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A prospective feasibility study of one-year administration of adjuvant S-1 therapy for resected biliary tract cancer in a multi-institutional trial (Tokyo Study Group for Biliary Cancer: TOSBIC01)

BACKGROUND: Although surgery is the definitive curative treatment for biliary tract cancer (BTC), outcomes after surgery alone have not been satisfactory. Adjuvant therapy with S-1 may improve survival in patients with BTC. This study examined the safety and efficacy of 1 year adjuvant S-1 therapy f...

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Autores principales: Itano, Osamu, Takemura, Yusuke, Kishida, Norihiro, Tamagawa, Eiji, Shinozaki, Hiroharu, Ikeda, Ken, Urakami, Hidejiro, Ei, Shigenori, Hayatsu, Shigeo, Suzuki, Keiichi, Sakuragawa, Tadayuki, Ishii, Masatsugu, Shito, Masaya, Aiura, Koichi, Fujisaki, Hiroto, Takano, Kiminori, Matsui, Junichi, Minagawa, Takuya, Shinoda, Masahiro, Kitago, Minoru, Abe, Yuta, Yagi, Hiroshi, Oshima, Go, Hori, Shutaro, Kitagawa, Yuko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7379785/
https://www.ncbi.nlm.nih.gov/pubmed/32703191
http://dx.doi.org/10.1186/s12885-020-07185-6
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author Itano, Osamu
Takemura, Yusuke
Kishida, Norihiro
Tamagawa, Eiji
Shinozaki, Hiroharu
Ikeda, Ken
Urakami, Hidejiro
Ei, Shigenori
Hayatsu, Shigeo
Suzuki, Keiichi
Sakuragawa, Tadayuki
Ishii, Masatsugu
Shito, Masaya
Aiura, Koichi
Fujisaki, Hiroto
Takano, Kiminori
Matsui, Junichi
Minagawa, Takuya
Shinoda, Masahiro
Kitago, Minoru
Abe, Yuta
Yagi, Hiroshi
Oshima, Go
Hori, Shutaro
Kitagawa, Yuko
author_facet Itano, Osamu
Takemura, Yusuke
Kishida, Norihiro
Tamagawa, Eiji
Shinozaki, Hiroharu
Ikeda, Ken
Urakami, Hidejiro
Ei, Shigenori
Hayatsu, Shigeo
Suzuki, Keiichi
Sakuragawa, Tadayuki
Ishii, Masatsugu
Shito, Masaya
Aiura, Koichi
Fujisaki, Hiroto
Takano, Kiminori
Matsui, Junichi
Minagawa, Takuya
Shinoda, Masahiro
Kitago, Minoru
Abe, Yuta
Yagi, Hiroshi
Oshima, Go
Hori, Shutaro
Kitagawa, Yuko
author_sort Itano, Osamu
collection PubMed
description BACKGROUND: Although surgery is the definitive curative treatment for biliary tract cancer (BTC), outcomes after surgery alone have not been satisfactory. Adjuvant therapy with S-1 may improve survival in patients with BTC. This study examined the safety and efficacy of 1 year adjuvant S-1 therapy for BTC in a multi-institutional trial. METHODS: The inclusion criteria were as follows: histologically proven BTC, Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1, R0 or R1 surgery performed, cancer classified as Stage IB to III. Within 10 weeks post-surgery, a 42-day cycle of treatment with S-1 (80 mg/m(2)/day orally twice daily on days 1–28 of each cycle) was initiated and continued up to 1 year post surgery. The primary endpoint was adjuvant therapy completion rate. The secondary endpoints were toxicities, disease-free survival (DFS), and overall survival (OS). RESULTS: Forty-six patients met the inclusion criteria of whom 19 had extrahepatic cholangiocarcinoma, 10 had gallbladder carcinoma, 9 had ampullary carcinoma, and 8 had intrahepatic cholangiocarcinoma. Overall, 25 patients completed adjuvant chemotherapy, with a 54.3% completion rate while the completion rate without recurrence during the 1 year administration was 62.5%. Seven patients (15%) experienced adverse events (grade 3/4). The median number of courses administered was 7.5. Thirteen patients needed dose reduction or temporary therapy withdrawal. OS and DFS rates at 1/2 years were 91.2/80.0% and 84.3/77.2%, respectively. Among patients who were administered more than 3 courses of S-1, only one patient discontinued because of adverse events. CONCLUSIONS: One-year administration of adjuvant S-1 therapy for resected BTC was feasible and may be a promising treatment for those with resected BTC. Now, a randomized trial to determine the optimal duration of S-1 is ongoing. TRIAL REGISTRATION: UMIN-CTR, UMIN000009029. Registered 5 October 2012-Retrospectively registered, https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000009347
