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在临床实践中多发性骨髓瘤患者的高危细胞遗传学异常和国际分期系统(R2-ISS)的第二次修订的临床相关性。

Clinical relevance of high-risk cytogenetic abnormalities and the second revision of the International Staging System (R2-ISS) in patients with multiple myeloma in clinical practice.

机构信息

Department of Hematology, Tokushima Prefecture Central Hospital, 1-10-3 Kuramoto, Tokushima, 770-8539, Japan.

Department of Internal Medicine, Tenma Hospital, 1-5-1 Kuramoto, Tokushima, 770-0042, Japan.

出版信息

Int J Hematol. 2023 May;117(5):718-728. doi: 10.1007/s12185-023-03541-x. Epub 2023 Jan 24.

Abstract

High-risk cytogenetic abnormalities (HRCAs) are the most critical factor affecting prognosis in multiple myeloma (MM). However, the clinical significance of HRCAs in routine practice has not been fully elucidated. We retrospectively analyzed clinical features and outcome in 60 newly diagnosed MM patients with or without HRCAs including t(4;14), t(14;16), del(17p), and 1q gain/amplification. The median age was 71 years (range, 35-90). Abnormalities with t(4;14), t(14;16), del(17p), and 1q gain/amplification were found in 10, 1, 6, and 21/14 patients, respectively, and 10 patients had ≥ 2 HRCAs. Patients with HRCAs exhibited progressive clinical features such as anemia, high β2-microglobulin, and high LDH. Symptomatic relapse was more common in patients with HRCAs. The median progression-free survival (PFS) by number of HRCAs (0, 1, and ≥ 2) was 51.7, 21.4, and 26.1 months (p = 0.011), and the median overall survival (OS) was not reached, 60.7, and 46.8 months (p = 0.045), respectively. Multivariate analysis revealed that HRCAs were an independent factor for PFS. Accordingly, the second revision of International Staging System (R2-ISS), which incorporates HRCA scores, was more useful for prognostic stratification (p = 0.0023). These results suggest that presence of multiple HRCAs including 1q gain/amplification is associated with advanced stage and poor prognosis in clinical practice as well.

摘要

高危细胞遗传学异常(HRCAs)是影响多发性骨髓瘤(MM)预后的最关键因素。然而,HRCAs 在常规实践中的临床意义尚未得到充分阐明。我们回顾性分析了 60 例新诊断的 MM 患者的临床特征和结局,这些患者中包括 t(4;14)、t(14;16)、del(17p)和 1q 增益/扩增。中位年龄为 71 岁(范围 35-90 岁)。10 例患者存在 t(4;14)、t(14;16)、del(17p)和 1q 增益/扩增异常,分别为 1、1、6 和 21/14 例,10 例患者存在≥2 种 HRCAs。HRCAs 患者表现出进行性临床特征,如贫血、高β2-微球蛋白和高乳酸脱氢酶。HRCAs 患者更易出现症状性复发。根据 HRCAs 数量(0、1 和≥2),无进展生存期(PFS)的中位数分别为 51.7、21.4 和 26.1 个月(p=0.011),总生存期(OS)未达到,分别为 60.7、46.8 个月(p=0.045)。多变量分析显示,HRCAs 是 PFS 的独立因素。因此,纳入 HRCA 评分的国际分期系统(ISS)第二修订版(R2-ISS)在预后分层方面更具价值(p=0.0023)。这些结果表明,在临床实践中,多种 HRCAs(包括 1q 增益/扩增)的存在与晚期和不良预后相关。

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