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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Veröffentlicht in:Journal of clinical oncology 2022-04, Vol.40 (11), p.1163-1173
Hauptverfasser: 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
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container_end_page 1173
container_issue 11
container_start_page 1163
container_title Journal of clinical oncology
container_volume 40
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
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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 &lt; 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, &lt; .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. 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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, &lt; .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. 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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 &lt; 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). 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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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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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