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Zidovudine and Interferon Alfa based regimens for the treatment of adult T-cell leukemia/lymphoma (ATLL): a systematic review and meta-analysis.

Authors :
Shafiee, Arman
Seighali, Niloofar
Taherzadeh-ghahfarokhi, Nooshin
Mardi, Shayan
Shojaeian, Sorour
Shadabi, Shahrzad
Hasani, Mahsa
Haghi, Sabahat
Mozhgani, Sayed-Hamidreza
Source :
Virology Journal; 6/7/2023, Vol. 20 Issue 1, p1-13, 13p
Publication Year :
2023

Abstract

Background: ATLL (Adult T-Cell Leukemia/Lymphoma) is an aggressive hematological malignancy. This T-cell non-Hodgkin lymphoma, caused by the human T-cell leukemia virus type 1 (HTLV-1), is challenging to treat. There is no known treatment for ATLL as of yet. However, it is recommended to use Zidovudine and Interferon Alfa-based regimens (AZT/IFN), chemotherapy, and stem cell transplant. This study aims to review the outcome of patients with different subtypes of ATLL treated with Zidovudine and Interferon Alfa-based regimens. Methods: A systematic search was carried out for articles evaluating outcomes of ATLL treatment by AZT/IFN agents on human subjects from January 1, 2004, until July 1, 2022. Researchers assessed all studies regarding the topic, followed by extracting the data. A random-effects model was used in the meta-analyses. Results: We obtained fifteen articles on the AZT/IFN treatment of 1101 ATLL patients. The response rate of the AZT/IFN regimen yielded an OR of 67% [95% CI: 0.50; 0.80], a CR of 33% [95% CI: 0.24; 0.44], and a PR of 31% [95% CI: 0.24; 0.39] among individuals who received this regimen at any point during their treatment. Our subgroup analyses' findings demonstrated that patients who received front-line and combined AZT/IFN therapy responded better than those who received AZT/IFN alone. It is significant to note that patients with indolent subtypes of disease had considerably higher response rates than individuals with aggressive disease. Conclusion: IFN/AZT combined with chemotherapy regimens is an effective treatment for ATLL patients, and its use in the early stages of the disease may result in a greater response rate. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
1743422X
Volume :
20
Issue :
1
Database :
Complementary Index
Journal :
Virology Journal
Publication Type :
Academic Journal
Accession number :
164150810
Full Text :
https://doi.org/10.1186/s12985-023-02077-0