Clinico-pathological predictors of clinical complete response in rectal cancer

Purpose: Prediction of clinical complete response in rectal cancer before neoadjuvant chemo-radiotherapy treatment enables treatment selection. Patients predicted to have complete response could have chemo-radiotherapy, and others could have additional doublet chemotherapy at this stage of their tre...

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Main Authors: P. Mbanu, E. Vasquez Osorio, H. Mistry, L. Malcomson, S. Yousif, M. Aznar, R. Kochhar, M. Van Herk, A.G. Renehan, M.P. Saunders
Format: Article
Language:English
Published: Elsevier 2022-01-01
Series:Cancer Treatment and Research Communications
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2468294222000314
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author P. Mbanu
E. Vasquez Osorio
H. Mistry
L. Malcomson
S. Yousif
M. Aznar
R. Kochhar
M. Van Herk
A.G. Renehan
M.P. Saunders
author_facet P. Mbanu
E. Vasquez Osorio
H. Mistry
L. Malcomson
S. Yousif
M. Aznar
R. Kochhar
M. Van Herk
A.G. Renehan
M.P. Saunders
author_sort P. Mbanu
collection DOAJ
description Purpose: Prediction of clinical complete response in rectal cancer before neoadjuvant chemo-radiotherapy treatment enables treatment selection. Patients predicted to have complete response could have chemo-radiotherapy, and others could have additional doublet chemotherapy at this stage of their treatment to improve their overall outcome. This work investigates the role of clinical variables in predicting clinical complete response. Method: Using the UK-based OnCoRe database (2008 to 2019), we performed a propensity-score matched study of 322 patients who received neoadjuvant chemoradiotherapy. We collected pre-treatment clinic-pathological, inflammatory and radiotherapy-related characteristics. We determined the odds for the occurrence of cCR using conditional logistic regression models. We derived the post-model Area under the Curve (AUC) as an indicator of discrimination performance and stated a priori that an AUC of 0.75 or greater was required for potential clinical utility. Results: Pre-treatment tumour diameter, mrT-stage, haemoglobin, alkaline phosphate and total radiotherapy depths were associated with cCR on univariable and multivariable analysis. Additionally, neutrophil to lymphocyte ratio (NLR), neutrophil-monocyte to lymphocyte ratio (NMLR), lymphocyte count and albumin were all significantly associated with cCR on multivariable analysis. A nomogram using the above parameters was developed with a resulting ROC AUC of 0.75. Conclusion: We identified routine clinic-pathological, inflammatory and radiotherapy-related variables which are independently associated with cCR. A nomogram was developed to predict cCR. The performance characteristics from this model were on the prior clinical utility threshold. Additional research is required to develop more associated variables to better select patients with rectal cancer undergoing chemoradiotherapy who may benefit from pursuing a W&W strategy.
