Hyperviscosity syndrome and central nervous system (CNS) involvement are common neurologic manifestations of MM that clinicians need to be aware of. Dizziness, frequent headache, tinnitus, and difficulty concentrating are typical presenting symptoms of hyperviscosity syndrome. For CNS involvement, the study authors note that although this is rare in MM, it typically occurs in the setting of progressive disease; therefore, they note the necessity of imaging via CT and MRI, as well as cerebral spinal fluid analysis to prevent neurological deterioration and optimize patient outcomes.
The study authors then highlighted how cardiovascular involvement with MM is either indirectly related to MM, such as through certain patient comorbidities (eg, diabetes, obesity); directly related (eg, hyperviscosity and high-output heart failure); or stemming from treatment toxicity, such as anthracyclines, alkylating agents, and immunomodulatory drugs. They believe it best that patient cardiac evaluation include an assessment of cardiac function, discussion of risk factors for cardiac toxicity, testing for potential AL amyloidosis, and monitoring/management during treatment.
Hemostatic abnormalities can include thrombotic complications, particularly venous thromboembolism (VTE), so clinicians should consistently monitor for risk factors that include recent surgery, trauma, previous VTE, and heart disease, among others. Hemorrhagic complications are also important to monitor for as a hemostatic abnormality; these usually happen in the setting of disease progression and are associated with thrombocytopenia, abnormal screening coagulation test results, and a history of bleeding.
The study authors highlight that bone disease complications connected to MM typically result from plasma cell proliferation and alterations to bone remodeling, which most frequently lead to bone pain. Managing this pain is primarily palliative in nature and meant to stabilize or improve patient quality of life. Palliative care in this setting is usually antiresorptive therapy with the goal of preventing new lesions, radiotherapy, surgery, corticosteroids, and analgesia. Other treatments to consider are vertebroplasty and kyphoplasty for pain associated with vertebral collapse.
Additional areas the authors cover in this guidance include chronic and acute pain, metabolic disorders, neuropsychiatric symptoms, ocular disorders, cutaneous lesions, gastrointestinal manifestations, second primary malignancies, teratogenic risk, toxicities associated with autologous stem cell transplant, and toxicities associated with T-cell engaging therapies.
Overall, the authors underscore the importance of recognizing and managing infections promptly in MM to minimize complication risk and optimize patient outcomes, and they emphasize that the high symptom burden and profound impact on quality of life from the disease and treatment-related toxicities make necessary treatment personalization and monitoring.
“Rapid and appropriate intervention on treatment-related adverse events and on worsening of comorbidities should be based on scientific evidence, consensus recommendations, clinical experience, and is of extreme importance for patients and their families,,” they conclude, “impacting the prognosis and quality of life of those who suffer daily with MM.”
Reference
Geraldes C, Roque A, Sarmento-Ribiero AB, et al. Practical management of disease-related manifestations and drug toxicities in patients with multiple myeloma. Front Oncol. 2024;14:1282300. doi:10.3389/fonc.2024.1282300