Latest advancement in Lung Cancer Clinical Research Part 3
Speakers: Prof. Byoung Chul Cho & Dr. Ross Soo
Document ID: SC-MY-00946
Speakers

Prof. Byoung Chul Cho
Prof. Byoung Chul Cho

MD, PhD, Professor Division of Medical Oncology

Yonsei Cancer Center, Korea Yonsei University College of Medicine

Dr. Ross Soo
Dr. Ross Soo

MBBS, FRACP, Senior Consultant Department Haematology-Oncology

National University Hospital National University Cancer Institute, Singapore

More Videos

Latest advancement in Lung Cancer Clinical Research Part 1

Speaker: Prof. Byoung Chul Cho

Latest advancement in Lung Cancer Clinical Research Part 2

Speaker: Dr. Ross Soo

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.