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

被引:25
作者
Goyal, Gaurav [1 ]
Bartley, Adam C. [2 ]
Funni, Shealeigh [3 ]
Inselman, Jonathan [3 ]
Shah, Nilay D. [3 ]
Marshall, Ariela L. [1 ]
Ashrani, Aneel A. [1 ]
Kapoor, Prashant [1 ]
Durani, Urshila [1 ]
Hashmi, Shahrukh K. [1 ]
Siddiqui, Mustaqeem A. [1 ]
Buadi, Francis K. [1 ]
Go, Ronald S. [1 ]
Kyle, Robert A. [1 ]
Kumar, Shaji [1 ]
Gonsalves, Wilson I. [1 ]
机构
[1] Mayo Clin, Div Hematol, Rochester, MN 55905 USA
[2] Mayo Clin, Div Biomed Stat & Informat, Rochester, MN USA
[3] Mayo Clin, Div Hlth Care Policy & Res, Rochester, MN USA
基金
美国国家卫生研究院;
关键词
SOLITARY EXTRAMEDULLARY PLASMACYTOMA; RARE-CANCER-NETWORK; UNITED-STATES; BONE; SURVIVAL; MYELOMA;
D O I
10.1038/s41375-018-0099-8
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
引用
收藏
页码:1414 / 1420
页数:7
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