Deintensified Chemoradiotherapy for Pretreatment Epstein-Barr Virus DNA-Selected Low-Risk Locoregionally Advanced Nasopharyngeal Carcinoma: A Phase II Randomized Noninferiority Trial
Cumulative doses of 200 mg/m for concurrent cisplatin (DDP) were indicated by retrospective studies as sufficient in conferring survival benefit for locoregionally advanced nasopharyngeal carcinoma (LA-NPC). We performed an open-label, phase II, randomized, controlled trial to test the noninferiorit...
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creator | Li, Xiao-Yun Luo, Dong-Hua Guo, Ling Mo, Hao-Yuan Sun, Rui Guo, Shan-Shan Liu, Li-Ting Yang, Zhen-Chong Yang, Jin-Hao Qiu, Fang Sun, Xue-Song Wang, Pan Liu, Qing Li, Ji-Bin Tang, Qing-Nan Lin, Chao Yang, Qi Liu, Sai-Lan Liang, Yu-Jing Jia, Guo-Dong Wen, Dong-Xiang Guo, Chun-Yan Yan, Jin-Jie Zhao, Chong Chen, Qiu-Yan Tang, Lin-Quan Mai, Hai-Qiang |
description | Cumulative doses of 200 mg/m
for concurrent cisplatin (DDP) were indicated by retrospective studies as sufficient in conferring survival benefit for locoregionally advanced nasopharyngeal carcinoma (LA-NPC). We performed an open-label, phase II, randomized, controlled trial to test the noninferiority of a two-cycle 100 mg/m
concurrent DDP regimen over three-cycle in patients with low-risk LA-NPC with pretreatment Epstein-Barr virus DNA levels < 4,000 copies/mL.
Eligible patients were randomly assigned 1:1 to receive two cycles or three cycles concurrent DDP-based chemoradiotherapy. The primary end point was 3-year progression-free survival (PFS). The secondary end points included overall survival, distant metastasis-free survival, locoregional relapse-free survival, etc.
Between September 2016 and October 2018, 332 patients were enrolled, with 166 in each arm. After a median follow-up of 37.7 months, the estimated 3-year PFS rates were 88.0% in the two-cycle group and 90.4% in the three-cycle group, with a difference of 2.4% (95% CI, -4.3 to 9.1,
= .014). No differences were observed between groups in terms of PFS, overall survival, and the cumulative incidences of locoregional relapse and distant metastasis. Patients in the three-cycle group developed significantly more grade 3-4 mucositis (41 [24.8%]
25 [15.1%]), hyponatremia (26 [15.8%]
14 [8.4%]), and dermatitis (9 [5.5%]
2 [1.2%]). The overall all-grade and grade 3-4 toxicity burdens were heavier in three-cycle group (T-scores, 12.33
10.57,
< .001 for all grades; 1.76
1.44,
= .05 for grade 3-4). Patients in the three-cycle group also showed more all-grade hearing impairment, dry mouth and skin fibrosis, and impaired long-term quality of life.
Intensity-modulated radiotherapy plus two cycles of concurrent 100 mg/m
DDP could be an alternative treatment option for patients with low-risk LA-NPC. |
doi_str_mv | 10.1200/JCO.21.01467 |
format | Article |
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for concurrent cisplatin (DDP) were indicated by retrospective studies as sufficient in conferring survival benefit for locoregionally advanced nasopharyngeal carcinoma (LA-NPC). We performed an open-label, phase II, randomized, controlled trial to test the noninferiority of a two-cycle 100 mg/m
concurrent DDP regimen over three-cycle in patients with low-risk LA-NPC with pretreatment Epstein-Barr virus DNA levels < 4,000 copies/mL.
Eligible patients were randomly assigned 1:1 to receive two cycles or three cycles concurrent DDP-based chemoradiotherapy. The primary end point was 3-year progression-free survival (PFS). The secondary end points included overall survival, distant metastasis-free survival, locoregional relapse-free survival, etc.
