Literature DB >> 17600466

Rituximab and escalated chemotherapy in elderly patients with aggressive diffuse large-cell lymphoma: a controlled clinical trial.

Agustin Avilés1, María Jesus Nambo, Claudia Castañeda, Sergio Cleto, Natividad Neri, Edgar Murillo, Judith Huerta-Guzmán, Margarita Contreras.   

Abstract

The treatment of elderly patients with aggressive malignant lymphoma has not been defined. The addition of rituximab to conventional chemotherapy has been reported to improve the outcome, but most patients have good prognostic factors (performance status < 2, no severe associated diseases, low or low-intermediate clinical risk). Thus, we developed a combined regimen, including escalated doses of anthracycline and rituximab. The endpoint was to improve event-free survival (EFS) and overall survival. Two hundred and four (204) patients were randomly assigned to receive an escalated chemotherapy regimen (CEOP) with escalated dose of epirubicin, compared to the same regimen and addition of rituximab. All patients had poor prognostic factors: high- or high-intermediate clinical risk, poor performance status, bulky disease, and more than 2 with extranodal involvement. In an intent-to-treat analysis, all patients were evaluable for efficacy and toxicity. The complete response rates were similar in both arms: 74% in chemotherapy and 78% in the rituximab + chemotherapy program. EFS and overall survival were similar: 77% and 84%, respectively, in combined chemotherapy and 75% and 81% in the rituximab-chemotherapy regimen. Toxicity was mild and well tolerated. In elderly patients with diffuse large-cell lymphoma and poor prognostic factors, rituximab did not improve their outcome.

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Year:  2007        PMID: 17600466     DOI: 10.1089/cbr.2006.360

Source DB:  PubMed          Journal:  Cancer Biother Radiopharm        ISSN: 1084-9785            Impact factor:   3.099


  6 in total

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Review 2.  NHL (diffuse large B-cell lymphoma).

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Journal:  Cochrane Database Syst Rev       Date:  2011-02-16

Review 4.  Meta-analysis of cardiovascular toxicity risks in cancer patients on selected targeted agents.

Authors:  C P Escalante; Y C Chang; K Liao; T Rouleau; J Halm; P Bossi; S Bhadriraju; N Brito-Dellan; S Sahai; S W Yusuf; A Zalpour; L S Elting
Journal:  Support Care Cancer       Date:  2016-06-25       Impact factor: 3.603

Review 5.  Risk of oral and gastrointestinal mucosal injury among patients receiving selected targeted agents: a meta-analysis.

Authors:  Linda S Elting; Yu-Chia Chang; Pratibha Parelkar; Christine B Boers-Doets; Marisol Michelet; Guido Hita; Tanya Rouleau; Catherine Cooksley; Josiah Halm; Madhuri Vithala; Paolo Bossi; Carmen Escalante; Michael T Brennan
Journal:  Support Care Cancer       Date:  2013-05-02       Impact factor: 3.603

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

  6 in total

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