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Extensive
experience of disease control with gefitinib and the role of prognostic markers
H
Cortes-Funes1 and H Soto Parra2
1Medical
Oncology Service, Hospital Universitario 12 de Octubre, Avda Córdoba Km 5,4,
Madrid 28041, Spain; 2Istituto
Clinico Humanitas, Rozzano 20089, Italy. Correspondence to: H Cortes-Funes, E-mail: hcortes.hdoc@salud.madrid.org.
Traditionally, the
efficacy of an anticancer agent has been measured by response rate.
With the development of biological molecular-targeted agents, which have a
different mechanism of action from conventional agents, it may be appropriate to
consider alternative criteria that reflect the positive effect of these
biological agents on disease control, palliation, symptom improvement and
quality of life.
One such targeted agent is the orally active epidermal growth factor receptor
tyrosine kinase inhibitor gefitinib ('Iressa', ZD1839).
This article reviews the clinical experience of patients with advanced/metastatic non-small-cell lung
cancer, who have received gefitinib as part of a clinical trial or through the
'Iressa' Expanded Access Programme.
Disease-control rates of ~50% were observed in some Expanded
Access Programme series, comparable with results obtained from Phase II
trials.
Symptom improvement was also reported.
Information that will help identify those patients most likely to respond to
treatment will become increasingly important.
Therefore, the possible role of prognostic markers and the relationship between
epidermal growth factor receptor status and response to gefitinib has been
investigated.
No clear association between epidermal growth factor receptor expression and
response was observed.
Future studies of other biomarkers in the epidermal growth factor receptor
pathway should help to identify which patients are likely to benefit most from
gefitinib.
Keywords: gefitinib ('Iressa',
ZD1839); EGFR; clinical benefit; disease control; prognostic marker
doi:10.1038/sj.bjc.6601476
© 2003 Cancer Research UK
Source: http://www.nature.com/cgi-taf/DynaPage.taf?file=/bjc/journal/v89/n2s/abs/6601476a.html
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