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 |
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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. |
doi_str_mv | 10.1038/sj.thj.6200374 |
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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.</description><identifier>ISSN: 1466-4860</identifier><identifier>EISSN: 1476-5632</identifier><identifier>DOI: 10.1038/sj.thj.6200374</identifier><identifier>PMID: 15048063</identifier><language>eng</language><publisher>England</publisher><subject><![CDATA[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]]></subject><ispartof>The hematology journal : the official journal of the European Haematology Association, 2004, Vol.5 (2), p.130-134</ispartof><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c293t-94fa1d4eaf71522dcfe284dd542cd0f93b2ddf7a8651b0934dfbdc090e7e0f353</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4024,27923,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15048063$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hermine, Olivier</creatorcontrib><creatorcontrib>Dombret, Hervé</creatorcontrib><creatorcontrib>Poupon, Joel</creatorcontrib><creatorcontrib>Arnulf, Bertrand</creatorcontrib><creatorcontrib>Lefrère, Francois</creatorcontrib><creatorcontrib>Rousselot, Phillippe</creatorcontrib><creatorcontrib>Damaj, Gandhi</creatorcontrib><creatorcontrib>Delarue, Richard</creatorcontrib><creatorcontrib>Fermand, Jean Paul</creatorcontrib><creatorcontrib>Brouet, Jean Claude</creatorcontrib><creatorcontrib>Degos, Laurent</creatorcontrib><creatorcontrib>Varet, Bruno</creatorcontrib><creatorcontrib>de Thé, Hugues</creatorcontrib><creatorcontrib>Bazarbachi, Ali</creatorcontrib><title>Phase II trial of arsenic trioxide and alpha interferon in patients with relapsed/refractory adult T-cell leukemia/lymphoma</title><title>The hematology journal : the official journal of the European Haematology Association</title><addtitle>Hematol J</addtitle><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.</description><subject>Adult</subject><subject>Anti-HIV Agents - administration & dosage</subject><subject>Antineoplastic Agents - administration & dosage</subject><subject>Arsenicals - administration & dosage</subject><subject>Female</subject><subject>Human T-lymphotropic virus 1 - drug effects</subject><subject>Humans</subject><subject>Injections, Intravenous</subject><subject>Interferon-alpha - administration & dosage</subject><subject>Leukemia-Lymphoma, Adult T-Cell - drug therapy</subject><subject>Leukemia-Lymphoma, Adult T-Cell - pathology</subject><subject>Leukemia-Lymphoma, Adult T-Cell - virology</subject><subject>Middle Aged</subject><subject>Oxides - administration & dosage</subject><subject>Prognosis</subject><subject>Recurrence</subject><subject>Treatment Outcome</subject><subject>Zidovudine - administration & dosage</subject><issn>1466-4860</issn><issn>1476-5632</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkN1LwzAUxYMoTqevPkr-gXZJk6btoww_BgN9mM_ltrmhrekHSYYO_3k7NvDpHi7nHA4_Qh44izkT-cp3cWi6WCWMiUxekBsuMxWlSiSXR61UJHPFFuTW-44xrnjGrsmCp0zmTIkb8vvRgEe62dDgWrB0NBScx6Gtj4_xp9VIYdAU7NQAbYeAzqAbh1nSCUKLQ_D0uw0NdWhh8qhXDo2DOozuQEHvbaC7qEZrqcX9F_YtrOyhn5qxhztyZcB6vD_fJfl8ed6t36Lt--tm_bSN6qQQISqkAa4lgsl4miS6NpjkUutUJrVmphBVorXJIFcpr1ghpDaVrlnBMENmRCqWJD711m70fp5XTq7twR1KzsojxdJ35UyxPFOcA4-nwLSvetT_9jM28Qeh4XHk</recordid><startdate>2004</startdate><enddate>2004</enddate><creator>Hermine, Olivier</creator><creator>Dombret, Hervé</creator><creator>Poupon, Joel</creator><creator>Arnulf, Bertrand</creator><creator>Lefrère, Francois</creator><creator>Rousselot, Phillippe</creator><creator>Damaj, Gandhi</creator><creator>Delarue, Richard</creator><creator>Fermand, Jean Paul</creator><creator>Brouet, Jean Claude</creator><creator>Degos, Laurent</creator><creator>Varet, Bruno</creator><creator>de Thé, Hugues</creator><creator>Bazarbachi, Ali</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>2004</creationdate><title>Phase II trial of arsenic trioxide and alpha interferon in patients with relapsed/refractory adult T-cell leukemia/lymphoma</title><author>Hermine, Olivier ; 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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.</abstract><cop>England</cop><pmid>15048063</pmid><doi>10.1038/sj.thj.6200374</doi><tpages>5</tpages></addata></record> |
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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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