Abstract
Purpose
Monoclonal gammopathy of undetermined significance (MGUS) is the precursor of multiple myeloma. This qualitative study described patient (n = 14) experiences and healthcare providers’ (n = 8) opinions and practices concerning care for patients with MGUS in the US.
Methods
Semi-structured, in-depth interviews were analyzed using thematic analysis.
Results
We identified six overarching themes related to the care pathway for patients with MGUS: (1) Process of MGUS diagnosis, (2) Providers’ explanations, (3) Patients’ understanding, (4) Impact of the diagnosis, (5) Follow-up/management, and (6) Factors influencing healthcare utilization. Patients demonstrated a basic understanding of MGUS. However, some patients felt anxiety around the diagnosis, which may affect other aspects of their lives. Non-hematologist providers report having less MGUS-specific knowledge. Older age, high-risk MGUS, and insurance coverage/healthcare costs influenced healthcare utilization.
Conclusion
Patients with MGUS may have difficulty processing this premalignant diagnosis. Non-hematologist providers may have gaps in knowledge around specific care for patients with MGUS.
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Data availability
Enquiries about data availability should be directed to the authors.
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Funding
This work was funded by the National Cancer Institute [Grant no. 1 F31 CA247105, 2020].
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Castañeda-Avila, M.A., Mazor, K.M., Lapane, K.L. et al. Patient and provider-level drivers of healthcare utilization related to a diagnosis of a precancerous condition: monoclonal gammopathy of undetermined significance (MGUS). Cancer Causes Control 34, 449–457 (2023). https://doi.org/10.1007/s10552-023-01675-1
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DOI: https://doi.org/10.1007/s10552-023-01675-1