Development of a comprehensive prognostic index for patients with chronic lymphocytic leukemia

被引:214
作者
Pflug, Natali [1 ,2 ]
Bahlo, Jasmin [1 ,2 ]
Shanafelt, Tait D. [3 ]
Eichhorst, Barbara F. [1 ,2 ]
Bergmann, Manuela A. [4 ]
Elter, Thomas [1 ,2 ]
Bauer, Kathrin [5 ]
Malchau, Gebhart [6 ]
Rabe, Kari G. [7 ]
Stilgenbauer, Stephan [8 ]
Doehner, Hartmut [8 ]
Jaeger, Ulrich [9 ,10 ]
Eckart, Michael J. [11 ]
Hopfinger, Georg [12 ]
Busch, Raymonde [13 ]
Fink, Anna-Maria [1 ,2 ]
Wendtner, Clemens-Martin [4 ]
Fischer, Kirsten [1 ,2 ]
Kay, Neil E. [3 ]
Hallek, Michael [1 ,2 ]
机构
[1] Univ Cologne, Dept Internal Med 1, D-50937 Cologne, Germany
[2] Univ Cologne, Ctr Integrated Oncol Cologne Bonn, D-50937 Cologne, Germany
[3] Mayo Clin, Dept Internal Med, Div Hematol, Rochester, MN USA
[4] Hosp Munchen Schwabing, Dept Internal Med 1, Munich, Germany
[5] Univ Cologne, Cochrane Hematol Malignancies Grp, D-50937 Cologne, Germany
[6] Univ Hosp Cologne, Inst Clin Chem, Cologne, Germany
[7] Mayo Clin, Dept Hlth Sci Res, Rochester, MN USA
[8] Univ Ulm, Dept Internal Med 3, D-89069 Ulm, Germany
[9] Med Univ Vienna, Dept Internal Med 1, Div Hematol & Haemostaseol, Vienna, Austria
[10] Med Univ Vienna, Ctr Comprehens Canc, Vienna, Austria
[11] Hamatol & Onkol Schwerpunktpraxis, Erlangen, Germany
[12] Univ Hosp Salzburg, Dept Internal Med 3, Salzburg, Austria
[13] Tech Univ Munich, Inst Med Stat & Epidemiol, D-80290 Munich, Germany
关键词
PREVIOUSLY UNTREATED PATIENTS; SERUM THYMIDINE KINASE; PHASE-II TRIAL; MUTATIONAL STATUS; PREDICTIVE-VALUE; SURVIVAL; FLUDARABINE; RITUXIMAB; NOTCH1; SF3B1;
D O I
10.1182/blood-2014-02-556399
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In addition to clinical staging, a number of biomarkers predicting overall survival (OS) have been identified in chronic lymphocytic leukemia (CLL). The multiplicity of markers, limited information on their independent prognostic value, and a lack of understanding of how to interpret discordant markers are major barriers to use in routine clinical practice. We therefore performed an analysis of 23 prognostic markers based on prospectively collected data from 1948 CLL patients participating in phase 3 trials of the German CLL Study Group to develop a comprehensive prognostic index. A multivariable Cox regression model identified 8 independent predictors of OS: sex, age, ECOG status, del(17p), del(11q), IGHV mutation status, serum beta(2)-microglobulin, and serum thymidine kinase. Using a weighted grading system, a prognostic index was derived that separated 4 risk categories with 5-year OS ranging from 18.7% to 95.2% and having a C-statistic of 0.75. The index stratified OS within all analyzed subgroups, including all Rai/Binet stages. The validity of the index was externally confirmed in a series of 676 newly diagnosed CLL patients from Mayo Clinic. Using this multistep process including external validation, we developed a comprehensive prognostic index with high discriminatory power and prognostic significance on the individual patient level. The studies were registered as follows: CLL1 trial (NCT00262782, http://clinicaltrials.gov), CLL4 trial (ISRCTN 75653261, http://www.controlled-trials.com), and CLL8 trial (NCT00281918, http://clinicaltrials.gov).
引用
收藏
页码:49 / 62
页数:14
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