Table 2

Randomized trials comparing ABVD or regimen of equivalent efficacy alone with treatment that includes RT

Accrual yearsProtocolNMedian follow-up, moTreatmentOS, %OS, yrPFFDP/FFTF/EFS, %FFDP/FFTF/EFS, yrP
Tata26  1993-1996  99* 63 ABVD × 6 98 .26 94 .29 
     ABVD × 6 + IFRT 100  97  
CCG28  1995-1998 5942 215 NR COPP-ABV × 4 100 NR 91 NR 
     COPP-ABV × 4 + IFRT 100  97  
MSKCC27  1990-2000  152 67 ABVD × 6 90 .08 81 .61 
     ABVD × 6 + RT 97  86  
NCIC CTG-ECOG 1994-2002 HD.6 399 136 ABVD × 4-6 94 12 .04 87 12 .05 
     EFRT (favorable cohort); ABVD × 2 + EFRT (unfavorable cohort) 87 12  92 12  
Accrual yearsProtocolNMedian follow-up, moTreatmentOS, %OS, yrPFFDP/FFTF/EFS, %FFDP/FFTF/EFS, yrP
Tata26  1993-1996  99* 63 ABVD × 6 98 .26 94 .29 
     ABVD × 6 + IFRT 100  97  
CCG28  1995-1998 5942 215 NR COPP-ABV × 4 100 NR 91 NR 
     COPP-ABV × 4 + IFRT 100  97  
MSKCC27  1990-2000  152 67 ABVD × 6 90 .08 81 .61 
     ABVD × 6 + RT 97  86  
NCIC CTG-ECOG 1994-2002 HD.6 399 136 ABVD × 4-6 94 12 .04 87 12 .05 
     EFRT (favorable cohort); ABVD × 2 + EFRT (unfavorable cohort) 87 12  92 12  

FFDP indicates freedom from disease progression; Tata, Tata Memorial Hospital, Mumbai; CCG, Children's Cancer Group; MSKCC, Memorial-Sloan Kettering Cancer Center; and NR, not reported.

*

Includes stage I or II patients only.

Includes group 1 patients only;

Control therapy.

Close Modal

or Create an Account

Close Modal
Close Modal