TY - JOUR
T1 - Gefitinib is active in patients with brain metastasis from non-small cell lung cancer
AU - Tsai, Chunming
AU - Chiu, Chaohua
AU - Liou, Jialing
AU - Tsai, Peijiun
AU - Perng, Reuryperng
PY - 2004/8
Y1 - 2004/8
N2 - Objective: To explore the efficacy of gefitinib to non-small cell lung cancer (NSCLC) patients irrespective of their performance status, number of prior treatment regimens and the presence of brain metastasis. Methods: A total of 76 patients were enrolled. Results: For all enrolled patients, the disease control rate was 63.2% (95% CI, 52.1%-74.3%) with a median Progression-free survival of 5.0 months (95% CI, 3.5-6.6 months) and median overall survival of 9.9 months (95% CI, 4.9-14.8 months). Fifty-seven patients had measurable lesions and the objective response rate was 33.3% (95% CI, 20.7%-46.0%). Twenty-one patients had simultineously assessable intracranial and extracranial lesions, 17 of them (81.0%) showed comparable tumor response. There was no survival difference between the patients with and without metastatic brain disease. Most drug-related adverse events were mild. Intolerable toxicities happened in 5 patients, 4 of them were interstitial pneumonia (5.8%). Conclusion: Gefitinib is active in patients with brain metastasis from NSCLC. It is feasible to conduct randomized trials to identify the role of gefitinib alone or in combination with other modality in the treatment of NSCLC patients who have metastatic brain lesion(s).
AB - Objective: To explore the efficacy of gefitinib to non-small cell lung cancer (NSCLC) patients irrespective of their performance status, number of prior treatment regimens and the presence of brain metastasis. Methods: A total of 76 patients were enrolled. Results: For all enrolled patients, the disease control rate was 63.2% (95% CI, 52.1%-74.3%) with a median Progression-free survival of 5.0 months (95% CI, 3.5-6.6 months) and median overall survival of 9.9 months (95% CI, 4.9-14.8 months). Fifty-seven patients had measurable lesions and the objective response rate was 33.3% (95% CI, 20.7%-46.0%). Twenty-one patients had simultineously assessable intracranial and extracranial lesions, 17 of them (81.0%) showed comparable tumor response. There was no survival difference between the patients with and without metastatic brain disease. Most drug-related adverse events were mild. Intolerable toxicities happened in 5 patients, 4 of them were interstitial pneumonia (5.8%). Conclusion: Gefitinib is active in patients with brain metastasis from NSCLC. It is feasible to conduct randomized trials to identify the role of gefitinib alone or in combination with other modality in the treatment of NSCLC patients who have metastatic brain lesion(s).
KW - Brain metastasis
KW - Gefitinib
KW - Non-small cell lung cancer
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M3 - Article
AN - SCOPUS:4344595740
SN - 1009-3419
VL - 7
SP - 298
EP - 304
JO - Chinese Journal of Lung Cancer
JF - Chinese Journal of Lung Cancer
IS - 4
ER -