Phase 2 study of the efficacy and safety of the combination of arsenic trioxide, interferon alpha, and zidovudine in newly diagnosed chronic adult T-cell leukemia/lymphoma (ATL)

Author:

Kchour Ghada1,Tarhini Mahdi2,Kooshyar Mohamad-Mehdi3,El Hajj Hiba4,Wattel Eric5,Mahmoudi Mahmoud1,Hatoum Hassan4,Rahimi Hossein3,Maleki Masoud6,Rafatpanah Houshang1,Rezaee S. A. Rahim7,Yazdi Mojtaba Tabatabaei8,Shirdel Abbas3,de Thé Hugues9,Hermine Olivier10,Farid Reza1,Bazarbachi Ali4

Affiliation:

1. Immunology Research Centre Bu-Ali Research Institute,

2. Department of Pathology and Laboratory Medicine, and

3. Department of Internal Medicine, Mashhad University of Medical Sciences, Mashhad, Iran;

4. Department of Internal Medicine, American University of Beirut, Beirut, Lebanon;

5. Oncovirologie et Biothérapies, Centre National de la Recherche Scientifique (CNRS) FRE 3011, Université Claude Bernard, Centre Léon Bérard, Hopital Edouard Herriot, Lyon, France;

6. Department of Dermatology, and

7. Microbiology and Virology Research Center, Bu-Ali Research institute, Mashhad University of Medical Sciences, Mashhad, Iran;

8. Department of Pharmaceutical Biotechnology, College of Pharmacy, Tehran University of Medical Science, Tehran, Iran;

9. CNRS Unité Mixte de Recherche (UMR) 7151, Laboratoire Associé au Comité de Paris de la Ligue contre le Cancer, Paris, France; and

10. CNRS UMR 8603 and Department of Hematology, Necker Hospital, Paris, France

Abstract

AbstractAdult T-cell leukemia/lymphoma (ATL) is resistant to chemotherapy and carries a dismal prognosis particularly for the acute and lymphoma subtypes. Promising results were obtained with the combination of zidovudine and interferon-alpha. Chronic ATL has a relatively better outcome, but poor long-term survival is noted when patients are managed with a watchful-waiting policy or with chemotherapy. In ATL cell lines, arsenic trioxide shuts off constitutive NF-κB activation and potentiates interferon-alpha apoptotic effects through proteasomal degradation of Tax. Clinically, arsenic/interferon therapy exhibits some efficacy in refractory aggressive ATL patients. These results prompted us to investigate the efficacy and safety of the combination of arsenic, interferon-alpha, and zidovudine in 10 newly diagnosed chronic ATL patients. An impressive 100% response rate was observed including 7 complete remissions, 2 complete remissions but with more than 5% circulating atypical lymphocytes, and 1 partial response. Responses were rapid and no relapse was noted. Side effects were moderate and mostly hematologic. In conclusion, treatment of chronic ATL with arsenic, interferon-alpha, and zidovudine is feasible and exhibits an impressive response rate with moderate toxicity. Long-term follow up will clarify whether this will translate to disease cure. Overall, these clinical results strengthen the concept of oncogene-targeted cancer therapy.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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