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Phase 2 study of perioperative chemotherapy with SOX and surgery for stage III colorectal cancer (SOS3 study)
This phase 2 study evaluated the safety and efficacy of perioperative chemotherapy with S-1 plus oxaliplatin (SOX) for stage III colorectal cancer (CRC). Patients with stage III CRC received surgery after neoadjuvant chemotherapy (NAC; SOX 4 cycles) and adjuvant chemotherapy (AC; SOX 4 cycles). The...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6851079/ https://www.ncbi.nlm.nih.gov/pubmed/31719583 http://dx.doi.org/10.1038/s41598-019-53096-3 |
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author | Aisu, Naoya Yoshida, Yoichiro Komono, Akira Sakamoto, Ryohei Kojima, Daibo Hasegawa, Suguru |
author_facet | Aisu, Naoya Yoshida, Yoichiro Komono, Akira Sakamoto, Ryohei Kojima, Daibo Hasegawa, Suguru |
author_sort | Aisu, Naoya |
collection | PubMed |
description | This phase 2 study evaluated the safety and efficacy of perioperative chemotherapy with S-1 plus oxaliplatin (SOX) for stage III colorectal cancer (CRC). Patients with stage III CRC received surgery after neoadjuvant chemotherapy (NAC; SOX 4 cycles) and adjuvant chemotherapy (AC; SOX 4 cycles). The primary endpoints were response rate and safety. We enrolled 30 patients. Their median age was 62 years (range: 43–87 years); 53% were women. They received a median of 4 cycles (range: 1–4) of NAC and a median 4 cycles (range: 0–4) of AC. Five patients interrupted NAC treatment because of toxicity (grade 3 diarrhoea [n = 1], grade 3 ileus [n = 1], and grade 3–4 thrombocytopenia [n = 3]). Patients’ responses were complete responses: n = 2 (6.6%), partial responses: n = 21 (70%), stable disease: n = 6 (20.0%), and progressive disease: n = 1 (3.3%; response rate: 73.3%). Curative resection was performed in 29 patients. No patients showed anastomotic leakage. Five-year overall survival and disease-free survival were 83.3% and 76.7%, respectively (median follow-up time: 48 months). NAC using SOX regimen is safe and effective, and may lead to reduced local recurrence and distant metastasis. Long-term outcomes are awaited to evaluate further the efficacy of this strategy (UMIN000006790). |
format | Online Article Text |
id | pubmed-6851079 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-68510792019-11-19 Phase 2 study of perioperative chemotherapy with SOX and surgery for stage III colorectal cancer (SOS3 study) Aisu, Naoya Yoshida, Yoichiro Komono, Akira Sakamoto, Ryohei Kojima, Daibo Hasegawa, Suguru Sci Rep Article This phase 2 study evaluated the safety and efficacy of perioperative chemotherapy with S-1 plus oxaliplatin (SOX) for stage III colorectal cancer (CRC). Patients with stage III CRC received surgery after neoadjuvant chemotherapy (NAC; SOX 4 cycles) and adjuvant chemotherapy (AC; SOX 4 cycles). The primary endpoints were response rate and safety. We enrolled 30 patients. Their median age was 62 years (range: 43–87 years); 53% were women. They received a median of 4 cycles (range: 1–4) of NAC and a median 4 cycles (range: 0–4) of AC. Five patients interrupted NAC treatment because of toxicity (grade 3 diarrhoea [n = 1], grade 3 ileus [n = 1], and grade 3–4 thrombocytopenia [n = 3]). Patients’ responses were complete responses: n = 2 (6.6%), partial responses: n = 21 (70%), stable disease: n = 6 (20.0%), and progressive disease: n = 1 (3.3%; response rate: 73.3%). Curative resection was performed in 29 patients. No patients showed anastomotic leakage. Five-year overall survival and disease-free survival were 83.3% and 76.7%, respectively (median follow-up time: 48 months). NAC using SOX regimen is safe and effective, and may lead to reduced local recurrence and distant metastasis. Long-term outcomes are awaited to evaluate further the efficacy of this strategy (UMIN000006790). Nature Publishing Group UK 2019-11-12 /pmc/articles/PMC6851079/ /pubmed/31719583 http://dx.doi.org/10.1038/s41598-019-53096-3 Text en © The Author(s) 2019 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Aisu, Naoya Yoshida, Yoichiro Komono, Akira Sakamoto, Ryohei Kojima, Daibo Hasegawa, Suguru Phase 2 study of perioperative chemotherapy with SOX and surgery for stage III colorectal cancer (SOS3 study) |
title | Phase 2 study of perioperative chemotherapy with SOX and surgery for stage III colorectal cancer (SOS3 study) |
title_full | Phase 2 study of perioperative chemotherapy with SOX and surgery for stage III colorectal cancer (SOS3 study) |
title_fullStr | Phase 2 study of perioperative chemotherapy with SOX and surgery for stage III colorectal cancer (SOS3 study) |
title_full_unstemmed | Phase 2 study of perioperative chemotherapy with SOX and surgery for stage III colorectal cancer (SOS3 study) |
title_short | Phase 2 study of perioperative chemotherapy with SOX and surgery for stage III colorectal cancer (SOS3 study) |
title_sort | phase 2 study of perioperative chemotherapy with sox and surgery for stage iii colorectal cancer (sos3 study) |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6851079/ https://www.ncbi.nlm.nih.gov/pubmed/31719583 http://dx.doi.org/10.1038/s41598-019-53096-3 |
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