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Systemic inflammatory prognostic scores in advanced pancreatic adenocarcinoma.

Authors :
Ma LX
Wang Y
Espin-Garcia O
Allen MJ
Jang GH
Zhang A
Dodd A
Ramotar S
Hutchinson S
Tehfe M
Ramjeesingh R
Biagi J
Wilson JM
Notta F
Fischer SE
Zogopoulos G
Gallinger S
Grant RC
Khokha R
Chan N
Grünwald BT
Knox JJ
O'Kane GM
Source :
British journal of cancer [Br J Cancer] 2023 May; Vol. 128 (10), pp. 1916-1921. Date of Electronic Publication: 2023 Mar 16.
Publication Year :
2023

Abstract

Background: Systemic inflammatory scores may aid prognostication and patient selection for trials. We compared five scores in advanced pancreatic adenocarcinoma (PDAC).<br />Methods: Unresectable/metastatic PDAC patients enrolled in the Comprehensive Molecular Characterisation of Advanced Pancreatic Ductal Adenocarcinoma for Better Treatment Selection trial (NCT02750657) were included. Patients had pre-treatment biopsies for whole genome and RNA sequencing. CD8 immunohistochemistry was available in a subset. The neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio, Prognostic Nutritional Index, Gustave Roussy Immune Score (GRIm-S), and Memorial Sloan Kettering Prognostic Score (MPS) were calculated. Overall survival (OS) was estimated using Kaplan-Meier methods. Associations between inflammatory scores, clinical/genomic characteristics, and OS were analysed.<br />Results: We analysed 263 patients. High-risk NLR, GRIm-S and MPS were poorly prognostic. The GRIm-S had the highest predictive ability: median OS 6.4 vs. 10 months for high risk vs. low-risk (P < 0.001); HR 2.26 (P < 0.001). ECOG ≥ 1, the basal-like subtype, and low-HRDetect were additional poor prognostic factors (P < 0.01). Inflammatory scores did not associate with RNA-based classifiers or homologous recombination repair deficiency genotypes. High-risk MPS (P = 0.04) and GRIm-S (P = 0.02) patients had lower median CD8 + tumour-infiltrating lymphocytes.<br />Conclusions: Inflammatory scores incorporating NLR have prognostic value in advanced PDAC. Understanding immunophenotypes of poor-risk patients and using these scores in trials will advance the field.<br /> (© 2023. The Author(s), under exclusive licence to Springer Nature Limited.)

Details

Language :
English
ISSN :
1532-1827
Volume :
128
Issue :
10
Database :
MEDLINE
Journal :
British journal of cancer
Publication Type :
Academic Journal
Accession number :
36927977
Full Text :
https://doi.org/10.1038/s41416-023-02214-0