Strategies in Managing EGFRM+ NSCLC
2 hours ago | Speaker: Dr. Lim Chun Sen
Document ID: PC-MY-101191
Watch Dr Lim Chun Sen elaborate on the clinical evidence of the 2nd generation EGFR-TKI, afatinib, which has a broad inhibitory profile of the ErbB receptor family. Learn which patient population is likely to receive maximum clinical benefit from afatinib as well as practical tips on optimizing afatinib dosing and managing its adverse events.
Speaker

Dr. Lim Chun Sen

Clinical Oncologist and Head of Department,
Oncology and Radiotherapy
Hospital Sultan Ismail, Johor Bahru, Johor

What is Afatinib (Giotrif®)?

Afatinib (Giotrif®) is an irreversible ErbB Family blocker approved in more than 70 countries. It is indicated for the treatment of patients with distinct types of epidermal growth factor receptor mutation-positive (EGFR M+) locally advanced or metastatic non-small cell lung cancer (NSCLC), and for the treatment of patients with locally advanced or metastatic NSCLC of squamous histology progressing on or after platinum-based chemotherapy. It is an oral, once-daily, targeted therapy.[1]

*Afatinib is approved in more than 70 countries including the EU, Japan, Taiwan, and Canada under the brand name Giotrif®, in the US under the brand name Gilotrif® and in India under the brand name Xovoltib®
 

IMPORTANT SAFETY INFORMATION

What is the most important information I should know about Afatinib (Giotrif®)?

The side effects of Afatinib are predictable, generally manageable and reversible. In studies to date, drug-related adverse events (AEs) were largely related to the gastrointestinal tract (diarrhoea) and skin disorders (rash), which is in line with EGFR tyrosine kinase inhibition.[1-4] For further details, please refer to the Local Prescribing Information.

References:
[1] GIOTRIF® Summary of Product Characteristics 2018
[2] Sequist L et al. J Clin Oncol 2013;31(27)3327–34.
[3] Wu YL et al. Lancet Oncol 2014;15(2):213–22.
[4] Park K et al. Lancet Oncol 2016;17(5):577–89.