Literature DB >> 9610711

A randomized comparison of the efficacy and toxicity of epirubicin and doxorubicin in the treatment of patients with non-Hodgkin's lymphoma.

R Nair1, G Ramakrishnan, N N Nair, T K Saikia, P M Parikh, S R Joshi, C S Soman, M Mukhadan, K T Dinshaw, S H Advani.   

Abstract

BACKGROUND: Combination chemotherapy consisting of methotrexate, doxorubicin, cyclophosphamide, vincristine, prednisolone, and bleomycin (MACOP-B) has been frequently used for the treatment of non-Hodgkin's lymphoma. This randomized study was undertaken to assess the efficacy and toxicity of this regimen when either doxorubicin or epirubicin was used as the anthracycline drug.
METHODS: Between April 1989 and December 1993, 211 previously untreated patients with intermediate grade and high grade non-Hodgkin's lymphoma were randomized to receive either doxorubicin (n=106) or epirubicin (n=105) with the MACOP-B regimen. These patients were followed through December 1996. Numerous clinical features predictive of response and survival were analyzed. Cardiac and noncardiac toxicity in the two treatment arms were compared.
RESULTS: The median age of the patients was 48 years. Complete remission was experienced by 122 patients (58.3%); 62 patients (58.5%) achieved complete remission in the doxorubicin arm and 60 (58.1%) in the epirubicin arm. Response rates, time to treatment failure, relapse data, and overall survival were comparable between the two arms. Morbidity due to mucositis, vomiting, peripheral neuropathy, and cardiotoxicity were also comparable. The overall mortality was 10%. Mortality due to neutropenic sepsis was considerably higher among patients who received epirubicin (10 patients) than among those who received doxorubicin (5 patients). Cardiac evaluation revealed no difference in toxicity between the two arms.
CONCLUSIONS: Epirubicin was as effective as doxorubicin in terms of patients' responses to therapy. There was no difference in cardiotoxicity between the two treatment arms. However, in this study, the mortality due to neutropenic sepsis was significantly higher among patients treated with epirubicin.

Entities:  

Mesh:

Substances:

Year:  1998        PMID: 9610711     DOI: 10.1002/(sici)1097-0142(19980601)82:11<2282::aid-cncr26>3.0.co;2-p

Source DB:  PubMed          Journal:  Cancer        ISSN: 0008-543X            Impact factor:   6.860


  7 in total

1.  Intensive chemotherapy in the treatment of aggressive diffuse large B-cell lymphoma: malignant lymphoma.

Authors:  Agustin Avilés; M Jesús Nambo; Natividad Neri; Alejandra Talavera; Claudia Castañeda; Edgar Murillo; Sergio Cleto; Judith Huerta-Guzmán
Journal:  Med Oncol       Date:  2004       Impact factor: 3.064

Review 2.  Monitoring chemotherapy-induced cardiotoxicity: role of cardiac nuclear imaging.

Authors:  Gurusher Singh Panjrath; Diwakar Jain
Journal:  J Nucl Cardiol       Date:  2006 May-Jun       Impact factor: 5.952

3.  Addition of rituximab to a CEOP regimen improved the outcome in the treatment of non-germinal center immunophenotype diffuse large B cell lymphoma cells with high Bcl-2 expression.

Authors:  Yan Li; Maimaitili Yimamu; Xiaomin Wang; Xiaoyan Zhang; Min Mao; Ling Fu; Aihemaitijiang Aisimitula; Yuling Nie; Qin Huang
Journal:  Int J Hematol       Date:  2013-11-21       Impact factor: 2.490

Review 4.  Different anthracycline derivates for reducing cardiotoxicity in cancer patients.

Authors:  Elvira C van Dalen; Erna Mc Michiels; Huib N Caron; Leontien Cm Kremer
Journal:  Cochrane Database Syst Rev       Date:  2010-05-12

5.  Phase II study of cyclophosphamide,epirubicin, vincristine, prednisone, and etoposide (CEOP-E) for aggressive non-Hodgkin 's lymphoma.

Authors:  Jong Gwang Kim; Sang Kyun Sohn; Dong Hwan Kim; Jin Ho Baek; Tae In Park; Kyu Bo Lee
Journal:  J Korean Med Sci       Date:  2004-12       Impact factor: 2.153

6.  Identification of potential surrogate end points in randomized clinical trials of aggressive and indolent non-Hodgkin's lymphoma: correlation of complete response, time-to-event and overall survival end points.

Authors:  L Lee; L Wang; M Crump
Journal:  Ann Oncol       Date:  2011-01-25       Impact factor: 32.976

7.  Cardiotoxicity as indicated by LVEF and troponin T sensitivity following two anthracycline-based regimens in lymphoma: Results from a randomized prospective clinical trial.

Authors:  Kai Xue; Juan J Gu; Qunling Zhang; Xiaojian Liu; Jiachen Wang; Xiao-Qiu Li; Jianfeng Luo; Francisco J Hernandez-Ilizaliturri; Stanley F Fernandez; Myron S Czuczman; Junning Cao; Xiaonan Hong; Ye Guo
Journal:  Oncotarget       Date:  2016-05-31
  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.