Comparing Paclitaxel Plus Fluorouracil Versus Cisplatin Plus Fluorouracil in Chemoradiotherapy for Locally Advanced Esophageal Squamous Cell Cancer: A Randomized, Multicenter, Phase III Clinical Trial
This trial aimed to assess the efficacy and safety of the paclitaxel plus fluorouracil regimen versus the cisplatin plus fluorouracil regimen in definitive concurrent chemoradiotherapy (dCRT) in patients with locally advanced esophageal squamous cell carcinoma (ESCC). Patients with locally advanced...
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Veröffentlicht in: | Journal of clinical oncology 2019-07, Vol.37 (20), p.1695-1703 |
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creator | Chen, Yun Ye, Jinjun Zhu, Zhengfei Zhao, Weixin Zhou, Jialiang Wu, Chaoyang Tang, Huarong Fan, Min Li, Ling Lin, Qin Xia, Yi Li, Yunhai Li, Jiancheng Jia, Huixun Lu, Saiquan Zhang, Zhen Zhao, Kuaile |
description | This trial aimed to assess the efficacy and safety of the paclitaxel plus fluorouracil regimen versus the cisplatin plus fluorouracil regimen in definitive concurrent chemoradiotherapy (dCRT) in patients with locally advanced esophageal squamous cell carcinoma (ESCC).
Patients with locally advanced ESCC were enrolled and randomly assigned to either the paclitaxel plus fluorouracil group or the cisplatin plus fluorouracil group. The patients in the paclitaxel plus fluorouracil group were treated with paclitaxel and fluorouracil one cycle per week in dCRT for five cycles followed by paclitaxel and fluorouracil one cycle per month in consolidation chemotherapy for two cycles. The patients in the cisplatin/5-fluorouracil group were treated with cisplatin and fluorouracil one cycle per month in dCRT for two cycles followed by two cycles in consolidation chemotherapy. The radiotherapy dose was 61.2 Gy delivered in 34 fractions. The primary end point was 3-year overall survival (OS).
Four hundred thirty-six patients with ESCC in six centers were recruited at a 1:1 ratio between April 2012 and July 2015. The median follow-up of the surviving patients was 48.7 months (interquartile range, 42.6-60.9). The 3-year OS was 55.4% in the paclitaxel plus fluorouracil group and 51.8% in the cisplatin plus fluorouracil group (hazard ratio, 0.905 [95% CI, 0.698 to 1.172];
= .448). The 3-year progression-free survival was also not significantly different between the paclitaxel plus fluorouracil group and the cisplatin plus fluorouracil group (43.7%
45.5%, respectively; hazard ratio, 0.973 [95% CI, 0.762 to 1.243];
= .828). Compared with the cisplatin plus fluorouracil group, the paclitaxel plus fluorouracil group had significantly lower incidences of acute grade 3 or higher anemia, thrombocytopenia, anorexia, nausea, vomiting, and fatigue (
< .05), but higher incidences of acute grade 3 or higher leukopenia, radiation dermatitis, and radiation pneumonitis (
< .05).
The paclitaxel plus fluorouracil regimen did not significantly prolong the OS compared with the standard cisplatin plus fluorouracil regimen in dCRT in patients with locally advanced ESCC. |
doi_str_mv | 10.1200/JCO.18.02122 |
format | Article |
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Patients with locally advanced ESCC were enrolled and randomly assigned to either the paclitaxel plus fluorouracil group or the cisplatin plus fluorouracil group. The patients in the paclitaxel plus fluorouracil group were treated with paclitaxel and fluorouracil one cycle per week in dCRT for five cycles followed by paclitaxel and fluorouracil one cycle per month in consolidation chemotherapy for two cycles. The patients in the cisplatin/5-fluorouracil group were treated with cisplatin and fluorouracil one cycle per month in dCRT for two cycles followed by two cycles in consolidation chemotherapy. The radiotherapy dose was 61.2 Gy delivered in 34 fractions. The primary end point was 3-year overall survival (OS).
