Calcitonin receptor-like (CALCRL) is a marker of stemness and an independent predictor of outcome in pediatric AML

Author:

Angenendt Linus1ORCID,Wöste Marius2ORCID,Mikesch Jan-Henrik1,Arteaga Maria Francisca1,Angenendt Adrian3,Sandmann Sarah2ORCID,Berdel Wolfgang E.1ORCID,Lenz Georg1,Dugas Martin24ORCID,Meshinchi Soheil5,Schliemann Christoph1,Rössig Claudia6ORCID

Affiliation:

1. Department of Medicine A, University Hospital Münster, Münster, Germany;

2. Institute of Medical Informatics, University of Münster, Münster, Germany;

3. Department of Biophysics, Faculty of Medicine, Centre for Integrative Physiology and Molecular Medicine (CIPMM), Saarland University, Homburg, Germany;

4. Institute of Medical Informatics, University Hospital Heidelberg, Heidelberg, Germany;

5. Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA; and

6. Department of Pediatric Hematology and Oncology, University Children’s Hospital Münster, Münster, Germany

Abstract

Abstract We have recently identified the G protein-coupled neuropeptide receptor calcitonin receptor-like (CALCRL) as an independent prognostic biomarker and a therapeutic target in more than 1500 adult patients with acute myeloid leukemia (AML). Here, we confirmed CALCRL expression as a prognostic factor in a cohort of 284 pediatric patients with AML. High CALCRL expression was independently associated with event-free survival (hazard ratio [HR], 1.87; 95% confidence interval [CI], 1.36-2.57; P = .0001), overall survival (HR, 1.55; 95% CI, 1.06-2.27; P = .025), and cumulative incidence of relapse (HR, 2.10; 95% CI, 1.49-1.96; P < .0001) when adjusting for age, white blood cell count, and genetic risk. Despite its association with leukemia stem cell signatures, CALCRL expression remained associated with all end points when compared with the 17-gene leukemic stem cell score. The strong association of CALCRL expression with the risk of relapse also in the pediatric population supports its role as novel age-independent master regulator of relapse-initiating, drug-tolerant AML cells in humans.

Publisher

American Society of Hematology

Subject

Hematology

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