Prognostic Value of Routinely Measured Inflammatory Biomarkers in Older Cancer Patients: Pooled Analysis of Three Cohorts.

biomarkers cancer mortality older patients

Journal

Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829

Informations de publication

Date de publication:
07 Dec 2021
Historique:
received: 28 10 2021
revised: 25 11 2021
accepted: 29 11 2021
entrez: 24 12 2021
pubmed: 25 12 2021
medline: 25 12 2021
Statut: epublish

Résumé

The prognostic assessment of older cancer patients is complicated by their heterogeneity. We aimed to assess the prognostic value of routine inflammatory biomarkers. A pooled analysis of prospective multicenter cohorts of cancer patients aged ≥70 was performed. We measured CRP and albumin, and calculated Glasgow Prognostic Score (GPS) and CRP/albumin ratio. The GPS has three levels (0 = CRP ≤ 10 mg/L, albumin ≥ 35 g/L, i.e., normal values; 1 = one abnormal value; 2 = two abnormal values). One-year mortality was assessed using Cox models. Discriminative power was assessed using Harrell's C index (C) and net reclassification improvement (NRI). Overall, 1800 patients were analyzed (mean age: 79 ± 6; males: 62%; metastases: 38%). The GPS and CRP/albumin ratio were independently associated with mortality in patients not at risk of frailty (hazard ratio [95% confidence interval] = 4.48 [2.03-9.89] for GPS1, 11.64 [4.54-29.81] for GPS2, and 7.15 [3.22-15.90] for CRP/albumin ratio > 0.215) and in patients at risk of frailty (2.45 [1.79-3.34] for GPS1, 3.97 [2.93-5.37] for GPS2, and 2.81 [2.17-3.65] for CRP/albumin ratio > 0.215). The discriminative power of the baseline clinical model (C = 0.82 [0.80-0.83]) was increased by adding GPS (C = 0.84 [0.82-0.85]; NRI events (NRI+) = 10% [2-16]) and CRP/albumin ratio (C = 0.83 [0.82-0.85]; NRI+ = 14% [2-17]). Routine inflammatory biomarkers add prognostic value to clinical factors in older cancer patients.

Sections du résumé

BACKGROUND BACKGROUND
The prognostic assessment of older cancer patients is complicated by their heterogeneity. We aimed to assess the prognostic value of routine inflammatory biomarkers.
METHODS METHODS
A pooled analysis of prospective multicenter cohorts of cancer patients aged ≥70 was performed. We measured CRP and albumin, and calculated Glasgow Prognostic Score (GPS) and CRP/albumin ratio. The GPS has three levels (0 = CRP ≤ 10 mg/L, albumin ≥ 35 g/L, i.e., normal values; 1 = one abnormal value; 2 = two abnormal values). One-year mortality was assessed using Cox models. Discriminative power was assessed using Harrell's C index (C) and net reclassification improvement (NRI).
RESULTS RESULTS
Overall, 1800 patients were analyzed (mean age: 79 ± 6; males: 62%; metastases: 38%). The GPS and CRP/albumin ratio were independently associated with mortality in patients not at risk of frailty (hazard ratio [95% confidence interval] = 4.48 [2.03-9.89] for GPS1, 11.64 [4.54-29.81] for GPS2, and 7.15 [3.22-15.90] for CRP/albumin ratio > 0.215) and in patients at risk of frailty (2.45 [1.79-3.34] for GPS1, 3.97 [2.93-5.37] for GPS2, and 2.81 [2.17-3.65] for CRP/albumin ratio > 0.215). The discriminative power of the baseline clinical model (C = 0.82 [0.80-0.83]) was increased by adding GPS (C = 0.84 [0.82-0.85]; NRI events (NRI+) = 10% [2-16]) and CRP/albumin ratio (C = 0.83 [0.82-0.85]; NRI+ = 14% [2-17]).
CONCLUSIONS CONCLUSIONS
Routine inflammatory biomarkers add prognostic value to clinical factors in older cancer patients.

