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Who could complete and benefit from the adjuvant chemotherapy regarding pancreatic ductal adenocarcinoma? A multivariate‐adjusted analysis at the pre‐adjuvant chemotherapy timing

BACKGROUND: The pre‐adjuvant chemotherapy (PAC) status of postoperative pancreatic ductal adenocarcinoma (PDAC) patients has not been studied and elaborated well previously. METHOD: The association of PAC variables and prognoses was explored using a multivariable Cox model, restricted cubic spline a...

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Autores principales: Fu, Ningzhen, Qin, Kai, Li, Jingfeng, Jin, Jiabin, Jiang, Yu, Deng, Xiaxing, Shen, Baiyong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9487870/
https://www.ncbi.nlm.nih.gov/pubmed/35434972
http://dx.doi.org/10.1002/cam4.4698
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author Fu, Ningzhen
Qin, Kai
Li, Jingfeng
Jin, Jiabin
Jiang, Yu
Deng, Xiaxing
Shen, Baiyong
author_facet Fu, Ningzhen
Qin, Kai
Li, Jingfeng
Jin, Jiabin
Jiang, Yu
Deng, Xiaxing
Shen, Baiyong
author_sort Fu, Ningzhen
collection PubMed
description BACKGROUND: The pre‐adjuvant chemotherapy (PAC) status of postoperative pancreatic ductal adenocarcinoma (PDAC) patients has not been studied and elaborated well previously. METHOD: The association of PAC variables and prognoses was explored using a multivariable Cox model, restricted cubic spline analysis, and correlation analysis. The main outcomes were overall survival (OS) and progression‐free survival (PFS). The secondary outcome was chemotherapy completeness (CHC). RESULTS: A total of 401 eligible patients were enrolled in sequential surgery and chemotherapy. The chemotherapy regimen, PAC fasting blood glucose (FBG), and elevated fasting blood glucose (eFBG) status were associated with CHC (regimen types: p = 0.005, continuous FBG: p = 0.014, eFBG status: p = 0.012). Early administration of adjuvant chemotherapy (<34 days) was a risk factor for the limited OS and PFS (OS: aHR: 1.61 [1.09–2.38], p = 0.016; PFS: aHR: 1.91 [1.29–2.82], p = 0.001). Patients with higher PAC body mass index (BMI), receiving Gemcap regimen, and with lower PAC tumor marker value were observed with better survival prognoses (PAC BMI: OS: 0.927 [0.875–0.983], p = 0.011; Gemcap: OS: 0.533 [0.312–0.913], p = 0.022; Gemcap: PFS: 0.560 [0.341–0.922], p = 0.023; PAC CA125: OS: 1.004 [1.002–1.006], p < 0.001; PAC CA125: PFS: 1.003 [1.000–1.005], p = 0.031; PAC CEA: OS: 1.050 [1.026–1.074], p < 0.001). The BMI decrease was mainly concentrated in the first 3 months of chemotherapy courses (first 3 months: p < 0.001; latter 3 months: p = 0.097). And CEA, compared to CA125 and CA199, was a better prognostic indicator (CEA: first 3 months: PFS p = 0.011, OS p < 0.001; latter 3 months: PFS p = 0.024, OS p = 0.041). CONCLUSION: PDAC patients should be treated with adjuvant chemotherapy over 34 postoperative days. PAC sarcopenia was a risk factor for OS, but not PFS and limited CHC. Those with higher PAC FBG levels were more likely to finish chemotherapy. CEA, compared to CA125 and CA199, was a better prognostic indicator.
