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Downsizing of rectal cancer following neoadjuvant radiotherapy (5 × 5 Gy) and long interval surgery evaluated using MRI semiautomated volumetric measurements, a retrospective study
INTRODUCTION: Neoadjuvant conventional chemoradiation (CRT) is the standard treatment for primary locally non-curatively resectable rectal cancer, as tumor downsizing may allow R0 resectability. Short-term neoadjuvant radiotherapy (5x5 Gy) followed by an interval before surgery (SRT- delay) is an al...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9981957/ https://www.ncbi.nlm.nih.gov/pubmed/36874463 http://dx.doi.org/10.3389/fsurg.2023.1106177 |
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author | Albrecht, Hendrik Christian Wagner, Sophie Sandbrink, Christoph Gretschel, Stephan |
author_facet | Albrecht, Hendrik Christian Wagner, Sophie Sandbrink, Christoph Gretschel, Stephan |
author_sort | Albrecht, Hendrik Christian |
collection | PubMed |
description | INTRODUCTION: Neoadjuvant conventional chemoradiation (CRT) is the standard treatment for primary locally non-curatively resectable rectal cancer, as tumor downsizing may allow R0 resectability. Short-term neoadjuvant radiotherapy (5x5 Gy) followed by an interval before surgery (SRT- delay) is an alternative for multimorbid patients who cannot tolerate CRT. This study examined the extent of tumor downsizing achieved with the SRT-delay approach in a limited cohort that underwent complete re-staging before surgery. METHODS: Between March 2018 and July 2021, 26 patients with locally advanced primary adenocarcinoma (>uT3 or/and N+) of the rectum were treated with SRT-delay. 22 patients underwent initial staging and complete re-staging (CT, endoscopy, MRI). Tumor downsizing was assessed by staging and re-staging data and pathologic findings. Semiautomated measurement of tumor volume was performed using mint Lesion™ 1.8 software to evaluate tumor regression. RESULTS: The mean tumor diameter determined on sagittal T2 MRI images decreased significantly from 54.1 (23–78) mm at initial staging to 37.9 (18–65) mm at re-staging before surgery (p <0.001) and to 25.5 (7–58) mm at pathologic examination (p <0.001). This corresponds to a mean reduction in tumor diameter of 28.9 (4.3–60.7) % at re-staging and 51.1 (8.7–86.5) % at pathology. Mean tumor volume determined from transverse T2 MR images mint Lesion(TM) 1.8 software significantly decreased from 27.5 (9.8 – 89.6) cm(3) at initial staging to 13.1 (3.7 – 32.8) cm(3) at re-staging (p <0.001), corresponding to a mean reduction of 50.8 (21.6 – 77) %. The frequency of positive circumferential resection margin (CRM) (less than 1mm) decreased from 45,5 % (10 patients) at initial staging to 18,2 % (4 patients) at re-staging. On pathologic examination, the CRM was negative in all cases. However, multivisceral resection for T4 tumors was required in 2 patients (9%). Tumor downstaging was noted in 15 of 22 patients after SRT-delay. CONCLUSION: In conclusion, the observed extent of downsizing is broadly comparable to the results of CRT, making SRT-delay a serious alternative for patients who cannot tolerate chemotherapy. |
format | Online Article Text |
id | pubmed-9981957 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-99819572023-03-04 Downsizing of rectal cancer following neoadjuvant radiotherapy (5 × 5 Gy) and long interval surgery evaluated using MRI semiautomated volumetric measurements, a retrospective study Albrecht, Hendrik Christian Wagner, Sophie Sandbrink, Christoph Gretschel, Stephan Front Surg Surgery INTRODUCTION: Neoadjuvant conventional chemoradiation (CRT) is the standard treatment for primary locally non-curatively resectable rectal cancer, as tumor downsizing may allow R0 resectability. Short-term neoadjuvant radiotherapy (5x5 Gy) followed by an interval before surgery (SRT- delay) is an alternative for multimorbid patients who cannot tolerate CRT. This study examined the extent of tumor downsizing achieved with the SRT-delay approach in a limited cohort that underwent complete re-staging before surgery. METHODS: Between March 2018 and July 2021, 26 patients with locally advanced primary adenocarcinoma (>uT3 or/and N+) of the rectum were treated with SRT-delay. 