High-Throughput Hybridization Assay as First-Line Diagnostic Test for Sarcomas: Clinical Assessment in a Tertiary Referral Center.

Carmen Salguero-Aranda, Marco Perez, María Victoria Vargas-Padilla, Amparo Beltrán-Povea, Daniel Delgado-Bellido, David Marcilla, Gema Civantos, Enrique de Álava, Juan Díaz-Martín
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Abstract

Context.—: Sarcomas are rare and highly heterogeneous mesenchymal tumors with deceptive morphologic features that pose a challenge for precise diagnostics. Chromosomal rearrangements generating pathognomonic gene fusions are useful diagnostic markers, traditionally tested using single-plex standard of care assays with limited diagnostic yield. NanoString nCounter technology has emerged as a robust solution with multiplexing capabilities.

Objective.—: To optimize NanoString effective coverage of specific entities and conduct a validation study to support its clinical implementation.

Design.—: We reconfigured a NanoString codeset by including a set of probes for detecting gene fusion variants of solitary fibrous tumors, low-grade fibromyxoid sarcomas/sclerosing epithelioid fibrosarcomas, and undifferentiated small round cell sarcomas, totaling 188 probes. A technical validation study was conducted with 96 retrospective samples. Additionally, 76 prospective samples were evaluated to assess the assay's clinical performance.

Results.—: Both technical and clinical validation studies showed that NanoString's codeset reached >88% sensitivity and 100% specificity, compared with standard of care methods, and superior diagnostic yield as a first-line test. Our design enabled the detection of almost all fusion variants of NGFI-A binding protein 2 (NAB2) with signal transducer and activator of transcription 6 (STAT6) in solitary fibrous tumors, as well as cAMP responsive element binding protein 3 like 1/2 (CREB3L1/2) rearrangements in all low-grade fibromyxoid sarcoma/sclerosing epithelioid fibrosarcoma cases. Identification of specific gene fusions of undifferentiated small round cell sarcoma was also improved, but additional strategies are necessary to attain full coverage.

Conclusions.—: The NanoString platform demonstrated good sensitivity, specificity, and superior diagnostic yield. It is a cost-effective assay with rapid turnaround time, low sample consumption, streamlined analysis, and easy customization. Therefore, it is a promising alternative first-line diagnostic tool for routine sarcoma testing.

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高通量杂交测定作为肉瘤的一线诊断检测:一家三级转诊中心的临床评估
背景肉瘤是一种罕见的高度异质性间质肿瘤,具有欺骗性的形态特征,给精确诊断带来了挑战。染色体重排产生的致病基因融合是有用的诊断标志物,传统上使用单倍标准检测法进行检测,诊断率有限。NanoString nCounter 技术是一种具有多重功能的强大解决方案:优化 NanoString 对特定实体的有效覆盖范围,并开展验证研究以支持其临床应用:我们重新配置了 NanoString 的代码集,加入了一组探针,用于检测单发纤维性肿瘤、低级别纤维肉瘤/硬化性上皮样纤维肉瘤和未分化小圆形细胞肉瘤的基因融合变异,探针总数为 188 个。对 96 份回顾性样本进行了技术验证研究。此外,还对 76 份前瞻性样本进行了评估,以评估该检测方法的临床表现:技术和临床验证研究均表明,与标准治疗方法相比,NanoString 的代码集灵敏度大于 88%,特异性大于 100%,作为一线检测方法具有更高的诊断率。我们的设计几乎能检测出单发纤维性肿瘤中所有的NGFI-A结合蛋白2(NAB2)与信号转导和转录激活因子6(STAT6)的融合变体,以及所有低级别纤维肉瘤/硬化性上皮样纤维肉瘤病例中的cAMP反应元件结合蛋白3 like 1/2 (CREB3L1/2)重排。对未分化小圆形细胞肉瘤特定基因融合的鉴定也有所改进,但要实现全面覆盖,还需要采取其他策略:结论:NanoString 平台具有良好的灵敏度、特异性和卓越的诊断率。它是一种具有成本效益的检测方法,周转时间快、样本消耗少、分析简便且易于定制。因此,它有望成为常规肉瘤检测的替代性一线诊断工具。
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