Four hundred thirty-six patients with ESCC in six centers were recruited at a 1:1 ratio between April 2012 and July 2015. The median follow-up of the surviving patients was 48.7 months (interquartile range, 42.6-60.9). The 3-year OS was 55.4% in the paclitaxel plus fluorouracil group and 51.8% in the cisplatin plus fluorouracil group (hazard ratio, 0.905 [95% CI, 0.698 to 1.172];
= .448). The 3-year progression-free survival was also not significantly different between the paclitaxel plus fluorouracil group and the cisplatin plus fluorouracil group (43.7%
45.5%, respectively; hazard ratio, 0.973 [95% CI, 0.762 to 1.243];
= .828). Compared with the cisplatin plus fluorouracil group, the paclitaxel plus fluorouracil group had significantly lower incidences of acute grade 3 or higher anemia, thrombocytopenia, anorexia, nausea, vomiting, and fatigue (
< .05), but higher incidences of acute grade 3 or higher leukopenia, radiation dermatitis, and radiation pneumonitis (
< .05).
The paclitaxel plus fluorouracil regimen did not significantly prolong the OS compared with the standard cisplatin plus fluorouracil regimen in dCRT in patients with locally advanced ESCC.</description><identifier>ISSN: 0732-183X</identifier><identifier>EISSN: 1527-7755</identifier><identifier>DOI: 10.1200/JCO.18.02122</identifier><identifier>PMID: 30920880</identifier><language>eng</language><publisher>United States: American Society of Clinical Oncology</publisher><subject>RAPID COMMUNICATION</subject><ispartof>Journal of clinical oncology, 2019-07, Vol.37 (20), p.1695-1703</ispartof><rights>2019 by American Society of Clinical Oncology 2019 American Society of Clinical Oncology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c493t-75830b6fb44224bc0447f31fc4279072e0a2256692613b9c65ff418231ac8e363</citedby><cites>FETCH-LOGICAL-c493t-75830b6fb44224bc0447f31fc4279072e0a2256692613b9c65ff418231ac8e363</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,3716,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30920880$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chen, Yun</creatorcontrib><creatorcontrib>Ye, Jinjun</creatorcontrib><creatorcontrib>Zhu, Zhengfei</creatorcontrib><creatorcontrib>Zhao, Weixin</creatorcontrib><creatorcontrib>Zhou, Jialiang</creatorcontrib><creatorcontrib>Wu, Chaoyang</creatorcontrib><creatorcontrib>Tang, Huarong</creatorcontrib><creatorcontrib>Fan, Min</creatorcontrib><creatorcontrib>Li, Ling</creatorcontrib><creatorcontrib>Lin, Qin</creatorcontrib><creatorcontrib>Xia, Yi</creatorcontrib><creatorcontrib>Li, Yunhai</creatorcontrib><creatorcontrib>Li, Jiancheng</creatorcontrib><creatorcontrib>Jia, Huixun</creatorcontrib><creatorcontrib>Lu, Saiquan</creatorcontrib><creatorcontrib>Zhang, Zhen</creatorcontrib><creatorcontrib>Zhao, Kuaile</creatorcontrib><title>Comparing Paclitaxel Plus Fluorouracil Versus Cisplatin Plus Fluorouracil in Chemoradiotherapy for Locally Advanced Esophageal Squamous Cell Cancer: A Randomized, Multicenter, Phase III Clinical Trial</title><title>Journal of clinical oncology</title><addtitle>J Clin Oncol</addtitle><description>This trial aimed to assess the efficacy and safety of the paclitaxel plus fluorouracil regimen versus the cisplatin plus fluorouracil regimen in definitive concurrent chemoradiotherapy (dCRT) in patients with locally advanced esophageal squamous cell carcinoma (ESCC).
Patients with locally advanced ESCC were enrolled and randomly assigned to either the paclitaxel plus fluorouracil group or the cisplatin plus fluorouracil group. The patients in the paclitaxel plus fluorouracil group were treated with paclitaxel and fluorouracil one cycle per week in dCRT for five cycles followed by paclitaxel and fluorouracil one cycle per month in consolidation chemotherapy for two cycles. The patients in the cisplatin/5-fluorouracil group were treated with cisplatin and fluorouracil one cycle per month in dCRT for two cycles followed by two cycles in consolidation chemotherapy. The radiotherapy dose was 61.2 Gy delivered in 34 fractions. The primary end point was 3-year overall survival (OS).
