Table 6

Results of RCTs comparing FDG-PET scanning to direct therapy

TrialIntervention control participantsOS, %FFTF, %PFS, %EFS, %Late AE, %Response, %Median follow-upReference
EORTC/LYSA/ FIL H10 (favorable) Arm A (control) (n = 223): 3 × ABVD + 30-Gy INRT (FDG-PET completed only for comparison in control arm) Arm B (intervention) (n = 221): 2 × ABVD + FDG-PET If FDG-PET negative: 2 × ABVD and no radiotherapy If FDG-PET positive: 2 × BEACOPP + 30-Gy INRT NR NR *100 vs 94.9 at 1 y NR NR NR 1.1 y 17, 27 
EORTC/LYSA/ FIL H10 (unfavorable) Arm A (control) (n = 346): 4 × ABVD + 30-Gy INRT (FDG-PET completed only for comparison) Arm B (intervention) (n = 347): 2 × ABVD + FDG-PET If FDG-PET negative: 4 × ABVD If FDG-PET positive: 2 × BEACOPP + 30-Gy INRT NR NR *97.3 vs 94.7 at 1y NR NR NR 1.1 y 17, 27 
RAPID 3 × ABVD + FDG-PET If FDG-PET negative: Arm A: IFRT (n = 209) Arm B: no further intervention (n = 211) If FDG-PET positive: 1 × ABVD + IFRT 97 vs 99.5 at 3 y (P values NR) NR *93.8 vs 90.7 at 3 y (risk difference of 2.9%; 95% CI: −10.7 to 1.4 (this exceeds the margin for noninferiority of −7%) NR NR NR 48 mo 18 
TrialIntervention control participantsOS, %FFTF, %PFS, %EFS, %Late AE, %Response, %Median follow-upReference
EORTC/LYSA/ FIL H10 (favorable) Arm A (control) (n = 223): 3 × ABVD + 30-Gy INRT (FDG-PET completed only for comparison in control arm) Arm B (intervention) (n = 221): 2 × ABVD + FDG-PET If FDG-PET negative: 2 × ABVD and no radiotherapy If FDG-PET positive: 2 × BEACOPP + 30-Gy INRT NR NR *100 vs 94.9 at 1 y NR NR NR 1.1 y 17, 27 
EORTC/LYSA/ FIL H10 (unfavorable) Arm A (control) (n = 346): 4 × ABVD + 30-Gy INRT (FDG-PET completed only for comparison) Arm B (intervention) (n = 347): 2 × ABVD + FDG-PET If FDG-PET negative: 4 × ABVD If FDG-PET positive: 2 × BEACOPP + 30-Gy INRT NR NR *97.3 vs 94.7 at 1y NR NR NR 1.1 y 17, 27 
RAPID 3 × ABVD + FDG-PET If FDG-PET negative: Arm A: IFRT (n = 209) Arm B: no further intervention (n = 211) If FDG-PET positive: 1 × ABVD + IFRT 97 vs 99.5 at 3 y (P values NR) NR *93.8 vs 90.7 at 3 y (risk difference of 2.9%; 95% CI: −10.7 to 1.4 (this exceeds the margin for noninferiority of −7%) NR NR NR 48 mo 18 

RAPID, PET Scan in Planning Treatment in Patients Undergoing Combination Chemotherapy For Stage IA or Stage IIA Hodgkin Lymphoma.

*

Primary outcome.

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