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Biomarkers of systemic inflammation predict survival with first-line immune checkpoint inhibitors in non-small-cell lung cancer.
Stares, M; Ding, T E; Stratton, C; Thomson, F; Baxter, M; Cagney, H; Cumming, K; Swan, A; Ross, F; Barrie, C; Maclennan, K; Campbell, S; Evans, T; Tufail, A; Harrow, S; Lord, H; Laird, B; MacKean, M; Phillips, I.
Afiliação
  • Stares M; Edinburgh Cancer Centre, NHS Lothian, Western General Hospital, Edinburgh; University of Edinburgh, Cancer Research UK Edinburgh Centre, Institute of Genetics and Cancer, Western General Hospital, Edinburgh.
  • Ding TE; Edinburgh Cancer Centre, NHS Lothian, Western General Hospital, Edinburgh.
  • Stratton C; University of Edinburgh, Cancer Research UK Edinburgh Centre, Institute of Genetics and Cancer, Western General Hospital, Edinburgh.
  • Thomson F; University of Edinburgh, Cancer Research UK Edinburgh Centre, Institute of Genetics and Cancer, Western General Hospital, Edinburgh.
  • Baxter M; Division of Molecular and Clinical Medicine, Ninewells Hospital and Medical School, University of Dundee, Dundee; Tayside Cancer Centre, Ninewells Hospital and Medical School, NHS Tayside, Dundee.
  • Cagney H; School of Medicine, Ninewells Hospital and Medical School, University of Dundee, Dundee, UK.
  • Cumming K; Edinburgh Cancer Centre, NHS Lothian, Western General Hospital, Edinburgh.
  • Swan A; Edinburgh Cancer Centre, NHS Lothian, Western General Hospital, Edinburgh.
  • Ross F; Edinburgh Cancer Centre, NHS Lothian, Western General Hospital, Edinburgh.
  • Barrie C; Edinburgh Cancer Centre, NHS Lothian, Western General Hospital, Edinburgh.
  • Maclennan K; Edinburgh Cancer Centre, NHS Lothian, Western General Hospital, Edinburgh.
  • Campbell S; Edinburgh Cancer Centre, NHS Lothian, Western General Hospital, Edinburgh.
  • Evans T; Edinburgh Cancer Centre, NHS Lothian, Western General Hospital, Edinburgh.
  • Tufail A; Edinburgh Cancer Centre, NHS Lothian, Western General Hospital, Edinburgh.
  • Harrow S; Edinburgh Cancer Centre, NHS Lothian, Western General Hospital, Edinburgh.
  • Lord H; Tayside Cancer Centre, Ninewells Hospital and Medical School, NHS Tayside, Dundee.
  • Laird B; University of Edinburgh, Cancer Research UK Edinburgh Centre, Institute of Genetics and Cancer, Western General Hospital, Edinburgh.
  • MacKean M; Edinburgh Cancer Centre, NHS Lothian, Western General Hospital, Edinburgh.
  • Phillips I; Edinburgh Cancer Centre, NHS Lothian, Western General Hospital, Edinburgh; University of Edinburgh, Cancer Research UK Edinburgh Centre, Institute of Genetics and Cancer, Western General Hospital, Edinburgh. Electronic address: Iain.phillips@nhslothian.scot.nhs.uk.
ESMO Open ; 7(2): 100445, 2022 04.
Article em En | MEDLINE | ID: mdl-35398717
ABSTRACT

INTRODUCTION:

Pembrolizumab is an established first-line option for patients with advanced non-small-cell lung cancer (NSCLC) expressing programmed death-ligand 1 ≥50%. Durable responses are seen in a subset of patients; however, many derive little clinical benefit. Biomarkers of the systemic inflammatory response predict survival in NSCLC. We evaluated their prognostic significance in patients receiving first-line pembrolizumab for advanced NSCLC.

METHODS:

Patients treated with first-line pembrolizumab for advanced NSCLC with programmed death-ligand 1 expression ≥50% at two regional Scottish cancer centres were identified. Pretreatment inflammatory biomarkers (white cell count, neutrophil count, neutrophil/lymphocyte ratio, platelet/lymphocyte ratio, albumin, prognostic nutritional index) were recorded. The relationship between these and progression-free survival (PFS) and overall survival (OS) were examined.

RESULTS:

Data were available for 219 patients. On multivariate analysis, albumin and neutrophil count were independently associated with PFS (P < 0.001, P = 0.002, respectively) and OS (both P < 0.001). A simple score combining these biomarkers was explored. The Scottish Inflammatory Prognostic Score (SIPS) assigned 1 point each for albumin <35 g/l and neutrophil count >7.5 × 109/l to give a three-tier categorical score. SIPS predicted PFS [hazard ratio 2.06, 95% confidence interval (CI) 1.68-2.52 (P < 0.001)] and OS [hazard ratio 2.33, 95% CI 1.86-2.92 (P < 0.001)]. It stratified PFS from 2.5 (SIPS2), to 8.7 (SIPS1) to 17.9 months (SIPS0) (P < 0.001) and OS from 5.1 (SIPS2), to 12.4 (SIPS1) to 28.7 months (SIPS0) (P < 0.001). The relative risk of death before 6 months was 2.96 (95% CI 1.98-4.42) in patients with SIPS2 compared with those with SIPS0-1 (P < 0.001).

CONCLUSIONS:

SIPS, a simple score combining albumin and neutrophil count, predicts survival in patients with NSCLC receiving first-line pembrolizumab. Unlike many proposed prognostic scores, SIPS uses only routinely collected pretreatment test results and provides a categorical score. It stratifies survival across clinically meaningful time periods that may assist clinicians and patients with treatment decisions. We advocate validation of the prognostic utility of SIPS in this and other immune checkpoint inhibitor treatment settings.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Carcinoma Pulmonar de Células não Pequenas / Neoplasias Pulmonares Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Carcinoma Pulmonar de Células não Pequenas / Neoplasias Pulmonares Idioma: En Ano de publicação: 2022 Tipo de documento: Article