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Outcomes of human immunodeficiency virus-associated Burkitt lymphoma and diffuse large B-cell lymphoma treated in Australia: A report from the Australasian Lymphoma Alliance
Authors:Kenneth J. C. Lim,Pietro Di   Ciaccio,Mark N. Polizzotto,Sam Milliken,Tara Cochrane,Zhong Goh,Briony Shaw,Evelyn Perry,Michael Gilbertson,William Kermode,Chan Y. Cheah,Maya Latimer,Nada Hamad,Matthew Ku
Affiliation:1. Department of Haematology, St Vincent's Hospital Melbourne, Sydney, Melbourne, Australia;2. Department of Haematology, St Vincent's Hospital Sydney, Fitzroy, New South Wales, Australia;3. College of Health and Medicine, Australian National University, Canberra, Australia

University of New South Wales, Sydney, New South Wales, Australia;4. Gold Coast University Hospital, Southport, Queensland, Australia;5. Gold Coast University Hospital, Southport, Queensland, Australia

Griffiths University, Nathan, Queensland, Australia;6. Monash Hospital, Clayton, Victoria, Australia;7. Sir Charles Gairdner Hospital, Nedlands, Western Australia, Australia;8. Canberra Hospital, Garran, Australian Capital Territory, Australia;9. Department of Haematology, St Vincent's Hospital Melbourne, Sydney, Melbourne, Australia

University of Melbourne, Melbourne, Victoria, Australia

Abstract:
Antiretroviral therapy (ART) has improved outcomes for human immunodeficiency virus-associated non-Hodgkin lymphoma (HIV-NHL). This is an analysis of 44 patients with HIV with Burkitt lymphoma (HIV-BL) and diffuse large B-cell lymphoma (HIV-DLBCL) treated in Australia over a 10-year period (2009–2019) during the ART and rituximab era. At HIV-NHL diagnosis, the majority of presenting patients had adequate CD4 counts and undetectable HIV viral load <50 copies/mL. More than 80% of patients received chemotherapy with curative intent, rituximab, and concurrent ART with chemotherapy (immunotherapy). R-CODOX-M/IVAC or R-Hyper-CVAD (55%) were most commonly used in HIV-BL. CHOP (58%) was the most commonly used chemotherapy backbone for HIV-DLBCL, although 45% of patients received more intense chemotherapy regimens. Overall, 93% of patients who received curative therapy completed their intended course. The 2-year progression-free survival (PFS) and overall survival (OS) for the HIV-BL cohort was 67% and 67% respectively. The 2-year PFS and OS for the HIV-DLBCL cohort was 77% and 81% respectively. Treatment related mortality was 5%. In all, 83% of patients achieved a CD4 count of >0.2 ×109/L 6 months after the end of treatment. Current Australian practice favours the treatment of HIV-BL and HIV-DLBCL similarly to the HIV-negative population with the use of concurrent ART, achieving outcomes comparable to the HIV-negative population.
Keywords:antiretroviral therapy  Burkitt lymphoma  diffuse large B-cell lymphoma  HIV  non-Hodgkin's lymphoma
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