Randomized phase 3 noninferiority trial of radiotherapy and cisplatin vs radiotherapy and cetuximab after docetaxel-cisplatin-fluorouracil induction chemotherapy in patients with locally advanced unresectable head and neck cancer

医学 西妥昔单抗 多西紫杉醇 氟尿嘧啶 放射治疗 肿瘤科 危险系数 内科学 放化疗 头颈部癌 临床终点 顺铂 诱导化疗 化疗 不利影响 随机对照试验 癌症 置信区间 结直肠癌
作者
Ricardo Hitt,Ricard Mesı́a,A. Lozano,Lara Iglesias Docampo,Juan J. Grau,Miren Taberna,Jordi Rubió‐Casadevall,Javier Martínez‐Trufero,E. del Barco,Carlos García Girón,Sergio Vázquez Estévez,Beatriz Cirauqui,Juan Jesús Cruz
出处
期刊:Oral Oncology [Elsevier BV]
卷期号:134: 106087-106087 被引量:8
标识
DOI:10.1016/j.oraloncology.2022.106087
摘要

Concurrent chemoradiotherapy is the standard treatment for patients with unresectable, locally advanced squamous cell carcinoma of the head and neck (LA-SCCHN); induction chemotherapy (ICT) may provide survival benefits in some patients. This study aimed to demonstrate the noninferiority of concomitant cetuximab plus radiotherapy (cet+RT) vs cisplatin plus radiotherapy (cis+RT) in patients with unresectable LA-SCCHN who were responsive to ICT.This randomized, open-label, phase 3 trial studied patients with unresectable LA-SCCHN who received 3 cycles of ICT (docetaxel, cisplatin, and 5-fluorouracil; TPF) followed by cis+RT (standard arm) or cet+RT (experimental arm). The primary endpoint was noninferiority of the experimental arm vs the standard arm in terms of overall survival (OS), based on a hazard ratio (HR) of < 1.3. Secondary endpoints included progression-free survival, overall response, safety, and quality of life (QOL).Between July 15, 2008, and July 5, 2013, 519 patients were recruited and started ICT; 407 patients received post-ICT treatment (cis+RT, n = 205; cet+RT, n = 202). At a median follow-up of 43.9 (cis+RT) and 41.1 (cet+RT) months, median OS was 63.6 and 42.9 months with cis+RT and cet+RT, respectively (HR [90% CI] = 1.106 [0.888-1.378], P =.4492). There were no differences in progression-free survival, overall response rates, or adverse event rates between groups. There was greater late neurotoxicity with cis+RT than cet+RT (P =.0058). Several QOL dimensions improved with cet+RT vs cis+RT (physical functioning, P =.0287; appetite loss, P =.0248; social contact, P =.0153).Noninferiority of cet+RT over cis+RT was not demonstrated.
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