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Phase 1/2 study of concurrent chemoradiotherapy with weekly irinotecan hydrochloride for advanced/recurrence uterine cancer: A multi-institutional study of Kansai Clinical Oncology Group

OBJECTIVE: Concurrent chemoradiotherapy using cisplatin was thought to be standard treatment for squamous cell carcinoma of cervix, but it had not been effective for adenocarcinoma. Concurrent chemoradiotherapy using irinotecan hydrochloride (CPT-11) had been effective for colorectal cancer, thus, w...

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Autores principales: Takeuchi, Satoshi, Kuroboshi, Haruo, Mori, Taisuke, Ito, Kimihiko, Kondo, Eiji, Tabata, Tsutomu, Itani, Yoshio, Kawaguchi, Ryuji, Takeuchi, Kyosuke, Soejima, Toshinori, Sasaki, Ryohei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7219098/
https://www.ncbi.nlm.nih.gov/pubmed/32410799
http://dx.doi.org/10.21147/j.issn.1000-9604.2020.02.09
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author Takeuchi, Satoshi
Kuroboshi, Haruo
Mori, Taisuke
Ito, Kimihiko
Kondo, Eiji
Tabata, Tsutomu
Itani, Yoshio
Kawaguchi, Ryuji
Takeuchi, Kyosuke
Soejima, Toshinori
Sasaki, Ryohei
author_facet Takeuchi, Satoshi
Kuroboshi, Haruo
Mori, Taisuke
Ito, Kimihiko
Kondo, Eiji
Tabata, Tsutomu
Itani, Yoshio
Kawaguchi, Ryuji
Takeuchi, Kyosuke
Soejima, Toshinori
Sasaki, Ryohei
author_sort Takeuchi, Satoshi
collection PubMed
description OBJECTIVE: Concurrent chemoradiotherapy using cisplatin was thought to be standard treatment for squamous cell carcinoma of cervix, but it had not been effective for adenocarcinoma. Concurrent chemoradiotherapy using irinotecan hydrochloride (CPT-11) had been effective for colorectal cancer, thus, we chose CPT-11 as a candidate for gynecologic adenocarcinoma. To evaluate the maximum tolerated dose (MTD) of weekly CPT-11 with external pelvic radiotherapy, a phase 1/2 study was conducted according to modified Fibonacci method. METHODS: Eligible patients were advanced uterine cancer with measurable diseases [performance score (PS): 0−2]. Study period was from August 1st, 2002 to December 31st, 2008. The starting dose level (DL) of CPT-11 was 30 mg/m(2) (DL1) given weekly for 4 weeks. Subsequently, dose escalation was scheduled in 10 mg/m(2) increments to 60 mg/m(2) (DL4). The fixed radiotherapy consisted of whole pelvic 1.8 Gy/d, once a day in weekday for five weeks and it amounted to 45 Gy (25 fractions) in total. RESULTS: Seventeen patients were enrolled. As for toxicities, one (1/17: 5.9%) grade (G) 4 neutropenia lasting 7 days had been seen in DL4. G2 diarrhea was identified in 35.3% (6/17) of the patients, and 11.8% (2/17) G3 diarrhea was observed in DL3 and DL4. Thus, the MTD of CPT-11 was defined as dose of 60 mg/m(2). The recommended dose was decided as 50 mg/m(2). The response rate was 88.2% [9 complete response (CR), 3 partial response (PR), 3 stable disease (SD), 2 not evaluable (NE)]. Disease control rate at 1 month after treatment completion was 100% but distant metastases were found in 24% (4/17) in longer outcome. CONCLUSIONS: MTD was 60 mg/m(2) and recommended dose was set as 50 mg/m(2). This concurrent chemoradiation using weekly CPT-11 was feasible at 50 mg/m(2), and it might be effective even in adenocarcinoma of the uterus.