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spelling pubmed-94878702022-09-30 Who could complete and benefit from the adjuvant chemotherapy regarding pancreatic ductal adenocarcinoma? A multivariate‐adjusted analysis at the pre‐adjuvant chemotherapy timing Fu, Ningzhen Qin, Kai Li, Jingfeng Jin, Jiabin Jiang, Yu Deng, Xiaxing Shen, Baiyong Cancer Med RESEARCH ARTICLES BACKGROUND: The pre‐adjuvant chemotherapy (PAC) status of postoperative pancreatic ductal adenocarcinoma (PDAC) patients has not been studied and elaborated well previously. METHOD: The association of PAC variables and prognoses was explored using a multivariable Cox model, restricted cubic spline analysis, and correlation analysis. The main outcomes were overall survival (OS) and progression‐free survival (PFS). The secondary outcome was chemotherapy completeness (CHC). RESULTS: A total of 401 eligible patients were enrolled in sequential surgery and chemotherapy. The chemotherapy regimen, PAC fasting blood glucose (FBG), and elevated fasting blood glucose (eFBG) status were associated with CHC (regimen types: p = 0.005, continuous FBG: p = 0.014, eFBG status: p = 0.012). Early administration of adjuvant chemotherapy (<34 days) was a risk factor for the limited OS and PFS (OS: aHR: 1.61 [1.09–2.38], p = 0.016; PFS: aHR: 1.91 [1.29–2.82], p = 0.001). Patients with higher PAC body mass index (BMI), receiving Gemcap regimen, and with lower PAC tumor marker value were observed with better survival prognoses (PAC BMI: OS: 0.927 [0.875–0.983], p = 0.011; Gemcap: OS: 0.533 [0.312–0.913], p = 0.022; Gemcap: PFS: 0.560 [0.341–0.922], p = 0.023; PAC CA125: OS: 1.004 [1.002–1.006], p < 0.001; PAC CA125: PFS: 1.003 [1.000–1.005], p = 0.031; PAC CEA: OS: 1.050 [1.026–1.074], p < 0.001). The BMI decrease was mainly concentrated in the first 3 months of chemotherapy courses (first 3 months: p < 0.001; latter 3 months: p = 0.097). And CEA, compared to CA125 and CA199, was a better prognostic indicator (CEA: first 3 months: PFS p = 0.011, OS p < 0.001; latter 3 months: PFS p = 0.024, OS p = 0.041). CONCLUSION: PDAC patients should be treated with adjuvant chemotherapy over 34 postoperative days. PAC sarcopenia was a risk factor for OS, but not PFS and limited CHC. Those with higher PAC FBG levels were more likely to finish chemotherapy. CEA, compared to CA125 and CA199, was a better prognostic indicator. John Wiley and Sons Inc. 2022-04-17 /pmc/articles/PMC9487870/ /pubmed/35434972 http://dx.doi.org/10.1002/cam4.4698 Text en © 2022 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle RESEARCH ARTICLES
Fu, Ningzhen
Qin, Kai
Li, Jingfeng
Jin, Jiabin
Jiang, Yu
Deng, Xiaxing
Shen, Baiyong
Who could complete and benefit from the adjuvant chemotherapy regarding pancreatic ductal adenocarcinoma? A multivariate‐adjusted analysis at the pre‐adjuvant chemotherapy timing
title Who could complete and benefit from the adjuvant chemotherapy regarding pancreatic ductal adenocarcinoma? A multivariate‐adjusted analysis at the pre‐adjuvant chemotherapy timing
title_full Who could complete and benefit from the adjuvant chemotherapy regarding pancreatic ductal adenocarcinoma? A multivariate‐adjusted analysis at the pre‐adjuvant chemotherapy timing
title_fullStr Who could complete and benefit from the adjuvant chemotherapy regarding pancreatic ductal adenocarcinoma? A multivariate‐adjusted analysis at the pre‐adjuvant chemotherapy timing
title_full_unstemmed Who could complete and benefit from the adjuvant chemotherapy regarding pancreatic ductal adenocarcinoma? A multivariate‐adjusted analysis at the pre‐adjuvant chemotherapy timing
title_short Who could complete and benefit from the adjuvant chemotherapy regarding pancreatic ductal adenocarcinoma? A multivariate‐adjusted analysis at the pre‐adjuvant chemotherapy timing
title_sort who could complete and benefit from the adjuvant chemotherapy regarding pancreatic ductal adenocarcinoma? a multivariate‐adjusted analysis at the pre‐adjuvant chemotherapy timing
topic RESEARCH ARTICLES
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9487870/
https://www.ncbi.nlm.nih.gov/pubmed/35434972
http://dx.doi.org/10.1002/cam4.4698
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