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Poor outcomes of immunoglobulin D multiple myeloma patients in the era of novel agents:a single-center experience 被引量:4
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作者 Qian Zhao Feng Li +8 位作者 Ping Song Xiaogang Zhou zhiming an Jiangang Mei Jingjing Shao Hanqing Li Xuli Wang Xing Guo Yongping Zhai 《Cancer Communications》 SCIE 2019年第1期460-465,共6页
Dear Editor, Multiple myeloma (MM) is a disease characterized by the clonal expansion of malignant plasma cells in the marrow, leading to anemia, hypercalcemia, bone lesion, and renal dysfunction [1]. Immunoglobulin D... Dear Editor, Multiple myeloma (MM) is a disease characterized by the clonal expansion of malignant plasma cells in the marrow, leading to anemia, hypercalcemia, bone lesion, and renal dysfunction [1]. Immunoglobulin D (IgD) myeloma is a rare subtype of MM, accounting for approximately 1% to 2% of all MM patients [2]. It occurs at a young age, often accom-panied with a high disease burden and short median sur-vival (18-21 months) [3, 4]. Several studies have suggested that in patients with IgD subtype, the outcomes of those who have had undergone autologous stem cell transplanta-tion (ASCT) were superior than those treated with chemo-therapy alone [5, 6]. However, these have been debatable as other reports have displayed opposite results [7, 8]. 展开更多
关键词 PATIENTS MYELOMA ANEMIA
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