Phase II trial of arsenic trioxide and alpha interferon in patients with relapsed/refractory adult T-cell leukemia/lymphoma

Human T-cell lymphotropic virus type 1 associated adult T-cell leukemia/lymphoma carries a very poor prognosis due to its intrinsic resistance to chemotherapy. Although zidovudine (AZT) and alpha-interferon (IFN) yield some responses and improve ATL prognosis, alternative therapies are needed. Arsen...

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Veröffentlicht in:The hematology journal : the official journal of the European Haematology Association 2004, Vol.5 (2), p.130-134
Hauptverfasser: Hermine, Olivier, Dombret, Hervé, Poupon, Joel, Arnulf, Bertrand, Lefrère, Francois, Rousselot, Phillippe, Damaj, Gandhi, Delarue, Richard, Fermand, Jean Paul, Brouet, Jean Claude, Degos, Laurent, Varet, Bruno, de Thé, Hugues, Bazarbachi, Ali
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container_issue 2
container_start_page 130
container_title The hematology journal : the official journal of the European Haematology Association
container_volume 5
creator Hermine, Olivier
Dombret, Hervé
Poupon, Joel
Arnulf, Bertrand
Lefrère, Francois
Rousselot, Phillippe
Damaj, Gandhi
Delarue, Richard
Fermand, Jean Paul
Brouet, Jean Claude
Degos, Laurent
Varet, Bruno
de Thé, Hugues
Bazarbachi, Ali
description Human T-cell lymphotropic virus type 1 associated adult T-cell leukemia/lymphoma carries a very poor prognosis due to its intrinsic resistance to chemotherapy. Although zidovudine (AZT) and alpha-interferon (IFN) yield some responses and improve ATL prognosis, alternative therapies are needed. Arsenic trioxide (As) dramatically synergizes with IFN to induce growth arrest and apoptosis of ATL leukemia cells in vitro. These results prompted us to initiate a phase II trial of As/IFN combination in seven patients with relapsed/refractory ATL (four acute and three lymphoma). Four patients exhibited a clear initial response (one complete remission and three partial remissions). Yet, the treatment was discontinued after a median of 22 days because of toxicity (three patients) or subsequent progression (four patients). Six patients eventually died from progressive disease (five patients) or infection (one patient), but the remaining patient is still alive and disease free at 32 months. Pharmacokinetic studies showed that maximum arsenic blood levels (median 0.46 microM) were slowly achieved (8-15 days). In conclusion, arsenic/IFN treatment is feasible and exhibits an anti-leukemia effect in very poor prognosis ATL patients despite a significant toxicity. Future studies should assess the best timing for arsenic therapy: frontline with IFN/AZT or as maintenance after induction.
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ispartof The hematology journal : the official journal of the European Haematology Association, 2004, Vol.5 (2), p.130-134
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subjects Adult
Anti-HIV Agents - administration & dosage
Antineoplastic Agents - administration & dosage
Arsenicals - administration & dosage
Female
Human T-lymphotropic virus 1 - drug effects
Humans
Injections, Intravenous
Interferon-alpha - administration & dosage
Leukemia-Lymphoma, Adult T-Cell - drug therapy
Leukemia-Lymphoma, Adult T-Cell - pathology
Leukemia-Lymphoma, Adult T-Cell - virology
Middle Aged
Oxides - administration & dosage
Prognosis
Recurrence
Treatment Outcome
Zidovudine - administration & dosage
title Phase II trial of arsenic trioxide and alpha interferon in patients with relapsed/refractory adult T-cell leukemia/lymphoma
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