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. 2007 Mar 20;96(8):1170–1177. doi: 10.1038/sj.bjc.6603686

Table 1. Details of the randomized controlled trials included in the individual patient data meta-analysis.

Category JFMC7-1 JFMC15-1 JFMC15-2 TAC-CR NSAS-CC Total
Additional chemotherapy Mitomycin C Mitomycin C+FU IV Mitomycin C+FU IV None None
Radiotherapy None None None None None
UFT dose/day 400 mg 400 mg 400 mg 400 mg 600 mga
 Period 12 months 12 months 12 months 24 months 12 months
Dates of accrual 1986–1988 1989 1990 1991–1994 1996–2001
No. of patients 834 447 391 143 276
Duration of accrual, months 35 24 24 36 54
             
Sex, No. of patients (male–female ratio)
 Male 521 (62.4%) 260 (58.1%) 244 (62.4%) 93 (65.0%) 167 (60.5%) 1285 (61.4%)
 Female 313 (37.6%) 187 (41.9%) 147 (37.6%) 50 (35.0%) 109 (39.5%) 806 (38.9%)
             
Duke's stage, No. of patients
 A 135 67 62 12 0 276
 B 326 175 139 53 0 693
 C 373 205 189 78 276 1121
             
Median age 57 60 59 62 58 58
Upper age limit, years 70 75 75 75 75

JFMC=Japanese Foundation for Multidisciplinary Treatment of Cancer; NSAS-CC=National Surgical Adjuvant Study of Colorectal Cancer; TAC–CR=Tokai Adjuvant Chemotherapy for Colorectal Cancer; UFT=Uracil–Tegafur.

a

400 mg m−2 day−1 for 5 days every 7 days.