原发性浆细胞白血病33例诊疗分析
车冠男, 王静, 张丽君中国医科大学附属第一医院血液内科, 沈阳 110001
收稿日期:
2022-05-07出版日期:
2023-06-30发布日期:
2023-05-31通讯作者:
张丽君E-mail:lzhang202003@163.com作者简介:
车冠男(1997-),女,硕士研究生关键词: 原发性, 浆细胞白血病, 治疗, 造血干细胞移植
Abstract: Objective To analyze the clinical characteristics,treatment,prognosis and other aspects of primary plasma cell leukemia (pPCL), and improve the understanding of the disease. Methods A total of 33 patients with pPCL admitted to The First Hospital of China Medical University between May 2009 and January 2022 were retrospectively analyzed based on clinical manifestations,laboratory tests,treatment and prognosis. Results The most common initial symptom in all 33 patients was fatigue. IgGλ was the most common immune type. Most patients,20/22 (90.9%) expressed both CD38 and CD138,and 12/17 (70.6%) patients expressed complex karyotypes. Nineteen patients received chemotherapy,and one had an autologous stem cell transplantation. The overall remission rate was 9/19 (47.4%). Conclusion As one of the malignant plasma cell diseases,pPCL is not sensitive to conventional chemotherapy. The combination of proteasome inhibitors and immunomodulatory drugs is the current,relatively advanced chemotherapy regimen,and hematopoietic stem cell transplantation is recommended for consolidation therapy. New therapeutics,such as CAR-T,CD38 monoclonal antibody and Bcl-2 inhibitors have brought new hope to patients.
Key words: primary, plasma cell leukemia, treatment, hematopoietic stem cell transplantation
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