Fusion transcripts as liquid biopsy markers in alveolar rhabdomyosarcoma and synovial sarcoma: A report of the Cooperative Weichteilsarkom Studiengruppe (CWS)

医学 活检 滑膜肉瘤 液体活检 病理 融合基因 肉瘤 横纹肌肉瘤 肺泡横纹肌肉瘤 骨髓 癌症 内科学 基因 生物 生物化学
作者
Sabine Stegmaier,Monika Sparber‐Sauer,Esther Aakcha‐Rudel,Petra Münch,Theresa Reeh,Simone Feuchtgruber,Erika Hallmen,Claudia Blattmann,Stefan Bielack,Thomas Klingebiel,Ewa Kościelniak
出处
期刊:Pediatric Blood & Cancer [Wiley]
卷期号:69 (9) 被引量:16
标识
DOI:10.1002/pbc.29652
摘要

Abstract Background The possible application of gene fusion transcripts as tumor‐specific noninvasive liquid biopsy biomarkers was investigated in blood plasma from patients with alveolar rhabdomyosarcoma (ARMS) and synovial sarcoma (SS). Methods Patients entered in the CWS Soft‐Tissue Sarcoma Registry (SoTiSaR) with tumors positive for fusion genes and available blood/plasma samples were included in our analysis. Cell‐free exosomal RNA was extracted and used to detect PAX‐FOXO1 or SYT‐SSX fusion transcripts by reverse transcription quantitative PCR (RT‐qPCR). Results The analysis included 112 ethylene diamine tetraacetic acid blood samples from 80 patients (65 with ARMS, 15 with SS; 34 with localized, 46 with metastatic disease). For patients with metastatic ARMS, 62% ( n = 18) of initial liquid biopsies were positive, and 16 (89%) of them showed initial bone marrow (BM) metastases. For all patients with primary localized ARMS, liquid biopsy was negative at diagnosis. Of the 48 plasma samples collected during therapy and follow‐up, five were positive. None of the liquid biopsies from patients with SS were positive. Conclusions This liquid biopsy assay based on the detection of fusion transcripts in cell‐free RNA from blood exosomes is suitable for analysis of patients with ARMS. Results showed good correlation with the initial tumor status; liquid biopsy was positive in 94% of patients with metastatic ARMS and initial BM involvement, whereas biopsies from all patients with localized tumors were negative. Prospective validation and optimization of the assay, as well as its application for other markers in diagnostics and monitoring of soft‐tissue sarcoma, are ongoing.
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