal:  J Support Oncol       Date:  2003 May-Jun

4.  Multi-institutional randomized phase II trial of gefitinib for previously treated patients with advanced non-small-cell lung cancer (The IDEAL 1 Trial) [corrected].

Authors:  Masahiro Fukuoka; Seiji Yano; Giuseppe Giaccone; Tomohide Tamura; Kazuhiko Nakagawa; Jean-Yves Douillard; Yutaka Nishiwaki; Johan Vansteenkiste; Shinzoh Kudoh; Danny Rischin; Richard Eek; Takeshi Horai; Kazumasa Noda; Ichiro Takata; Egbert Smit; Steven Averbuch; Angela Macleod; Andrea Feyereislova; Rui-Ping Dong; José Baselga
Journal:  J Clin Oncol       Date:  2003-05-14       Impact factor: 44.544

5.  Gefitinib in combination with paclitaxel and carboplatin in advanced non-small-cell lung cancer: a phase III trial--INTACT 2.

Authors:  Roy S Herbst; Giuseppe Giaccone; Joan H Schiller; Ronald B Natale; Vincent Miller; Christian Manegold; Giorgio Scagliotti; Rafael Rosell; Ira Oliff; James A Reeves; Michael K Wolf; Annetta D Krebs; Steven D Averbuch; Judith S Ochs; John Grous; Abderrahim Fandi; David H Johnson
Journal:  J Clin Oncol       Date:  2004-03-01       Impact factor: 44.544

Review 6.  Targeting growth factors in lung cancer.

Authors:  Philip S Hodkinson; Alison Mackinnon; Tariq Sethi
Journal:  Chest       Date:  2008-05       Impact factor: 9.410

7.  Phase III study of erlotinib in combination with cisplatin and gemcitabine in advanced non-small-cell lung cancer: the Tarceva Lung Cancer Investigation Trial.

Authors:  Ulrich Gatzemeier; Anna Pluzanska; Aleksandra Szczesna; Eckhard Kaukel; Jaromir Roubec; Flavio De Rosa; Janusz Milanowski; Hanna Karnicka-Mlodkowski; Milos Pesek; Piotr Serwatowski; Rodryg Ramlau; Terezie Janaskova; Johan Vansteenkiste; Janos Strausz; Georgy Moiseevich Manikhas; Joachim Von Pawel
Journal:  J Clin Oncol       Date:  2007-04-20       Impact factor: 44.544

8.  Correlation between development of rash and efficacy in patients treated with the epidermal growth factor receptor tyrosine kinase inhibitor erlotinib in two large phase III studies.

Authors:  Bret Wacker; Tina Nagrani; Jacqueline Weinberg; Karsten Witt; Gary Clark; Pablo J Cagnoni
Journal:  Clin Cancer Res       Date:  2007-07-01       Impact factor: 12.531

9.  Clinical Significance of Skin Toxicity due to EGFR-Targeted Therapies.

Authors:  Monica Giovannini; Vanesa Gregorc; Carmen Belli; Elisa Roca; Chiara Lazzari; Maria Grazia Viganò; Anna Serafico; Eugenio Villa
Journal:  J Oncol       Date:  2009-06-22       Impact factor: 4.375

10.  Prevention and management of chemotherapy-induced diarrhea in patients with colorectal cancer: a consensus statement by the Canadian Working Group on Chemotherapy-Induced Diarrhea.

Authors:  J A Maroun; L B Anthony; N Blais; R Burkes; S D Dowden; G Dranitsaris; B Samson; A Shah; M P Thirlwell; M D Vincent; R Wong
Journal:  Curr Oncol       Date:  2007-02       Impact factor: 3.677

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  43 in total

Review 1.  Management of egfr tki-induced dermatologic adverse events.

Authors:  B Melosky; N B Leighl; J Rothenstein; R Sangha; D Stewart; K Papp
Journal:  Curr Oncol       Date:  2015-04       Impact factor: 3.677

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.  Rash management and treatment persistence of cancer patients treated with epidermal growth factor receptor inhibitors in the Truven MarketScan® research database.

Authors:  Lei Chen; Jacqueline Brown; Dale Quentin Marmaduke; Carlos Mayo; Gerrit Grau; Yiu-Keung Lau; Coleman K Obasaju
Journal:  Support Care Cancer       Date:  2018-02-08       Impact factor: 3.603

4.  Systems biology analysis identifies molecular determinants of chemotherapy-induced diarrhoea.

Authors:  Andreas U Lindner; Alexa J Resler; Steven Carberry; Kasia Oficjalska; Orna Bacon; Chun Seng Lee; Abdurehman Choudhry; John P Burke; Kieran Sheahan; Mattia Cremona; Bryan T Hennessy; Deborah McNamara; Glen Doherty; Elizabeth J Ryan; Jochen H M Prehn
Journal:  J Mol Med (Berl)       Date:  2019-12-17       Impact factor: 4.599

Review 5.  Tyrosine kinase inhibitors: their on-target toxicities as potential indicators of efficacy.

Authors:  Devron R Shah; Rashmi R Shah; Joel Morganroth
Journal:  Drug Saf       Date:  2013-06       Impact factor: 5.606

6.  A personalized approach to treatment: use of EGFR tyrosine kinase inhibitors for the treatment of non-small-cell lung cancer in Canada.

Authors:  V Hirsh; B Melosky; G Goss; D Morris; W Morzycki
Journal:  Curr Oncol       Date:  2012-04       Impact factor: 3.677

7.  Management of diarrhea induced by epidermal growth factor receptor tyrosine kinase inhibitors.

Authors:  V Hirsh; N Blais; R Burkes; S Verma; K Croitoru
Journal:  Curr Oncol       Date:  2014-12       Impact factor: 3.677

8.  Pharmacokinetics of afatinib, a selective irreversible ErbB family blocker, in patients with advanced solid tumours.

Authors:  Sven Wind; Marion Schmid; Julia Erhardt; Rainer-Georg Goeldner; Peter Stopfer
Journal:  Clin Pharmacokinet       Date:  2013-12       Impact factor: 6.447

Review 9.  Towards personalized treatment for early stage HER2-positive breast cancer.

Authors:  Kristina Goutsouliak; Jamunarani Veeraraghavan; Vidyalakshmi Sethunath; Carmine De Angelis; C Kent Osborne; Mothaffar F Rimawi; Rachel Schiff
Journal:  Nat Rev Clin Oncol       Date:  2019-12-13       Impact factor: 66.675

Review 10.  Skin problems and EGFR-tyrosine kinase inhibitor.

Authors:  Toshiyuki Kozuki
Journal:  Jpn J Clin Oncol       Date:  2016-01-29       Impact factor: 3.019

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