Literature DB >> 28357672

Overview of Targeted Therapies for Adult T-Cell Leukemia/Lymphoma.

Rihab Nasr1, Ambroise Marçais2, Olivier Hermine2, Ali Bazarbachi3,4.   

Abstract

Adult T-Cell Leukemia/lymphoma (ATL) is the first human malignancy associated with a chronic infection by a retrovirus, the human T-cell lymphotropic virus type I (HTLV-I). ATL occurs, after a long latency period, only in about 5% of 10-20 millions infected individuals. ATL has a dismal prognosis with a median survival of less than 1 year, mainly due to its resistance to chemotherapy and to a profound immunosuppression. The viral oncoprotein, Tax, plays a major role in ATL oncogenic transformation by interfering with cell proliferation, cell cycle, apoptosis, and DNA repair. The diversity in ATL clinical features and prognosis led to Shimoyama classification of ATL into four clinical subtypes (acute, lymphoma, chronic, and smoldering) requiring different therapeutic strategies. Clinical trials, mainly conducted in Japan, demonstrated that combination of chemotherapy could induce acceptable response rate in the lymphoma subtype but not in acute ATL. However, long-term prognosis remains poor for both subtypes, due to a high relapse rate. Similarly, whether managed by a watchful waiting or treated with chemotherapy, the indolent forms (smoldering and chronic) have a poor long-term outcome. An international meta-analysis showed improved survival in the leukemic subtypes of ATL (chronic, smoldering as well as a subset of the acute subtype) with the use of two antiviral agents, zidovudine and interferon-alpha, and accordingly, this combination should be considered the standard first-line treatment in this context. ATL patients with lymphoma subtype benefit from induction chemotherapy, given simultaneously or sequentially with an antiviral combination of zidovudine and interferon-alpha. Allogeneic hematopoietic stem cells transplantation remains a promising and potentially curative approach but is limited to a small number of patients. Novel drugs such as arsenic trioxide in combination with interferon-alpha or monoclonal antibodies such as anti-CXCR4 have shown promising results and warrant further investigation.

Entities:  

Keywords:  ATL; Antiviral drugs; Shimoyama classification; Therapeutic strategies

Mesh:

Substances:

Year:  2017        PMID: 28357672     DOI: 10.1007/978-1-4939-6872-5_15

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  7 in total

1.  HTLV-1 HBZ Viral Protein: A Key Player in HTLV-1 Mediated Diseases.

Authors:  Marco Baratella; Greta Forlani; Roberto S Accolla
Journal:  Front Microbiol       Date:  2017-12-22       Impact factor: 5.640

Review 2.  Viral Oncology: Molecular Biology and Pathogenesis.

Authors:  Uyen Ngoc Mui; Christopher T Haley; Stephen K Tyring
Journal:  J Clin Med       Date:  2017-11-29       Impact factor: 4.241

Review 3.  The Anti-Angiogenic Effects of Anti-Human Immunodeficiency Virus Drugs.

Authors:  Giovanni Barillari
Journal:  Front Oncol       Date:  2020-05-21       Impact factor: 6.244

4.  JAG1 overexpression contributes to Notch1 signaling and the migration of HTLV-1-transformed ATL cells.

Authors:  Marcia Bellon; Ramona Moles; Hassiba Chaib-Mezrag; Joanna Pancewicz; Christophe Nicot
Journal:  J Hematol Oncol       Date:  2018-09-19       Impact factor: 17.388

5.  HTLV-1 Tax-specific memory cytotoxic T lymphocytes in long-term survivors of aggressive-type adult T-cell leukemia/lymphoma.

Authors:  Tatsuro Jo; Kazuhiro Noguchi; Takahiro Sakai; Ritsuko Kubota-Koketsu; Sadaharu Irie; Masatoshi Matsuo; Jun Taguchi; Kuniko Abe; Kazuto Shigematsu
Journal:  Cancer Med       Date:  2022-03-22       Impact factor: 4.711

Review 6.  Mouse Models That Enhanced Our Understanding of Adult T Cell Leukemia.

Authors:  Sara Moodad; Abdou Akkouche; Rita Hleihel; Nadine Darwiche; Marwan El-Sabban; Ali Bazarbachi; Hiba El Hajj
Journal:  Front Microbiol       Date:  2018-03-28       Impact factor: 5.640

7.  Ectonucleotidase CD39 is highly expressed on ATLL cells and is responsible for their immunosuppressive function.

Authors:  Yasuhiro Nagate; Sachiko Ezoe; Jiro Fujita; Daisuke Okuzaki; Daisuke Motooka; Tomohiko Ishibashi; Michiko Ichii; Akira Tanimura; Masako Kurashige; Eiichi Morii; Takuya Fukushima; Youko Suehiro; Takafumi Yokota; Hirohiko Shibayama; Kenji Oritani; Yuzuru Kanakura
Journal:  Leukemia       Date:  2020-03-20       Impact factor: 11.528

  7 in total

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