Recent advances in the treatment of adult T‐cell leukemia‐lymphomas
Open accessAbstract
Recent advances in treatment for adult T‐cell leukemia‐lymphoma (ATL) are reviewed herein. It is currently possible to select a therapeutic strategy for ATL and predict prognosis by classification of patients by clinical subtypes and clinicopathological factors. Although the overall survival (OS) of patients with ATL has increased marginally because of advances in chemotherapy, further prolongation of survival might be difficult with conventional chemotherapy alone. Promising results have been reported for antiviral therapy using zidovudine and interferon‐α, and, indeed, antiviral therapy is currently the standard treatment for patients with ATL in western countries. Remarkably, the 5‐year OS rates are 100% for both the smoldering‐type and chronic‐type ATL. Recently, treatments for ATL have included allogeneic hematopoietic stem cell transplantation and molecular targeted therapies. Furthermore, the anti‐CCR4 monoclonal antibody mogamulizumab has been shown to have marked cytotoxic effects on ATL cells, especially in the leukemic type of ATL. In the lymphoma type of ATL, the response rate may be improved by combining mogamulizumab with chemotherapy. It should be recognized that prevention of infection from carriers of human T‐cell leukemia virus type‐I and transfer of the virus from mother to infant are crucial issues for the eradication of ATL.
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ATL therapeutic strategies for patients are determined largely by clinical subtype (acute, lymphoma, chronic, and smouldering).
“ATL therapeutic strategies for patients are determined largely by clinical subtype (acute, lymphoma, chronic, and smouldering) [12,193].”
From Current State of Therapeutics for HTLV-1 (2024) · cites this paper as [193]
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Current State of Therapeutics for HTLV-1
Wang, T. T., Hirons, A., Doerflinger, M., Morris, K. V., Ledger, S., Purcell, D. F. J., Kelleher, A. D., & Ahlenstiel, C. L. (2024) · Viruses · doi:10.3390/v16101616 · Cited by 22 · see citing works
“Long-term corticosteroid therapy [265] HTLV-1-associated inflammatory myositis Currently no available therapeutic; myositis is resistant to corticosteroids and immunomodulatory therapies such as cyclosporin [266,267] Table 5.”
BackgroundInfluential
- Authors
- Utsunomiya, A., Choi, I., Chihara, D., & Seto, M.
- Affiliations
- Imamura Hospital (JP)
- National Hospital Organization Kyushu Cancer Center (JP)
- Aichi Cancer Center (JP)
- Kurume University (JP)
- Corresponding author
- Utsunomiya, Atae
- Venue
- Cancer Science
- Publisher
- Wiley
- Published
- 2015-03-06
- Volume
- 106
- Issue
- 4
- Pages
- 344-351
- ISSN
- 1347-9032 (ISSN-L)
- 1349-7006
- PMC
- PMC4409876
- OpenAlex
- W2032605246
- Cited by
- 103
- References
- 1
- Citations by year
- 2026: 3 · 2025: 1 · 2024: 6 · 2023: 4 · 2022: 8 · 2021: 8 · 2020: 12 · 2019: 13 · 2018: 10 · 2017: 15 · 2016: 15 · 2015: 7
- FWCI
- 1.47
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Cancer Science (publishedVersion, cc-by-nc)
- Europe PMC (PubMed Central) (publishedVersion, cc-by-nc)
- PubMed Central (publishedVersion, cc-by-nc)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and Retrovirus Studies
- Health Sciences › Medicine › Oncology › Viral-associated cancers and disorders
- Health Sciences › Medicine › Dermatology › Cutaneous lymphoproliferative disorders research
- Keywords
- adult T-cell leukemia/lymphoma, antiviral therapy, zidovudine, interferon-alpha, allogeneic hematopoietic stem cell transplantation, targeted therapy, mogamulizumab, CCR4, overall survival, prognostic stratification, human T-cell leukemia virus type I, mother-to-child transmission, infection control
- MeSH terms
- Antiviral Agents, Humans, Immunotherapy, Zidovudine, Human T-lymphotropic virus 1, Leukemia-Lymphoma, Adult T-Cell, HTLV-I Infections, Interferon-alpha, Hematopoietic Stem Cell Transplantation, Reverse Transcriptase Inhibitors, Receptors, CCR4, Molecular Targeted Therapy, Antibodies, Monoclonal, Humanized, Cell- and Tissue-Based Therapy
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