A prognostic score including mutation profile and clinical features for patients with CMML undergoing stem cell transplantation

被引:27
作者
Gagelmann, Nico [1 ]
Badbaran, Anita [1 ]
Beelen, Dietrich W. [2 ]
Salit, Rachel B. [3 ]
Stoelzel, Friedrich [4 ]
Rautenberg, Christina [5 ]
Becker, Heiko [6 ]
Radujkovic, Aleksandar [7 ]
Panagiota, Victoria [8 ]
Bogdanov, Rashit [2 ]
Christopeit, Maximilian [1 ]
Park, Yong [3 ]
Nibourel, Olivier [9 ]
Luft, Thomas [7 ]
Koldehoff, Michael [2 ]
Corsten, Maarten [10 ]
Heuser, Michael [8 ]
Finke, Jurgen [6 ]
Kobbe, Guido [5 ]
Platzbecker, Uwe [11 ]
Robin, Marie [12 ]
Scott, Bart L. [3 ]
Kroeger, Nicolaus [1 ]
机构
[1] Univ Med Ctr Hamburg Eppendorf, Dept Stem Cell Transplantat, Martinistr 52, D-20246 Hamburg, Germany
[2] Univ Hosp Essen, West German Canc Ctr, Dept Bone Marrow Transplantat, Essen, Germany
[3] Fred Hutchinson Canc Res Ctr, 1124 Columbia St, Seattle, WA 98104 USA
[4] Tech Univ Dresden, Univ Hosp Carl Gustav Carus, Med Clin 1, Dresden, Germany
[5] Heinrich Heine Univ Duesseldorf, Med Fac, Dept Hematol Oncol & Clin Immunol, Dusseldorf, Germany
[6] Univ Freiburg, Med Ctr, Dept Med 1, Freiburg, Germany
[7] Univ Hosp Heidelberg, Dept Internal Med 5, Heidelberg, Germany
[8] Hannover Med Sch, Dept Hematol Hemostasis Oncol & Stem Cell Transpl, Hannover, Germany
[9] Ctr Hosp Reg Univ Lille, Lille, France
[10] Radboud Univ Nijmegen, Med Ctr, Nijmegen, Netherlands
[11] Leipzig Univ Hosp, Med Clin & Policlin 1, Hematol & Cellular Therapy, Leipzig, Germany
[12] Univ Paris, Hop St Louis, AP HP, Paris, France
关键词
D O I
10.1182/bloodadvances.2020003600
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The inclusion of mutation status improved risk stratification for newly diagnosed patients with chronic myelomonocytic leukemia (CMML). Stem cell transplantation is a potentially curative treatment option, and patient selection is critical because of relevant transplant-related morbidity and mortality. We aimed to evaluate the impact of mutation status together with clinical presentations on posttransplant outcome. Our study included 240 patients with a median follow-up of 5.5 years. A significant association with worse survival was identified for the presence of mutations in ASXL1 and/or NRAS. In multivariable analysis, ASXL1- and/or NRAS-mutated genotype (hazard ratio [HR], 1.63), marrow blasts >2% (HR, 1.70), and increasing comorbidity index (continuous HR, 1.16) were independently associated with worse survival. A prognostic score (CMML transplant score) was developed, and the following points were assigned: 4 points for an ASXL1- and/or NRAS-mutated genotype or blasts >2% and 1 point each for an increase of 1 in the comorbidity index. The CMML transplant score (range, 0-20) was predictive of survival and nonrelapse mortality (P < .001 for both). Up to 5 risk groups were identified, showing 5-year survival of 81% for a score of 0 to 1, 49% for a score of 2 to 4, 43% for a score of 5 to 7, 31% for a score of 8 to 10, and 19% for a score >10. The score retained performance after validation (concordance index, 0.68) and good accuracy after calibration. Predictions were superior compared with existing scores designed for the nontransplant setting, which resulted in significant risk reclassification. This CMML transplant score, which incorporated mutation and clinical information, was prognostic in patients specifically undergoing transplantation and may facilitate personalized counseling.
引用
收藏
页码:1760 / 1769
页数:10
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