Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer · 2009
Efficacy of erlotinib for brain and leptomeningeal metastases in patients with lung adenocarcinoma who showed initial good response to gefitinib.
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Katayama Tatsuya, Shimizu Junichi, Suda Kenichi, Onozato Ryoichi, Fukui Takayuki, Ito Simon, Hatooka Shunzo, Sueda Taijiro, Hida Toyoaki, Yatabe Yasushi, Mitsudomi Tetsuya
Аннотация
INTRODUCTION: The efficacy of high-dose (1250 mg/d) gefitinib for the treatment of leptomeningeal metastasis in a patient with lung cancer harboring a mutation in the epidermal growth factor receptor (EGFR) gene was previously reported. We speculate that erlotinib, instead of high dose of gefitinib, may be also effective for the treatment of central nervous system (CNS) lesions, as trough serum concentration of erlotinib is nine times higher than that of gefitinib.
PATIENTS AND METHODS: Patients with lung cancer in whom CNS lesions developed after an initial good response to gefitinib for extra CNS lesions were enrolled in the study. Tumor response, performance status, neurologic symptoms, and survival were retrospectively evaluated.
RESULTS: All seven patients had EGFR mutations in their primary tumors except one patient. The median interval between gefitinib withdrawal and erlotinib administration was 5 days. Three patients showed partial response, three had stable disease, and one had progressive disease. Performance status and symptoms improved in five patients. The overall survival from the initiation of erlotinib treatment ranged from 15 to 530 days (median, 88 days).
CONCLUSIONS: Erlotinib was a reasonable option for the treatment of CNS diseases that appeared after a good initial response of extra CNS disease to gefitinib.
PATIENTS AND METHODS: Patients with lung cancer in whom CNS lesions developed after an initial good response to gefitinib for extra CNS lesions were enrolled in the study. Tumor response, performance status, neurologic symptoms, and survival were retrospectively evaluated.
RESULTS: All seven patients had EGFR mutations in their primary tumors except one patient. The median interval between gefitinib withdrawal and erlotinib administration was 5 days. Three patients showed partial response, three had stable disease, and one had progressive disease. Performance status and symptoms improved in five patients. The overall survival from the initiation of erlotinib treatment ranged from 15 to 530 days (median, 88 days).
CONCLUSIONS: Erlotinib was a reasonable option for the treatment of CNS diseases that appeared after a good initial response of extra CNS disease to gefitinib.
Предметные рубрики MeSH
AdenocarcinomaAgedAged, 80 and overAntineoplastic AgentsBiomarkers, TumorBrain NeoplasmsDNA, NeoplasmErbB ReceptorsErlotinib HydrochlorideFemaleFollow-Up StudiesGefitinibHumansLung NeoplasmsMaleMeningeal NeoplasmsMiddle AgedMutationProtein Kinase InhibitorsQuinazolinesRetrospective StudiesSpinal Cord NeoplasmsTreatment Outcome