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. 2010 May 3;1:9–22. doi: 10.2147/lctt.s6075

Table 1.

Phase III randomized trials of platin-based doublets

Reference Patients Treatment RR (%) OS (mo) 1 Year (%) P (OS)
Kelly16 408 VNR/CDDP 28 8.1 36
CBDCA/PAC 25 8.6 38 0.87
Rosell17 618 PAC/CDDP 28 9.8 38
PAC/CBDCA 25 8.2 33 0.019
Scagliotti18 612 GEM/CDDP 30 9.8 37
CBDCA/PAC 32 9.9 43 0.484a
VNR/CDDP 30 9.5 37 0.105a
Ohe19 602 CDDP/CPT-11 31 13.9 59.2
CBDCA/PAC 32.4 12.3 51 0.465
CDDP/GEM 30.1 14 59.6 0.949
CDDP/VNR 33.1 11.4 48.3 0.242
Schiller15 1207 PAC/CDDP 21 7.8 31
GEM/CDDP 22 8.1 36 NSb
DOC/CDDP 17 7.4 31 NS
CBDCA/PAC 17 8.1 34 NS
Fossella4 1218 VNR/CDDP 24.5 10.1 41
DOC/CDDP 31.6 11.3 46 0.044
VNR/CDDP 24.5 9.9 40
DOC/CBDCA 23.9 9.4 38 0.657

Notes: If more than two regimens were compared in one study, the topmost regimen was the reference regimen and P value is based on comparison to the reference regimen.

a

P value for 1-year survival rate.

b

P value was not reported.

Abbreviations: RR, response rate; OS, overall survival; 1 Yr, one-year survival; VNR, vinorelbine; CDDP, cisplatin; CBDCA, carboplatin; PAC, paclitaxel; GEM, gemcitabine; CPT-11, irinotecan; DOC, docetaxel; NS, not significant.