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Icotinib With Concurrent Radiotherapy vs Radiotherapy Alone in Older Adults With Unresectable Esophageal Squamous Cell Carcinoma: A Phase II Randomized Clinical Trial
IMPORTANCE: Palliative radiotherapy (RT) is generally recommended for older patients with esophageal squamous cell carcinoma (ESCC) with poor prognosis. A new combination treatment is therefore needed. OBJECTIVE: To assess the efficacy and toxicity of RT plus icotinib vs RT alone in older patients w...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Medical Association
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7542309/ https://www.ncbi.nlm.nih.gov/pubmed/33026449 http://dx.doi.org/10.1001/jamanetworkopen.2020.19440 |
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author | Luo, Honglei Jiang, Wei Ma, Li Chen, Peng Fang, Min Ding, Lingyu Hua, Yuhui Du, Dexi Jing, Zhao Xie, Ruifei Song, Yaqi Wang, Jiayang Zhou, Rongjing Tian, Zhifeng Wu, Shixiu |
author_facet | Luo, Honglei Jiang, Wei Ma, Li Chen, Peng Fang, Min Ding, Lingyu Hua, Yuhui Du, Dexi Jing, Zhao Xie, Ruifei Song, Yaqi Wang, Jiayang Zhou, Rongjing Tian, Zhifeng Wu, Shixiu |
author_sort | Luo, Honglei |
collection | PubMed |
description | IMPORTANCE: Palliative radiotherapy (RT) is generally recommended for older patients with esophageal squamous cell carcinoma (ESCC) with poor prognosis. A new combination treatment is therefore needed. OBJECTIVE: To assess the efficacy and toxicity of RT plus icotinib vs RT alone in older patients with ESCC. DESIGN, SETTING, AND PARTICIPANTS: This randomized, multicenter, open-label, phase II clinical trial was conducted in China, with enrollment between January 1, 2015, and October 31, 2016. Patients aged 70 years or older with clinical stage T2 to T4, N0/1, M0/1a unresectable (because of comorbidities, T4 disease, unresectable lymph node, or refused surgery) ESCC were randomized 1:1 to receive RT plus icotinib or RT alone. Radiation was prescribed at 60 Gy in 30 fractions in both groups, and icotinib was administered at a dosage of 125 mg 3 times a day in the RT plus icotinib group. The last follow-up was completed on June 30, 2019, and data were analyzed from July 1 to September 30, 2019. INTERVENTIONS: Patients were randomized to either RT plus icotinib or RT alone. MAIN OUTCOMES AND MEASURES: The primary end point was overall survival (OS). Treatment-related toxic effects were evaluated. Immunohistochemistry was performed to analyze epidermal growth factor receptor (EGFR) expression if available. RESULTS: A total of 127 patients (median age, 76 years [range, 70-91 years]; 76 men [59.8%]) were enrolled and were eligible for survival analysis. Median OS was 24.0 (95% CI, 22.2-25.8) months in the RT plus icotinib group vs 16.3 (95% CI, 13.8-18.8) months in the RT group (hazard ratio, 0.53; 95% CI, 0.33-0.87; P = .008). No difference was observed in grades 3 or 4 adverse events. Patients with EGFR overexpression had a significantly better median overall survival (not reached vs 16.3 months [range, 2.6-45.1 months]; P = .03) in the RT plus icotinib group. CONCLUSIONS AND RELEVANCE: In this randomized clinical trial, icotinib plus RT was well tolerated and improved OS in older patients with ESCC relative to RT alone. Patients with EGFR overexpression benefitted more from icotinib with RT. TRIAL REGISTRATION: ClinicalTrials.gov Identifier: NCT02375581 |
format | Online Article Text |
id | pubmed-7542309 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Medical Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-75423092020-10-19 Icotinib With Concurrent Radiotherapy vs Radiotherapy Alone in Older Adults With Unresectable Esophageal Squamous Cell Carcinoma: A Phase II Randomized Clinical Trial Luo, Honglei Jiang, Wei Ma, Li Chen, Peng Fang, Min Ding, Lingyu Hua, Yuhui Du, Dexi Jing, Zhao Xie, Ruifei Song, Yaqi Wang, Jiayang Zhou, Rongjing Tian, Zhifeng Wu, Shixiu JAMA Netw Open Original Investigation IMPORTANCE: Palliative radiotherapy (RT) is generally recommended for older patients with