Conditional survival to assess prognosis in patients with chronic lymphocytic leukemia

被引:1
|
作者
Schlosser, Pascal [1 ,2 ,3 ,4 ]
Schiwitza, Annett [5 ]
Klaus, Jonas [6 ]
Hieke-Schulz, Stefanie [2 ,7 ,8 ]
Szic, Katarzyna Szarc vel [6 ]
Duyster, Justus [6 ]
Trepel, Martin [2 ,5 ]
Zirlik, Katja [6 ,9 ]
Schumacher, Martin [7 ]
Claus, Rainer [5 ,6 ,10 ,11 ]
机构
[1] Univ Freiburg, Inst Genet Epidemiol, Fac Med, Freiburg, Germany
[2] Univ Freiburg, Med Ctr, Freiburg, Germany
[3] Johns Hopkins Bloomberg Sch Publ Hlth, Dept Epidemiol, Baltimore, MD USA
[4] Univ Freiburg, Ctr Integrat Biol Signalling Studies CIBSS, Freiburg, Germany
[5] Univ Augsburg, Fac Med, Hematol Oncol, Augsburg, Germany
[6] Univ Med Ctr Freiburg, Dept Hematol, Oncol & Stem Cell Transplantat, Freiburg, Germany
[7] Univ Freiburg, Inst Med Biometry & Med Informat, Fac Med, Freiburg, Germany
[8] Roche Pharm AG, Grenzach Wyhlen, Germany
[9] Tumor Und BrustZentrum Ostschweiz, Chur, Switzerland
[10] Univ Augsburg, Fac Med, Pathol, Augsburg, Germany
[11] Univ Augsburg, Fac Med, Comprehens Canc Ctr, Stenglin str 2, D-86156 Augsburg, Germany
关键词
CLL; Conditional survival; Prognostic biomarker; Mortality; IGHV mutation status; OPEN-LABEL; CANCER-PATIENTS; COMORBIDITY; PHASE-3; CYCLOPHOSPHAMIDE; CHLORAMBUCIL; OBINUTUZUMAB; FLUDARABINE; METHYLATION; VALIDATION;
D O I
10.1007/s00277-024-05627-w
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Biomarkers in chronic lymphocytic leukemia (CLL) allow assessment of prognosis. However, the validity of current prognostic biomarkers based on a single assessment point remains unclear for patients who have survived one or more years. Conditional survival (CS) studies that address how prognosis may change over time, especially in prognostic subgroups, are still rare. We performed CS analyses to estimate 5-year survival in 1-year increments, stratified by baseline disease characteristics and known risk factors in two community-based cohorts of CLL patients (Freiburg University Hospital (n = 316) and Augsburg University Hospital (n = 564)) diagnosed between 1984 and 2021. We demonstrate that 5-year CS probability is stable (app. 75%) for the entire CLL patient cohort over 10 years. While age, sex, and stage have no significant impact on CS, patients with high-risk disease features such as non-mutated IGHV, deletion 17p, and high-risk CLL-IPI have a significantly worse prognosis at diagnosis, and 5-year CS steadily decreases with each additional year survived. Our results confirm that CLL patients have a stable survival probability with excess mortality and that the prognosis of high-risk CLL patients declines over time. We infer that CS-based prognostic information is relevant for disease management and counseling of CLL patients.
引用
收藏
页码:1613 / 1622
页数:10
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