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spelling pubmed-73797852020-08-04 A prospective feasibility study of one-year administration of adjuvant S-1 therapy for resected biliary tract cancer in a multi-institutional trial (Tokyo Study Group for Biliary Cancer: TOSBIC01) Itano, Osamu Takemura, Yusuke Kishida, Norihiro Tamagawa, Eiji Shinozaki, Hiroharu Ikeda, Ken Urakami, Hidejiro Ei, Shigenori Hayatsu, Shigeo Suzuki, Keiichi Sakuragawa, Tadayuki Ishii, Masatsugu Shito, Masaya Aiura, Koichi Fujisaki, Hiroto Takano, Kiminori Matsui, Junichi Minagawa, Takuya Shinoda, Masahiro Kitago, Minoru Abe, Yuta Yagi, Hiroshi Oshima, Go Hori, Shutaro Kitagawa, Yuko BMC Cancer Research Article BACKGROUND: Although surgery is the definitive curative treatment for biliary tract cancer (BTC), outcomes after surgery alone have not been satisfactory. Adjuvant therapy with S-1 may improve survival in patients with BTC. This study examined the safety and efficacy of 1 year adjuvant S-1 therapy for BTC in a multi-institutional trial. METHODS: The inclusion criteria were as follows: histologically proven BTC, Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1, R0 or R1 surgery performed, cancer classified as Stage IB to III. Within 10 weeks post-surgery, a 42-day cycle of treatment with S-1 (80 mg/m(2)/day orally twice daily on days 1–28 of each cycle) was initiated and continued up to 1 year post surgery. The primary endpoint was adjuvant therapy completion rate. The secondary endpoints were toxicities, disease-free survival (DFS), and overall survival (OS). RESULTS: Forty-six patients met the inclusion criteria of whom 19 had extrahepatic cholangiocarcinoma, 10 had gallbladder carcinoma, 9 had ampullary carcinoma, and 8 had intrahepatic cholangiocarcinoma. Overall, 25 patients completed adjuvant chemotherapy, with a 54.3% completion rate while the completion rate without recurrence during the 1 year administration was 62.5%. Seven patients (15%) experienced adverse events (grade 3/4). The median number of courses administered was 7.5. Thirteen patients needed dose reduction or temporary therapy withdrawal. OS and DFS rates at 1/2 years were 91.2/80.0% and 84.3/77.2%, respectively. Among patients who were administered more than 3 courses of S-1, only one patient discontinued because of adverse events. CONCLUSIONS: One-year administration of adjuvant S-1 therapy for resected BTC was feasible and may be a promising treatment for those with resected BTC. Now, a randomized trial to determine the optimal duration of S-1 is ongoing. TRIAL REGISTRATION: UMIN-CTR, UMIN000009029. Registered 5 October 2012-Retrospectively registered, https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000009347 BioMed Central 2020-07-23 /pmc/articles/PMC7379785/ /pubmed/32703191 http://dx.doi.org/10.1186/s12885-020-07185-6 Text en © The Author(s) 2020 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/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Itano, Osamu
Takemura, Yusuke
Kishida, Norihiro
Tamagawa, Eiji
Shinozaki, Hiroharu
Ikeda, Ken
Urakami, Hidejiro
Ei, Shigenori
Hayatsu, Shigeo
Suzuki, Keiichi
Sakuragawa, Tadayuki
Ishii, Masatsugu
Shito, Masaya
Aiura, Koichi
Fujisaki, Hiroto
Takano, Kiminori
Matsui, Junichi
Minagawa, Takuya
Shinoda, Masahiro
Kitago, Minoru
Abe, Yuta
Yagi, Hiroshi
Oshima, Go
Hori, Shutaro
Kitagawa, Yuko
A prospective feasibility study of one-year administration of adjuvant S-1 therapy for resected biliary tract cancer in a multi-institutional trial (Tokyo Study Group for Biliary Cancer: TOSBIC01)
title A prospective feasibility study of one-year administration of adjuvant S-1 therapy for resected biliary tract cancer in a multi-institutional trial (Tokyo Study Group for Biliary Cancer: TOSBIC01)
title_full A prospective feasibility study of one-year administration of adjuvant S-1 therapy for resected biliary tract cancer in a multi-institutional trial (Tokyo Study Group for Biliary Cancer: TOSBIC01)
title_fullStr A prospective feasibility study of one-year administration of adjuvant S-1 therapy for resected biliary tract cancer in a multi-institutional trial (Tokyo Study Group for Biliary Cancer: TOSBIC01)
title_full_unstemmed A prospective feasibility study of one-year administration of adjuvant S-1 therapy for resected biliary tract cancer in a multi-institutional trial (Tokyo Study Group for Biliary Cancer: TOSBIC01)
title_short A prospective feasibility study of one-year administration of adjuvant S-1 therapy for resected biliary tract cancer in a multi-institutional trial (Tokyo Study Group for Biliary Cancer: TOSBIC01)
title_sort prospective feasibility study of one-year administration of adjuvant s-1 therapy for resected biliary tract cancer in a multi-institutional trial (tokyo study group for biliary cancer: tosbic01)
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7379785/
https://www.ncbi.nlm.nih.gov/pubmed/32703191
http://dx.doi.org/10.1186/s12885-020-07185-6
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