Between September 2016 and October 2018, 332 patients were enrolled, with 166 in each arm. After a median follow-up of 37.7 months, the estimated 3-year PFS rates were 88.0% in the two-cycle group and 90.4% in the three-cycle group, with a difference of 2.4% (95% CI, -4.3 to 9.1,
= .014). No differences were observed between groups in terms of PFS, overall survival, and the cumulative incidences of locoregional relapse and distant metastasis. Patients in the three-cycle group developed significantly more grade 3-4 mucositis (41 [24.8%]
25 [15.1%]), hyponatremia (26 [15.8%]
14 [8.4%]), and dermatitis (9 [5.5%]
2 [1.2%]). The overall all-grade and grade 3-4 toxicity burdens were heavier in three-cycle group (T-scores, 12.33
10.57,
< .001 for all grades; 1.76
1.44,
= .05 for grade 3-4). Patients in the three-cycle group also showed more all-grade hearing impairment, dry mouth and skin fibrosis, and impaired long-term quality of life.
Intensity-modulated radiotherapy plus two cycles of concurrent 100 mg/m
DDP could be an alternative treatment option for patients with low-risk LA-NPC.</description><identifier>ISSN: 0732-183X</identifier><identifier>EISSN: 1527-7755</identifier><identifier>DOI: 10.1200/JCO.21.01467</identifier><identifier>PMID: 34990291</identifier><language>eng</language><publisher>United States</publisher><subject>Antineoplastic Combined Chemotherapy Protocols - adverse effects ; Chemoradiotherapy - adverse effects ; Cisplatin ; DNA - therapeutic use ; Epstein-Barr Virus Infections ; Herpesvirus 4, Human - genetics ; Humans ; Nasopharyngeal Carcinoma - drug therapy ; Nasopharyngeal Neoplasms - pathology ; Neoplasm Recurrence, Local - drug therapy ; Quality of Life ; Retrospective Studies</subject><ispartof>Journal of clinical oncology, 2022-04, Vol.40 (11), p.1163-1173</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c206t-b4d289c27bfa1ca1a746c1aa60cd13e0e7597db3ed92724ee04aba30d2403fb33</citedby><cites>FETCH-LOGICAL-c206t-b4d289c27bfa1ca1a746c1aa60cd13e0e7597db3ed92724ee04aba30d2403fb33</cites><orcidid>0000-0002-9613-7305 ; 0000-0003-3271-5783 ; 0000-0003-0214-203X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,3727,27922,27923</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34990291$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Xiao-Yun</creatorcontrib><creatorcontrib>Luo, Dong-Hua</creatorcontrib><creatorcontrib>Guo, Ling</creatorcontrib><creatorcontrib>Mo, Hao-Yuan</creatorcontrib><creatorcontrib>Sun, Rui</creatorcontrib><creatorcontrib>Guo, Shan-Shan</creatorcontrib><creatorcontrib>Liu, Li-Ting</creatorcontrib><creatorcontrib>Yang, Zhen-Chong</creatorcontrib><creatorcontrib>Yang, Jin-Hao</creatorcontrib><creatorcontrib>Qiu, Fang</creatorcontrib><creatorcontrib>Sun, Xue-Song</creatorcontrib><creatorcontrib>Wang, Pan</creatorcontrib><creatorcontrib>Liu, Qing</creatorcontrib><creatorcontrib>Li, Ji-Bin</creatorcontrib><creatorcontrib>Tang, Qing-Nan</creatorcontrib><creatorcontrib>Lin, Chao</creatorcontrib><creatorcontrib>Yang, Qi</creatorcontrib><creatorcontrib>Liu, Sai-Lan</creatorcontrib><creatorcontrib>Liang, Yu-Jing</creatorcontrib><creatorcontrib>Jia, Guo-Dong</creatorcontrib><creatorcontrib>Wen, Dong-Xiang</creatorcontrib><creatorcontrib>Guo, Chun-Yan</creatorcontrib><creatorcontrib>Yan, Jin-Jie</creatorcontrib><creatorcontrib>Zhao, Chong</creatorcontrib><creatorcontrib>Chen, Qiu-Yan</creatorcontrib><creatorcontrib>Tang, Lin-Quan</creatorcontrib><creatorcontrib>Mai, Hai-Qiang</creatorcontrib><title>Deintensified Chemoradiotherapy for Pretreatment Epstein-Barr Virus DNA-Selected Low-Risk Locoregionally Advanced Nasopharyngeal Carcinoma: A Phase II Randomized Noninferiority Trial</title><title>Journal of clinical oncology</title><addtitle>J Clin Oncol</addtitle><description>Cumulative doses of 200 mg/m
for concurrent cisplatin (DDP) were indicated by retrospective studies as sufficient in conferring survival benefit for locoregionally advanced nasopharyngeal carcinoma (LA-NPC). We performed an open-label, phase II, randomized, controlled trial to test the noninferiority of a two-cycle 100 mg/m
concurrent DDP regimen over three-cycle in patients with low-risk LA-NPC with pretreatment Epstein-Barr virus DNA levels < 4,000 copies/mL.
