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Intensified 12-week CHOP (I-CHOP) plus G-CSF compared with standard 24-week CHOP (CHOP-21) for patients with intermediate-risk aggressive non-Hodgkin lymphoma: a phase 3 trial of the Dutch-Belgian Hemato-Oncology Cooperative Group (HOVON).

Abstract
Optimal dose and timing of CHOP (cyclophosphamide, doxorubicin, vincristine, and prednisone) chemotherapy for aggressive non-Hodgkin lymphoma (NHL) is still an unresolved issue. We assessed whether dose intensifications with cyclophosphamide and doxorubicin might improve outcome in younger patients with intermediate-risk aggressive NHL. Previously untreated patients were assigned to receive either 8 courses of standard CHOP (n = 239) or 6 courses of intensified (I)-CHOP (n = 238). Although there was a tendency in favor of I-CHOP for overall survival (OS), disease-free survival (DFS), and event-free survival (EFS), the differences were not significant. However, although these analyses were not planned, when the intermediate-risk group was divided into low-intermediate- and high-intermediate-risk patients according to the International Prognostic Index (IPI), low-intermediate-risk patients had improved 6-year OS (67% vs 52%; P = .05), DFS (58% vs 45%; P = .06), and EFS (41% vs 30%; P = .21) when they were treated with I-CHOP compared with standard CHOP. On the other hand, high-intermediate-risk patients seem to have no benefit from I-CHOP. Although clinically relevant side effects occurred more often in the I-CHOP arm, treatment-related mortality was similar. These data suggest that I-CHOP might be preferable to standard CHOP in younger patients with low-intermediate-risk aggressive NHL.
AuthorsLeo F Verdonck, Annelise Notenboom, Daphne D de Jong, Marius A MacKenzie, Gregor E G Verhoef, Mark H H Kramer, Gert J Ossenkoppele, Jeanette K Doorduijn, Pieter Sonneveld, Gustaaf W van Imhoff
JournalBlood (Blood) Vol. 109 Issue 7 Pg. 2759-66 (Apr 01 2007) ISSN: 0006-4971 [Print] United States
PMID17132720 (Publication Type: Clinical Trial, Phase III, Comparative Study, Journal Article, Multicenter Study, Randomized Controlled Trial)
Chemical References
  • Recombinant Proteins
  • Granulocyte Colony-Stimulating Factor
  • Vincristine
  • Doxorubicin
  • Cyclophosphamide
  • Prednisone
Topics
  • Adolescent
  • Adult
  • Antineoplastic Combined Chemotherapy Protocols (administration & dosage, adverse effects)
  • Belgium
  • Child
  • Cyclophosphamide (administration & dosage, adverse effects)
  • Disease-Free Survival
  • Doxorubicin (administration & dosage, adverse effects)
  • Drug Administration Schedule
  • Female
  • Granulocyte Colony-Stimulating Factor (administration & dosage, adverse effects)
  • Humans
  • Lymphoma, Non-Hodgkin (drug therapy)
  • Male
  • Middle Aged
  • Netherlands
  • Prednisone (administration & dosage, adverse effects)
  • Prognosis
  • Recombinant Proteins
  • Risk Factors
  • Vincristine (administration & dosage, adverse effects)

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