Detailed Information

Cited 34 time in webofscience Cited 0 time in scopus
Metadata Downloads

Efficacy and Safety of Erlotinib in 1242 East/South-East Asian Patients with Advanced Non-small Cell Lung Cancer

Authors
Mok, T[Mok, Tony]Wu, YL[Wu, Yi-long]Au, JSK[Au, Joseph Siu-kie]Zhou, CC[Zhou, Caicun]Zhang, L[Zhang, Li]Perng, RP[Perng, Reury-Perng]Park, K[Park, Keunchil]
Issue Date
Oct-2010
Publisher
LIPPINCOTT WILLIAMS & WILKINS
Keywords
Erlotinib; NSCLC; Phase IV; Asia; TRUST
Citation
JOURNAL OF THORACIC ONCOLOGY, v.5, no.10, pp.1609 - 1615
Indexed
SCIE
SCOPUS
Journal Title
JOURNAL OF THORACIC ONCOLOGY
Volume
5
Number
10
Start Page
1609
End Page
1615
URI
https://scholarworks.bwise.kr/skku/handle/2021.sw.skku/73176
ISSN
1556-0864
Abstract
Introduction: Erlotinib is an epidermal growth factor receptor tyrosine kinase inhibitor that significantly increases survival for patients with previously treated advanced non-small cell lung cancer. Epidermal growth factor receptor tyrosine kinase inhibitors have been reported to be particularly effective in Asian patients and may have a distinct safety profile in this population compared with non-Asian patients. We report safety and efficacy data from a subpopulation of East/South-East (E/SE) Asian patients enrolled in a global, open-label, phase IV trial of erlotinib (Tarceva Lung Cancer Survival Treatment study). Methods: Patients who had previously failed on chemotherapy or radiotherapy, or were unsuitable for these treatments, were treated with oral erlotinib (150 mg/d) until disease progression or unacceptable toxicity. Results: Best response data were available for 1118 E/SE Asian and 4276 non-E/SE Asian patients. The overall response rates were 27% versus 10%, respectively (p < 0.0001). The disease control rates were 78% versus 66%, respectively (p < 0.0001). Survival data were available for 1242 E/SE Asian and 5338 non-E/SE Asian patients. The median progression-free survival times were 5.78 months versus 2.92 months, respectively (hazard ratio = 0.66, p < 0.0001). The median overall survival times were 14.7 months versus 6.8 months, respectively (hazard ratio = 0.57, p < 0.0001). One-year survival rates were 58.3% and 32.7%, respectively. Safety data were available for 1242 E/SE Asian patients. Seventeen percent of these patients experienced one or more erlotinib-related adverse event (AE) (other than the most frequently occurring AEs prespecified in the protocol) and 2% experienced an erlotinib-related serious AE. Dose reductions were reported for 171 (14%) patients. Conclusion: Erlotinib is an effective and well-tolerated treatment for Asian patients with advanced non-small cell lung cancer.
Files in This Item
There are no files associated with this item.
Appears in
Collections
Medicine > Department of Medicine > 1. Journal Articles

qrcode

Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.

Altmetrics

Total Views & Downloads

BROWSE