Lacas Benjamin, Bourhis Jean, Overgaard Jens, Zhang Qiang, Grégoire Vincent, Nankivell Matthew, Zackrisson Björn, Szutkowski Zbigniew, Suwiński Rafał, Poulsen Michael, O'Sullivan Brian, Corvò Renzo, Laskar Sarbani Ghosh, Fallai Carlo, Yamazaki Hideya, Dobrowsky Werner, Cho Kwan Ho, Beadle Beth, Langendijk Johannes A, Viegas Celia Maria Pais, Hay John, Lotayef Mohamed, Parmar Mahesh K B, Aupérin Anne, van Herpen Carla, Maingon Philippe, Trotti Andy M, Grau Cai, Pignon Jean-Pierre, Blanchard Pierre
Ligue Nationale Contre le Cancer Meta-Analysis Platform, Service de Biostatistique et d'Epidémiologie, Gustave Roussy Cancer Campus, INSERM U1018, CESP, Université Paris-Sud, Université Paris-Saclay, Villejuif, France.
Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland.
Lancet Oncol. 2017 Sep;18(9):1221-1237. doi: 10.1016/S1470-2045(17)30458-8. Epub 2017 Jul 27.
The Meta-Analysis of Radiotherapy in squamous cell Carcinomas of Head and neck (MARCH) showed that altered fractionation radiotherapy is associated with improved overall and progression-free survival compared with conventional radiotherapy, with hyperfractionated radiotherapy showing the greatest benefit. This update aims to confirm and explain the superiority of hyperfractionated radiotherapy over other altered fractionation radiotherapy regimens and to assess the benefit of altered fractionation within the context of concomitant chemotherapy with the inclusion of new trials.
For this updated meta-analysis, we searched bibliography databases, trials registries, and meeting proceedings for published or unpublished randomised trials done between Jan 1, 2009, and July 15, 2015, comparing primary or postoperative conventional fractionation radiotherapy versus altered fractionation radiotherapy (comparison 1) or conventional fractionation radiotherapy plus concomitant chemotherapy versus altered fractionation radiotherapy alone (comparison 2). Eligible trials had to start randomisation on or after Jan 1, 1970, and completed accrual before Dec 31, 2010; had to have been randomised in a way that precluded prior knowledge of treatment assignment; and had to include patients with non-metastatic squamous cell carcinoma of the oral cavity, oropharynx, hypopharynx, or larynx undergoing first-line curative treatment. Trials including a non-conventional radiotherapy control group, investigating hypofractionated radiotherapy, or including mostly nasopharyngeal carcinomas were excluded. Trials were grouped in three types of altered fractionation: hyperfractionated, moderately accelerated, and very accelerated. Individual patient data were collected and combined with a fixed-effects model based on the intention-to-treat principle. The primary endpoint was overall survival.
Comparison 1 (conventional fractionation radiotherapy vs altered fractionation radiotherapy) included 33 trials and 11 423 patients. Altered fractionation radiotherapy was associated with a significant benefit on overall survival (hazard ratio [HR] 0·94, 95% CI 0·90-0·98; p=0·0033), with an absolute difference at 5 years of 3·1% (95% CI 1·3-4·9) and at 10 years of 1·2% (-0·8 to 3·2). We found a significant interaction (p=0·051) between type of fractionation and treatment effect, the overall survival benefit being restricted to the hyperfractionated group (HR 0·83, 0·74-0·92), with absolute differences at 5 years of 8·1% (3·4 to 12·8) and at 10 years of 3·9% (-0·6 to 8·4). Comparison 2 (conventional fractionation radiotherapy plus concomitant chemotherapy versus altered fractionation radiotherapy alone) included five trials and 986 patients. Overall survival was significantly worse with altered fractionation radiotherapy compared with concomitant chemoradiotherapy (HR 1·22, 1·05-1·42; p=0·0098), with absolute differences at 5 years of -5·8% (-11·9 to 0·3) and at 10 years of -5·1% (-13·0 to 2·8).
This update confirms, with more patients and a longer follow-up than the first version of MARCH, that hyperfractionated radiotherapy is, along with concomitant chemoradiotherapy, a standard of care for the treatment of locally advanced head and neck squamous cell cancers. The comparison between hyperfractionated radiotherapy and concomitant chemoradiotherapy remains to be specifically tested.
Institut National du Cancer; and Ligue Nationale Contre le Cancer.
头颈部鳞状细胞癌放疗的Meta分析(MARCH)表明,与传统放疗相比,改变分割放疗可改善总生存期和无进展生存期,其中超分割放疗获益最大。本次更新旨在确认并解释超分割放疗相对于其他改变分割放疗方案的优势,并在纳入新试验的情况下评估同步化疗背景下改变分割放疗的获益。
对于本次更新的Meta分析,我们检索了文献数据库、试验注册库和会议论文集,以查找2009年1月1日至2015年7月15日期间开展的已发表或未发表的随机试验,这些试验比较了原发性或术后常规分割放疗与改变分割放疗(比较1),或常规分割放疗加同步化疗与单纯改变分割放疗(比较2)。符合条件的试验必须在1970年1月1日或之后开始随机分组,并在2010年12月31日前完成入组;必须以排除治疗分配先验知识的方式进行随机分组;必须纳入接受一线根治性治疗的口腔、口咽、下咽或喉非转移性鳞状细胞癌患者。排除包括非常规放疗对照组、研究低分割放疗或主要纳入鼻咽癌患者的试验。试验分为三种改变分割类型:超分割、适度加速和非常加速。收集个体患者数据,并根据意向性治疗原则采用固定效应模型进行合并。主要终点为总生存期。
比较1(常规分割放疗与改变分割放疗)纳入33项试验和11423例患者。改变分割放疗与总生存期显著获益相关(风险比[HR]0.94,95%CI 0.90 - 0.98;p = 0.0033),5年时绝对差异为3.1%(95%CI 1.3 - 4.9),10年时为1.2%(-0.8至3.2)。我们发现分割类型与治疗效果之间存在显著交互作用(p = 0.051),总生存期获益仅限于超分割组(HR 0.83,0.74 - 0.92),5年时绝对差异为8.1%(3.4至12.8),10年时为3.9%(-0.6至8.4)。比较2(常规分割放疗加同步化疗与单纯改变分割放疗)纳入5项试验和986例患者。与同步放化疗相比,改变分割放疗的总生存期显著更差(HR 1.22,1.05 - 1.42;p = 0.0098),5年时绝对差异为-5.8%(-11.9至0.3),10年时为-5.1%(-13.0至2.8)。
本次更新纳入了更多患者且随访时间更长,证实了超分割放疗与同步放化疗一样,是局部晚期头颈部鳞状细胞癌治疗的标准治疗方法。超分割放疗与同步放化疗之间的比较仍有待专门检验。
法国国家癌症研究所;法国抗癌联盟。