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Predictors of Complete Response and Disease Recurrence Following Chemoradiation for Rectal Cancer

OBJECTIVE: Approximately 10–40% of rectal patients have a complete response (CR) to neoadjuvant chemoradiation (CRT), and these patients have improved survival. Thus, non-operative management (“watch-and-wait” approach) may be an option for select patients. We aimed to identify clinical predictors o...

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Autores principales: Bitterman, Danielle S., Resende Salgado, Lucas, Moore, Harvey G., Sanfilippo, Nicholas J., Gu, Ping, Hatzaras, Ioannis, Du, Kevin L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4686647/
https://www.ncbi.nlm.nih.gov/pubmed/26734570
http://dx.doi.org/10.3389/fonc.2015.00286
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author Bitterman, Danielle S.
Resende Salgado, Lucas
Moore, Harvey G.
Sanfilippo, Nicholas J.
Gu, Ping
Hatzaras, Ioannis
Du, Kevin L.
author_facet Bitterman, Danielle S.
Resende Salgado, Lucas
Moore, Harvey G.
Sanfilippo, Nicholas J.
Gu, Ping
Hatzaras, Ioannis
Du, Kevin L.
author_sort Bitterman, Danielle S.
collection PubMed
description OBJECTIVE: Approximately 10–40% of rectal patients have a complete response (CR) to neoadjuvant chemoradiation (CRT), and these patients have improved survival. Thus, non-operative management (“watch-and-wait” approach) may be an option for select patients. We aimed to identify clinical predictors of CR following CRT. METHODS: Patients treated with definitive CRT for T3–T4, locally unresectable T1–T2, low-lying T2, and/or node-positive rectal cancer from August 2004 to February 2015 were retrospectively reviewed. Most patients were treated with 50.4 Gy radiation and concurrent 5-fluoruracil or capecitabine. Patients were considered to have a CR if surgical pathology revealed ypT0N0M0 (operative management), or if they had no evidence of residual disease on clinical and radiographic assessment (non-operative management). Statistical analysis was carried out to determine predictors of CR and long-term outcomes. RESULTS: Complete records were available on 138 patients. The median follow-up was 24.5 months. Thirty-six patients (26.3%) achieved a CR; 30/123 operatively managed patients (24.5%) and 6/15 (40%) non-operatively managed patients. None of the 10 patients with mucinous adenocarcinoma achieved a CR. Carcinoembryonic antigen (CEA) ≥5 μg/L at diagnosis (OR 0.190, 95% CI 0.037–0.971, p = 0.046), tumor size ≥3 cm (OR 0.123, 95% CI 0.020–0.745, p = 0.023), distance of tumor from the anal verge ≥3 cm (OR 0.091, 95% CI 0.013–0.613, p = 0.014), clinically node-positive disease at diagnosis (OR 0.201, 95% CI 0.045–0.895, p = 0.035), and interval from CRT to surgery ≥8 weeks (OR 5.267, 95% CI 1.068–25.961, p = 0.041) were independent predictors of CR. The CR group had longer 3-year distant metastasis-free survival (DMFS) (93.7 vs. 63.7%, p = 0.016) and 3-year disease-free survival (DFS) (91.1 vs. 67.8%, p = 0.038). Three-year locoregional control (LRC) (96.6 vs. 81.3%, p = 0.103) and overall survival (97.2 vs. 87.5%, p = 0.125) were higher in the CR group but this did not achieve statistical significance. CR was not an independent predictor of LRC, DMFS, or DFS. CONCLUSION: CEA at diagnosis, tumor size, tumor distance from the anal verge, node positivity at diagnosis, and interval from CRT to surgery were predictors of CR. These clinical variables may offer insight into patient selection and timing of treatment response evaluation in the watch-and-wait approach.
