Study (reference) | RR(n/N) | OS (HR, 95% CI) | Toxicity |
---|---|---|---|
Goekkurt 2006 [11] | CC: 10/28; CT+TT: 3/22 | NR | NR |
Ruzzo 2006 [14] | CC: 13/34; CT+TT: 57/141 | NR | NR |
Lu 2004 [25] | CC: 2/24; CT+TT: 20/51 | NR | Nausea/vomiting: P=0.002 |
Shitara 2010 [27] | NR | TT/(CT+CC): 0.57 (0.33, 0.97) | NSS |
Huang 2009 [28] | NR | TT/(CT+CC): 0.595 (0.349, 1.012) | NR |
Goekkurt 2009 [31] | CC: 18/59; CT+TT: 34/75 | NR | NSS |
Ott 2006 [32] | CC: 16/50; CT+TT: 17/85 | CT/CC: 1.8 (1.13, 2.88); TT/CC: 0.93 (0.54, 1.62) | NR |
Ott 2011 [33] | NR | CT/CC: 0.8 (0.50, 1.36); TT/CC: 0.5 (0.18, 1.49) | NR |
Lee 2005 [34] | NR | CT/CC: 0.91 (0.58, 1.43); TT/CC: 1.16 (0.65, 2.08) | NR |
Combined analysis (OR/HR, 95CI %) | OR: (CT+TT)/CC | CT/CC (total): 1.10 (0.67, 1.79); | ___ |
Total: 1.12 (0.49, 2.55); RECIST subgroup: 0.28 (0.07, 1.20); | CT/CC (Asian subgroup): 0.91 (0.58, 1.43); | Â | |
WHO subgroup: 7.1 (1.5, 33.53); | CT/CC (European subgroup): 1.21 (0.54, 2.67); | Â | |
Others subgroup: 1.05 (0.51, 2.16); | CT/CC (Palliative subgroup): 0.91 (0.58, 1.43); | Â | |
Asian subgroup: 7.1 (1.5, 33.53); | CT/CC (Neoadjuvant subgroup): 1.21 (0.54, 2.67) TT/CC (total): 0.94 (0.65, 1.37); | Â | |
European subgroup: 0.85 (0.41, 1.77) | TT/CC (Asian subgroup): 1.16 (0.65, 2.08); | Â | |
Palliative subgroup: 1.40 (0.55, 3.60); | TT/CC (European subgroup): 0.81 (0.50, 1.33); | Â | |
Neoadjuvant subgroup: 1.12 (0.49, 2.55) | TT/CC (Palliative subgroup): 1.16 (0.65, 2.08); | Â | |
 | TT/CC (Neoadjuvant subgroup): 0.81 (0.50, 1.33) |  |