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临床风险评分无法准确识别弥漫性大 B 细胞淋巴瘤的极高风险人群:对 386 例葡萄牙患者的分析。

Clinical risk scores do not accurately identify a very high risk population with diffuse large B cell lymphoma-an analysis of 386 Portuguese patients.

机构信息

Department of Hematology, Centro Hospitalar Universitário do Porto, Porto, Portugal.

Department of Hematology, Instituto Português de Oncologia de Lisboa Francisco Gentil, E.P.E., Lisbon, Portugal.

出版信息

Ann Hematol. 2019 Aug;98(8):1937-1946. doi: 10.1007/s00277-019-03676-0. Epub 2019 Apr 4.

DOI:10.1007/s00277-019-03676-0
PMID:30949752
Abstract

The identification of high-risk patients deserving alternative first-line treatments to R-CHOP is a research priority in diffuse large B cell lymphoma (DLBCL). Despite the increasing recognition of biological features underlying aggressive behavior, clinical scores remain the basis for prognostic evaluation and treatment stratification in DLBCL. We performed a retrospective analysis of patients with DLBCL uniformly treated with immunochemotherapy with the aim of assessing the discriminative power of the NCCN international prognostic index (IPI) and the GELTAMO-IPI scores in risk group stratification and compared them with the IPI. Additionally, we investigated if bulky disease, gender, beta-2 microglobulin (β2m), body mass index, and B-symptoms have independent prognostic impact. We confirmed the discriminative ability of the three prognostic scores in terms of progression-free survival and overall survival and found that the NCCN-IPI performs better in the identification of a high-risk population compared to the IPI and the GELTAMO scores. In an attempt to improve the prognostic power of the NCCN-IPI we analyzed additional clinical variables. Bulky disease and elevated β2m were found to be independent predictors of prognosis when controlling for the NCCN-IPI risk groups. However, they seem to bring no incremental power to the latter in the identification of poor outcome patients. We support the use of the NCCN-IPI for the clinical identification of high-risk patients in DLBCL. Future studies to unravel the biological heterogeneity within NCCN-IPI groups are needed to improve risk prediction and design targeted therapies for poor prognosis patients.

摘要

确定需要替代 R-CHOP 的一线治疗的高危患者是弥漫性大 B 细胞淋巴瘤 (DLBCL) 的研究重点。尽管人们越来越认识到侵袭性行为的生物学特征,但临床评分仍然是 DLBCL 预后评估和治疗分层的基础。我们对接受免疫化学治疗的 DLBCL 患者进行了回顾性分析,目的是评估 NCCN 国际预后指数 (IPI) 和 GELTAMO-IPI 评分在风险分层中的区分能力,并将其与 IPI 进行比较。此外,我们还研究了肿块大小、性别、β-2 微球蛋白 (β2m)、体重指数和 B 症状是否具有独立的预后影响。我们证实了三种预后评分在无进展生存期和总生存期方面的区分能力,并发现 NCCN-IPI 在识别高危人群方面优于 IPI 和 GELTAMO 评分。为了提高 NCCN-IPI 的预后能力,我们分析了其他临床变量。在控制 NCCN-IPI 风险组后,发现肿块大小和升高的β2m 是预后的独立预测因子。然而,在识别预后不良的患者方面,它们似乎并没有给后者带来额外的能力。我们支持在 DLBCL 中使用 NCCN-IPI 来临床识别高危患者。需要进一步的研究来阐明 NCCN-IPI 组内的生物学异质性,以改善风险预测并为预后不良的患者设计靶向治疗。

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