Study protocol: a multicentre, prospective, phase II trial of isotoxic hypofractionated concurrent chemoradiotherapy for non-small cell lung cancer
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作者:
Liu, Yue-E
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Hebei Med Univ, North China Petr Bur Gen Hosp, Dept Oncol, Renqiu, Hebei, Peoples R ChinaHebei Med Univ, North China Petr Bur Gen Hosp, Dept Oncol, Renqiu, Hebei, Peoples R China
Liu, Yue-E
[1
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Xue, Xiao-Ying
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Hebei Med Univ, Hosp 2, Dept Radiotherapy, Shijiazhuang, Hebei, Peoples R ChinaHebei Med Univ, North China Petr Bur Gen Hosp, Dept Oncol, Renqiu, Hebei, Peoples R China
Xue, Xiao-Ying
[2
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Zhang, Rui
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Hebei Med Univ, North China Petr Bur Gen Hosp, Dept Oncol, Renqiu, Hebei, Peoples R ChinaHebei Med Univ, North China Petr Bur Gen Hosp, Dept Oncol, Renqiu, Hebei, Peoples R China
Zhang, Rui
[1
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Chen, Xue-Ji
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Hebei Med Univ, North China Petr Bur Gen Hosp, Dept Oncol, Renqiu, Hebei, Peoples R ChinaHebei Med Univ, North China Petr Bur Gen Hosp, Dept Oncol, Renqiu, Hebei, Peoples R China
Chen, Xue-Ji
[1
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Ding, Yu-Xia
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Hebei Med Univ, North China Petr Bur Gen Hosp, Dept Oncol, Renqiu, Hebei, Peoples R ChinaHebei Med Univ, North China Petr Bur Gen Hosp, Dept Oncol, Renqiu, Hebei, Peoples R China
Ding, Yu-Xia
[1
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Liu, Chao-Xing
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1 Hosp Shijiazhuang City, Dept Oncol, Shijiazhuang, Hebei, Peoples R ChinaHebei Med Univ, North China Petr Bur Gen Hosp, Dept Oncol, Renqiu, Hebei, Peoples R China
Liu, Chao-Xing
[3
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Qin, Yue-Liang
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Hebei Med Univ, North China Petr Bur Gen Hosp, Dept Oncol, Renqiu, Hebei, Peoples R ChinaHebei Med Univ, North China Petr Bur Gen Hosp, Dept Oncol, Renqiu, Hebei, Peoples R China
Qin, Yue-Liang
[1
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Li, Wei-Qian
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Hebei Med Univ, North China Petr Bur Gen Hosp, Dept Oncol, Renqiu, Hebei, Peoples R ChinaHebei Med Univ, North China Petr Bur Gen Hosp, Dept Oncol, Renqiu, Hebei, Peoples R China
Li, Wei-Qian
[1
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Ren, Xiao-Cang
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Hebei Med Univ, North China Petr Bur Gen Hosp, Dept Oncol, Renqiu, Hebei, Peoples R ChinaHebei Med Univ, North China Petr Bur Gen Hosp, Dept Oncol, Renqiu, Hebei, Peoples R China
Ren, Xiao-Cang
[1
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Lin, Qiang
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Hebei Med Univ, North China Petr Bur Gen Hosp, Dept Oncol, Renqiu, Hebei, Peoples R China
Hebei Med Univ, Shijiazhuang, Hebei, Peoples R ChinaHebei Med Univ, North China Petr Bur Gen Hosp, Dept Oncol, Renqiu, Hebei, Peoples R China
Lin, Qiang
[1
,4
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机构:
[1] Hebei Med Univ, North China Petr Bur Gen Hosp, Dept Oncol, Renqiu, Hebei, Peoples R China
[2] Hebei Med Univ, Hosp 2, Dept Radiotherapy, Shijiazhuang, Hebei, Peoples R China
[3] 1 Hosp Shijiazhuang City, Dept Oncol, Shijiazhuang, Hebei, Peoples R China
[4] Hebei Med Univ, Shijiazhuang, Hebei, Peoples R China
Introduction Concurrent chemoradiotherapy with conventional fractionation has been acknowledged as one of the standard treatments for locally advanced non-small cell lung cancer (NSCLC). The radiotherapy dose of 60 Gy is far from enough for local tumour control. Due to this fact, hypofractionated radiotherapy can shorten the total treatment duration, partially counteract the accelerated repopulation of tumour cells and deliver a higher biological effective dose, it has been increasingly used for NSCLC. In theory, concurrent hypofractionated chemoradiotherapy can result in an enhanced curative effect. To date, the vast majority of radiotherapy prescriptions assign a uniform radiotherapy dose to all patients. However this kind of uniform radiotherapy prescription may lead to two consequences: excess damage to normal tissues for large tumours and insufficient dose for small tumours. Our study aims to evaluate whether delivering individualised radiotherapy dose is feasible using intensity-modulated radiotherapy. Methods and analysis Our study of individualised radiotherapy is a multicenter phase II trial. From April 2019, a total of 30 patients from three Chinese centres, with a proven histological or cytological diagnosis of inoperable NSCLC, will be recruited. The dose of radiation will be increased until one or more of the organs at risk tolerance or the maximum dose of 69 Gy is reached. The primary end point is feasibility, with response rates, progression-free survival and overall survival as secondary end points. The concurrent chemotherapy regimen will be docetaxel plus lobaplatin. Ethics and dissemination The study has been approved by medical ethics committees from three research centres. The trial is conducted in accordance with the Declaration of Helsinki. The trial results will be disseminated through academic conference presentations and peer-reviewed publications.
机构:
Krankenhaus Martha Maria Halle Doelau, Klin Innere Med 2, Halle, GermanyKrankenhaus Martha Maria Halle Doelau, Klin Innere Med 2, Halle, Germany
Schuette, Wolfgang
Krzakowski, Maciej J.
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Maria Sklodowska Curie Inst Oncol, Warsaw, PolandKrankenhaus Martha Maria Halle Doelau, Klin Innere Med 2, Halle, Germany
Krzakowski, Maciej J.
Massuti, Bartomeu
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Hosp Gen Alicante, Med Oncol Serv, Alicante, SpainKrankenhaus Martha Maria Halle Doelau, Klin Innere Med 2, Halle, Germany
Massuti, Bartomeu
Otterson, Gregory A.
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Ohio State Univ, Columbus, OH 43210 USAKrankenhaus Martha Maria Halle Doelau, Klin Innere Med 2, Halle, Germany
Otterson, Gregory A.
Lizambri, Richard
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Amgen Inc, Thousand Oaks, CA 91320 USAKrankenhaus Martha Maria Halle Doelau, Klin Innere Med 2, Halle, Germany
Lizambri, Richard
Wei, Helen
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Amgen Inc, Thousand Oaks, CA 91320 USAKrankenhaus Martha Maria Halle Doelau, Klin Innere Med 2, Halle, Germany
Wei, Helen
Berger, Dietmar P.
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Amgen Inc, Thousand Oaks, CA 91320 USAKrankenhaus Martha Maria Halle Doelau, Klin Innere Med 2, Halle, Germany
Berger, Dietmar P.
Chen, Yuhchyau
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机构:
Univ Rochester, James P Wilmot Canc Ctr, Dept Radiat Oncol, Rochester, NY USAKrankenhaus Martha Maria Halle Doelau, Klin Innere Med 2, Halle, Germany