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Postoperative Inflammatory Marker Surveillance in Colorectal Peritoneal Carcinomatosis
BACKGROUND: The prognostic significance of inflammatory markers in solid cancers is well-established, albeit with considerable heterogeneity. This study sought to investigate the postoperative inflammatory marker trend in peritoneal carcinomatosis (PC), with a focus on colorectal PC (CPC), and to pr...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8460570/ https://www.ncbi.nlm.nih.gov/pubmed/33655363 http://dx.doi.org/10.1245/s10434-020-09544-w |
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author | Thiagarajan, Sasinthiran Tan, Joey Wee-Shan Zhou, Siqin Tan, Qiu Xuan Hendrikson, Josephine Ng, Wai Har Ng, Gillian Liu, Ying Tan, Grace Hwei Ching Soo, Khee Chee Teo, Melissa Ching Ching Chia, Claramae Shulyn Ong, Chin-Ann Johnny |
author_facet | Thiagarajan, Sasinthiran Tan, Joey Wee-Shan Zhou, Siqin Tan, Qiu Xuan Hendrikson, Josephine Ng, Wai Har Ng, Gillian Liu, Ying Tan, Grace Hwei Ching Soo, Khee Chee Teo, Melissa Ching Ching Chia, Claramae Shulyn Ong, Chin-Ann Johnny |
author_sort | Thiagarajan, Sasinthiran |
collection | PubMed |
description | BACKGROUND: The prognostic significance of inflammatory markers in solid cancers is well-established, albeit with considerable heterogeneity. This study sought to investigate the postoperative inflammatory marker trend in peritoneal carcinomatosis (PC), with a focus on colorectal PC (CPC), and to propose optimal surveillance periods and cutoffs. METHODS: Data were collected from a prospectively maintained database of PC patients treated at the authors’ institution from April 2001 to March 2019. The platelet–lymphocyte ratio (PLR), the neutrophil–lymphocyte ratio (NLR), and the lymphocyte–monocyte ratio (LMR) were collected preoperatively and on postoperative days 0, 1 to 3, 4 to 7, 8 to 21, 22 to 56, and 57 to 90 as averages. Optimal surveillance periods and cutoffs for each marker were determined by maximally selected rank statistics. The Kaplan–Meier method and Cox proportional hazard regression models were used to investigate the association of inflammatory markers with 1-year overall survival (OS) and recurrence-free survival (RFS) using clinicopathologic parameters. RESULTS: The postoperative inflammatory marker trend and levels did not differ between the patients with and those without hyperthermic intraperitoneal chemotherapy (HIPEC). Low postoperative LMR (days 4–7), high postoperative NLR (days 8–21), and high postoperative PLR (days 22–56) were optimal for prognosticating poor 1-year OS, whereas high postoperative PLR and NLR (days 57–90) and low postoperative LMR (days 8–21) were associated with poor 1-year RFS. A composite score of these three markers was prognostic for OS in CPC. CONCLUSIONS: The reported cutoffs should be validated in a larger population of CPC patients. Future studies should account for the inflammatory response profile when selecting appropriate surveillance periods. SUPPLEMENTARY INFORMATION: The online version of this article (10.1245/s10434-020-09544-w) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-8460570 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-84605702021-10-07 Postoperative Inflammatory Marker Surveillance in Colorectal Peritoneal Carcinomatosis Thiagarajan, Sasinthiran Tan, Joey Wee-Shan Zhou, Siqin Tan, Qiu Xuan Hendrikson, Josephine Ng, Wai Har Ng, Gillian Liu, Ying Tan, Grace Hwei Ching Soo, Khee Chee Teo, Melissa Ching Ching Chia, Claramae Shulyn Ong, Chin-Ann Johnny Ann Surg Oncol Gastrointestinal Oncology BACKGROUND: The prognostic significance of inflammatory markers in solid cancers is well-established, albeit with considerable heterogeneity. This study sought to investigate the postoperative inflammatory marker trend in peritoneal carcinomatosis (PC), with a focus on colorectal PC (CPC), and to propose optimal surveillance periods and cutoffs. METHODS: Data were collected from a prospectively maintained database of PC patients treated at the authors’ institution from April 2001 to March 2019. The platelet–lymphocyte ratio (PLR), the neutrophil–lymphocyte ratio (NLR), and the lymphocyte–monocyte ratio (LMR) were collected preoperatively and on postoperative days 0, 1 to 3, 4 to 7, 8 to 21, 22 to 56, and 57 to 90 as averages. Optimal surveillance periods and cutoffs for each marker were determined by maximally selected rank statistics. The Kaplan–Meier method and Cox proportional hazard regression models were used to investigate the association of inflammatory markers with 1-year overall survival (OS) and recurrence-free survival (RFS) using clinicopathologic parameters. RESULTS: The postoperative inflammatory marker trend and levels did not differ between the patients with and those without hyperthermic intraperitoneal chemotherapy (HIPEC). Low postoperative LMR (days 4–7), high postoperative NLR (days 8–21), and high postoperative PLR (days 22–56) were optimal for prognosticating poor 1-year OS, whereas high postoperative PLR and NLR (days 57–90) and low postoperative LMR (days 8–21) were associated with poor 1-year RFS. A composite score of these three markers was prognostic for OS in CPC. CONCLUSIONS: The reported cutoffs should be validated in a larger population of CPC patients. Future studies should account for the inflammatory response profile when selecting appropriate surveillance periods. SUPPLEMENTARY INFORMATION: The online version of this article (10.1245/s10434-020-09544-w) contains supplementary material, which is available to authorized users. Springer International Publishing 2021-03-02 2021 /pmc/articles/PMC8460570/ /pubmed/33655363 http://dx.doi.org/10.1245/s10434-020-09544-w Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Gastrointestinal Oncology Thiagarajan, Sasinthiran Tan, Joey Wee-Shan Zhou, Siqin Tan, Qiu Xuan Hendrikson, Josephine Ng, Wai Har Ng, Gillian Liu, Ying Tan, Grace Hwei Ching Soo, Khee Chee Teo, Melissa Ching Ching Chia, Claramae Shulyn Ong, Chin-Ann Johnny Postoperative Inflammatory Marker Surveillance in Colorectal Peritoneal Carcinomatosis |
title | Postoperative Inflammatory Marker Surveillance in Colorectal Peritoneal Carcinomatosis |
title_full | Postoperative Inflammatory Marker Surveillance in Colorectal Peritoneal Carcinomatosis |
title_fullStr | Postoperative Inflammatory Marker Surveillance in Colorectal Peritoneal Carcinomatosis |
title_full_unstemmed | Postoperative Inflammatory Marker Surveillance in Colorectal Peritoneal Carcinomatosis |
title_short | Postoperative Inflammatory Marker Surveillance in Colorectal Peritoneal Carcinomatosis |
title_sort | postoperative inflammatory marker surveillance in colorectal peritoneal carcinomatosis |
topic | Gastrointestinal Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8460570/ https://www.ncbi.nlm.nih.gov/pubmed/33655363 http://dx.doi.org/10.1245/s10434-020-09544-w |
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