A phase II study of concurrent chemoradiotherapy with 5-fluorouracil and mitomycin-C for squamous cell carcinoma of the anal canal (the JROSG 10–2 trial)
This study assessed the efficacy of chemoradiotherapy for squamous cell carcinoma of the anal canal (SCCAC). Patients with T1–4N0-3M0 SCCAC received chemoradiotherapy with 5-fluorouracil (5-FU, 800 mg/m2/day, 96-h infusion) and mitomycin-C (MMC, 10 mg/m2 bolus). Patients treated with 3-dimensional c...
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Veröffentlicht in: | Journal of radiation research 2023-01, Vol.64 (1), p.154-161 |
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creator | Murofushi, Keiko Nemoto Itasaka, Satoshi Shimokawa, Mototsugu Murakami, Yuji Yamamoto, Takaya Nishimura, Yasumasa Kudo, Shigehiro Sakamoto, Takashi Ariga, Takuro Ogo, Etsuyo Taguchi, Kentaro Jingu, Keiichi Ogawa, Kazuhiko |
description | This study assessed the efficacy of chemoradiotherapy for squamous cell carcinoma of the anal canal (SCCAC). Patients with T1–4N0-3M0 SCCAC received chemoradiotherapy with 5-fluorouracil (5-FU, 800 mg/m2/day, 96-h infusion) and mitomycin-C (MMC, 10 mg/m2 bolus). Patients treated with 3-dimensional conformal radiotherapy (3D-CRT) or intensity-modulated radiotherapy (IMRT) were administered 36.0 Gy in 20 fractions or 49.5 Gy in 33 fractions for elective nodal irradiation and 59.4 Gy in 33 fractions for primary tumor and metastatic nodal irradiation. The sample size was considered sufficient to estimate 95% confidence intervals (CIs) for the true 2-year disease-free survival (DFS) within a width of +15% when the expected true 2-year DFS was 70%. The primary endpoint was 2-year DFS. The secondary endpoints were 2-year overall survival (OS), locoregional control (LC), colostomy-free survival (CFS) and adverse events. Thirty-one patients were enrolled between January 2014 and July 2019. The median follow-up was 33.3 months (range, 16.2–65.8 months). Among the 31 patients, 13%, 32%, 16% and 39% had stage I, II, IIIA and IIIB disease, respectively. Thirty patients were treated with IMRT. Complete response (CR) was achieved in 27 patients. The 2-year DFS, OS, LC and CFS rates were 77.4% (95% CI, 58.4–88.5%), 93.5% (95% CI, 76.6–98.3%), 83.9% (95% CI, 65.5–92.9%) and 80.6% (95% CI, 61.9–90.8%), respectively. One patient experienced grade 3 late adverse events; however, no grade ≥ 4 late adverse events occurred. Good DFS with a low rate of late adverse events was observed. Chemoradiotherapy with 5-FU and MMC was effective for SCCAC. |
doi_str_mv | 10.1093/jrr/rrac069 |
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Patients with T1–4N0-3M0 SCCAC received chemoradiotherapy with 5-fluorouracil (5-FU, 800 mg/m2/day, 96-h infusion) and mitomycin-C (MMC, 10 mg/m2 bolus). Patients treated with 3-dimensional conformal radiotherapy (3D-CRT) or intensity-modulated radiotherapy (IMRT) were administered 36.0 Gy in 20 fractions or 49.5 Gy in 33 fractions for elective nodal irradiation and 59.4 Gy in 33 fractions for primary tumor and metastatic nodal irradiation. The sample size was considered sufficient to estimate 95% confidence intervals (CIs) for the true 2-year disease-free survival (DFS) within a width of +15% when the expected true 2-year DFS was 70%. The primary endpoint was 2-year DFS. The secondary endpoints were 2-year overall survival (OS), locoregional control (LC), colostomy-free survival (CFS) and adverse events. Thirty-one patients were enrolled between January 2014 and July 2019. The median follow-up was 33.3 months (range, 16.2–65.8 months). Among the 31 patients, 13%, 32%, 16% and 39% had stage I, II, IIIA and IIIB disease, respectively. Thirty patients were treated with IMRT. Complete response (CR) was achieved in 27 patients. The 2-year DFS, OS, LC and CFS rates were 77.4% (95% CI, 58.4–88.5%), 93.5% (95% CI, 76.6–98.3%), 83.9% (95% CI, 65.5–92.9%) and 80.6% (95% CI, 61.9–90.8%), respectively. One patient experienced grade 3 late adverse events; however, no grade ≥ 4 late adverse events occurred. Good DFS with a low rate of late adverse events was observed. Chemoradiotherapy with 5-FU and MMC was effective for SCCAC.