My NCBISign In

Display Settings:

Format

Send to:

Choose Destination

    J Hematol Oncol. 2009 Mar 24;2:14.

    R-CHOP versus R-CVP in the treatment of follicular lymphoma: a meta-analysis and critical appraisal of current literature.

    Siddhartha G, Vijay P.

    Division of Hematology/Oncology, Department of Medicine, University of Kansas Medical Center, Kansas City, Kansas, USA. sganguly@kumc.edu

    PURPOSE: R-CHOP (rituximab with cyclophosphamide, doxorubicin, vincristine and prednisone) and R-CVP (rituximab with cyclophosphamide, vincristine and prednisone) have both been used successfully in the treatment of patients with symptomatic follicular lymphoma (FL). No study has compared the efficacy of the two treatment modalities and attempted to evaluate the role of anthracyclines in the management of patients with FL. We conducted a meta-analysis of relevant literature comparing the two treatment arms for FL with response being the final endpoint. PATIENTS AND METHODS: TWO ANALYSES WERE CONDUCTED: The first analysis compared R-CHOP to R-CVP as frontline agents for the treatment of FL, and the second analysis included both untreated and relapsed patients. RESULTS: For both studies, R-CVP was superior to R-CHOP when evaluating for complete response (CR). Odds ratios were 2.86 (95% CI, 1.81-4.51) in the first analysis and 1.48 (95% CI, 0.991-2.22) in the second analysis. However for overall response (CR+Partial response, PR), R-CHOP was superior, with odds ratios of 5.45 (95% CI: 2.51 - 11.83) and 5.54 (95% CI: 2.69 - 11.40), for the first and second analyses, respectively. CONCLUSION: R-CHOP and R-CVP protocols achieve excellent overall response. In patients with known cardiac history, omission of anthracyclines is reasonable and R-CVP provides a competitive CR rate. In younger patients with FL where cumulative cardio-toxicity may be of importance in the long term and in whom future stem cell transplantation is an option, again R-CVP may be a more appealing option.

    PMID: 19309523 [PubMed - in process]

    PMCID: PMC2669150

    Supplemental Content

    Click here to read Click here to read
    Write to the Help Desk