Eligible patients were randomly assigned 1:1 to receive two cycles or three cycles concurrent DDP-based chemoradiotherapy. The primary end point was 3-year progression-free survival (PFS). The secondary end points included overall survival, distant metastasis-free survival, locoregional relapse-free survival, etc.
Between September 2016 and October 2018, 332 patients were enrolled, with 166 in each arm. After a median follow-up of 37.7 months, the estimated 3-year PFS rates were 88.0% in the two-cycle group and 90.4% in the three-cycle group, with a difference of 2.4% (95% CI, -4.3 to 9.1,
= .014). No differences were observed between groups in terms of PFS, overall survival, and the cumulative incidences of locoregional relapse and distant metastasis. Patients in the three-cycle group developed significantly more grade 3-4 mucositis (41 [24.8%]
25 [15.1%]), hyponatremia (26 [15.8%]
14 [8.4%]), and dermatitis (9 [5.5%]
2 [1.2%]). The overall all-grade and grade 3-4 toxicity burdens were heavier in three-cycle group (T-scores, 12.33
10.57,
< .001 for all grades; 1.76
1.44,
= .05 for grade 3-4). Patients in the three-cycle group also showed more all-grade hearing impairment, dry mouth and skin fibrosis, and impaired long-term quality of life.
Intensity-modulated radiotherapy plus two cycles of concurrent 100 mg/m
DDP could be an alternative treatment option for patients with low-risk LA-NPC.</description><subject>Antineoplastic Combined Chemotherapy Protocols - adverse effects</subject><subject>Chemoradiotherapy - adverse effects</subject><subject>Cisplatin</subject><subject>DNA - therapeutic use</subject><subject>Epstein-Barr Virus Infections</subject><subject>Herpesvirus 4, Human - genetics</subject><subject>Humans</subject><subject>Nasopharyngeal Carcinoma - drug therapy</subject><subject>Nasopharyngeal Neoplasms - pathology</subject><subject>Neoplasm Recurrence, Local - drug therapy</subject><subject>Quality of Life</subject><subject>Retrospective Studies</subject><issn>0732-183X</issn><issn>1527-7755</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kU1v1DAQQC0Eokvhxhn5yIEs_kjihNs2bWHRqq1KQdyiiT3pGhI72F6q5Yfx-8jSwmnm8OZJo0fIS86WXDD29mNzuRR8yXheqkdkwQuhMqWK4jFZMCVFxiv59Yg8i_Ebm5lKFk_JkczrmomaL8jvU7QuoYu2t2hos8XRBzDWpy0GmPa094FeBUwBIY3oEj2bYppvshMIgX6xYRfp6cUq-4QD6jQrNv4uu7bx-7xoH_DWegfDsKcr8xOcnoELiH7aQti7W4SBNhC0dX6Ed3RFr7YQka7X9Bqc8aP9deC9s67HYH2waU9vgoXhOXnSwxDxxcM8Jp_Pz26aD9nm8v26WW0yLViZsi43oqq1UF0PXAMHlZeaA5RMGy6RoSpqZTqJphZK5Igshw4kMyJnsu-kPCav771T8D92GFM72qhxGMCh38VWlLwSoir4AX1zj-rgYwzYt1Ow4_xmy1l7KNXOpVrB27-lZvzVg3nXjWj-w__SyD-pzZKI</recordid><startdate>20220410</startdate><enddate>20220410</enddate><creator>Li, Xiao-Yun</creator><creator>Luo, Dong-Hua</creator><creator>Guo, Ling</creator><creator>Mo, Hao-Yuan</creator><creator>Sun, Rui</creator><creator>Guo, Shan-Shan</creator><creator>Liu, Li-Ting</creator><creator>Yang, Zhen-Chong</creator><creator>Yang, Jin-Hao</creator><creator>Qiu, Fang</creator><creator>Sun, Xue-Song</creator><creator>Wang, Pan</creator><creator>Liu, Qing</creator><creator>Li, Ji-Bin</creator><creator>Tang, Qing-Nan</creator><creator>Lin, Chao</creator><creator>Yang, Qi</creator><creator>Liu, Sai-Lan</creator><creator>Liang, Yu-Jing</creator><creator>Jia, Guo-Dong</creator><creator>Wen, Dong-Xiang</creator><creator>Guo, Chun-Yan</creator><creator>Yan, Jin-Jie</creator><creator>Zhao, Chong</creator><creator>Chen, Qiu-Yan</creator><creator>Tang, Lin-Quan</creator><creator>Mai, Hai-Qiang</creator><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><orcidid>https://orcid.org/0000-0002-9613-7305</orcidid><orcidid>https://orcid.org/0000-0003-3271-5783</orcidid><orcidid>https://orcid.org/0000-0003-0214-203X</orcidid></search><sort><creationdate>20220410</creationdate><title>Deintensified