Four hundred thirty-six patients with ESCC in six centers were recruited at a 1:1 ratio between April 2012 and July 2015. The median follow-up of the surviving patients was 48.7 months (interquartile range, 42.6-60.9). The 3-year OS was 55.4% in the paclitaxel plus fluorouracil group and 51.8% in the cisplatin plus fluorouracil group (hazard ratio, 0.905 [95% CI, 0.698 to 1.172];
= .448). The 3-year progression-free survival was also not significantly different between the paclitaxel plus fluorouracil group and the cisplatin plus fluorouracil group (43.7%
45.5%, respectively; hazard ratio, 0.973 [95% CI, 0.762 to 1.243];
= .828). Compared with the cisplatin plus fluorouracil group, the paclitaxel plus fluorouracil group had significantly lower incidences of acute grade 3 or higher anemia, thrombocytopenia, anorexia, nausea, vomiting, and fatigue (
< .05), but higher incidences of acute grade 3 or higher leukopenia, radiation dermatitis, and radiation pneumonitis (
< .05).
The paclitaxel plus fluorouracil regimen did not significantly prolong the OS compared with the standard cisplatin plus fluorouracil regimen in dCRT in patients with locally advanced ESCC.</description><subject>RAPID COMMUNICATION</subject><issn>0732-183X</issn><issn>1527-7755</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNptkU1v1DAQhi0Eokvhxhn5yGGz-CNOHA5Iq6gtixZ1BQVxsyaOs2vkxKmdVGx_IT-LhJYKJE4jzTx6ZuwXoZeUrCgj5M2H8nJF5YowytgjtKCC5UmeC_EYLUjOWUIl_3aCnsX4nRCaSi6eohNOCkakJAv0s_RtD8F2e7wD7ewAP4zDOzdGfO5GH_wYQFuHv5oQp15pY-9gsN1_kKlZHkzrA9TWDwcToD_ixge89RqcO-J1fQOdNjU-i74_wN6Aw5-vR2j9bDbO4XKeh7d4jT9BV_vW3pp6iT-ObrDadIMJS7w7QDR4s9ng0tnOTmZ8FSy45-hJAy6aF_f1FH05P7sq3yfby4tNud4mOi34kORCclJlTZWmjKWVJmmaN5w2OmV5QXJmCDAmsqxgGeVVoTPRNCmVjFPQ0vCMn6J3d95-rFpTz2cFcKoPtoVwVB6s-nfS2YPa-xuVZVyKYha8vhcEfz2aOKjWRj29HjozfYRiU6i5ZIKICV3eoTr4GINpHtZQoubw1RS-olL9Dn_CX_192gP8J23-C7_dres</recordid><startdate>20190710</startdate><enddate>20190710</enddate><creator>Chen, Yun</creator><creator>Ye, Jinjun</creator><creator>Zhu, Zhengfei</creator><creator>Zhao, Weixin</creator><creator>Zhou, Jialiang</creator><creator>Wu, Chaoyang</creator><creator>Tang, Huarong</creator><creator>Fan, Min</creator><creator>Li, Ling</creator><creator>Lin, Qin</creator><creator>Xia, Yi</creator><creator>Li, Yunhai</creator><creator>Li, Jiancheng</creator><creator>Jia, Huixun</creator><creator>Lu, Saiquan</creator><creator>Zhang, Zhen</creator><creator>Zhao, Kuaile</creator><general>American Society of Clinical Oncology</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20190710</creationdate><title>Comparing Paclitaxel Plus Fluorouracil Versus Cisplatin Plus Fluorouracil in Chemoradiotherapy for Locally Advanced Esophageal Squamous Cell Cancer: A Randomized, Multicenter, Phase III Clinical Trial</title><author>Chen, Yun ; Ye, Jinjun ; Zhu, Zhengfei ; Zhao, Weixin ; Zhou, Jialiang ; Wu, Chaoyang ; Tang, Huarong ; Fan, Min ; Li, Ling ; Lin, Qin ; Xia, Yi ; Li, Yunhai ; Li, Jiancheng ; Jia, Huixun ; Lu, Saiquan ; Zhang, Zhen ; Zhao, Kuaile</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c493t-75830b6fb44224bc0447f31fc4279072e0a2256692613b9c65ff418231ac8e363</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>RAPID COMMUNICATION</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chen, Yun</creatorcontrib><creatorcontrib>Ye, Jinjun</creatorcontrib><creatorcontrib>Zhu, Zhengfei</creatorcontrib><creatorcontrib>Zhao, Weixin</creatorcontrib><creatorcontrib>Zhou, Jialiang</creatorcontrib><creatorcontrib>Wu, Chaoyang</creatorcontrib><creatorcontrib>Tang, Huarong</creatorcontrib><creatorcontrib>Fan, Min</creatorcontrib><creatorcontrib>Li, Ling</creatorcontrib><creatorcontrib>Lin, Qin</creatorcontrib><creatorcontrib>Xia, Yi</creatorcontrib><creatorcontrib>Li, Yunhai</creatorcontrib><creatorcontrib>Li, Jiancheng</creatorcontrib><creatorcontrib>Jia, Huixun</creatorcontrib><creatorcontrib>Lu, Saiquan</creatorcontrib><creatorcontrib>Zhang, Zhen</creatorcontrib><creatorcontrib>Zhao, Kuaile</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of