Outcomes and patterns of failure in solitary plasmacytoma: A multicenter Rare Cancer Network study of 258 patients
Journal Article
·
· International Journal of Radiation Oncology, Biology and Physics
- Dept. of Radiation Oncology, Centre Hospitalier Universitaire Vaudois, Lausanne (Switzerland)
- Dept. of Radiation Oncology, Princess Margaret Hospital, Toronto, ON (Canada)
- Dept. of Radiation Oncology, Dr. Bernard Verbeeten Institute, Tilburg (Netherlands)
- Dept. of Radiation Oncology, Hopital Tenon, Paris (France)
- Dept. of Radiation Oncology, Centre Hospitalier Universitaire, Grenoble (France)
- Dept. of Radiation Oncology, Istanbul University Cerrahpasa School of Medicine, Istanbul (Turkey)
- Dept. of Radiation Oncology, Kantonsspital, Basel (Switzerland)
- Dept. of Radiation Oncology, Centre Oscar-Lambret, Lille (France)
- Dept. of Radiation Oncology, MAASTRO, Maastricht (Netherlands)
- Dept. of Radiation Oncology, Inselspital, Bern (Switzerland)
- Dept. of Radiation Oncology, Lahey Clinic, Burlington, MA (United States)
- Dept. of Radiation Oncology, Medical University, Gdansk (Poland)
- Dept. of Radiation Oncology, Ege University Medical School, Izmir (Turkey)
- Dept. of Radiation Oncology, Barmherzige Schwestern Hospital, Linz (Austria)
- Dept. of Radiation Oncology, Institut Jean-Godinot, Reims (France)
- University Hospital, Zurich (Switzerland)
- Dept. of Radiation Oncology, Dokuz Eyluel University Medical School, Izmir (Turkey)
- Dept. of Radiation Oncology, Marmara University Hospital, Istanbul (Turkey)
- Dept. of Radiation Oncology, Ospedale Sant' Anna, Como (Italy)
Purpose: To assess the outcomes and patterns of failure in solitary plasmacytoma (SP). Methods and Materials: The data from 258 patients with bone (n = 206) or extramedullary (n = 52) SP without evidence of multiple myeloma (MM) were collected. A histopathologic diagnosis was obtained for all patients. Most (n = 214) of the patients received radiotherapy (RT) alone; 34 received chemotherapy and RT, and 8 surgery alone. The median radiation dose was 40 Gy. The median follow-up was 56 months (range 7-245). Results: The median time to MM development was 21 months (range 2-135), with a 5-year probability of 45%. The 5-year overall survival, disease-free survival, and local control rate was 74%, 50%, and 86%, respectively. On multivariate analyses, the favorable factors were younger age and tumor size <4 cm for survival; younger age, extramedullary localization, and RT for disease-free survival; and small tumor and RT for local control. Bone localization was the only predictor of MM development. No dose-response relationship was found for doses >30 Gy, even for larger tumors. Conclusion: Progression to MM remains the main problem. Patients with extramedullary SP had the best outcomes, especially when treated with moderate-dose RT. Chemotherapy and/or novel therapies should be investigated for bone or bulky extramedullary SP.
- OSTI ID:
- 20788287
- Journal Information:
- International Journal of Radiation Oncology, Biology and Physics, Journal Name: International Journal of Radiation Oncology, Biology and Physics Journal Issue: 1 Vol. 64; ISSN IOBPD3; ISSN 0360-3016
- Country of Publication:
- United States
- Language:
- English
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