Gutierrez Antonio, Bento Leyre, Diaz-Lopez Antonio, Barranco Gilberto, Garcia-Recio Marta, Lopez-Guillermo Armando, Dlouhy Ivan, Rovira Jordina, Rodriguez Mario, Sanchez Pina Jose María, Baile Monica, Martín Alejandro, Novelli Silvana, Sancho Juan-Manuel, García Olga, Salar Antonio, Bastos-Oreiro Mariana, Rodriguez-Salazar Mª José, Fernandez Ruben, de la Cruz Fatima, Queizan Jose Antonio, González de Villambrosia Sonia, Cordoba Raul, López Andres, Luzardo Hugo, García Daniel, Sastre-Serra Jordi, Garcia Juan Fernando, Montalban Carlos, Cabanillas Fernando, Rodríguez Jose
Lymphoma Unit, Department of Hematology, Hospital Universitari Son Espases/IdISBa, Palma, Spain.
Department of Translational Research, MD Anderson Cancer Center, Madrid, Spain.
Eur J Haematol. 2020 May;104(5):400-408. doi: 10.1111/ejh.13364. Epub 2020 Feb 18.
Diffuse large B-cell lymphoma (DLBCL) is an aggressive heterogeneous lymphoma with standard treatment. However, 30%-40% of patients still fail, so we should know which patients are candidates for alternative therapies. IPI is the main prognostic score but, in the rituximab era, it cannot identify a very high-risk (HR) subset. The MD Anderson Cancer Center reported a score in the prerituximab era exclusively considering tumor-related variables: Tumor Score (TS). We aim to validate TS in the rituximab era and to analyze its current potential role.
From GELTAMO DLBCL registry, we selected those patients homogeneously treated with R-CHOP (n = 1327).
Five-years PFS and OS were 62% and 74%. All variables retained an independent prognostic role in the revised TS (R-TS), identifying four different risk groups, with 5-years PFS of 86%, 71%, 50%, and very HR (28%). With a further categorization of three variables of the original TS (Ann Arbor Stage, LDH and B2M), we generated a new index that allowed an improvement in HR assessment.
(a) All variables of the original TS retain an independent prognostic role, and R-TS remains predictive in the rituximab era; (b) R-TS and additional categorization of LDH, B2M, and AA stage (enhanced TS) increased the ability to identify HR subsets.
弥漫性大B细胞淋巴瘤(DLBCL)是一种侵袭性异质性淋巴瘤,有标准治疗方案。然而,30%-40%的患者仍治疗失败,因此我们应了解哪些患者适合替代疗法。国际预后指数(IPI)是主要的预后评分,但在利妥昔单抗时代,它无法识别出极高风险(HR)亚组。MD安德森癌症中心在仅考虑肿瘤相关变量的利妥昔单抗前时代报告了一个评分:肿瘤评分(TS)。我们旨在验证利妥昔单抗时代的TS,并分析其当前的潜在作用。
从GELTAMO DLBCL登记处,我们选择了接受R-CHOP同质治疗的患者(n = 1327)。
五年无进展生存期(PFS)和总生存期(OS)分别为62%和74%。所有变量在修订后的TS(R-TS)中均保留独立预后作用,识别出四个不同风险组,五年PFS分别为86%、71%、50%和极高风险组(28%)。通过对原始TS的三个变量(Ann Arbor分期、乳酸脱氢酶(LDH)和β2微球蛋白(B2M))进一步分类,我们生成了一个新指数,可改善HR评估。
(a)原始TS的所有变量均保留独立预后作用,且R-TS在利妥昔单抗时代仍具有预测性;(b)R-TS以及对LDH、B2M和Ann Arbor分期的额外分类(增强型TS)提高了识别HR亚组的能力。