clinical oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chen, Yun</au><au>Ye, Jinjun</au><au>Zhu, Zhengfei</au><au>Zhao, Weixin</au><au>Zhou, Jialiang</au><au>Wu, Chaoyang</au><au>Tang, Huarong</au><au>Fan, Min</au><au>Li, Ling</au><au>Lin, Qin</au><au>Xia, Yi</au><au>Li, Yunhai</au><au>Li, Jiancheng</au><au>Jia, Huixun</au><au>Lu, Saiquan</au><au>Zhang, Zhen</au><au>Zhao, Kuaile</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparing Paclitaxel Plus Fluorouracil Versus Cisplatin Plus Fluorouracil in Chemoradiotherapy for Locally Advanced Esophageal Squamous Cell Cancer: A Randomized, Multicenter, Phase III Clinical Trial</atitle><jtitle>Journal of clinical oncology</jtitle><addtitle>J Clin Oncol</addtitle><date>2019-07-10</date><risdate>2019</risdate><volume>37</volume><issue>20</issue><spage>1695</spage><epage>1703</epage><pages>1695-1703</pages><issn>0732-183X</issn><eissn>1527-7755</eissn><abstract>This trial aimed to assess the efficacy and safety of the paclitaxel plus fluorouracil regimen versus the cisplatin plus fluorouracil regimen in definitive concurrent chemoradiotherapy (dCRT) in patients with locally advanced esophageal squamous cell carcinoma (ESCC).
Patients with locally advanced ESCC were enrolled and randomly assigned to either the paclitaxel plus fluorouracil group or the cisplatin plus fluorouracil group. The patients in the paclitaxel plus fluorouracil group were treated with paclitaxel and fluorouracil one cycle per week in dCRT for five cycles followed by paclitaxel and fluorouracil one cycle per month in consolidation chemotherapy for two cycles. The patients in the cisplatin/5-fluorouracil group were treated with cisplatin and fluorouracil one cycle per month in dCRT for two cycles followed by two cycles in consolidation chemotherapy. The radiotherapy dose was 61.2 Gy delivered in 34 fractions. The primary end point was 3-year overall survival (OS).
Four hundred thirty-six patients with ESCC in six centers were recruited at a 1:1 ratio between April 2012 and July 2015. The median follow-up of the surviving patients was 48.7 months (interquartile range, 42.6-60.9). The 3-year OS was 55.4% in the paclitaxel plus fluorouracil group and 51.8% in the cisplatin plus fluorouracil group (hazard ratio, 0.905 [95% CI, 0.698 to 1.172];
= .448). The 3-year progression-free survival was also not significantly different between the paclitaxel plus fluorouracil group and the cisplatin plus fluorouracil group (43.7%
45.5%, respectively; hazard ratio, 0.973 [95% CI, 0.762 to 1.243];
= .828). Compared with the cisplatin plus fluorouracil group, the paclitaxel plus fluorouracil group had significantly lower incidences of acute grade 3 or higher anemia, thrombocytopenia, anorexia, nausea, vomiting, and fatigue (
< .05), but higher incidences of acute grade 3 or higher leukopenia, radiation dermatitis, and radiation pneumonitis (
< .05).
The paclitaxel plus fluorouracil regimen did not significantly prolong the OS compared with the standard cisplatin plus fluorouracil regimen in dCRT in patients with locally advanced ESCC.</abstract><cop>United States</cop><pub>American Society of Clinical Oncology</pub><pmid>30920880</pmid><doi>10.1200/JCO.18.02122</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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source | American Society of Clinical Oncology Online Journals; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection |
subjects | RAPID COMMUNICATION |
title | Comparing Paclitaxel Plus Fluorouracil Versus Cisplatin Plus Fluorouracil in Chemoradiotherapy for Locally Advanced Esophageal Squamous Cell Cancer: A Randomized, Multicenter, Phase III Clinical Trial |
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