Biomarker Detection in Lung Cancer: The Pros and Cons of Multiplex Testing Part3
29th April, 2020 | Speaker: Herbert Ho-Fung LOONG
Document ID: SC-SG-00608
Speaker

Herbert Ho-Fung LOONG
Herbert Ho-Fung LOONG

MBBS(HK), PDipMDPath(HK),
MRCP(UK), FHKCP, FHKAM(Medicine)
The Chinese University of Hong Kong,
Department of Clinical Oncology

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Biomarker Detection in Lung Cancer: The Pros and Cons of Multiplex Testing Part1
 

Biomarker Detection in Lung Cancer: The Pros and Cons of Multiplex Testing - Part1

29th April, 2020

Speaker: Herbert Ho-Fung LOONG

Biomarker Detection in Lung Cancer: The Pros and Cons of Multiplex Testing Part2
 

Biomarker Detection in Lung Cancer: The Pros and Cons of Multiplex Testing - Part2

29th April, 2020

Speaker: Herbert Ho-Fung LOONG

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.