</description><identifier>ISSN: 0449-3060</identifier><identifier>EISSN: 1349-9157</identifier><identifier>DOI: 10.1093/jrr/rrac069</identifier><identifier>PMID: 36280895</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>Anal Canal - pathology ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Anus Neoplasms - therapy ; Cancer ; Carcinoma, Squamous Cell - therapy ; Care and treatment ; Chemoradiotherapy - adverse effects ; Clinical trials ; Fluorouracil ; Fluorouracil - therapeutic use ; Humans ; Metastasis ; Mitomycin - therapeutic use ; Radiotherapy ; Radiotherapy, Intensity-Modulated - methods ; Regular paper ; Squamous cell carcinoma</subject><ispartof>Journal of radiation research, 2023-01, Vol.64 (1), p.154-161</ispartof><rights>The Author(s) 2022. Published by Oxford University Press on behalf of The Japanese Radiation Research Society and Japanese Society for Radiation Oncology. 2022</rights><rights>The Author(s) 2022. Published by Oxford University Press on behalf of The Japanese Radiation Research Society and Japanese Society for Radiation Oncology.</rights><rights>COPYRIGHT 2023 Oxford University Press</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c503t-4fc5dba3c1ce19842853aae62b3b4806e7e2bffac9ad2c85dc34154195827d843</citedby><cites>FETCH-LOGICAL-c503t-4fc5dba3c1ce19842853aae62b3b4806e7e2bffac9ad2c85dc34154195827d843</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9855315/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9855315/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,1598,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36280895$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Murofushi, Keiko Nemoto</creatorcontrib><creatorcontrib>Itasaka, Satoshi</creatorcontrib><creatorcontrib>Shimokawa, Mototsugu</creatorcontrib><creatorcontrib>Murakami, Yuji</creatorcontrib><creatorcontrib>Yamamoto, Takaya</creatorcontrib><creatorcontrib>Nishimura, Yasumasa</creatorcontrib><creatorcontrib>Kudo, Shigehiro</creatorcontrib><creatorcontrib>Sakamoto, Takashi</creatorcontrib><creatorcontrib>Ariga, Takuro</creatorcontrib><creatorcontrib>Ogo, Etsuyo</creatorcontrib><creatorcontrib>Taguchi, Kentaro</creatorcontrib><creatorcontrib>Jingu, Keiichi</creatorcontrib><creatorcontrib>Ogawa, Kazuhiko</creatorcontrib><title>A phase II study of concurrent chemoradiotherapy with 5-fluorouracil and mitomycin-C for squamous cell carcinoma of the anal canal (the JROSG 10–2 trial)</title><title>Journal of radiation research</title><addtitle>J Radiat Res</addtitle><description>This study assessed the efficacy of chemoradiotherapy for squamous cell carcinoma of the anal canal (SCCAC). Patients with T1–4N0-3M0 SCCAC received chemoradiotherapy with 5-fluorouracil (5-FU, 800 mg/m2/day, 96-h infusion) and mitomycin-C (MMC, 10 mg/m2 bolus). Patients treated with 3-dimensional conformal radiotherapy (3D-CRT) or intensity-modulated radiotherapy (IMRT) were administered 36.0 Gy in 20 fractions or 49.5 Gy in 33 fractions for elective nodal irradiation and 59.4 Gy in 33 fractions for primary tumor and metastatic nodal irradiation. The sample size was considered sufficient to estimate 95% confidence intervals (CIs) for the true 2-year disease-free survival (DFS) within a width of +15% when the expected true 2-year DFS was 70%. The primary endpoint was 2-year DFS. The secondary endpoints were 2-year overall survival (OS), locoregional control (LC), colostomy-free survival (CFS) and adverse events. Thirty-one patients were enrolled between January 2014 and July 2019. The median follow-up was 33.3 months (range, 16.2–65.8 months). Among the 31 patients, 13%, 32%, 16% and 39% had stage I, II, IIIA and IIIB disease, respectively. Thirty patients were treated with IMRT. Complete response (CR) was achieved in 27 patients. The 2-year DFS, OS, LC and CFS rates were 77.4% (95% CI, 58.4–88.5%), 93.5% (95% CI, 76.6–98.3%), 83.9% (95% CI, 65.5–92.9%) and 80.6% (95% CI, 61.9–90.8%), respectively. One patient experienced grade 3 late adverse events; however, no grade ≥ 4 late adverse events occurred. Good DFS with a low rate of late adverse events was observed. Chemoradiotherapy with 5-FU and MMC was effective for SCCAC.