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The application of the Glasgow prognostic score to predict the survival in patients with metastatic pancreatic carcinoma

OBJECTIVES: Thither is a more pressing effort to think about chemotherapy (CTx) in second-line and beyond in patients with metastatic pancreatic cancer (mPC). The current work aimed to evaluate the value of the Glasgow prognostic score (GPS) and modified Glasgow prognostic score (mGPS) to predict th...

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Autores principales: Mohammed, Amrallah A., Al-Zahrani, Omar, Elsayed, Fifi Mostafa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Scientific Scholar 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9699916/
https://www.ncbi.nlm.nih.gov/pubmed/36447500
http://dx.doi.org/10.25259/IJPC_81_2021
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author Mohammed, Amrallah A.
Al-Zahrani, Omar
Elsayed, Fifi Mostafa
author_facet Mohammed, Amrallah A.
Al-Zahrani, Omar
Elsayed, Fifi Mostafa
author_sort Mohammed, Amrallah A.
collection PubMed
description OBJECTIVES: Thither is a more pressing effort to think about chemotherapy (CTx) in second-line and beyond in patients with metastatic pancreatic cancer (mPC). The current work aimed to evaluate the value of the Glasgow prognostic score (GPS) and modified Glasgow prognostic score (mGPS) to predict the survival in patients receiving second-line CTx protocol. MATERIAL AND METHODS: We retrospectively reviewed the patients’ medical files with mPC who received second-line CTx protocol between September 2013 and December 2017. The GPS/mGPS graded from 0 to 2 based on C-reactive protein and serum albumin. RESULTS: One hundred and sixty-nine patients with mPC were eligible. Survival of patients with Score 0 (GPS/mGPS) was better than that of Score 1 (GPS/mGPS) or Score 2 (GPS/mGPS), which was statistically significant (P < 0.001). Of 78 patients who died, only 16 patients belonged to Score 0 (GPS/mGPS), compared to 30 patients belonged to Score 1 (GPS/mGPS) and 32 patients belonged to Score 2 (GPS/mGPS). Univariate analysis showed that high GPS/mGPS (P < 0.000) as well as poor Eastern Cooperative Oncology Group Performance Status (P < 0.000) and metastasis either to the liver (P < 0.01) or lung (P < 0.04) were linked with worse prognosis. A statistically significant association was detected between the two scores. Cohen’s Kappa coefficient (k) was 0.9, SD = 0.03; 95% CI (0.787–0.922; P < 0.001). CONCLUSION: Our data suggested that GPS/mGPS is an easy and applicable index that may be used in daily practice and may help in the prognostic stratification of mPC patients to avert overtreatment in frail patients and raise the best supportive treatment concept.
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spelling pubmed-96999162022-11-28 The application of the Glasgow prognostic score to predict the survival in patients with metastatic pancreatic carcinoma Mohammed, Amrallah A. Al-Zahrani, Omar Elsayed, Fifi Mostafa Indian J Palliat Care Original Article OBJECTIVES: Thither is a more pressing effort to think about chemotherapy (CTx) in second-line and beyond in patients with metastatic pancreatic cancer (mPC). The current work aimed to evaluate the value of the Glasgow prognostic score (GPS) and modified Glasgow prognostic score (mGPS) to predict the survival in patients receiving second-line CTx protocol. MATERIAL AND METHODS: We retrospectively reviewed the patients’ medical files with mPC who received second-line CTx protocol between September 2013 and December 2017. The GPS/mGPS graded from 0 to 2 based on C-reactive protein and serum albumin. RESULTS: One hundred and sixty-nine patients with mPC were eligible. Survival of patients with Score 0 (GPS/mGPS) was better than that of Score 1 (GPS/mGPS) or Score 2 (GPS/mGPS), which was statistically significant (P < 0.001). Of 78 patients who died, only 16 patients belonged to Score 0 (GPS/mGPS), compared to 30 patients belonged to Score 1 (GPS/mGPS) and 32 patients belonged to Score 2 (GPS/mGPS). Univariate analysis showed that high GPS/mGPS (P < 0.000) as well as poor Eastern Cooperative Oncology Group Performance Status (P < 0.000) and metastasis either to the liver (P < 0.01) or lung (P < 0.04) were linked with worse prognosis. A statistically significant association was detected between the two scores. Cohen’s Kappa coefficient (k) was 0.9, SD = 0.03; 95% CI (0.787–0.922; P < 0.001). CONCLUSION: Our data suggested that GPS/mGPS is an easy and applicable index that may be used in daily practice and may help in the prognostic stratification of mPC patients to avert overtreatment in frail patients and raise the best supportive treatment concept. Scientific Scholar 2022-11-23 2022 /pmc/articles/PMC9699916/ /pubmed/36447500 http://dx.doi.org/10.25259/IJPC_81_2021 Text en © 2022 Published by Scientific Scholar on behalf of Indian Journal of Palliative Care https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-Share Alike 4.0 License, which allows others to remix, transform, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Original Article
Mohammed, Amrallah A.
Al-Zahrani, Omar
Elsayed, Fifi Mostafa
The application of the Glasgow prognostic score to predict the survival in patients with metastatic pancreatic carcinoma
title The application of the Glasgow prognostic score to predict the survival in patients with metastatic pancreatic carcinoma
title_full The application of the Glasgow prognostic score to predict the survival in patients with metastatic pancreatic carcinoma
title_fullStr The application of the Glasgow prognostic score to predict the survival in patients with metastatic pancreatic carcinoma
title_full_unstemmed The application of the Glasgow prognostic score to predict the survival in patients with metastatic pancreatic carcinoma
title_short The application of the Glasgow prognostic score to predict the survival in patients with metastatic pancreatic carcinoma
title_sort application of the glasgow prognostic score to predict the survival in patients with metastatic pancreatic carcinoma
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9699916/
https://www.ncbi.nlm.nih.gov/pubmed/36447500
http://dx.doi.org/10.25259/IJPC_81_2021
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