Table I.
A, Unmatched dataset | |||
---|---|---|---|
Characteristics | Chemotherapy-bevacizumab (n=43) | Chemotherapy alone (n=122) | P-value |
Age, years | 0.844 | ||
Median (range) | 52 (37–72) | 56 (27–76) | |
≤60 | 32 | 88 | |
>60 | 11 | 34 | |
Sex, n | 0.287 | ||
Male | 19 | 67 | |
Female | 24 | 55 | |
Smoking history, n | 0.583 | ||
Current/previous | 14 | 47 | |
Never | 29 | 75 | |
Histology, n | 0.800 | ||
Adenocarcinoma | 38 | 105 | |
Squamous cell/adenosquamous carcinoma | 5 | 17 | |
EGFR mutation status | 0.716 | ||
Mutant typea | 17 | 44 | |
Wild-type/unknown | 26 | 78 | |
Number of prior regimensb, n | 0.009 | ||
Median (range) | 3 (2–5) | 2 (2–5) | |
≤3 | 28 | 103 | |
>3 | 15 | 19 | |
Chemotherapy regimen, n | <0.0001 | ||
Gemcitabine | 30 | 39 | |
Pemetrexed | 5 | 31 | |
Paclitaxel | 3 | 8 | |
Docetaxel | 5 | 44 | |
B, Matched (1:1) dataset | |||
Characteristics | Chemotherapy-bevacizumab (n=38) | Chemotherapy alone (n=38) | P-value |
Age, years | 1.000 | ||
Median (range) | 52 (40–71) | 49 (38–76) | |
≤60 | 30 | 31 | |
>60 | 8 | ||
Sex | 0.492 | ||
Male | 17 | 21 | |
Female | 21 | 17 | |
Smoking history, n | 0.240 | ||
Current/previous | 26 | 20 | |
Never | 12 | 18 | |
Histology, n | 1.000 | ||
Adenocarcinoma | 34 | 35 | |
Squamous cell/ | 4 | 3 | |
adenosquamous carcinoma | |||
EGFR mutation status | 0.641 | ||
Mutant typea | 17 | 14 | |
Wild-type/unknown | 21 | 24 | |
Number of prior regimensb, n | 1.000 | ||
Median (range) | 3 (2–5) | 3 (2–4) | |
≤3 | 28 | 28 | |
>3 | 10 | 10 | |
Chemotherapy regimen, n | 1.000 | ||
Gemcitabine | 25 | 25 | |
Pemetrexed | 5 | 5 | |
Paclitaxel | 3 | 3 | |
Docetaxel | 5 | 5 |
EGFR, epidermal growth factor receptor.
Mutant type included the exon 19 deletion and exon 21 L858R mutations.
Prior regimens included chemotherapy, EGFR tyrosine kinase inhibitors and anaplastic lymphoma kinase inhibitors.