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A prognostic profile of hypoxia-induced genes for localised high-grade soft tissue sarcoma.
Aggerholm-Pedersen, Ninna; Sørensen, Brita Singers; Overgaard, Jens; Toustrup, Kasper; Baerentzen, Steen; Nielsen, Ole Steen; Maretty-Kongstad, Katja; Nordsmark, Marianne; Alsner, Jan; Safwat, Akmal.
Affiliation
  • Aggerholm-Pedersen N; Department of Experimental Clinical Oncology, Aarhus University Hospital, Norrebrogade 44, Aarhus C 8000, Denmark.
  • Sørensen BS; Department of Experimental Clinical Oncology, Aarhus University Hospital, Norrebrogade 44, Aarhus C 8000, Denmark.
  • Overgaard J; Department of Experimental Clinical Oncology, Aarhus University Hospital, Norrebrogade 44, Aarhus C 8000, Denmark.
  • Toustrup K; Department of Oncology, Aarhus University Hospital, Norrebrogade 44, Aarhus C 8000, Denmark.
  • Baerentzen S; Department of Pathology, Aarhus University Hospital, Norrebrogade 44, Aarhus C 8000, Denmark.
  • Nielsen OS; Faculty of Health, Aarhus University, Nordre Ringgade 1, Aarhus C 8000, Denmark.
  • Maretty-Kongstad K; Department of Experimental Clinical Oncology, Aarhus University Hospital, Norrebrogade 44, Aarhus C 8000, Denmark.
  • Nordsmark M; Department of Oncology, Aarhus University Hospital, Norrebrogade 44, Aarhus C 8000, Denmark.
  • Alsner J; Department of Experimental Clinical Oncology, Aarhus University Hospital, Norrebrogade 44, Aarhus C 8000, Denmark.
  • Safwat A; Department of Oncology, Aarhus University Hospital, Norrebrogade 44, Aarhus C 8000, Denmark.
Br J Cancer ; 115(9): 1096-1104, 2016 Oct 25.
Article in En | MEDLINE | ID: mdl-27701385
BACKGROUND: For decades, tumour hypoxia has been pursued as a cancer treatment target. However, prognostic and predictive biomarkers are essential for the use of this target in the clinic. This study investigates the prognostic value of a hypoxia-induced gene profile in localised soft tissue sarcoma (STS). METHODS: The hypoxia-induced gene quantification was performed by real-time quantitative PCR (RT-qPCR) of formalin-fixed, paraffin-embedded tissue samples. The gene expression cut-points were determined in a test cohort of 55 STS patients and used to allocate each patient into a more or a less hypoxic group. The cut-points found in the test cohort were applied to a cohort of 77 STS patients for validation. RESULTS: For patients with localised high-grade STS treated with surgery with or without postoperative radiation therapy, the prognostic value of the hypoxia-induced gene profile was proved in the test cohort and confirmed in the validation cohort. After adjustment for confounders, the hazard ratio (HR) was 3.2 (95% CI: 1.5; 7.0) for patients with more hypoxic tumours compared with patients with less hypoxic tumours regarding disease-specific survival. Moreover, for the development of metastatic disease, the HR was 2.61 (95% CI: 1.27; 5.33). CONCLUSIONS: The hypoxia-induced gene profile is a validated independent prognostic marker that may help identify STS patients needing more aggressive or different adjuvant treatment.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Sarcoma / Biomarkers, Tumor / Tumor Hypoxia Type of study: Prognostic_studies Limits: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Language: En Journal: Br J Cancer Year: 2016 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Sarcoma / Biomarkers, Tumor / Tumor Hypoxia Type of study: Prognostic_studies Limits: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Language: En Journal: Br J Cancer Year: 2016 Document type: Article Affiliation country: Country of publication: