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Morphologic Classification Is an Important Prognostic Factor in Patients with Newly Diagnosed Multiple Myeloma Treated with Bortezomib or Lenalidomide.

作者信息

Takakuwa Teruhito, Araki Taku, Nakamura Koji, Fukuyama Tomoko, Miura Akiko, Fujitani Yotaro, Hisanabe Akari, Kaieda Anna, Fukada Erina, Yamamura Ryosuke

机构信息

Department of Hematology, Osaka Saiseikai Nakatsu Hospital, Osaka, Japan

Department of Hematology, Osaka Saiseikai Nakatsu Hospital, Osaka, Japan.

出版信息

Ann Clin Lab Sci. 2020 May;50(3):333-341.

PMID:32581022
Abstract

The morphological classification of multiple myeloma (MM) has long been known to have an impact on its clinical course. We retrospectively analyzed 30 cases of newly diagnosed MM initially treated with bortezomib or lenalidomide between November 2014 and November 2018. The morphological bone marrow types were assessed on the basis of the Greipp classification. The patients' median age was 74.5 years (range, 49-88), and the male-to-female ratio was 0.67. The International Staging System stages were as follows: stages I, II, and III accounted for 3.3%, 46.7%, and 50.0% of patients, respectively. The M-proteins were IgG (n=21) and non-IgG (n=9). The median progression free survival (PFS) was not reached. The proportion of plasma, immature, and plasmablastic cells in the bone marrow was significantly affected by PFS. When scored with 1 point each, PFS could be stratified into three groups. All patients who had ≥5% of immature cells had a complex karyotype. This study shows that the visual morphological classification of plasma cells is an important prognostic factor even when bortezomib or lenalidomide is used as induction therapy. Further research is expected to reveal the optimal treatment strategy for immature and plasmablastic MM.

摘要

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引用本文的文献

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[The significance of bone marrow immature plasma cell burden in the prognosis of newly diagnosed multiple myeloma patients].[骨髓未成熟浆细胞负荷在新诊断的多发性骨髓瘤患者预后中的意义]
Zhonghua Xue Ye Xue Za Zhi. 2022 Jan 14;43(1):70-74. doi: 10.3760/cma.j.issn.0253-2727.2022.01.014.