esophageal squamous cell carcinoma (ESCC) with poor prognosis. A new combination treatment is therefore needed. OBJECTIVE: To assess the efficacy and toxicity of RT plus icotinib vs RT alone in older patients with ESCC. DESIGN, SETTING, AND PARTICIPANTS: This randomized, multicenter, open-label, phase II clinical trial was conducted in China, with enrollment between January 1, 2015, and October 31, 2016. Patients aged 70 years or older with clinical stage T2 to T4, N0/1, M0/1a unresectable (because of comorbidities, T4 disease, unresectable lymph node, or refused surgery) ESCC were randomized 1:1 to receive RT plus icotinib or RT alone. Radiation was prescribed at 60 Gy in 30 fractions in both groups, and icotinib was administered at a dosage of 125 mg 3 times a day in the RT plus icotinib group. The last follow-up was completed on June 30, 2019, and data were analyzed from July 1 to September 30, 2019. INTERVENTIONS: Patients were randomized to either RT plus icotinib or RT alone. MAIN OUTCOMES AND MEASURES: The primary end point was overall survival (OS). Treatment-related toxic effects were evaluated. Immunohistochemistry was performed to analyze epidermal growth factor receptor (EGFR) expression if available. RESULTS: A total of 127 patients (median age, 76 years [range, 70-91 years]; 76 men [59.8%]) were enrolled and were eligible for survival analysis. Median OS was 24.0 (95% CI, 22.2-25.8) months in the RT plus icotinib group vs 16.3 (95% CI, 13.8-18.8) months in the RT group (hazard ratio, 0.53; 95% CI, 0.33-0.87; P = .008). No difference was observed in grades 3 or 4 adverse events. Patients with EGFR overexpression had a significantly better median overall survival (not reached vs 16.3 months [range, 2.6-45.1 months]; P = .03) in the RT plus icotinib group. CONCLUSIONS AND RELEVANCE: In this randomized clinical trial, icotinib plus RT was well tolerated and improved OS in older patients with ESCC relative to RT alone. Patients with EGFR overexpression benefitted more from icotinib with RT. TRIAL REGISTRATION: ClinicalTrials.gov Identifier: NCT02375581 American Medical Association 2020-10-07 /pmc/articles/PMC7542309/ /pubmed/33026449 http://dx.doi.org/10.1001/jamanetworkopen.2020.19440 Text en Copyright 2020 Luo H et al. JAMA Network Open. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the CC-BY License. |
spellingShingle | Original Investigation Luo, Honglei Jiang, Wei Ma, Li Chen, Peng Fang, Min Ding, Lingyu Hua, Yuhui Du, Dexi Jing, Zhao Xie, Ruifei Song, Yaqi Wang, Jiayang Zhou, Rongjing Tian, Zhifeng Wu, Shixiu Icotinib With Concurrent Radiotherapy vs Radiotherapy Alone in Older Adults With Unresectable Esophageal Squamous Cell Carcinoma: A Phase II Randomized Clinical Trial |
title | Icotinib With Concurrent Radiotherapy vs Radiotherapy Alone in Older Adults With Unresectable Esophageal Squamous Cell Carcinoma: A Phase II Randomized Clinical Trial |
title_full | Icotinib With Concurrent Radiotherapy vs Radiotherapy Alone in Older Adults With Unresectable Esophageal Squamous Cell Carcinoma: A Phase II Randomized Clinical Trial |
title_fullStr | Icotinib With Concurrent Radiotherapy vs Radiotherapy Alone in Older Adults With Unresectable Esophageal Squamous Cell Carcinoma: A Phase II Randomized Clinical Trial |
title_full_unstemmed | Icotinib With Concurrent Radiotherapy vs Radiotherapy Alone in Older Adults With Unresectable Esophageal Squamous Cell Carcinoma: A Phase II Randomized Clinical Trial |
title_short | Icotinib With Concurrent Radiotherapy vs Radiotherapy Alone in Older Adults With Unresectable Esophageal Squamous Cell Carcinoma: A Phase II Randomized Clinical Trial |
title_sort | icotinib with concurrent radiotherapy vs radiotherapy alone in older adults with unresectable esophageal squamous cell carcinoma: a phase ii randomized clinical trial |
topic | Original Investigation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7542309/ https://www.ncbi.nlm.nih.gov/pubmed/33026449 http://dx.doi.org/10.1001/jamanetworkopen.2020.19440 |
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