This is a multi-center phase III randomized controlled study to assess the efficacy of Gefitinib alone and Gefitinib combination with Pemetrexed/platinum on patients with brain metastasis from non-small cell lung cancer(NSCLC) harboring EGFR mutation type by intracranial PFS(iPFS),also PFS ,DCR and OS.The side effect is evaluated as well.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
160
Gefitinib 250mg is Taken Orally on day 1-28,combined Pemetrexed (D1)+cisplatin (D1-3) or Pemetrexed (D1) + nedaplatin (D1) chemotherapy, every 28 days
Gefitinib 250mg is Taken Orally everyday
Sun Yat-sen University of Cancer Center
Guangzhou, Guangdong, China
RECRUITINGiPFS(intracranial progression free survival
defined as time from randomization to intracranial progressive disease or death.
Time frame: 2 years
ORR
proportion of patients with complete or partial response of overall lesions
Time frame: 2 years
intracranial objective response rate (iORR)
proportion of patients with complete or partial response of intracranial lesions
Time frame: 2 years
PFS(Progression Free Survival)
time from randomization to overall disease progression or death
Time frame: 2 years
OS(Overall Survival)
time from randomization to death from any cause
Time frame: 3 years
adverse events
adverse events were evaluated according to NCI-CTCAE 4.0.
Time frame: 3 years
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