Identifiants

pubmed: 34944774
pii: cancers13246154
doi: 10.3390/cancers13246154
pmc: PMC8699299
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Nadia Oubaya (N)

University Paris Est Creteil, INSERM, IMRB, F-94010 Créteil, France.
Department of Public Health, Henri Mondor Hospital, AP-HP, F-94010 Créteil, France.

Pierre Soubeyran (P)

Department of Medical Oncology, Institut Bergonié, University of Bordeaux, Inserm U1218, F-33000 Bordeaux, France.

Nicoleta Reinald (N)

University Paris Est Creteil, INSERM, IMRB, F-94010 Créteil, France.

Marianne Fonck (M)

Department of Medical Oncology, Institut Bergonié, University of Bordeaux, Inserm U1218, F-33000 Bordeaux, France.

Mylène Allain (M)

University Paris Est Creteil, INSERM, IMRB, F-94010 Créteil, France.
Clinical Research Unit, Henri Mondor Hospital, AP-HP, F-94010 Créteil, France.

Sonia Zebachi (S)

University Paris Est Creteil, INSERM, IMRB, F-94010 Créteil, France.

Damien Heitz (D)

Oncology and Hematology Unit, Strasbourg University Hospital, Hautepierre Hospital, F-67200 Strasbourg, France.

Marie Laurent (M)

University Paris Est Creteil, INSERM, IMRB, F-94010 Créteil, France.
Department of Geriatrics, Henri Mondor Hospital, AP-HP, F-94010 Créteil, France.

Cécile Delattre (C)

Supportive Care Unit, Institut de Cancérologie of Lorraine Alexis Vautrin, F-54500 Vandoeuvre les Nancy, France.

Philippe Caillet (P)

University Paris Est Creteil, INSERM, IMRB, F-94010 Créteil, France.
Department of Geriatrics, Hôpital Européen Georges Pompidou, AP-HP, F-75015 Paris, France.

Jérôme Dauba (J)

Department of Oncology, Dax Hospital, F-40100 Dax, France.

Sylvie Bastuji-Garin (S)

University Paris Est Creteil, INSERM, IMRB, F-94010 Créteil, France.
Department of Public Health, Henri Mondor Hospital, AP-HP, F-94010 Créteil, France.

Gilles Albrand (G)

Department of Geriatrics, Centre Hospitalier Lyon Sud, Hospices Civils de Lyon, F-69310 Pierre-Bénite, France.

Michael Bringuier (M)

Department of Medical Oncology, Institut Curie, F-92210 Saint-Cloud, France.

Muriel Rainfray (M)

Department of Geriatrics, Bordeaux University Hospital, F-33000 Bordeaux, France.

Etienne Brain (E)

Department of Medical Oncology, Institut Curie, F-92210 Saint-Cloud, France.

Thomas Grellety (T)

Department of Medical Oncology, Institut Bergonié, University of Bordeaux, Inserm U1218, F-33000 Bordeaux, France.

Elena Paillaud (E)

University Paris Est Creteil, INSERM, IMRB, F-94010 Créteil, France.
Department of Geriatrics, Hôpital Européen Georges Pompidou, AP-HP, F-75015 Paris, France.

Simone Mathoulin-Pélissier (S)

Epicene Team, Bordeaux Population Health Research Center, University Bordeaux, INSERM, UMR 1219, F-33000 Bordeaux, France.
Clinical and Epidemiological Research Unit, Comprehensive Cancer Center, INSERM, CIC1401, Institut Bergonié, F-33000 Bordeaux, France.

Carine Bellera (C)

Epicene Team, Bordeaux Population Health Research Center, University Bordeaux, INSERM, UMR 1219, F-33000 Bordeaux, France.
Clinical and Epidemiological Research Unit, Comprehensive Cancer Center, INSERM, CIC1401, Institut Bergonié, F-33000 Bordeaux, France.

Florence Canouï-Poitrine (F)

University Paris Est Creteil, INSERM, IMRB, F-94010 Créteil, France.
Department of Public Health, Henri Mondor Hospital, AP-HP, F-94010 Créteil, France.

Classifications MeSH