Chemoradiotherapy for Pretreatment Epstein-Barr Virus DNA-Selected Low-Risk Locoregionally Advanced Nasopharyngeal Carcinoma: A Phase II Randomized Noninferiority Trial</title><author>Li, Xiao-Yun ; Luo, Dong-Hua ; Guo, Ling ; Mo, Hao-Yuan ; Sun, Rui ; Guo, Shan-Shan ; Liu, Li-Ting ; Yang, Zhen-Chong ; Yang, Jin-Hao ; Qiu, Fang ; Sun, Xue-Song ; Wang, Pan ; Liu, Qing ; Li, Ji-Bin ; Tang, Qing-Nan ; Lin, Chao ; Yang, Qi ; Liu, Sai-Lan ; Liang, Yu-Jing ; Jia, Guo-Dong ; Wen, Dong-Xiang ; Guo, Chun-Yan ; Yan, Jin-Jie ; Zhao, Chong ; Chen, Qiu-Yan ; Tang, Lin-Quan ; Mai, Hai-Qiang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c206t-b4d289c27bfa1ca1a746c1aa60cd13e0e7597db3ed92724ee04aba30d2403fb33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Antineoplastic Combined Chemotherapy Protocols - adverse effects</topic><topic>Chemoradiotherapy - adverse effects</topic><topic>Cisplatin</topic><topic>DNA - therapeutic use</topic><topic>Epstein-Barr Virus Infections</topic><topic>Herpesvirus 4, Human - genetics</topic><topic>Humans</topic><topic>Nasopharyngeal Carcinoma - drug therapy</topic><topic>Nasopharyngeal Neoplasms - pathology</topic><topic>Neoplasm Recurrence, Local - drug therapy</topic><topic>Quality of Life</topic><topic>Retrospective Studies</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Xiao-Yun</creatorcontrib><creatorcontrib>Luo, Dong-Hua</creatorcontrib><creatorcontrib>Guo, Ling</creatorcontrib><creatorcontrib>Mo, Hao-Yuan</creatorcontrib><creatorcontrib>Sun, Rui</creatorcontrib><creatorcontrib>Guo, Shan-Shan</creatorcontrib><creatorcontrib>Liu, Li-Ting</creatorcontrib><creatorcontrib>Yang, Zhen-Chong</creatorcontrib><creatorcontrib>Yang, Jin-Hao</creatorcontrib><creatorcontrib>Qiu, Fang</creatorcontrib><creatorcontrib>Sun, Xue-Song</creatorcontrib><creatorcontrib>Wang, Pan</creatorcontrib><creatorcontrib>Liu, Qing</creatorcontrib><creatorcontrib>Li, Ji-Bin</creatorcontrib><creatorcontrib>Tang, Qing-Nan</creatorcontrib><creatorcontrib>Lin, Chao</creatorcontrib><creatorcontrib>Yang, Qi</creatorcontrib><creatorcontrib>Liu, Sai-Lan</creatorcontrib><creatorcontrib>Liang, Yu-Jing</creatorcontrib><creatorcontrib>Jia, Guo-Dong</creatorcontrib><creatorcontrib>Wen, Dong-Xiang</creatorcontrib><creatorcontrib>Guo, Chun-Yan</creatorcontrib><creatorcontrib>Yan, Jin-Jie</creatorcontrib><creatorcontrib>Zhao, Chong</creatorcontrib><creatorcontrib>Chen, Qiu-Yan</creatorcontrib><creatorcontrib>Tang, Lin-Quan</creatorcontrib><creatorcontrib>Mai, Hai-Qiang</creatorcontrib><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><jtitle>Journal of clinical oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Xiao-Yun</au><au>Luo, Dong-Hua</au><au>Guo, Ling</au><au>Mo, Hao-Yuan</au><au>Sun, Rui</au><au>Guo, Shan-Shan</au><au>Liu, Li-Ting</au><au>Yang, Zhen-Chong</au><au>Yang, Jin-Hao</au><au>Qiu, Fang</au><au>Sun, Xue-Song</au><au>Wang, Pan</au><au>Liu, Qing</au><au>Li, Ji-Bin</au><au>Tang, Qing-Nan</au><au>Lin, Chao</au><au>Yang, Qi</au><au>Liu, Sai-Lan</au><au>Liang, Yu-Jing</au><au>Jia, Guo-Dong</au><au>Wen, Dong-Xiang</au><au>Guo, Chun-Yan</au><au>Yan, Jin-Jie</au><au>Zhao, Chong</au><au>Chen, Qiu-Yan</au><au>Tang, Lin-Quan</au><au>Mai, Hai-Qiang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Deintensified Chemoradiotherapy for Pretreatment Epstein-Barr Virus DNA-Selected Low-Risk Locoregionally Advanced Nasopharyngeal Carcinoma: A Phase II Randomized Noninferiority Trial</atitle><jtitle>Journal of clinical oncology</jtitle><addtitle>J Clin Oncol</addtitle><date>2022-04-10</date><risdate>2022</risdate><volume>40</volume><issue>11</issue><spage>1163</spage><epage>1173</epage><pages>1163-1173</pages><issn>0732-183X</issn><eissn>1527-7755</eissn><abstract>Cumulative doses of 200 mg/m
