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The prognostic value of derived neutrophil to lymphocyte ratio in oesophageal cancer treated with definitive chemoradiotherapy

The prognostic value of derived neutrophil to lymphocyte ratio in oesophageal cancer treated with definitive chemoradiotherapy
The prognostic value of derived neutrophil to lymphocyte ratio in oesophageal cancer treated with definitive chemoradiotherapy
Background and purpose: the derived neutrophil–lymphocyte ratio (dNLR) is a validated prognostic biomarker for cancer survival but has not been extensively studied in locally-advanced oesophageal cancer treated with definitive chemoradiotherapy (dCRT). We aimed to identify the prognostic value of dNLR in patients recruited to the SCOPE1 trial.

Materials and methods: 258 patients were randomised to receive dCRT ± cetuximab. Kaplan–Meier’s curves and both univariable and multivariable Cox regression models were calculated for overall survival (OS), progression free survival (PFS), local PFS inside the radiation volume (LPFSi), local PFS outside the radiation volume (LPFSo), and distant PFS (DPFS).

Results: an elevated pre-treatment dNLR ≥ 2 was significantly associated with decreased OS in univariable (HR 1.74 [95% CI 1.29–2.35], p < 0.001) and multivariable analyses (HR 1.64 [1.17–2.29], p = 0.004). Median OS was 36 months (95% CI 27.8–42.4) if dNLR < 2 and 18.4 months (95% CI 14.1–24.9) if dNLR ≥ 2. All measures of PFS were also significantly reduced with an elevated dNLR. dNLR was prognostic for OS in cases of squamous cell carcinoma with a non-significant trend for adenocarcinoma/undifferentiated tumours.

Conclusions: an elevated pre-treatment dNLR may be an independent prognostic biomarker for OS and PFS in oesophageal cancer patients treated with definitive CRT. dNLR is a simple, inexpensive and readily available tool for risk-stratification and should be considered for use in future oesophageal cancer clinical trials.

The SCOPE1 trial was an International Standard Randomised Controlled Trial [number 47718479].
0167-8140
154-159
Cox, Samantha
117f793c-6211-4e30-a14b-fcd8025148c9
Hurt, Christopher
bf8b37a0-8f08-4b47-b3f3-6fc65f7ab87f
Grenader, Tal
00e7206f-5f87-427c-9117-195df52521bc
Mukherjee, Somnath
81b82408-8d54-4983-a412-81969f5edfdd
Bridgewater, John
3eef73bb-d714-40ae-bd9b-cd9c4a9df6c6
Crosby, Thomas
03643ef4-1539-4a22-914d-b3da1eaa67e8
Cox, Samantha
117f793c-6211-4e30-a14b-fcd8025148c9
Hurt, Christopher
bf8b37a0-8f08-4b47-b3f3-6fc65f7ab87f
Grenader, Tal
00e7206f-5f87-427c-9117-195df52521bc
Mukherjee, Somnath
81b82408-8d54-4983-a412-81969f5edfdd
Bridgewater, John
3eef73bb-d714-40ae-bd9b-cd9c4a9df6c6
Crosby, Thomas
03643ef4-1539-4a22-914d-b3da1eaa67e8

Cox, Samantha, Hurt, Christopher, Grenader, Tal, Mukherjee, Somnath, Bridgewater, John and Crosby, Thomas (2017) The prognostic value of derived neutrophil to lymphocyte ratio in oesophageal cancer treated with definitive chemoradiotherapy. Radiotherapy and Oncology, 125 (1), 154-159. (doi:10.1016/j.radonc.2017.08.023).

Record type: Article

Abstract

Background and purpose: the derived neutrophil–lymphocyte ratio (dNLR) is a validated prognostic biomarker for cancer survival but has not been extensively studied in locally-advanced oesophageal cancer treated with definitive chemoradiotherapy (dCRT). We aimed to identify the prognostic value of dNLR in patients recruited to the SCOPE1 trial.

Materials and methods: 258 patients were randomised to receive dCRT ± cetuximab. Kaplan–Meier’s curves and both univariable and multivariable Cox regression models were calculated for overall survival (OS), progression free survival (PFS), local PFS inside the radiation volume (LPFSi), local PFS outside the radiation volume (LPFSo), and distant PFS (DPFS).

Results: an elevated pre-treatment dNLR ≥ 2 was significantly associated with decreased OS in univariable (HR 1.74 [95% CI 1.29–2.35], p < 0.001) and multivariable analyses (HR 1.64 [1.17–2.29], p = 0.004). Median OS was 36 months (95% CI 27.8–42.4) if dNLR < 2 and 18.4 months (95% CI 14.1–24.9) if dNLR ≥ 2. All measures of PFS were also significantly reduced with an elevated dNLR. dNLR was prognostic for OS in cases of squamous cell carcinoma with a non-significant trend for adenocarcinoma/undifferentiated tumours.

Conclusions: an elevated pre-treatment dNLR may be an independent prognostic biomarker for OS and PFS in oesophageal cancer patients treated with definitive CRT. dNLR is a simple, inexpensive and readily available tool for risk-stratification and should be considered for use in future oesophageal cancer clinical trials.

The SCOPE1 trial was an International Standard Randomised Controlled Trial [number 47718479].

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Accepted/In Press date: 29 August 2017
e-pub ahead of print date: 8 September 2017
Published date: 18 October 2017

Identifiers

Local EPrints ID: 488224
URI: http://eprints.soton.ac.uk/id/eprint/488224
ISSN: 0167-8140
PURE UUID: 74c482f1-cd98-4b0f-9a12-ec01bdd06abb
ORCID for Christopher Hurt: ORCID iD orcid.org/0000-0003-1206-8355

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Date deposited: 18 Mar 2024 18:00
Last modified: 23 Mar 2024 03:13

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Contributors

Author: Samantha Cox
Author: Christopher Hurt ORCID iD
Author: Tal Grenader
Author: Somnath Mukherjee
Author: John Bridgewater
Author: Thomas Crosby

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