4.7 Article

Identification of prognostic factors in 61 patients with posttransplantation lymphoproliferative disorders

Journal

JOURNAL OF CLINICAL ONCOLOGY
Volume 19, Issue 3, Pages 772-778

Publisher

AMER SOC CLINICAL ONCOLOGY
DOI: 10.1200/JCO.2001.19.3.772

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Purpose: Prognostic studies of posttransplantation lymphoproliferative disorders (PTLDs) are hindered by the small number of cases at each transplant center. We analyzed prognostic factors and long-term outcome according to clinical manifestations, pathologic features, and treatment and investigated the prognostic value of the non-Hodgkin's lymphoma International Prognostic Index (IPI) in 61 patients with PTLD. Patients and Methods: We studied 61 patients in two institutions who developed PTLD and analyzed factors influencing the complete remission and survival rates. Results: In univariate analysis, factors predictive of failure to achieve complete remission were performance status (PS) greater than or equal to (P = .0001) and nondetection of Epstein-Barr virus (EBV) in the tumor (P = .01). Only a negative link with PS greater than or equal to 2 was observed in multivariate analysis. In univariate analysis, factors predictive of lower survival were PS greater than or equal to 2, the number of sites (one v > one), primary CNS localization, T cell origin, monoclonality, nondetection of EBV, and treatment with chemotherapy. The IPI failed to identify a patient subgroup with better survival and was less predictive of the response rate than was a specific index using two risk factors (PS and number of involved sites), which defined three groups of patients: low risk patients whose median survival time has not yet been reached, intermediate-risk patients with a median survival time of 34 months, and high-risk patients with a median survival time of 1 month. Conclusion: PS and the number of involved sites defined three risk groups in our population. The value of these prognostic factors needs to be confirmed in larger cohorts of patients treated in prospective multicenter studies. (C) 2001 by American Society of Clinical Oncology.

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