Significantly, PFS improvement in doublets in EGFR wild-type ( p < 0.0001), KRAS mutant ( p < 0.00001), KRAS wild-type ( p = 0.03) was observed; While, PFS in EGFR -mutant patients showed a trend in favor of single-agent erlotinib (HR 1.09, 95%CI 0.63-1.88).
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Erlotinib-based doublet targeted therapy versus erlotinib alone in previously treated advanced non-small-cell lung cancer: a meta-analysis from 24 randomized controlled trials.
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