22 patients underwent initial staging and complete re-staging (CT, endoscopy, MRI). Tumor downsizing was assessed by staging and re-staging data and pathologic findings. Semiautomated measurement of tumor volume was performed using mint Lesion™ 1.8 software to evaluate tumor regression. RESULTS: The mean tumor diameter determined on sagittal T2 MRI images decreased significantly from 54.1 (23–78) mm at initial staging to 37.9 (18–65) mm at re-staging before surgery (p <0.001) and to 25.5 (7–58) mm at pathologic examination (p <0.001). This corresponds to a mean reduction in tumor diameter of 28.9 (4.3–60.7) % at re-staging and 51.1 (8.7–86.5) % at pathology. Mean tumor volume determined from transverse T2 MR images mint Lesion(TM) 1.8 software significantly decreased from 27.5 (9.8 – 89.6) cm(3) at initial staging to 13.1 (3.7 – 32.8) cm(3) at re-staging (p <0.001), corresponding to a mean reduction of 50.8 (21.6 – 77) %. The frequency of positive circumferential resection margin (CRM) (less than 1mm) decreased from 45,5 % (10 patients) at initial staging to 18,2 % (4 patients) at re-staging. On pathologic examination, the CRM was negative in all cases. However, multivisceral resection for T4 tumors was required in 2 patients (9%). Tumor downstaging was noted in 15 of 22 patients after SRT-delay. CONCLUSION: In conclusion, the observed extent of downsizing is broadly comparable to the results of CRT, making SRT-delay a serious alternative for patients who cannot tolerate chemotherapy. Frontiers Media S.A. 2023-02-17 /pmc/articles/PMC9981957/ /pubmed/36874463 http://dx.doi.org/10.3389/fsurg.2023.1106177 Text en © 2023 Albrecht, Wagner, Sandbrink and Gretschel. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY) (https://creativecommons.org/licenses/by/4.0/) . The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Surgery Albrecht, Hendrik Christian Wagner, Sophie Sandbrink, Christoph Gretschel, Stephan Downsizing of rectal cancer following neoadjuvant radiotherapy (5 × 5 Gy) and long interval surgery evaluated using MRI semiautomated volumetric measurements, a retrospective study |
title | Downsizing of rectal cancer following neoadjuvant radiotherapy (5 × 5 Gy) and long interval surgery evaluated using MRI semiautomated volumetric measurements, a retrospective study |
title_full | Downsizing of rectal cancer following neoadjuvant radiotherapy (5 × 5 Gy) and long interval surgery evaluated using MRI semiautomated volumetric measurements, a retrospective study |
title_fullStr | Downsizing of rectal cancer following neoadjuvant radiotherapy (5 × 5 Gy) and long interval surgery evaluated using MRI semiautomated volumetric measurements, a retrospective study |
title_full_unstemmed | Downsizing of rectal cancer following neoadjuvant radiotherapy (5 × 5 Gy) and long interval surgery evaluated using MRI semiautomated volumetric measurements, a retrospective study |
title_short | Downsizing of rectal cancer following neoadjuvant radiotherapy (5 × 5 Gy) and long interval surgery evaluated using MRI semiautomated volumetric measurements, a retrospective study |
title_sort | downsizing of rectal cancer following neoadjuvant radiotherapy (5 × 5 gy) and long interval surgery evaluated using mri semiautomated volumetric measurements, a retrospective study |
topic | Surgery |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9981957/ https://www.ncbi.nlm.nih.gov/pubmed/36874463 http://dx.doi.org/10.3389/fsurg.2023.1106177 |
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