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Biomarkers of systemic inflammation provide additional prognostic stratification in cancers of unknown primary.
Harvey, Svenja; Stares, Mark; Scott, Julie-Anne; Thottiyil, Tharun Joseph Vattam; Conway, Alicia-Marie; Haigh, Rachel; Brown, Jackie; Knowles, Gillian; Dasgupta, Sonali; Shiu, Kai-Keen; Mitchell, Claire; Barrie, Colin; Cook, Natalie; Clive, Sally.
Afiliação
  • Harvey S; University of Edinburgh, Cancer Research UK Edinburgh Centre, Institute of Genetics and Cancer, Western General Hospital, Edinburgh, UK.
  • Stares M; University of Edinburgh, Cancer Research UK Edinburgh Centre, Institute of Genetics and Cancer, Western General Hospital, Edinburgh, UK.
  • Scott JA; Edinburgh Cancer Centre, NHS Lothian, Western General Hospital, Edinburgh, UK.
  • Thottiyil TJV; Experimental Cancer Medicine Team (ECMT), The Christie NHS Foundation Trust, Manchester, UK.
  • Conway AM; University College London Hospitals NHS Foundation Trust, London, UK.
  • Haigh R; The University of Manchester, Cancer Research UK Manchester Institute, Manchester, UK.
  • Brown J; The Christie NHS Foundation Trust, Manchester, UK.
  • Knowles G; Edinburgh Cancer Centre, NHS Lothian, Western General Hospital, Edinburgh, UK.
  • Dasgupta S; Edinburgh Cancer Centre, NHS Lothian, Western General Hospital, Edinburgh, UK.
  • Shiu KK; Edinburgh Cancer Centre, NHS Lothian, Western General Hospital, Edinburgh, UK.
  • Mitchell C; Velindre University NHS Trust, Cardiff, UK.
  • Barrie C; University College London Hospitals NHS Foundation Trust, London, UK.
  • Cook N; The Christie NHS Foundation Trust, Manchester, UK.
  • Clive S; Edinburgh Cancer Centre, NHS Lothian, Western General Hospital, Edinburgh, UK.
Cancer Med ; 13(3): e6988, 2024 Feb.
Article em En | MEDLINE | ID: mdl-38404120
ABSTRACT

BACKGROUND:

Biomarkers of systemic inflammation have been shown to predict outcomes in patients with cancer of unknown primary (CUP). We sought to validate these findings in patients with confirmed CUP (cCUP) and explore their role alongside existing clinicopathological prognostic categories. PATIENTS AND

METHODS:

CUP oncologist from across the United Kingdom were invited to include patients with cCUP referred to their local CUP multidisciplinary team. Patient demographics, clinical, pathological and outcome data were recorded and analysed.

RESULTS:

Data were available for 548 patients from four CUP services. 23% (n = 124) of patients met clinicopathological criteria for favourable-risk cCUP. On multivariate analysis c-reactive protein (CRP) (p < 0.001) and the Scottish Inflammatory Prognostic Score (SIPS combining albumin and neutrophil count) (p < 0.001) were independently predictive of survival. CRP and SIPS effectively stratified survival in patients with both favourable-risk and poor-risk cCUP based on clinicopathological features.

CONCLUSIONS:

Biomarkers of systemic inflammation are reliable prognostic factors in patients with cCUP, regardless of clinicopathological subgroup. We recommend that CRP or SIPS are incorporated into routine clinical assessments of patients with cCUP as a tool to aid investigation and/or treatment decision-making across all groups. Established clinicopathological factors can then be used to inform management pathways and specific systemic anticancer therapy selection.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Primárias Desconhecidas Limite: Humans Idioma: En Revista: Cancer Med Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Primárias Desconhecidas Limite: Humans Idioma: En Revista: Cancer Med Ano de publicação: 2024 Tipo de documento: Article