Table 2.
Toxicity events |
Pairwise meta-analysis | |||
---|---|---|---|---|
Included studies | Comparisons | Treatment1 | Treatment2 | OR (95%CI) |
Non-hematologic (all grades) | ||||
Rash | ||||
1 study | A vs. B | 43/308 | 43/305 | 0.99 (0.63–1.56) |
1 study | A vs. C | 20/80 | 38/80 | 0.37 (0.19–0.72) |
1 study | A vs. F | 29/280 | 72/282 | 0.34 (0.21–0.54) |
1 study | A vs. G | 15/342 | 18/331 | 0.80 (0.40–1.61) |
Diarrhea | ||||
1 study | A vs. B | 68/308 | 101/305 | 0.57 (0.40–0.82) |
1 study | A vs. C | 22/80 | 43/80 | 0.33 (0.17–0.63) |
1 study | A vs. D | 29/52 | 49/50 | 0.03 (0.00–0.20) |
1 study | A vs. F | 41/280 | 56/282 | 0.69 (0.44–1.08) |
1 study | A vs. G | 25/342 | 37/331 | 0.63 (0.37–1.07) |
Stomatitis | ||||
1 study | A vs. B | 12/308 | 52/305 | 0.20 (0.10–0.38) |
1 study | A vs. C | 22/80 | 43/80 | 0.17 (0.07–0.37) |
1 study | A vs. D | 29/52 | 49/50 | 0.06 (0.02–0.18) |
1 study | A vs. F | 41/280 | 56/282 | 0.59 (0.30–1.18) |
Non-hematologic (grade≥3) | ||||
Rash | ||||
1 study | A vs. B | 3/308 | 3/305 | 0.99 (0.20–4.94) |
1 study | A vs. C | 0/80 | 5/80 | 0.09 (0.00–1.57) |
1 study | A vs. F | 1/280 | 6/282 | 0.16 (0.02–1.38) |
1 study | A vs. G | 1/342 | 2/331 | 0.48 (0.04–5.35) |
Diarrhea | ||||
1 study | A vs. B | 6/308 | 3/305 | 2.00 (0.50–8.07) |
1 study | A vs. C | 1/80 | 6/80 | 0.16 (0.02–1.33) |
1 study | A vs. D | 6/52 | 4/50 | 1.50 (0.40–5.67) |
1 study | A vs. F | 2/280 | 6/282 | 0.33 (0.07–1.65) |
1 study | A vs. G | 3/342 | 4/331 | 0.72 (0.16–3.26) |
Stomatitis | ||||
1 study | A vs. B | 1/308 | 1/305 | 0.99 (0.06–15.90) |
1 study | A vs. C | 0/80 | 2/80 | 0.20 (0.01–4.13) |
1 study | A vs. D | 0/52 | 4/50 | 0.10 (0.01–1.88) |
1 study | A vs. F | 1/280 | 1/282 | 1.01 (0.06–1.18) |
Notes: OR = odds ratio; 95%CI = 95% confidence intervals; A = Gemcitabine+Placebo; B = Gemcitabine+Axitinib; C = Gemcitabine+Trametinib; D = Gemcitabine+Sorafenib; F = Gemcitabine+Erlotinib; G = Gemcitabine+Tipifarnib.