Acute Myeloid Leukemia in Patients Living with HIV Infection: Several Questions, Fewer Answers
- PMID: 32041199
- PMCID: PMC7036847
- DOI: 10.3390/ijms21031081
Acute Myeloid Leukemia in Patients Living with HIV Infection: Several Questions, Fewer Answers
Abstract
Both human immunodeficiency virus (HIV) infection and acute myeloid leukemia (AML) may be considered relatively uncommon disorders in the general population, but the precise incidence of AML in people living with HIV infection (PLWH) is uncertain. However, life expectancy of newly infected HIV-positive patients receiving anti-retroviral therapy (ART) is gradually increasing, rivaling that of age-matched HIV-negative individuals, so that the occurrence of AML is also expected to progressively increase. Even if HIV is not reported to be directly mutagenic, several indirect leukemogenic mechanisms, mainly based on bone marrow microenvironment disruption, have been proposed. Despite a well-controlled HIV infection under ART should no longer be considered per se a contraindication to intensive chemotherapeutic approaches, including allogeneic hematopoietic stem cell transplantation, in selected fit patients with AML, survival outcomes are still generally unsatisfactory. We discussed several controversial issues about pathogenesis and clinical management of AML in PLWH, but few evidence-based answers may currently be provided, due to the limited number of cases reported in the literature, mainly as case reports or small retrospective case series. Prospective multicenter clinical trials are warranted to more precisely investigate epidemiology and cytogenetic/molecular features of AML in PLWH, but also to standardize and further improve its therapeutic management.
Keywords: AIDS; HIV infection; acute myeloid leukemia; acute promyelocytic leukemia; anti-retroviral therapy; hematopoietic stem cell transplantation; myelodysplastic syndrome.
Conflict of interest statement
FF served on advisory boards for Jannsen on the clinical use of decitabine, for Novartis on the clinical use of midostaurin and received travel grants from Jazz Pharmaceuticals; ML served on advisory boards for Novartis on the clinical use of midostaurin, for AbbVie, on the clinical use of venetoclax, for Jazz Pharmaceuticals, on the clinical use of Vyxeos, for Gilead Sci., on the clinical use of Ambisome, for MSD, on the clinical use of letermovir, for Sanofi, on the clinical use of caplacizumab, from Daiichi-Sankyo, for the clinical use of quizartinib and received travel grants from Gilead Sci. The other authors declare no potential conflicts of interest.
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