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Clinical Characteristics and Outcomes of Newly Diagnosed Patients with Human Immunodeficiency Virus-associated Burkitt Lymphoma: the Central and Western China AIDS Lymphoma League 002 Study (CALL-002 Study)

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Publisher Biomed Central
Date 2023 Dec 5
PMID 38053186
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Abstract

Background: Despite the introduction of combined antiretroviral therapy, the clinical outcomes of HIV-associated Burkitt lymphoma (BL) remain poor.

Methods: To evaluate the clinical characteristics, prognostic factors, and outcomes of HIV-associated BL, we conducted a retrospective analysis of patients from multiple centers in China.

Results: The study included 41 patients from 8 medical centers. Among the included population, male patients accounted for 87.8%, with 75.6% in advanced stages. Notably, 46.3% of cases involved bone marrow, while 19.5% involved the central nervous system (CNS). The most commonly used chemotherapy regimen was DA-EPOCH ± R, accounting for 53.6% of cases. The overall response rates for patients receiving DA-EPOCH ± R and R-Hyper-CVAD were 59% and 58.2%, respectively. Interestingly, patients receiving regimens containing rituximab had similar complete remission rates (25% vs. 23.5%) and overall survival time (45.69 ± 11.58 vs. 47.79 ± 11.72 months, P = 0.907) compared to those without rituximab, but differed in progression rates (33.3% vs. 47.1%). For the entire cohort, the 1-year progression-free survival (PFS) and overall survival (OS) rates were 52% and 67%, respectively. CNS involvement was independent risk factors for survival, with 1-year PFS and OS rates of 0% and 38% for patients with CNS involvement, and PFS and OS rates of 66% and 75% for patients without CNS involvement.

Conclusions: HIV-associated BL patients in China have poor prognosis and show limited response to current treatment regimens. The absence of CNS involvement significantly improves clinical outcomes. The use of rituximab is not significantly associated with improved outcomes but can reduce disease progression.

References
1.
Alwan F, He A, Montoto S, Kassam S, Mee M, Burns F . Adding rituximab to CODOX-M/IVAC chemotherapy in the treatment of HIV-associated Burkitt lymphoma is safe when used with concurrent combination antiretroviral therapy. AIDS. 2015; 29(8):903-10. DOI: 10.1097/QAD.0000000000000623. View

2.
Kimani S, Painschab M, Horner M, Muchengeti M, Fedoriw Y, Shiels M . Epidemiology of haematological malignancies in people living with HIV. Lancet HIV. 2020; 7(9):e641-e651. PMC: 10199168. DOI: 10.1016/S2352-3018(20)30118-1. View

3.
Roschewski M, Dunleavy K, Abramson J, Powell B, Link B, Patel P . Multicenter Study of Risk-Adapted Therapy With Dose-Adjusted EPOCH-R in Adults With Untreated Burkitt Lymphoma. J Clin Oncol. 2020; 38(22):2519-2529. PMC: 7392744. DOI: 10.1200/JCO.20.00303. View

4.
Wang E, Straus D, Teruya-Feldstein J, Qin J, Portlock C, Moskowitz C . Intensive chemotherapy with cyclophosphamide, doxorubicin, high-dose methotrexate/ifosfamide, etoposide, and high-dose cytarabine (CODOX-M/IVAC) for human immunodeficiency virus-associated Burkitt lymphoma. Cancer. 2003; 98(6):1196-205. DOI: 10.1002/cncr.11628. View

5.
Zayac A, Evens A, Danilov A, Smith S, Jagadeesh D, Leslie L . Outcomes of Burkitt lymphoma with central nervous system involvement: evidence from a large multicenter cohort study. Haematologica. 2021; 106(7):1932-1942. PMC: 8252937. DOI: 10.3324/haematol.2020.270876. View