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TERT promoter mutation is an objective clinical marker for disease progression in chondrosarcoma.
Zhang, Yifan; Chen, Yi; Yang, Chen; Seger, Nelly; Hesla, Asle C; Tsagkozis, Panagiotis; Larsson, Olle; Lin, Yingbo; Haglund, Felix.
Afiliação
  • Zhang Y; Department of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden.
  • Chen Y; Department of Clinical Pathology and Cytology, Karolinska University Hospital Solna, Stockholm, Sweden.
  • Yang C; Department of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden.
  • Seger N; Department of Clinical Pathology and Cytology, Karolinska University Hospital Solna, Stockholm, Sweden.
  • Hesla AC; Department of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden.
  • Tsagkozis P; Department of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden.
  • Larsson O; Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.
  • Lin Y; Department of Orthopedic Surgery, Karolinska University Hospital Solna, Stockholm, Sweden.
  • Haglund F; Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.
Mod Pathol ; 34(11): 2020-2027, 2021 11.
Article em En | MEDLINE | ID: mdl-34108637
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.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Limite: Adolescent / Adult / Aged / Aged80 / Child / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Limite: Adolescent / Adult / Aged / Aged80 / Child / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2021 Tipo de documento: Article