</description><subject>Anal Canal - pathology</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Anus Neoplasms - therapy</subject><subject>Cancer</subject><subject>Carcinoma, Squamous Cell - therapy</subject><subject>Care and treatment</subject><subject>Chemoradiotherapy - adverse effects</subject><subject>Clinical trials</subject><subject>Fluorouracil</subject><subject>Fluorouracil - therapeutic use</subject><subject>Humans</subject><subject>Metastasis</subject><subject>Mitomycin - therapeutic use</subject><subject>Radiotherapy</subject><subject>Radiotherapy, Intensity-Modulated - methods</subject><subject>Regular paper</subject><subject>Squamous cell carcinoma</subject><issn>0449-3060</issn><issn>1349-9157</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>TOX</sourceid><sourceid>EIF</sourceid><recordid>eNp9kl2L1DAUhoso7rh65b0EBFmR7uajaZObhWHQdWRhwY_rcJom2yxt001aZe78D1767_wlpsy4uCASyMfJc97kJG-WPSf4lGDJzm5COAsBNC7lg2xFWCFzSXj1MFvhIs0ZLvFR9iTGG4xphTl-nB2xkgosJF9lP9dobCEatN2iOM3NDnmLtB_0HIIZJqRb0_sAjfNTawKMO_TNTS3iue1mH_ycznUdgqFBvZt8v9NuyDfI-oDi7Qy9nyPSpuuQhpC2fA-LfpJKKbBEl_5kWX_4ePXpAhH86_sPiqbgoHv9NHtkoYvm2WE8zr68e_t58z6_vLrYbtaXueaYTXlhNW9qYJpoQ6QoqOAMwJS0ZnUhcGkqQ2trQUtoqBa80awgvCCSC1o1omDH2fled5zr3jQ61R2gU2NwPYSd8uDU_Z3Bteraf1VScM4ITwInB4Hgb2cTJ9W7uJQNg0kvoGhFRVHyitOEvtyj19AZ5Qbrk6JecLWuSkkIJUIk6vQfVGqN6V36HWNdit9LeLNP0MHHGIy9uz3BanGJSi5RB5ck-sXfBd-xf2yRgFd7wM_jf5V-A_9MyKg</recordid><startdate>20230120</startdate><enddate>20230120</enddate><creator>Murofushi, Keiko Nemoto</creator><creator>Itasaka, Satoshi</creator><creator>Shimokawa, Mototsugu</creator><creator>Murakami, Yuji</creator><creator>Yamamoto, Takaya</creator><creator>Nishimura, Yasumasa</creator><creator>Kudo, Shigehiro</creator><creator>Sakamoto, Takashi</creator><creator>Ariga, Takuro</creator><creator>Ogo, Etsuyo</creator><creator>Taguchi, Kentaro</creator><creator>Jingu, Keiichi</creator><creator>Ogawa, Kazuhiko</creator><general>Oxford University Press</general><scope>TOX</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20230120</creationdate><title>A phase II study of concurrent chemoradiotherapy with 5-fluorouracil and mitomycin-C for squamous cell carcinoma of the anal canal (the JROSG 10–2 trial)</title><author>Murofushi, Keiko Nemoto ; Itasaka, Satoshi ; Shimokawa, Mototsugu ; Murakami, Yuji ; Yamamoto, Takaya ; Nishimura, Yasumasa ; Kudo, Shigehiro ; Sakamoto, Takashi ; Ariga, Takuro ; Ogo, Etsuyo ; Taguchi, Kentaro ; Jingu, Keiichi ; Ogawa, Kazuhiko</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c503t-4fc5dba3c1ce19842853aae62b3b4806e7e2bffac9ad2c85dc34154195827d843</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Anal Canal - pathology</topic><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>Anus Neoplasms - therapy</topic><topic>Cancer</topic><topic>Carcinoma, Squamous Cell - therapy</topic><topic>Care and treatment</topic><topic>Chemoradiotherapy - adverse effects</topic><topic>Clinical trials</topic><topic>Fluorouracil</topic><topic>Fluorouracil - therapeutic use</topic><topic>Humans</topic><topic>Metastasis</topic><topic>Mitomycin - therapeutic use</topic><topic>Radiotherapy</topic><topic>Radiotherapy, Intensity-Modulated - methods</topic><topic>Regular paper</topic><topic>Squamous cell carcinoma</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Murofushi, Keiko