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Validation of a novel risk score to predict early and late recurrence in solitary fibrous tumour.
Georgiesh, Tatiana; Aggerholm-Pedersen, Ninna; Schöffski, Patrick; Zhang, Yifan; Napolitano, Andrea; Bovée, Judith V M G; Hjelle, Åse; Tang, Gordon; Spalek, Mateusz; Nannini, Margherita; Swanson, David; Baad-Hansen, Thomas; Sciot, Raf; Hesla, Asle C; Huang, Paul; Dorleijn, Desiree; Haugland, Hans Kristian; Lacambra, Maribel; Skoczylas, Jacek; Pantaleo, Maria A; Haas, Rick L; Meza-Zepeda, Leonardo A; Haller, Florian; Czarnecka, Anna M; Loong, Herbert; Jebsen, Nina L; van de Sande, Michiel; Jones, Robin L; Haglund, Felix; Timmermans, Iris; Safwat, Akmal; Bjerkehagen, Bodil; Boye, Kjetil.
Afiliação
  • Georgiesh T; Department of Pathology, Oslo University Hospital, Oslo, Norway.
  • Aggerholm-Pedersen N; Department of Tumour Biology, Institute for Cancer Research, Oslo University Hospital, Oslo, Norway.
  • Schöffski P; Department of Oncology, Aarhus University Hospital, Aarhus, Denmark.
  • Zhang Y; Department of General Medical Oncology, University Hospitals Leuven, Leuven, Belgium.
  • Napolitano A; Department of Oncology-Pathology, Karolinska Institutet and Clinical Pathology and Cancer Diagnostics, Karolinska University Hospital, Stockholm, Sweden.
  • Bovée JVMG; Sarcoma Unit, The Royal Marsden Hospital and The Institute of Cancer Research, London, UK.
  • Hjelle Å; Department of Pathology, Leiden University Medical Center, Leiden, The Netherlands.
  • Tang G; Department of Oncology, Haukeland University Hospital, Bergen, Norway.
  • Spalek M; Department of Clinical Oncology, Prince of Wales Hospital, Hong Kong SAR, China.
  • Nannini M; Department of Soft Tissue/Bone Sarcoma and Melanoma, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
  • Swanson D; Division of Oncology, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
  • Baad-Hansen T; Oslo Centre for Biostatistics and Epidemiology, Oslo University Hospital, Oslo, Norway.
  • Sciot R; Department of Orthopedic Surgery, Aarhus University Hospital, Aarhus, Denmark.
  • Hesla AC; Department of Pathology, University Hospitals Leuven, Leuven, Belgium.
  • Huang P; Department of Molecular Medicine and Surgery, Karolinska Institutet and Clinical Orthopaedics, Karolinska University Hospital, Stockholm, Sweden.
  • Dorleijn D; Division of Molecular Pathology, The Institute of Cancer Research, London, UK.
  • Haugland HK; Department of Orthopedic Surgery, Bone and Soft Tissue Tumor Unit, Leiden University Medical Center, Leiden, The Netherlands.
  • Lacambra M; Department of Pathology, Haukeland University Hospital, Bergen, Norway.
  • Skoczylas J; Department of Clinical Oncology, The Chinese University of Hong Kong, Hong Kong SAR, China.
  • Pantaleo MA; Department of Soft Tissue/Bone Sarcoma and Melanoma, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
  • Haas RL; Department of Experimental, Diagnostic and Specialty Medicine, University of Bologna, Bologna, Italy.
  • Meza-Zepeda LA; Department of Radiotherapy, the Netherlands Cancer Institute, Amsterdam, The Netherlands and Department of Radiotherapy, the Leiden University Medical Center, Leiden, The Netherlands.
  • Haller F; Department of Tumour Biology, Institute for Cancer Research, Oslo University Hospital, Oslo, Norway.
  • Czarnecka AM; Department of Core Facilities, Institute for Cancer Research, Oslo University Hospital, Oslo, Norway.
  • Loong H; Institute of Pathology, University Hospital Erlangen, Friedrich-Alexander University Erlangen-Nuremberg, Erlangen, Germany.
  • Jebsen NL; Department of Soft Tissue/Bone Sarcoma and Melanoma, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
  • van de Sande M; Department of Clinical Oncology, The Chinese University of Hong Kong, Hong Kong SAR, China.
  • Jones RL; Department of Oncology, Haukeland University Hospital, Bergen, Norway.
  • Haglund F; Department of Orthopedic Surgery, Bone and Soft Tissue Tumor Unit, Leiden University Medical Center, Leiden, The Netherlands.
  • Timmermans I; Sarcoma Unit, The Royal Marsden Hospital and The Institute of Cancer Research, London, UK.
  • Safwat A; Department of Oncology-Pathology, Karolinska Institutet and Clinical Pathology and Cancer Diagnostics, Karolinska University Hospital, Stockholm, Sweden.
  • Bjerkehagen B; Department of General Medical Oncology, University Hospitals Leuven, Leuven, Belgium.
  • Boye K; Department of Oncology, Aarhus University Hospital, Aarhus, Denmark.
Br J Cancer ; 127(10): 1793-1798, 2022 Nov.
Article em En | MEDLINE | ID: mdl-36030294
ABSTRACT

BACKGROUND:

Current risk models in solitary fibrous tumour (SFT) were developed using cohorts with short follow-up and cannot reliably identify low-risk patients. We recently developed a novel risk model (G-score) to account for both early and late recurrences. Here, we aimed to validate the G-score in a large international cohort with long-term follow-up.

METHODS:

Data were collected from nine sarcoma referral centres worldwide. Recurrence-free interval (RFi) was the primary endpoint.

RESULTS:

The cohort comprised 318 patients with localised extrameningeal SFTs. Disease recurrence occurred in 96 patients (33%). The estimated 5-year RFi rate was 72%, and the 10-year RFi rate was 52%. G-score precisely predicted recurrence risk with estimated 10-year RFi rate of 84% in low risk, 54% in intermediate risk and 36% in high risk (p < 0.001; C-index 0.691). The mDemicco (p < 0.001; C-index 0.749) and SalasOS (p < 0.001; C-index 0.674) models also predicted RFi but identified low-risk patients less accurate with 10-year RFi rates of 72% and 70%, respectively.

CONCLUSIONS:

G-score is a highly significant predictor of early and late recurrence in SFT and is superior to other models to predict patients at low risk of relapse. A less intensive follow-up schedule could be considered for patients at low recurrence risk according to G-score.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Tumores Fibrosos Solitários / Recidiva Local de Neoplasia Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Br J Cancer Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Noruega

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Tumores Fibrosos Solitários / Recidiva Local de Neoplasia Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Br J Cancer Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Noruega