Abstract

Abstract 1641 Background:The World Health Organization (WHO) classification allocates indolent follicular lymphoma to grades 1, 2 or 3A according to the proportions of small centrocytes and large centroblasts in the neoplastic follicles. The prognostic value of the WHO's grading system in indolent follicular lymphoma has not been investigated in patients given the anti-CD20 monoclonal antibody rituximab without chemotherapy. Methods:We prospectively reviewed the follicular lymphoma grades in 276 grade 1–3A patients who received upfront rituximab without chemotherapy in two randomized trials. Flow cytometry analyses of malignant and nonmalignant lymphocyte subsets in lymph nodes and blood were also assessed. Results:In these patients given upfront rituximab-containing therapy, increasing grades of 1, 2, and 3A correlated with longer time to treatment-failure (P =0.002) and overall survival (P =0.045), independently of clinical factors (including the follicular lymphoma international prognostic index). The grades' impact was also independent of the levels of CD3+, CD4+, and CD8+ T cells in lymph nodes and in blood. Conclusion:Increasing grades of indolent follicular lymphoma correlate with better outcome in patients treated upfront with rituximab without chemotherapy, independently of clinical and immunologic factors. This suggests that treatment with rituximab acts differentially in tumors depending on the centrocyte/centroblast ratio.Table 1Independent prognostic factors for time to treatment-failureCategoryTime to treatment-failureHR95% CIPB symptoms1.71.2 to 2.40.005Elevated lactate dehydrogenase1.81.2 to 2.80.0003World Health Organization grades0.002Grade 11Grade 20.710.51 to 0.99Grade 3A0.180.05 to 0.76Abbreviations: HR, hazard ratio and CI, confidence interval. The number of observations was 276. [Display omitted] Disclosures:No relevant conflicts of interest to declare.

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