Clinical outcome of Mantle Cell Lymphoma patients with high-risk disease (high-risk MIPI-c or high p53 expression)

被引:29
作者
Scheubeck, Gabriel [1 ]
Jiang, Linmiao [2 ]
Hermine, Olivier [3 ]
Kluin-Nelemans, Hanneke C. [4 ]
Schmidt, Christian [1 ]
Unterhalt, Michael [1 ]
Rosenwald, Andreas [5 ]
Klapper, Wolfram [6 ]
Evangelista, Andrea [7 ,8 ]
Ladetto, Marco [9 ]
Jerkeman, Mats [10 ]
Ferrero, Simone [11 ]
Dreyling, Martin [1 ]
Hoster, Eva [1 ,2 ]
机构
[1] LMU Univ Hosp, Dept Med 3, Munich, Germany
[2] Ludwig Maximilians Univ Munchen, Inst Med Informat Proc Biometry & Epidemiol, Munich, Germany
[3] Univ Hosp, Paris, France
[4] Univ Groningen, Univ Med Ctr Groningen, Dept Hematol, Groningen, Netherlands
[5] Univ Wurzburg, Inst Pathol, Wurzburg, Germany
[6] Univ Hosp Schleswig Holstein, Dept Pathol, Hematopathol Sect, Campus Kiel, Kiel, Germany
[7] Azienda Osped Univ Citta Salute & Sci, Unit Clin Epidemiol, Turin, Italy
[8] CPO Piemonte, Turin, Italy
[9] Azienda Osped SS Antonio & Biagio & Cesare Arrigo, Hematol, Alessandria, Italy
[10] Skane Univ Hosp, Lund, Sweden
[11] Univ Torino, Dept Mol Biotechnol & Hlth Sci, Div Hematol, AOU Citta Salute & Sci Torino, Turin, Italy
关键词
HIGH-DOSE CYTARABINE; PROGNOSTIC INDEX; OLDER PATIENTS; FOLLOW-UP; KI-67; TP53; IMMUNOCHEMOTHERAPY; TRANSPLANTATION; MUTATIONS; YOUNGER;
D O I
10.1038/s41375-023-01977-y
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Currently, treatment allocation of patients with Mantle Cell Lymphoma (MCL) is mainly based on age and medical fitness. The combined MCL International Prognostic Index (MIPI-c) allows to predict prognosis using clinical factors (MIPI) and the Ki-67 index. However, high p53 expression as surrogate for TP53 alterations has demonstrated to be an independent predictor for poor outcome. We aimed to define a clear high-risk group based on the combination of MIPI, Ki-67 and p53 expression/TP53 alteration. A total of 684 patients from the prospective European MCL-Younger and MCL-Elderly trials were evaluable. The classification of high-risk disease (HRD) as high-risk MIPI-c or p53 expression >50% versus low-risk disease (LRD) as low, low-intermediate or high-intermediate MIPI-c and p53 expression & LE;50% allowed to characterize two distinct groups with highly divergent outcome. Patients with HRD had significantly shorter median failure-free survival (FFS) (1.1 vs. 5.6 years, p < 0.0001) and overall survival (OS) (2.2 vs. 13.2 years, p < 0.0001) compared to those with LRD. These major differences were confirmed in two validation cohorts from the Italian MCL0208 and the Nordic-MCL4 trials. The results suggest that this subset of HRD patients is not sufficiently managed with the current standard treatment and is asking for novel treatment strategies.
引用
收藏
页码:1887 / 1894
页数:8
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