Simple acute phase protein score to predict long-term survival in patients with acute myeloid leukemia

被引:10
作者
Heini, Alexander D. [1 ,2 ]
Hugo, Rebecca [1 ,2 ]
Berger, Martin D. [1 ,2 ]
Novak, Urban [1 ,2 ]
Bacher, Ulrike [2 ,3 ,4 ]
Pabst, Thomas [1 ,2 ]
机构
[1] Univ Hosp, Dept Med Oncol, Bern, Switzerland
[2] Univ Bern, Bern, Switzerland
[3] Univ Hosp, Dept Hematol, Bern, Switzerland
[4] Univ Hosp, Inselspital, Ctr Lab Med, Bern, Switzerland
关键词
acute myeloid leukemia; acute phase protein; albumin; C-reactive protein; fibrinogen; prognosis; outcome; C-REACTIVE-PROTEIN; GLASGOW PROGNOSTIC SCORE; PROTEIN/ALBUMIN RATIO; PANCREATIC-CANCER; INFLAMMATION; DIAGNOSIS; AML; RECOMMENDATIONS; FIBRINOGEN; OUTCOMES;
D O I
10.1002/hon.2696
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
High levels of acute phase reactants can be associated with adverse outcome in patients with various solid tumor types. For patients with acute myeloid leukemia (AML), this correlation is unknown. We retrospectively investigated the prognostic value of pretreatment acute phase protein levels in 282 consecutive newly diagnosed AML patients undergoing at least one cycle of intensive induction chemotherapy. We applied a new score integrating pre-treatment C-reactive protein (CRP), fibrinogen, and albumin levels termed the CFA ratio, and we stratified patients into two groups: Patients with a CFA ratio below 3.06 had decisively better progression-free (26.2 vs 7.7 months; P < .001), disease-free (56.4 vs 8.7 months; P < .001), and overall survival (61.2 vs 13.8 months; P < .001). Results remained significant when adjusting for confounders including European Leukemia Network risk group. Early mortality also tended to be lower in the low CFA ratio group. Finally, patients with lower modified Glasgow prognostic score (mGPS) similarly had better outcome. In conclusion, our data suggest that an elevated CFA ratio as well as a high mGPS are associated with adverse outcome in patients with newly diagnosed AML undergoing intensive induction. These parameters should undergo prospective evaluation for their contribution to risk profiling in AML patients.
引用
收藏
页码:74 / 81
页数:8
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