Fu K K, Cooper J S, Marcial V A, Laramore G E, Pajak T F, Jacobs J, Al-Sarraf M, Forastiere A A, Cox J D
University of California, San Francisco, CA, USA.
Int J Radiat Oncol Biol Phys. 1996 Jun 1;35(3):425-38. doi: 10.1016/s0360-3016(96)80003-4.
During the past 25 years, the Radiation Therapy Oncology Group (RTOG) has played a major role in head and neck cancer clinical research. The major research themes for recent and currently active trials have been: (a) combined modality therapy, (b) altered fractionation radiotherapy, (c) hypoxic cell sensitizers, (d) organ preservation, (e) chemoprevention, and (f) clinical/laboratory correlations. For advanced operable disease, the RTOG showed improved local-regional control with postoperative radiotherapy as compared to preoperative radiotherapy for carcinoma of the supraglottic larynx and hypopharynx. This established the use of surgery followed by postoperative radiotherapy as the standard treatment in subsequent RTOG and Intergroup trials for operable disease. For advanced inoperable disease, the RTOG demonstrated the feasibility of testing altered fractionation radiotherapy in a multiinstitutional clinical trials setting. A Phase III trial comparing hyperfractionation and accelerated fractionation to conventional fractionation is now in progress. Phase I/II combined modality studies established the efficacy of concurrent high-dose cisplatin and radiotherapy in the treatment of advanced disease and provided the basis for further testing in Phase III trials for nasopharyngeal carcinoma, larynx preservation, and high-risk advanced operable disease. Analysis of the extensive RTOG Head and Neck Cancer database established the incidence of second malignancies and their adverse impact on patients whose initial tumors were cured by radiotherapy, and provided the basis for chemoprevention trials. Recursive partitioning analysis identified 6 distinct prognostically homogeneous patient groups based on pretreatment tumor or patient characteristics and/or treatment variables. Retrospective analysis identified tumor p105 antigen density as an independent prognostic indicator in patients irradiated for head and neck cancer. Future trials will continue to focus on the reduction of morbidity and mortality, and improvement of the quality of life of head and neck cancer patients through innovative radiotherapy delivery, multimodality approaches, use of chemical and biological modifiers, and other novel therapies, identification of clinical and biological prognostic indicators, and prevention or diminution of acute morbidity and late complications of the disease and its treatment.
在过去25年里,放射治疗肿瘤学组(RTOG)在头颈癌临床研究中发挥了重要作用。近期及当前正在进行的试验的主要研究主题包括:(a)综合治疗模式;(b)改变分割放疗;(c)乏氧细胞增敏剂;(d)器官保留;(e)化学预防;以及(f)临床/实验室相关性研究。对于晚期可手术疾病,RTOG研究表明,与术前放疗相比,声门上喉癌和下咽癌术后放疗可改善局部区域控制。这确立了手术加术后放疗作为后续RTOG和协作组可手术疾病试验的标准治疗方法。对于晚期不可手术疾病,RTOG证明了在多机构临床试验环境中测试改变分割放疗的可行性。一项比较超分割放疗和加速分割放疗与常规分割放疗的III期试验正在进行中。I/II期综合治疗模式研究确立了高剂量顺铂同步放疗治疗晚期疾病的疗效,并为鼻咽癌、喉保留和高危晚期可手术疾病的III期试验进一步测试提供了依据。对RTOG广泛的头颈癌数据库的分析确定了第二原发恶性肿瘤的发生率及其对初始肿瘤经放疗治愈的患者的不良影响,并为化学预防试验提供了依据。递归分割分析根据治疗前肿瘤或患者特征和/或治疗变量确定了6个不同的预后同质患者组。回顾性分析确定肿瘤p105抗原密度是头颈癌放疗患者的独立预后指标。未来的试验将继续聚焦于通过创新的放疗方式、多模式方法、使用化学和生物调节剂及其他新疗法来降低发病率和死亡率,改善头颈癌患者的生活质量,确定临床和生物学预后指标,以及预防或减少该疾病及其治疗的急性发病率和晚期并发症。