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CHOEP versus Alternating hCHOP/IVEP for High Grade Non-Hodgkin’s Lymphomas: A Randomized Multicentre Trial

 

作者: H. Köppler,   K.H. Pflüger,   I. Eschenbach,   R. Pfab,   J. Birkmann,   W. Zeller,   E.U. Steinhauer,   C. Gropp,   S. Oehl,   E. Lötzke,   H. Kuhn,   P. Drings,   H.H. Großmann,   K. Lennert,   H. Stein,   M. Khoury,   W. Heinzelmann,   K. Havemann,  

 

期刊: Onkologie  (Karger Available online 1991)
卷期: Volume 14, issue 2  

页码: 181-184

 

ISSN:0378-584X

 

年代: 1991

 

DOI:10.1159/000216968

 

出版商: S. Karger GmbH

 

关键词: High grade non-Hodgkin’s lymphoma;Combination drug therapy;Radiotherapy;Multicentre randomized trial

 

数据来源: Karger

 

摘要:

185 patients with high grade non-Hodgkin’s lymphoma stages II-IV entered this multicentre trial and were randomized to receive either four cycles of CHOEP (cyclophosphamide 750mg/m2 i.v. d 1, dox-orubicin 50 mg/m2 i.v. d 1, vincristine 2 mg i.v. d 1, etoposide 100 mg/ m2 i.v. d 3–5, prednisolone 100 mg p.o. d 1–5) (treatment arm A), or four cycles of chemotherapy with hCHOP (cyclophosphamide 1,200 mg/m2 i.v. d 1, doxorubicin 40 mg/m2 i.v. d 1 + 2, vincristine 2mg i.v. d 1, prednisolone 100 mg p.o. d 1–5) alternating with IVEP (ifosfamide 1,500 mg/m2 i.v. d 1–5, vindesine 3 mg/m2 i.v. d 1, etoposide 120mg/m2 70 years after hCHOP. Main side effects were mild nausea/vomiting, leukopenia and fever/infection associated with leukopenia. In conclusion, both treatment modalities produced high complete remission rates. A longer follow-up will be needed to exclude differences in overall and diseas

 

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