1.1 D(M)FS increment ‐ nearest to 3 years (25 trials) |
25 |
8479 |
Prevented Fraction (IV, Random, 95% CI) |
0.28 [0.19, 0.36] |
1.1.1 Placebo control |
15 |
5671 |
Prevented Fraction (IV, Random, 95% CI) |
0.21 [0.15, 0.28] |
1.1.2 No‐treatment control |
10 |
2808 |
Prevented Fraction (IV, Random, 95% CI) |
0.38 [0.24, 0.52] |
1.2 D(M)FT increment ‐ nearest to 3 years (10 trials) |
10 |
3198 |
Prevented Fraction (IV, Random, 95% CI) |
0.32 [0.19, 0.46] |
1.2.1 Placebo control |
4 |
1525 |
Prevented Fraction (IV, Random, 95% CI) |
0.18 [0.09, 0.27] |
1.2.2 No‐treatment control |
6 |
1673 |
Prevented Fraction (IV, Random, 95% CI) |
0.43 [0.29, 0.57] |
1.3 d(e/m)fs increment ‐ nearest to 3 years (3 trials) |
3 |
1254 |
Prevented fraction (IV, Random, 95% CI) |
0.20 [0.01, 0.38] |
1.3.1 Placebo control |
3 |
1254 |
Prevented fraction (IV, Random, 95% CI) |
0.20 [0.01, 0.38] |
1.3.2 No‐treatment control |
0 |
0 |
Prevented fraction (IV, Random, 95% CI) |
Not estimable |
1.4 Signs of acute toxicity ‐ nausea, vomiting (2 trials) |
2 |
490 |
Risk Difference (M‐H, Random, 95% CI) |
0.01 [‐0.01, 0.02] |
1.5 Dropouts or withdrawals |
19 |
8695 |
Risk Ratio (M‐H, Random, 95% CI) |
1.03 [0.89, 1.19] |
1.5.1 Placebo control |
11 |
6067 |
Risk Ratio (M‐H, Random, 95% CI) |
1.05 [0.91, 1.22] |
1.5.2 No‐treatment control |
8 |
2628 |
Risk Ratio (M‐H, Random, 95% CI) |
1.03 [0.73, 1.47] |