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spelling doaj.art-e846fce02d3e42ca95954ef928b174fa2022-12-22T02:29:59ZengElsevierCancer Treatment and Research Communications2468-29422022-01-0131100540Clinico-pathological predictors of clinical complete response in rectal cancerP. Mbanu0E. Vasquez Osorio1H. Mistry2L. Malcomson3S. Yousif4M. Aznar5R. Kochhar6M. Van Herk7A.G. Renehan8M.P. Saunders9Department of Clinical Oncology, Christie NHS Foundation Trust, Manchester, United Kingdom; Corresponding author at: Department of Clinical Oncology, Christie NHS Foundation Trust, 450 Wilmslow Road, Manchester, M20 4BX United KingdomDivision of Cancer Sciences, School of Medical Sciences, Faculty of Biology, Medicine and Health, Manchester Academic Health Science Centre, University of Manchester, Manchester, United KingdomDivision of Cancer Sciences, School of Medical Sciences, Faculty of Biology, Medicine and Health, Manchester Academic Health Science Centre, University of Manchester, Manchester, United Kingdom; Division of Pharmacy, University of Manchester, Manchester, United KingdomDivision of Cancer Sciences, School of Medical Sciences, Faculty of Biology, Medicine and Health, Manchester Academic Health Science Centre, University of Manchester, Manchester, United Kingdom; Colorectal and Peritoneal Oncology Centre, Christie NHS Foundation Trust, Manchester, United KingdomDepartment of Clinical Oncology, Lancashire Teaching Hospital, Preston, United KingdomDivision of Cancer Sciences, School of Medical Sciences, Faculty of Biology, Medicine and Health, Manchester Academic Health Science Centre, University of Manchester, Manchester, United KingdomDepartment of Radiological Oncology, Christie NHS Foundation Trust, Manchester, United KingdomDivision of Cancer Sciences, School of Medical Sciences, Faculty of Biology, Medicine and Health, Manchester Academic Health Science Centre, University of Manchester, Manchester, United KingdomDivision of Cancer Sciences, School of Medical Sciences, Faculty of Biology, Medicine and Health, Manchester Academic Health Science Centre, University of Manchester, Manchester, United Kingdom; Colorectal and Peritoneal Oncology Centre, Christie NHS Foundation Trust, Manchester, United KingdomDepartment of Clinical Oncology, Christie NHS Foundation Trust, Manchester, United KingdomPurpose: Prediction of clinical complete response in rectal cancer before neoadjuvant chemo-radiotherapy treatment enables treatment selection. Patients predicted to have complete response could have chemo-radiotherapy, and others could have additional doublet chemotherapy at this stage of their treatment to improve their overall outcome. This work investigates the role of clinical variables in predicting clinical complete response. Method: Using the UK-based OnCoRe database (2008 to 2019), we performed a propensity-score matched study of 322 patients who received neoadjuvant chemoradiotherapy. We collected pre-treatment clinic-pathological, inflammatory and radiotherapy-related characteristics. We determined the odds for the occurrence of cCR using conditional logistic regression models. We derived the post-model Area under the Curve (AUC) as an indicator of discrimination performance and stated a priori that an AUC of 0.75 or greater was required for potential clinical utility. Results: Pre-treatment tumour diameter, mrT-stage, haemoglobin, alkaline phosphate and total radiotherapy depths were associated with cCR on univariable and multivariable analysis. Additionally, neutrophil to lymphocyte ratio (NLR), neutrophil-monocyte to lymphocyte ratio (NMLR), lymphocyte count and albumin were all significantly associated with cCR on multivariable analysis. A nomogram using the above parameters was developed with a resulting ROC AUC of 0.75. Conclusion: We identified routine clinic-pathological, inflammatory and radiotherapy-related variables which are independently associated with cCR. A nomogram was developed to predict cCR. The performance characteristics from this model were on the prior clinical utility threshold. Additional research is required to develop more associated variables to better select patients with rectal cancer undergoing chemoradiotherapy who may benefit from pursuing a W&W strategy.http://www.sciencedirect.com/science/article/pii/S2468294222000314Rectal cancerClinical complete responseChemoradiotherapy
spellingShingle P. Mbanu
E. Vasquez Osorio
H. Mistry
L. Malcomson
S. Yousif
M. Aznar
R. Kochhar
M. Van Herk
A.G. Renehan
M.P. Saunders
Clinico-pathological predictors of clinical complete response in rectal cancer
Cancer Treatment and Research Communications
Rectal cancer
Clinical complete response
Chemoradiotherapy
title Clinico-pathological predictors of clinical complete response in rectal cancer
title_full Clinico-pathological predictors of clinical complete response in rectal cancer
title_fullStr Clinico-pathological predictors of clinical complete response in rectal cancer
title_full_unstemmed Clinico-pathological predictors of clinical complete response in rectal cancer
title_short Clinico-pathological predictors of clinical complete response in rectal cancer
title_sort clinico pathological predictors of clinical complete response in rectal cancer
topic Rectal cancer
Clinical complete response
Chemoradiotherapy
url http://www.sciencedirect.com/science/article/pii/S2468294222000314
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