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      Standard International prognostic index remains a valid predictor of outcome for patients with aggressive CD20+ B-cell lymphoma in the rituximab era.

      Journal of clinical oncology : official journal of the American Society of Clinical Oncology
      Adolescent, Adult, Aged, Aged, 80 and over, Antibodies, Monoclonal, administration & dosage, Antibodies, Monoclonal, Murine-Derived, Antigens, CD20, immunology, Antineoplastic Combined Chemotherapy Protocols, Computer Simulation, Cyclophosphamide, Disease Progression, Disease-Free Survival, Doxorubicin, Female, Health Status Indicators, Humans, Kaplan-Meier Estimate, Lymphoma, B-Cell, diagnosis, drug therapy, mortality, Male, Middle Aged, Predictive Value of Tests, Prednisone, Proportional Hazards Models, Prospective Studies, Risk Assessment, Risk Factors, Time Factors, Treatment Outcome, Vincristine, Young Adult

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          Abstract

          The International Prognostic Index (IPI) is widely used for risk stratification of patients with aggressive B-cell lymphoma. The introduction of rituximab has markedly improved outcome, and R-CHOP (rituximab + cyclophosphamide, doxorubicin, vincristine, prednisone) has become the standard treatment for CD20(+) diffuse large B-cell lymphoma. To investigate whether the IPI has maintained its power for risk stratification when rituximab is combined with CHOP, we analyzed the prognostic relevance of IPI in three prospective clinical trials. In total, 1,062 patients treated with rituximab were included (MabThera International Trial [MInT], 380 patients; dose-escalated regimen of cyclophosphamide, doxorubicin, vincristine, etoposide, and prednisone (MegaCHOEP) trial, 72 patients; CHOP + rituximab for patients older than age 60 years [RICOVER-60] trial, 610 patients). A multivariate proportional hazards modeling was performed for single IPI factors under rituximab on event-free, progression-free, and overall survival. IPI score was significant for all three end points. Rituximab significantly improved treatment outcome within each IPI group resulting in a quenching of the Kaplan-Meier estimators. However, IPI was a significant prognostic factor in all three end points and the ordering of the IPI groups remained valid. The relative risk estimates of single IPI factors and their order in patients treated with R-CHOP were similar to those found with CHOP. The effects of rituximab were superimposed on the effects of CHOP with no interactions between chemotherapy and antibody therapy. These results demonstrate that the IPI is still valid in the R-CHOP era.

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