Department of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden.
Department of Clinical Pathology and Cytology, Karolinska University Hospital Solna, Stockholm, Sweden.
Mod Pathol. 2021 Nov;34(11):2020-2027. doi: 10.1038/s41379-021-00848-0. Epub 2021 Jun 9.
Chondrosarcomas are the second most common malignant bone tumor. Activating promoter mutations in telomerase reverse transcriptase (TERT) was recently described by us and others as a frequent mutation in high-grade chondrosarcoma. In this study, we investigate the prognostic significance of TERT promoter mutations in 241 chondrosarcomas from 190 patients collected over 24 years (1994-2017). The TERT promoter was sequenced after microdissection of 135 chondrosarcomas from 106 patients in addition to data from our previous cohort. The TERT promoter mutation at -124 C > T was found in 45% of all patients and was significantly associated (p > 0,001) with higher tumor grade, shorter metastasis-free survival, and disease-specific survival. Additionally, TERT promoter-mutated tumors were associated with a more aggressive metastatic pattern. Shorter survival was observed in patients with wild-type primary tumors who developed a mutated metastasis indicative of tumor progression. Primary tumor genetic heterogeneity and altering mutational status between nonsynchronous metastatic lesions suggests that chondrosarcoma is a multiclonal disease progressing through a branching evolution. Conclusion: TERT promoter mutation seems to be a central event in chondrosarcoma progression with association to metastatic disease and disease-related mortality. As an easily analyzed marker, there is future potential to utilize TERT promoter mutation status as a prognostic marker and investigate telomerase-targeted therapy in chondrosarcomas.
软骨肉瘤是第二常见的恶性骨肿瘤。端粒酶逆转录酶(TERT)启动子突变最近被我们和其他人描述为高级别软骨肉瘤的常见突变。在这项研究中,我们调查了 241 例软骨肉瘤患者(190 名患者,收集时间超过 24 年[1994-2017])中 TERT 启动子突变的预后意义。在微切割 106 名患者的 135 例软骨肉瘤后,对 TERT 启动子进行测序,此外还对我们之前的队列数据进行了测序。在所有患者中,发现 TERT 启动子-124 C> T 突变的比例为 45%,与较高的肿瘤分级、无转移生存时间较短和疾病特异性生存时间较短显著相关(p>0.001)。此外,TERT 启动子突变的肿瘤与侵袭性更高的转移模式相关。在发生突变转移的野生型原发性肿瘤患者中观察到较短的生存时间,提示肿瘤进展。原发性肿瘤遗传异质性和非同步转移病变之间的突变状态改变提示软骨肉瘤是一种通过分支进化进展的多克隆疾病。结论:TERT 启动子突变似乎是软骨肉瘤进展中的一个核心事件,与转移性疾病和疾病相关死亡率相关。作为一种易于分析的标志物,未来有可能利用 TERT 启动子突变状态作为预后标志物,并研究软骨肉瘤中的端粒酶靶向治疗。