Nemoto</creatorcontrib><creatorcontrib>Itasaka, Satoshi</creatorcontrib><creatorcontrib>Shimokawa, Mototsugu</creatorcontrib><creatorcontrib>Murakami, Yuji</creatorcontrib><creatorcontrib>Yamamoto, Takaya</creatorcontrib><creatorcontrib>Nishimura, Yasumasa</creatorcontrib><creatorcontrib>Kudo, Shigehiro</creatorcontrib><creatorcontrib>Sakamoto, Takashi</creatorcontrib><creatorcontrib>Ariga, Takuro</creatorcontrib><creatorcontrib>Ogo, Etsuyo</creatorcontrib><creatorcontrib>Taguchi, Kentaro</creatorcontrib><creatorcontrib>Jingu, Keiichi</creatorcontrib><creatorcontrib>Ogawa, Kazuhiko</creatorcontrib><collection>Oxford Journals Open Access Collection</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of radiation research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Murofushi, Keiko Nemoto</au><au>Itasaka, Satoshi</au><au>Shimokawa, Mototsugu</au><au>Murakami, Yuji</au><au>Yamamoto, Takaya</au><au>Nishimura, Yasumasa</au><au>Kudo, Shigehiro</au><au>Sakamoto, Takashi</au><au>Ariga, Takuro</au><au>Ogo, Etsuyo</au><au>Taguchi, Kentaro</au><au>Jingu, Keiichi</au><au>Ogawa, Kazuhiko</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A phase II study of concurrent chemoradiotherapy with 5-fluorouracil and mitomycin-C for squamous cell carcinoma of the anal canal (the JROSG 10–2 trial)</atitle><jtitle>Journal of radiation research</jtitle><addtitle>J Radiat Res</addtitle><date>2023-01-20</date><risdate>2023</risdate><volume>64</volume><issue>1</issue><spage>154</spage><epage>161</epage><pages>154-161</pages><issn>0449-3060</issn><eissn>1349-9157</eissn><abstract>This study assessed the efficacy of chemoradiotherapy for squamous cell carcinoma of the anal canal (SCCAC). Patients with T1–4N0-3M0 SCCAC received chemoradiotherapy with 5-fluorouracil (5-FU, 800 mg/m2/day, 96-h infusion) and mitomycin-C (MMC, 10 mg/m2 bolus). Patients treated with 3-dimensional conformal radiotherapy (3D-CRT) or intensity-modulated radiotherapy (IMRT) were administered 36.0 Gy in 20 fractions or 49.5 Gy in 33 fractions for elective nodal irradiation and 59.4 Gy in 33 fractions for primary tumor and metastatic nodal irradiation. The sample size was considered sufficient to estimate 95% confidence intervals (CIs) for the true 2-year disease-free survival (DFS) within a width of +15% when the expected true 2-year DFS was 70%. The primary endpoint was 2-year DFS. The secondary endpoints were 2-year overall survival (OS), locoregional control (LC), colostomy-free survival (CFS) and adverse events. Thirty-one patients were enrolled between January 2014 and July 2019. The median follow-up was 33.3 months (range, 16.2–65.8 months). Among the 31 patients, 13%, 32%, 16% and 39% had stage I, II, IIIA and IIIB disease, respectively. Thirty patients were treated with IMRT. Complete response (CR) was achieved in 27 patients. The 2-year DFS, OS, LC and CFS rates were 77.4% (95% CI, 58.4–88.5%), 93.5% (95% CI, 76.6–98.3%), 83.9% (95% CI, 65.5–92.9%) and 80.6% (95% CI, 61.9–90.8%), respectively. One patient experienced grade 3 late adverse events; however, no grade ≥ 4 late adverse events occurred. Good DFS with a low rate of late adverse events was observed. Chemoradiotherapy with 5-FU and MMC was effective for SCCAC.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>36280895</pmid><doi>10.1093/jrr/rrac069</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Anal Canal - pathology Antineoplastic Combined Chemotherapy Protocols - therapeutic use Anus Neoplasms - therapy Cancer Carcinoma, Squamous Cell - therapy Care and treatment Chemoradiotherapy - adverse effects Clinical trials Fluorouracil Fluorouracil - therapeutic use Humans Metastasis Mitomycin - therapeutic use Radiotherapy Radiotherapy, Intensity-Modulated - methods Regular paper Squamous cell carcinoma |
title | A phase II study of concurrent chemoradiotherapy with 5-fluorouracil and mitomycin-C for squamous cell carcinoma of the anal canal (the JROSG 10–2 trial) |
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