Research Department of Pathology, University College London, UCL Cancer Institute, London, UK.
Medical Genomics Research Group, University College London, UCL Cancer Institute, London, UK.
Mol Oncol. 2021 Dec;15(12):3679-3690. doi: 10.1002/1878-0261.13102. Epub 2021 Sep 30.
Chondrosarcoma (CS) is a rare tumour type and the most common primary malignant bone cancer in adults. The prognosis, currently based on tumour grade, imaging and anatomical location, is not reliable, and more objective biomarkers are required. We aimed to determine whether the level of circulating tumour DNA (ctDNA) in the blood of CS patients could be used to predict outcome. In this multi-institutional study, we recruited 145 patients with cartilaginous tumours, of which 41 were excluded. ctDNA levels were assessed in 83 of the remaining 104 patients, whose tumours harboured a hotspot mutation in IDH1/2 or GNAS. ctDNA was detected pre-operatively in 31/83 (37%) and in 12/31 (39%) patients postoperatively. We found that detection of ctDNA was more accurate than pathology for identification of high-grade tumours and was associated with a poor prognosis; ctDNA was never associated with CS grade 1/atypical cartilaginous tumours (ACT) in the long bones, in neoplasms sited in the small bones of the hands and feet or in tumours measuring less than 80 mm. Although the results are promising, they are based on a small number of patients, and therefore, introduction of this blood test into clinical practice as a complementary assay to current standard-of-care protocols would allow the assay to be assessed more stringently and developed for a more personalised approach for the treatment of patients with CS.
软骨肉瘤(CS)是一种罕见的肿瘤类型,也是成年人中最常见的原发性恶性骨癌。目前,基于肿瘤分级、影像学和解剖位置的预后并不可靠,需要更客观的生物标志物。我们旨在确定 CS 患者血液中循环肿瘤 DNA(ctDNA)的水平是否可用于预测预后。在这项多机构研究中,我们招募了 145 名软骨瘤患者,其中 41 名被排除在外。对其余 104 名患者中的 83 名患者评估了 ctDNA 水平,其肿瘤存在 IDH1/2 或 GNAS 的热点突变。术前检测到 31/83(37%)和术后 12/31(39%)患者的 ctDNA。我们发现,ctDNA 的检测比病理学更准确地识别高级别肿瘤,并与预后不良相关;ctDNA 从未与长骨中的 CS 1 级/非典型软骨肿瘤(ACT)、手部和足部小骨中的肿瘤或小于 80mm 的肿瘤相关。尽管结果很有希望,但它们基于少数患者,因此,将这种血液检测作为当前标准治疗方案的补充检测引入临床实践,将允许更严格地评估该检测,并开发出更个性化的方法来治疗 CS 患者。