HIV and multiple myeloma: do patients present at a younger age? A perspective from a South African orthopaedic oncology unit
DOI:
https://doi.org/10.17159/2309-%208309/2025/v24n4a5Keywords:
multiple myeloma, myeloma bone disease, skeletal-related events, HIV, pathological fractureAbstract
Background: Multiple myeloma (MM) is the third most common haematological malignancy and the most common malignancy affecting the skeletal systems of the elderly. Skeletal-related events (SREs) such as hypercalcaemia, bone pain, spinal cord compression, and pathological fracture are common sequelae of multiple myeloma bone disease (MMBD) and are the reasons patients might consult an orthopaedic surgeon. It has been established that infection with the human immunodeficiency virus (HIV) increases one’s risk of developing haematological malignancies. However, there is scant literature on how HIV infection affects MMBD, particularly from a South African perspective. We hypothesised that MMBD presents at a younger age and with more advanced disease in HIV-positive individuals.
Methods: A retrospective single-centre descriptive study was undertaken of patients with newly diagnosed MM presenting with SREs to an orthopaedic oncology unit between 1 January 2016 and 31 December 2020. Patient demographic data (e.g., age, race and sex), biochemical and histopathological results, and whole-body X-rays (WBXR) were collected for each participant.
Results: Twenty-seven patients were included. The median age at presentation was 56 years (interquartile range [IQR]: 49‒47). Regarding HIV infection, 19% (n = 5) were HIV-positive, 45% (n = 12) were HIV-negative, and 37% (n = 10) had an unknown status due to absent screening. The age at presentation in HIV-positive patients was 44 years (IQR: 41–51); in HIV-negative patients, it was 58 years (IQR: 48–66). The difference in age at presentation between HIV-positive and HIV-negative patients was statistically significant, with a Kruskal-Wallis p-value of 0.041. Among HIV-positive patients, 60% (n = 3) presented with International Staging System (ISS) stage III disease, while 50% (n = 10) of HIV-negative patients presented with ISS stage II disease, with the Fisher’s exact p-value = 0.836 indicating an insignificant difference. The presenting complaint was mainly a pathological fracture in 67% (n = 20), predominantly affecting the femur in 50% (n = 10).
Conclusion: The majority of MM patients present to the orthopaedic surgeon with pathological fractures and commonly have more advanced disease. In our setting, when treating a young HIV-infected individual with a pathological fracture, one should always consider MM as a likely diagnosis.
Level of evidence: 4
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