[中国高危多发性骨髓瘤诊治专家共识(2024 年)]。

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引用次数: 0

摘要

高危多发性骨髓瘤(HRMM)是指在目前的标准化诊断和治疗下,总生存期少于2-3年的多发性骨髓瘤患者。通过结合各种静态和动态预后因素,进行风险分层,早期识别HRMM患者,并采取个性化策略进行治疗,旨在显著改善HRMM患者的不良生存预后。尽管近年来国内对HRMM的临床价值已达成共识,但在HRMM的定义、高危因素、风险分层和治疗等方面仍存在混乱和模糊之处,有必要进行标准化。为提高我国医生对HRMM的诊治能力,中国抗癌协会血液恶性肿瘤专业委员会(CACA)和中国临床肿瘤学会多发性骨髓瘤专家委员会(CSCO)组织相关专家制定了本共识。本共识旨在明确多发性骨髓瘤的定义、高危因素和风险分层体系,为多发性骨髓瘤的治疗提供建议,从而改善中国多发性骨髓瘤患者的生活质量和预后。
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[Chinese expert consensus on diagnosis and treatment of high risk multiple myeloma (2024)].

High-risk multiple myeloma (HRMM) refers to patients with multiple myeloma whose overall survival time is less than 2-3 years under current standardized diagnosis and treatment. By combining various static and dynamic prognostic factors, risk stratification is performed to identify HRMM patients early and treat patients with personalized strategies, with the aim of significantly improving adverse survival outcomes in HRMM patients. Although the clinical value of HRMM has reached a consensus domestically in recent years, there still exist confusions and ambiguities in the definition, high-risk factors, risk stratification, and treatment of HRMM, necessitating standardization. In order to enhance the diagnostic and treatment capabilities of Chinese physicians in HRMM, the Professional Committee of Hematologic Malignancies of the Chinese Anti-Cancer Association (CACA) and the Multiple Myeloma Expert Committee of the Chinese Society of Clinical Oncology (CSCO) have organized relevant experts to develop this consensus. This consensus aims to clarify the definition of HRMM, high-risk factors, and risk stratification system, and provide treatment recommendations for HRMM, thereby improving the quality of life and prognosis of Chinese HRMM patients.

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来源期刊
CiteScore
0.80
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发文量
100
期刊最新文献
[Research on the clinical characteristics and prognosis of children with chronic myeloid leukemia in the blast phase]. [Single-center study of COVID-19 in patients with chronic lymphocytic leukemia]. [The advancement of cuproptosis in hematological tumors]. [Phylogenetic analysis and pathogenesis study of a new deletion mutation causing inherited FⅩ deficiency]. [Prognostic analysis of 19 newly treated multiple myeloma patients with t(14; 16)].
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