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E-Poster Display

62P - Prognostic significance of baseline neutrophil lymphocyte ratio (NLR), platelet lymphocyte ratio (PLR) and systemic immune-inflammation index (SII) in patients (pts) with biliary tract cancer (BTC)

Date

17 Sep 2020

Session

E-Poster Display

Topics

Tumour Site

Hepatobiliary Cancers

Presenters

Noor-Ul-Ain Tariq

Citation

Annals of Oncology (2020) 31 (suppl_4): S260-S273. 10.1016/annonc/annonc259

Authors

N. Tariq1, H. Raja2, X. Wang3, S. Mehta4, A. Lamarca5, R. Hubner3, M.G. McNamara3, J.W. Valle6

Author affiliations

  • 1 Medical Oncology Department, Clatterbridge Cancer Center, Wirral - NHS Foundation Trust, CH63 4JY - Birkenhead/GB
  • 2 Medical Oncology, Luton and Dunstable University Hospital, LU40DZ - Luton/GB
  • 3 Statistics, The Christie Foundation Trust, M20 - BX/GB
  • 4 Clinical Oncology Department, Clatterbridge Cancer Center, Wirral - NHS Foundation Trust, CH63 4JY - Birkenhead/GB
  • 5 Dept. Medical Oncology, The Christie NHS Foundation Trust, M20 4BX - Manchester/GB
  • 6 Medical Oncology Department, The Christie NHS Foundation Trust, M20 4BX - Manchester/GB

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Abstract 62P

Background

Biliary tract cancer is a poor prognosis disease. Due to the role of chronic inflammation in the development of BTC, inflammatory markers such as NLR, PLR, and SII might be useful as prognostic markers in this disease group.

Methods

Data from sequential pts with BTC referred to The Christie (Jan 2012 - Aug 2017) were reviewed retrospectively. Median (med) value was used to dichotomise subgroups for baseline NLR, PLR and SII (Platelets x Neutrophils/Lymphocytes) for balanced division of patients. The Kaplan-Meier survival method was used and association of overall survival (OS) with different co-variables was analysed using Cox proportional hazard regression.

Results

Data from 591 pts were included; median age was 69 years, 46% were males, Eastern Co-operative Oncology Group performance status (ECOG PS) 1 was the commonest PS (51.1%). Patients had extrahepatic cholangiocarcinoma (CCA): 32.3%, intrahepatic CCA: 28.7%, gallbladder carcinoma: 20.6%, or ampulla of Vater carcinoma: 15.9%. Stage: 54.2% stage IV, 32.5% stage III, and 13.2% stage I/II; 89% of pts had died at time of analysis. The cut-off for NLR was ≥3.64, PLR was ≥193.3 and SII was ≥1082.1. The median OS for the entire cohort was 13.4 months (mths) (95% Confidence Interval [CI] 12-14.8); the 5-year survival rate was 5.1% (95%CI 3.3-7.9). The multivariable analysis was adjusted for gender, age, stage, ECOG PS, treatment type, and NLR, PLR and SII at baseline as these were significant at univariate analysis. On multivariable analysis, NLR (HR 1.34, 95%CI 1.1-1.7, p=0.01) and SII (HR 1.57, 95%CI 1.2-2.0, p<0.001) were both independent prognostic factors, with better OS in patients with lower NLR (med OS 17.7 mths vs 9.2 mths, [95% CI 16.66-22.3], p<0.001) and lower SII (med OS 17.9 mths vs 8.6 mths [95% CI 16.26-22.16], p<0.001).

Conclusions

Lower baseline NLR and SII were prognostic for better OS in pts with BTC. Prospective studies are needed to explore the clinical prognostic relevance of these markers.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

The authors.

Funding

Has not received any funding.

Disclosure

N-U-A. Tariq: Honoraria (self), Travel/Accommodation/Expenses: Boehringer-Ingelheim; Travel/Accommodation/Expenses: Roche; Honoraria (self): AstraZeneca. A. Lamarca: Advisory/Consultancy: EISAI; Advisory/Consultancy: Nutricia; Advisory/Consultancy, Speaker Bureau/Expert testimony, Travel/Accommodation/Expenses: Ipsen; Advisory/Consultancy: QED; Advisory/Consultancy: Roche; Speaker Bureau/Expert testimony: Merck; Speaker Bureau/Expert testimony, Travel/Accommodation/Expenses: Pfizer; Speaker Bureau/Expert testimony: Incyte; Speaker Bureau/Expert testimony, Travel/Accommodation/Expenses: AAA; Travel/Accommodation/Expenses: Bayer; Travel/Accommodation/Expenses: SirtEx; Travel/Accommodation/Expenses: Novartis; Travel/Accommodation/Expenses: Mylan and Declath. R. Hubner: Advisory/Consultancy, Travel/Accommodation/Expenses: Roche; Advisory/Consultancy: Eisai; Advisory/Consultancy, Travel/Accommodation/Expenses: BMS; Advisory/Consultancy: Ipsen; Advisory/Consultancy: BTG; Speaker Bureau/Expert testimony: Prime Oncology; Travel/Accommodation/Expenses: Bayer. M.G. McNamara: Research grant/Funding (self): Servier; Honoraria (self), Advisory/Consultancy, Speaker Bureau/Expert testimony, Research grant/Funding (self), Travel/Accommodation/Expenses: Ipsen; Honoraria (self), Speaker Bureau/Expert testimony, Research grant/Funding (self): Nucana; Honoraria (self), Speaker Bureau/Expert testimony: Pfizer; Travel/Accommodation/Expenses: Bayer; Advisory/Consultancy: Celgene; Advisory/Consultancy: Sirtex; Advisory/Consultancy: Baxalta; Advisory/Consultancy: Incyte. J.W. Valle: Honoraria (self), Advisory/Consultancy, Speaker Bureau/Expert testimony: Ipsen; Advisory/Consultancy: Agios; Advisory/Consultancy: AstraZeneca; Advisory/Consultancy: Debiopharm; Advisory/Consultancy: Delcath Systems; Advisory/Consultancy: GenoScience Pharma; Advisory/Consultancy, Speaker Bureau/Expert testimony: Imaging Equipment Ltd; Advisory/Consultancy: Incyte; Advisory/Consultancy: Keocyt; Advisory/Consultancy: Merck; Advisory/Consultancy: Mundipharma EDO; Advisory/Consultancy, Speaker Bureau/Expert testimony: Novartis; Advisory/Consultancy, Speaker Bureau/Expert testimony, Travel/Accommodation/Expenses: Nucana; Advisory/Consultancy: PCI Biotech; Advisory/Consultancy: Pieris Pharmaceuticals; Advisory/Consultancy, Travel/Accommodation/Expenses: Pfizer; Advisory/Consultancy: QED; Advisory/Consultancy: Servier; Advisory/Consultancy: Wren Laboratories; Travel/Accommodation/Expenses: Celgene. All other authors have declared no conflicts of interest.

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