Calderon B, Guerder C, Resbeut M, Fakhry N, Dupuis C, Cowen D
Service de radiothérapie, centre hospitalier universitaire de la Timone, 264, rue Saint-Pierre, 13005 Marseille, France.
Centre de radiothérapie Saint-Louis, Croix-Rouge française, quartier Sainte-Musse, rue André-Blondel, 83100 Toulon, France.
Cancer Radiother. 2016 Apr;20(2):83-90. doi: 10.1016/j.canrad.2015.10.001. Epub 2016 Mar 8.
Retrospectively evaluate the safety, feasibility and efficacy of concomitant chemoradiotherapy after induction chemotherapy by docetaxel, cisplatin and 5-fluoro-uracil for locally advanced head and neck cancers.
Patients' data from three radiotherapy centres in South of France, with locally advanced head and neck cancers, and treated between December 2007 and July 2013 by concomitant chemoradiotherapy, after induction chemotherapy by docetaxel, cisplatin and 5-fluoro-uracil, were analysed. Adverse effects were graduated according to CTCAE v3.0 criteria. Overall survival and disease-free survival were calculated according to Kaplan-Meier method.
One hundred and sixty-eight patients, mostly oropharynx (38%) T4 (46%) N2 (54%) tumors, received, after induction chemotherapy by docetaxel, cisplatin and 5-fluoro-uracil, a concomitant chemoradiotherapy with platin or cetuximab, which delivered 66 to 70Gy. Grade 3-4 adverse effects were less frequent in the group of patients who received cisplatin (with or withour 5-fluoro-uracil) at 100mg/m(2) each 21 days compared to cetuximab (radiomucositis: 32.5% vs 61%, P=0.018; radioepithelitis: 13% vs 61 %, P<0.0001). Chemopotentiation was incomplete for 21% of patients without impacting survival. Two years overall survival and disease-free survival were respectively of 81% and 64%. Lymph nodes status and WHO status significantly influenced these survivals (overall survival 84% if N<3 vs 56% if N3, P=0.017 and 85 % if WHO status ≤ 1 vs 50% if WHO status>1, P=0.006; disease-free survival 66% if N<3 vs 47% if N3, P=0.046).
The association of induction chemotherapy by docetaxel, cisplatin and 5-fluoro-uracil and concomitant chemoradiotherapy shows satisfying results with an acceptable toxicity. The terms of the chemopotentiation and its superiority to a single concomitant chemoradiotherapy treatment still remain to be clarified.
回顾性评估多西他赛、顺铂和5-氟尿嘧啶诱导化疗后同步放化疗治疗局部晚期头颈癌的安全性、可行性和疗效。
分析了法国南部三个放疗中心2007年12月至2013年7月期间收治的局部晚期头颈癌患者的数据,这些患者在接受多西他赛、顺铂和5-氟尿嘧啶诱导化疗后接受了同步放化疗。根据CTCAE v3.0标准对不良反应进行分级。采用Kaplan-Meier法计算总生存期和无病生存期。
168例患者,多数为口咽癌(38%),T4期(46%),N2期(54%)肿瘤,在接受多西他赛、顺铂和5-氟尿嘧啶诱导化疗后,接受了铂类或西妥昔单抗同步放化疗,放疗剂量为66至70Gy。与西妥昔单抗组相比,每21天接受100mg/m²顺铂(加或不加5-氟尿嘧啶)的患者3-4级不良反应发生率较低(放射性粘膜炎:32.5%对61%,P=0.018;放射性上皮炎:13%对61%,P<0.0001)。21%的患者化疗增敏不完全,但不影响生存率。两年总生存期和无病生存期分别为81%和64%。淋巴结状态和世界卫生组织状态显著影响这些生存率(如果N<3,总生存期为84%,如果N≥3,则为56%,P=0.017;如果世界卫生组织状态≤1,总生存期为85%,如果世界卫生组织状态>1,则为50%,P=0.006;如果N<3,无病生存期为66%,如果N≥3,则为47%,P=0.046)。
多西他赛、顺铂和5-氟尿嘧啶诱导化疗与同步放化疗联合应用显示出令人满意的结果,毒性可接受。化疗增敏的情况及其相对于单纯同步放化疗的优势仍有待阐明。