for concurrent cisplatin (DDP) were indicated by retrospective studies as sufficient in conferring survival benefit for locoregionally advanced nasopharyngeal carcinoma (LA-NPC). We performed an open-label, phase II, randomized, controlled trial to test the noninferiority of a two-cycle 100 mg/m
concurrent DDP regimen over three-cycle in patients with low-risk LA-NPC with pretreatment Epstein-Barr virus DNA levels < 4,000 copies/mL.
Eligible patients were randomly assigned 1:1 to receive two cycles or three cycles concurrent DDP-based chemoradiotherapy. The primary end point was 3-year progression-free survival (PFS). The secondary end points included overall survival, distant metastasis-free survival, locoregional relapse-free survival, etc.
Between September 2016 and October 2018, 332 patients were enrolled, with 166 in each arm. After a median follow-up of 37.7 months, the estimated 3-year PFS rates were 88.0% in the two-cycle group and 90.4% in the three-cycle group, with a difference of 2.4% (95% CI, -4.3 to 9.1,
= .014). No differences were observed between groups in terms of PFS, overall survival, and the cumulative incidences of locoregional relapse and distant metastasis. Patients in the three-cycle group developed significantly more grade 3-4 mucositis (41 [24.8%]
25 [15.1%]), hyponatremia (26 [15.8%]
14 [8.4%]), and dermatitis (9 [5.5%]
2 [1.2%]). The overall all-grade and grade 3-4 toxicity burdens were heavier in three-cycle group (T-scores, 12.33
10.57,
< .001 for all grades; 1.76
1.44,
= .05 for grade 3-4). Patients in the three-cycle group also showed more all-grade hearing impairment, dry mouth and skin fibrosis, and impaired long-term quality of life.
Intensity-modulated radiotherapy plus two cycles of concurrent 100 mg/m
DDP could be an alternative treatment option for patients with low-risk LA-NPC.</abstract><cop>United States</cop><pmid>34990291</pmid><doi>10.1200/JCO.21.01467</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0002-9613-7305</orcidid><orcidid>https://orcid.org/0000-0003-3271-5783</orcidid><orcidid>https://orcid.org/0000-0003-0214-203X</orcidid></addata></record> |
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language | eng |
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source | MEDLINE; American Society of Clinical Oncology Online Journals; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection |
subjects | Antineoplastic Combined Chemotherapy Protocols - adverse effects Chemoradiotherapy - adverse effects Cisplatin DNA - therapeutic use Epstein-Barr Virus Infections Herpesvirus 4, Human - genetics Humans Nasopharyngeal Carcinoma - drug therapy Nasopharyngeal Neoplasms - pathology Neoplasm Recurrence, Local - drug therapy Quality of Life Retrospective Studies |
title | Deintensified Chemoradiotherapy for Pretreatment Epstein-Barr Virus DNA-Selected Low-Risk Locoregionally Advanced Nasopharyngeal Carcinoma: A Phase II Randomized Noninferiority Trial |
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