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spelling pubmed-46866472016-01-05 Predictors of Complete Response and Disease Recurrence Following Chemoradiation for Rectal Cancer Bitterman, Danielle S. Resende Salgado, Lucas Moore, Harvey G. Sanfilippo, Nicholas J. Gu, Ping Hatzaras, Ioannis Du, Kevin L. Front Oncol Oncology OBJECTIVE: Approximately 10–40% of rectal patients have a complete response (CR) to neoadjuvant chemoradiation (CRT), and these patients have improved survival. Thus, non-operative management (“watch-and-wait” approach) may be an option for select patients. We aimed to identify clinical predictors of CR following CRT. METHODS: Patients treated with definitive CRT for T3–T4, locally unresectable T1–T2, low-lying T2, and/or node-positive rectal cancer from August 2004 to February 2015 were retrospectively reviewed. Most patients were treated with 50.4 Gy radiation and concurrent 5-fluoruracil or capecitabine. Patients were considered to have a CR if surgical pathology revealed ypT0N0M0 (operative management), or if they had no evidence of residual disease on clinical and radiographic assessment (non-operative management). Statistical analysis was carried out to determine predictors of CR and long-term outcomes. RESULTS: Complete records were available on 138 patients. The median follow-up was 24.5 months. Thirty-six patients (26.3%) achieved a CR; 30/123 operatively managed patients (24.5%) and 6/15 (40%) non-operatively managed patients. None of the 10 patients with mucinous adenocarcinoma achieved a CR. Carcinoembryonic antigen (CEA) ≥5 μg/L at diagnosis (OR 0.190, 95% CI 0.037–0.971, p = 0.046), tumor size ≥3 cm (OR 0.123, 95% CI 0.020–0.745, p = 0.023), distance of tumor from the anal verge ≥3 cm (OR 0.091, 95% CI 0.013–0.613, p = 0.014), clinically node-positive disease at diagnosis (OR 0.201, 95% CI 0.045–0.895, p = 0.035), and interval from CRT to surgery ≥8 weeks (OR 5.267, 95% CI 1.068–25.961, p = 0.041) were independent predictors of CR. The CR group had longer 3-year distant metastasis-free survival (DMFS) (93.7 vs. 63.7%, p = 0.016) and 3-year disease-free survival (DFS) (91.1 vs. 67.8%, p = 0.038). Three-year locoregional control (LRC) (96.6 vs. 81.3%, p = 0.103) and overall survival (97.2 vs. 87.5%, p = 0.125) were higher in the CR group but this did not achieve statistical significance. CR was not an independent predictor of LRC, DMFS, or DFS. CONCLUSION: CEA at diagnosis, tumor size, tumor distance from the anal verge, node positivity at diagnosis, and interval from CRT to surgery were predictors of CR. These clinical variables may offer insight into patient selection and timing of treatment response evaluation in the watch-and-wait approach. Frontiers Media S.A. 2015-12-22 /pmc/articles/PMC4686647/ /pubmed/26734570 http://dx.doi.org/10.3389/fonc.2015.00286 Text en Copyright © 2015 Bitterman, Resende Salgado, Moore, Sanfilippo, Gu, Hatzaras and Du. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor 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 Oncology
Bitterman, Danielle S.
Resende Salgado, Lucas
Moore, Harvey G.
Sanfilippo, Nicholas J.
Gu, Ping
Hatzaras, Ioannis
Du, Kevin L.
Predictors of Complete Response and Disease Recurrence Following Chemoradiation for Rectal Cancer
title Predictors of Complete Response and Disease Recurrence Following Chemoradiation for Rectal Cancer
title_full Predictors of Complete Response and Disease Recurrence Following Chemoradiation for Rectal Cancer
title_fullStr Predictors of Complete Response and Disease Recurrence Following Chemoradiation for Rectal Cancer
title_full_unstemmed Predictors of Complete Response and Disease Recurrence Following Chemoradiation for Rectal Cancer
title_short Predictors of Complete Response and Disease Recurrence Following Chemoradiation for Rectal Cancer
title_sort predictors of complete response and disease recurrence following chemoradiation for rectal cancer
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4686647/
https://www.ncbi.nlm.nih.gov/pubmed/26734570
http://dx.doi.org/10.3389/fonc.2015.00286
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