Randomized trial comparing two methods of re-irradiation after salvage surgery in head and neck squamous cell carcinoma: Once daily split-course radiotherapy with concomitant chemotherapy or twice daily radiotherapy with cetuximab

被引:15
作者
Tao, Yungan [1 ]
Faivre, Laura [1 ]
Laprie, Anne [2 ]
Boisselier, Pierre [3 ]
Ferron, Christophe [4 ]
Jung, Guy Michel [5 ]
Racadot, Severine [6 ]
Gery, Bernard [7 ]
Even, Caroline [1 ]
Breuskin, Ingrid [1 ]
Bourhis, Jean [8 ]
Janot, Francois [1 ]
机构
[1] Gustave Roussy Canc Campus, Villejuif, France
[2] Inst Claudius Regaud, Toulouse, France
[3] Inst Canc Val Aurelle, Montpellier, France
[4] CHU Nantes, Nantes, France
[5] Ctr Paul Strauss, Strasbourg, France
[6] Ctr Leon Berard, Lyon, France
[7] Ctr Francois Baclesse, Caen, France
[8] CHU Vaudois, Lausanne, Switzerland
关键词
Cetuximab; Re-irradiation; Head and neck squamous cell carcinoma; Recurrent or second primary; Hyperfractionation; PHASE-II; CANCER; SURVIVAL;
D O I
10.1016/j.radonc.2018.05.005
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: A previous randomized trial in recurrent Head and Neck squamous-cell carcinoma (HNSCC) has shown re-irradiation combined with chemotherapy after salvage surgery significantly improved disease-free survival (DFS). The objective of this randomized trial was to compare two methods of re-irradiation in terms of toxicity and survival. Patients and methods: Patients with recurrence/second primary in previously irradiated area were randomly allocated to receive either 60 Gy over 11 weeks with concomitant 5FU - hydroxyurea (VP-arm), or 60 Gy (1.2 Gy twice daily) over 5 weeks with cetuximab (HFR-arm). Primary endpoint was treatment interruption >15 days (acute toxicity). Results: Twenty-six patients were included in VP-arm and 27 in HFR-arm. One patient in VP-arm experienced >15 days interruption due to toxicity, and none in HFR-arm. In both arms, all patients received at least 60 Gy. In VP-arm, 8/26 patients had chemotherapy delay and/or dose reduction. In HFR-arm, 4/27 patients had <6 cycles cetuximab. There was no significant difference in overall survival (Median OS: 37.4 months vs 21.9 months, p = 0.12). Toxicities and DFS were not different between 2 arms. Conclusions: Twice daily schedule of re-irradiation of 60 Gy/5 weeks with cetuximab was tolerable and no significant difference in treatment delays occurred between two arms. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:467 / 471
页数:5
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