Abstract:P=0.005) was significantly associated with the higher response rate to gefitinib. Progression-free survival (6.6 vs. 3.3 months; p=0.246) and overall survival (8.1 vs. 8.6 months; p=0.397) were similar between patients with EGFR mutations and those with wild-type EGFR. Conclusion: Clinical response to gefitinib in this study was linked to the presence of EGFR mutations. Given the limitation of small sample size, EGFR mutations were not associated with the specific clinical predictors for gefitinib responsive… Show more
“…b One study 25 was excluded because it did not have detail information about performance status. c Seven studies 10,11,14,15,19,26,28 were excluded because they contained both chemotherapy-naïve patients and chemotherapy-received patients.…”
We found a significant relationship between RR and MST in clinical trials with EGFR-TKIs. RR could be an independent surrogate marker for MST in the current response criteria in the clinical trials of EGFR-TKIs.
“…b One study 25 was excluded because it did not have detail information about performance status. c Seven studies 10,11,14,15,19,26,28 were excluded because they contained both chemotherapy-naïve patients and chemotherapy-received patients.…”
We found a significant relationship between RR and MST in clinical trials with EGFR-TKIs. RR could be an independent surrogate marker for MST in the current response criteria in the clinical trials of EGFR-TKIs.
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