Effect of immune modulation in relapsed peripheral T-cell lymphomas after post-allogeneic stem cell transplantation: a study by the Société Française de Greffe de Moelle et de Thérapie Cellulaire (SFGM-TC)

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Mamez, A.-C. | Levy, V. | Chevallier, P. | Blaise, D. | Vigouroux, S. | Xhaard, A. | Fegueux, N. | Contentin, N. | Beguin, Y. | Ifrah, N. | Bulabois, C.-E. | Suarez, F. | Yakoub-Agha, I. | Turlure, P. | Deconink, E. | Lamy, T. | Cahn, J. Y. | Huynh, A. | Maury, S. | Fornecker, L. M. | Ouzegdouh, M. | Bay, J.-O. | Guillerm, G. | Maillard, N. | Michallet, M. | Malfuson, J.-V. | Bourhis, J.-H. | Rialland, F. | Oumedaly, R. | Jubert, C. | Leblond, V. | Boubaya, M. | Mohty, M. | Nguyen, Son

Edité par CCSD ; Nature Publishing Group -

International audience. Peripheral T-cell lymphoma carries a poor prognosis. To document a possible graft-versus-lymphoma effect in this setting, we evaluated the impact of immunomodulation in 63 patients with peripheral T-cell lymphoma who relapsed after allogeneic transplant in 27 SFGM-TC centers. Relapse occurred after a median of 2.8 months. Patients were then treated with non-immunologic strategies (chemotherapy, radiotherapy) and/or immune modulation (donor lymphocyte infusions (DLI) and/or discontinuation of immunosuppressive therapy). Median overall survival (OS) after relapse was 6.1 months (DLI group: 23.6 months, non-DLI group: 3.6 months). Among the 14 patients who received DLI, 9 responded and 2 had stable disease. Among the remaining 49 patients, a complete response accompanied by extensive chronic GvHD was achieved in two patients after tapering of immunosuppressive drugs. Thirty patients received radio-chemotherapy, with an overall response rate of 50%. In multivariate analysis, chronic GvHD (odds ratio: 11.25 (2.68–48.21), P=0.0009) and skin relapse (odds ratio: 4.15 (1.04–16.50), P=0.043) were associated with a better response to treatment at relapse. In a time-dependent analysis, the only factor predictive of OS was the time from transplantation to relapse (hazards ratio: 0.33 (0.17–0.640), P=0.0009). This large series provides encouraging evidence of a true GvL effect in this disease

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