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C
Christopher M. Nutting *
C
Clare Griffin
P
Paul Sanghera
B
Bernadette Foran
M
Matthew Beasley
D
David Bernstein
C
Catherine West
A
Amen Sibtain
T
Teresa Guerrero Urbano
M
Mohammed Rizwanullah
K
Katie Wood
S
S. Ramkumar
E
Elizabeth Junor
A
Audrey Cook
T
Tom Roques
C
Christopher Scrase
S
Shreerang Bhide
D
Dorothy M. Gujral
K
Kevin J. Harrington
H
Hisham Mehanna
A
Aisha Miah
M
Marie A. Emson
D
Deborah Gardiner
J
James P. Morden
E
Emma Hall
DOI:10.1016/j.ejca.2021.05.021delete
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摘要

摘要

En 中文
Background: Radical (chemo)radiotherapy offers potentially curative treatment for patients with locally advanced laryngeal or hypopharyngeal cancer. We aimed to show that dose-escalated intensity-modulated radiotherapy (DE-IMRT) improved locoregional control. Methods: We performed a phase III open-label randomised controlled trial in patients with laryngeal or hypopharyngeal cancer (AJCC III-IVa/b, TNM 7). Patients were randomised (1:1) to DE-IMRT or standard dose IMRT (ST-IMRT) using a minimisation algorithm, balancing for centre, tumour site, nodal status and chemotherapy use. DE-IMRT was 67.2 gray (Gy) in 28 fractions (f) to the primary tumour and 56Gy/28f to at-risk nodes; STIMRT was 65Gy/30f to primary tumour and 54Gy/30f to at-risk nodes. Suitable patients received 2 cycles of concomitant cisplatin and up to 3 cycles of platinum-based induction chemotherapy. The primary end-point was time to locoregional failure analysed by intention-to-treat analysis using competing risk methodology. Findings: Between February 2011 and October 2015, 276 patients (138 ST-IMRT; 138 DEIMRT) were randomised. A preplanned interim futility analysis met the criterion for early closure. After a median follow-up of 47.9 months (interquartile range 37.5-60.5), there were locoregional failures in 38 of 138 (27.5%) ST-IMRT patients and 42 of 138 (30.4%) DE-IMRT patients; an adjusted subhazard ratio of 1.16 (95% confidence interval: 0.74-1.83, p Z 0.519) indicated no evidence of benefit with DE-IMRT. Acute grade 2 pharyngeal mucositis was reported more frequently with DE-IMRT than with ST-IMRT (42% vs. 32%). No differences in grade >3 acute or late toxicity rates were seen. Conclusion: DE-IMRT did not improve locoregional control in patients with laryngeal or hypopharyngeal cancer. The trial is registered: ISRCTN01483375. 2021 Published by Elsevier Ltd.
Keyword:
Head and neck cancer
IMRT
Dose escalation
Clinical outcomes
Toxicity
Phase III
Randomised controlled trial
Larynx cancer
Hypopharynx cancer
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European Journal of Cancer 封面图
European Journal of Cancer
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7.1
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2.6W
被引数:
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Velindre Cancer Centre
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weston park hospital
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institute of cancer research - uk
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University of Manchester
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