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spelling pubmed-72190982020-05-14 Phase 1/2 study of concurrent chemoradiotherapy with weekly irinotecan hydrochloride for advanced/recurrence uterine cancer: A multi-institutional study of Kansai Clinical Oncology Group Takeuchi, Satoshi Kuroboshi, Haruo Mori, Taisuke Ito, Kimihiko Kondo, Eiji Tabata, Tsutomu Itani, Yoshio Kawaguchi, Ryuji Takeuchi, Kyosuke Soejima, Toshinori Sasaki, Ryohei Chin J Cancer Res Original Article OBJECTIVE: Concurrent chemoradiotherapy using cisplatin was thought to be standard treatment for squamous cell carcinoma of cervix, but it had not been effective for adenocarcinoma. Concurrent chemoradiotherapy using irinotecan hydrochloride (CPT-11) had been effective for colorectal cancer, thus, we chose CPT-11 as a candidate for gynecologic adenocarcinoma. To evaluate the maximum tolerated dose (MTD) of weekly CPT-11 with external pelvic radiotherapy, a phase 1/2 study was conducted according to modified Fibonacci method. METHODS: Eligible patients were advanced uterine cancer with measurable diseases [performance score (PS): 0−2]. Study period was from August 1st, 2002 to December 31st, 2008. The starting dose level (DL) of CPT-11 was 30 mg/m(2) (DL1) given weekly for 4 weeks. Subsequently, dose escalation was scheduled in 10 mg/m(2) increments to 60 mg/m(2) (DL4). The fixed radiotherapy consisted of whole pelvic 1.8 Gy/d, once a day in weekday for five weeks and it amounted to 45 Gy (25 fractions) in total. RESULTS: Seventeen patients were enrolled. As for toxicities, one (1/17: 5.9%) grade (G) 4 neutropenia lasting 7 days had been seen in DL4. G2 diarrhea was identified in 35.3% (6/17) of the patients, and 11.8% (2/17) G3 diarrhea was observed in DL3 and DL4. Thus, the MTD of CPT-11 was defined as dose of 60 mg/m(2). The recommended dose was decided as 50 mg/m(2). The response rate was 88.2% [9 complete response (CR), 3 partial response (PR), 3 stable disease (SD), 2 not evaluable (NE)]. Disease control rate at 1 month after treatment completion was 100% but distant metastases were found in 24% (4/17) in longer outcome. CONCLUSIONS: MTD was 60 mg/m(2) and recommended dose was set as 50 mg/m(2). This concurrent chemoradiation using weekly CPT-11 was feasible at 50 mg/m(2), and it might be effective even in adenocarcinoma of the uterus. AME Publishing Company 2020-04 /pmc/articles/PMC7219098/ /pubmed/32410799 http://dx.doi.org/10.21147/j.issn.1000-9604.2020.02.09 Text en Copyright © 2020 Chinese Journal of Cancer Research. All rights reserved. http://creativecommons.org/licenses/by-nc-sa/4.0/ This work is licensed under a Creative Commons Attribution-Non Commercial-Share Alike 4.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/
spellingShingle Original Article
Takeuchi, Satoshi
Kuroboshi, Haruo
Mori, Taisuke
Ito, Kimihiko
Kondo, Eiji
Tabata, Tsutomu
Itani, Yoshio
Kawaguchi, Ryuji
Takeuchi, Kyosuke
Soejima, Toshinori
Sasaki, Ryohei
Phase 1/2 study of concurrent chemoradiotherapy with weekly irinotecan hydrochloride for advanced/recurrence uterine cancer: A multi-institutional study of Kansai Clinical Oncology Group
title Phase 1/2 study of concurrent chemoradiotherapy with weekly irinotecan hydrochloride for advanced/recurrence uterine cancer: A multi-institutional study of Kansai Clinical Oncology Group
title_full Phase 1/2 study of concurrent chemoradiotherapy with weekly irinotecan hydrochloride for advanced/recurrence uterine cancer: A multi-institutional study of Kansai Clinical Oncology Group
title_fullStr Phase 1/2 study of concurrent chemoradiotherapy with weekly irinotecan hydrochloride for advanced/recurrence uterine cancer: A multi-institutional study of Kansai Clinical Oncology Group
title_full_unstemmed Phase 1/2 study of concurrent chemoradiotherapy with weekly irinotecan hydrochloride for advanced/recurrence uterine cancer: A multi-institutional study of Kansai Clinical Oncology Group
title_short Phase 1/2 study of concurrent chemoradiotherapy with weekly irinotecan hydrochloride for advanced/recurrence uterine cancer: A multi-institutional study of Kansai Clinical Oncology Group
title_sort phase 1/2 study of concurrent chemoradiotherapy with weekly irinotecan hydrochloride for advanced/recurrence uterine cancer: a multi-institutional study of kansai clinical oncology group
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7219098/
https://www.ncbi.nlm.nih.gov/pubmed/32410799
http://dx.doi.org/10.21147/j.issn.1000-9604.2020.02.09
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