Volume 130, Issue 4 pp. 536-541

Comparison of CHOP versus CIOP in good prognosis younger patients with histologically aggressive non-Hodgkin lymphoma

C. Burton

C. Burton

Lymphoma Trials Office, University College London and CRUK Clinical Trials Centre, London

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P. Smith

P. Smith

Lymphoma Trials Office, University College London and CRUK Clinical Trials Centre, London

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G. Vaughan-Hudson

G. Vaughan-Hudson

Lymphoma Trials Office, University College London and CRUK Clinical Trials Centre, London

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W. Qian

W. Qian

Department of Statistics, MRC Clinical Trials Centre, London

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P. Hoskin

P. Hoskin

Mount Vernon Centre for Cancer Treatment, Mount Vernon Hospital, Northwood

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D. Cunningham

D. Cunningham

Department of Oncology, Royal Marsden Hospital, Sutton

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B. Hancock

B. Hancock

Department of Oncology, Weston Park Hospital, Sheffield

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D. Linch

D. Linch

Lymphoma Trials Office, University College London and CRUK Clinical Trials Centre, London

Department of Haematology, University College London, London, UK

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First published: 20 July 2005
Citations: 15
David Linch, Department of Haematology, University College London, 98 Chenies Mews, London WC1E 8HX, UK.
E-mail: [email protected]

Summary

CHOP (cyclophosphamide, doxorubicin, vincristine and prednisolone) has been the standard chemotherapy regimen used for diffuse large cell lymphomas for over 30 years. Idarubicin is a 4-demethoxy-anthracycline analogue of daunorubicin that has proven activity in non-Hodgkin lymphoma, and has been reported to cause less cardiotoxicity. We therefore initiated a randomised trial of standard dose CHOP versus CIOP (cyclophosphamide, idarubicin, vincristine and prednisolone), in which doxorubicin 50 mg/m2 was substituted by idarubicin 10 mg/m2, a dose thought to have equivalent anti-lymphoma activity. This trial was closed prematurely after 211 patients had completed therapy when a lower complete remission (CR) rate was noted in the CIOP arm. The formal results with long-term follow up are now reported. Overall response rate was 84% in the CHOP arm and 78% in the CIOP arm, CR rates were 70% and 52% respectively in all patients (P = 0·013) and 73% and 52% respectively for the eligible patients (P = 0·0084). At a median of 8 years follow-up, 4-year progression-free survival for all patients was 56% in the CHOP arm and 40% in the CIOP arm (P = 0·0096). Overall survival for all patients was 65% in the CHOP arm and 56% in the CIOP arm (P = 0·14). Results for eligible patients were comparable. CIOP containing idarubicin at a dose of 10 mg/m2 is clearly inferior to standard CHOP.

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