| Autor: |
Eskelinen V; Department of Medicine, University of Oulu, 90220 Oulu, Finland., Nivakoski E; Department of Medicine, University of Oulu, 90220 Oulu, Finland., Launonen K; Department of Hematology, Oulu University Hospital, 90220 Oulu, Finland., Partanen A; Department of Hematology, Kuopio University Hospital, 70290 Kuopio, Finland., Kakko S; Department of Medicine, University of Oulu, 90220 Oulu, Finland., Kuusisto MEL; Cancer and Translational Research Unit, University of Oulu, 90220 Oulu, Finland.; Department of Internal Medicine, Länsi-Pohja Central Hospital, 94100 Kemi, Finland.; Medical Research Unit, Oulu University Hospital, 90220 Oulu, Finland. |
| Abstrakt: |
The present study provides real-world evidence on the treatment of multiple myeloma (MM) bone disease with various bisphosphonates combined for different myeloma-specific treatments as no validated data regarding the best combination treatment for bone disease associated with MM are available. We examined retrospectively 345 MM patients treated with autologous stem cell transplantation in Finland during 1996-2020. The median age of the patients was 60 years with a median follow-up time of 50 months (1-339). At diagnosis, 72.1% of the patients had myeloma-associated bone disease and 45.8% had fractures. Most patients (58.8%) received proteasome inhibitor (PI)-containing treatment at first line. MM bone disease was treated in 91.6% of the patients; 49.9% received zoledronic acid (ZA) and 29.9% pamidronate. Inferior overall survival was associated with MM bone disease at diagnosis ( p = 0.005) or a fracture at diagnosis ( p = 0.003). A later fracture was identified in 29% of the patients, and in those patients without MM bone disease at diagnosis later fractures were less common after ZA treatment ( p = 0.049). PI-based treatment plus ZA ( p = 0.019) seemed to be the best combination to prevent later fractures, even though the same patient subgroup was more likely to experience relapse ( p = 0.018), and also when excluding patients with previous induction therapy without novel agents ( p = 0.008). To conclude, this study suggests that the best therapy to prevent later fractures in MM might be PI-based treatment combined with ZA. |
