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. 2018 Jun;32(6):1414-1420.
doi: 10.1038/s41375-018-0099-8. Epub 2018 Mar 21.

Treatment approaches and outcomes in plasmacytomas: analysis using a national dataset

Affiliations

Treatment approaches and outcomes in plasmacytomas: analysis using a national dataset

Gaurav Goyal et al. Leukemia. 2018 Jun.

Abstract

Solitary plasmacytomas are uncommon plasma cell disorders, which may present as a single bone lesion (P-bone) or extramedullary plasmacytoma (P-EM). There is a paucity of large studies analyzing prognostic factors and outcomes of plasmacytomas. While the treatment of choice is radiation therapy (RT), there is a lack of data evaluating optimal RT dose. In this study, we sought to answer these questions by utilizing the National Cancer Database plasmacytoma data from 2000 to 2011. A total of 5056 patients were included in the study (median age 62 years; range 52-72). To obtain a pure plasmacytoma cohort, potential multiple myeloma patients were excluded from the study (bone marrow involvement, systemic chemotherapy use). P-bone constituted 70% of the patients. The median overall survival (OS) of P-EM was significantly longer than P-bone (132 vs. 85 months), and for soft/connective tissue it was worse than remainder of P-EM (82 vs. 148 months). On multivariable analysis, factors associated with worse OS included older age (≥65), presence of P-bone, and treatment with a radiation dose <40 Gy.

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Figures

Figure 1.
Figure 1.
CONSORT diagram for cohort selection.
Figure 2.
Figure 2.
Overall survival (OS) based on location of plasmacytoma (A) Extramedullary plasmacytoma (P-EM) compared to bone plasmacytoma; (B) Plasmacytoma of soft/connective tissue compared to others (P-EM other than connective/soft tissue or P-bone).
Figure 3.
Figure 3.
Regression tree for upper aero-digestive tract site subgroup analysis of radiation dose.

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