Comprehensive characterization of circulating tumor cells and cell‐free DNA in patients with metastatic melanoma

Author:

Bos Manouk K.1ORCID,Kraan Jaco1,Starmans Martijn P. A.2,Helmijr Jean C. A.1,Verschoor Noortje1ORCID,De Jonge Maja J. A.1,Joosse Arjen1,van der Veldt Astrid A. M.12,te Boekhorst Peter A. W.3,Martens John W. M.1ORCID,Sleijfer Stefan1,Wilting Saskia M.1

Affiliation:

1. Department of Medical Oncology Erasmus MC Cancer Institute, University Medical Center Rotterdam The Netherlands

2. Department of Radiology and Nuclear Medicine Erasmus MC Rotterdam The Netherlands

3. Department of Hematology Erasmus MC Cancer Institute, University Medical Center Rotterdam The Netherlands

Abstract

Advances in therapeutic approaches for melanoma urge the need for biomarkers that can identify patients at risk for recurrence and to guide treatment. The potential use of liquid biopsies in identifying biomarkers is increasingly being recognized. Here, we present a head‐to‐head comparison of several techniques to analyze circulating tumor cells (CTCs) and cell‐free DNA (cfDNA) in 20 patients with metastatic melanoma. In this study, we investigated whether diagnostic leukapheresis (DLA) combined with multimarker flow cytometry (FCM) increased the detection of CTCs in blood compared to the CellSearch platform. Additionally, we characterized cfDNA at the level of somatic mutations, extent of aneuploidy and genome‐wide DNA methylation. Both CTCs and cfDNA measures were compared to tumor markers and extracranial tumor burden on radiological imaging. Compared to the CellSearch method applied on peripheral blood, DLA combined with FCM increased the proportion of patients with detectable CTCs from 35% to 70% (P = 0.06). However, the median percentage of cells that could be recovered by the DLA procedure was 29%. Alternatively, cfDNA mutation and methylation analysis detected tumor load in the majority of patients (90% and 93% of samples successfully analyzed, respectively). The aneuploidy score was positive in 35% of all patients. From all tumor measurements in blood, lactate dehydrogenase (LDH) levels were significantly correlated to variant allele frequency (P = 0.004). Furthermore, the presence of CTCs in DLA was associated with tumor burden (P < 0.001), whereas the presence of CTCs in peripheral blood was associated with number of lesions on radiological imaging (P < 0.001). In conclusion, DLA tended to increase the proportion of patients with detectable CTCs but was also associated with low recovery. Both cfDNA and CTCs were correlated with clinical parameters such as LDH levels and extracranial tumor burden.

Funder

KWF kankerbestrijding

Publisher

Wiley

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