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. 2017 Oct 10;1(22):1945–1958. doi: 10.1182/bloodadvances.2017008748

Table 1.

Pediatric HL trials

Reference Trial acronym Stage Risk Treatment EFS OS
Survival % Survival %
94 CCG-P9426 I, IIA, IIIA ABVE × 4 + IFRT 8-y 86 8-y 97
23 GPOH-HD-2002 I, IIA (treatment group 1) OEPA × 2 (M); OPPA × 2 (F) 3-y 90 3-y 97.9
IIB, IIE, IIIA (treatment group 2) OEPA × 2, COPDAC × 2 (M); OPPA × 2, COPP × 2 (F) 3-y 91.1 (M); 87.7 (F)
IIBE, IIIBE, IIIB, IV (treatment group 3) OEPA × 2, COPDAC × 4 (M); OPPA × 2, COPP × 4 (F)
95 CCG 5942 IA, IB, IIA Low COPP/ABV × 4 ± IFRT 10-y 83.5 92.5
96 IA, IB, IIA (with adverse features), IIB, III Intermediate COPP/ABV × 6 10-y (IFRT) 91.2 97.1
IV High COPP/ABV, CHOP, etoposide/cytarabine × 2 10-y (no IFRT) 82.9 95.9
97 COG-AHOD0431 IA, IIA (no bulk) AVPC × 3 ± IFRT 4-y 79 4-y 99.6
98 Stanford, Dana-Farber, and St. Jude Consortium IA, IIA (no bulk) VAMP × 4 ± IFRT 2-y 90.8 2-y 100
22 P9425 IB, IIA/IIIA1 (with large mediastinal adenopathy) or IIIA2 Intermediate ABVE-PC × 3 5-y 84 5-y 95
IIB, IIIB, IV High RER: IFRT SER: ABVE-PC × 2 + IFRT
24 COG-59704 IIB/IIIB (with bulk), IV High BEACOPP × 4; RER (F): COPP/ABV × 4; RER (M): ABVD × 2 + IFRT; SER: BEACOPP × 4 + IFRT 5-y 93 5-y 97
25 COG-AHOD0031 IB, IA/IIA (with bulk), IIB, IIIA, IVA ABVE-PC × 2 RER: ABVE × 2 ± IFRT; SER: ABVE-PC × 2 ± DECA × 2 + IFRT 4-y All 85 RER 86.9 SER 77.4 4-y All 97.8 RER 98.5 SER 95.3
24 AHOD0831 IIIB, IVB Very high ABVE-PC × 2 RER: ABVE-PC × 2 + RT (bulk only) SER: ABVE-PC × 2 + ifosfamide/vinorelbine + ABVE-PC × 2 + RT (bulk and PET2-positive sites) 4-y 80.2 4-y 95.9

ABV, doxorubicin, bleomycin, and vinblastine; CCG, Children’s Oncology Group; CHOP, cyclophosphamide, doxorubicin, vincristine, and prednisone; COPDAC, cyclophosphamide, vincristine, prednisone, and dacarbazine; COPP, cyclophosphamide, vincristine, procarbazine, and prednisone; F, female; GPOH, German Society of Pediatric Oncology and Hematology; M, male; RER, rapid early responder; SER, slow early responder.