Department of Radiation Oncology, Erasmus MC-Daniel den Hoed Cancer Center, Groene Hilledijk, Rotterdam, the Netherlands.
Int J Radiat Oncol Biol Phys. 2012 Mar 15;82(4):1494-500. doi: 10.1016/j.ijrobp.2011.05.019. Epub 2011 Jul 26.
To prospectively assess the outcome and toxicity of frameless stereotactic body radiotherapy (SBRT) as a treatment option for boosting primary oropharyngeal cancers (OPC) in patients who not suitable for the standard brachytherapy boost (BTB).
Between 2005 and 2010, 51 patients with Stage I to IV biopsy-proven OPC who were not suitable for BTB received boosts by means of SBRT (3 times 5.5 Gy, prescribed to the 80% isodose line), after 46 Gy of IMRT to the primary tumor and neck (when indicated). Endpoints of the study were local control (LC), disease-free survival (DFS), overall survival (OS), and acute and late toxicity.
After a median follow-up of 18 months (range, 6-65 months), the 2-year actuarial rates of LC, DFS, and OS were 86%, 80%, and 82%, respectively, and the 3-year rates were 70%, 66%, and 54%, respectively. The treatment was well tolerated, as there were no treatment breaks and no Grade 4 or 5 toxicity reported, either acute or chronic. The overall 2-year cumulative incidence of Grade ≥2 late toxicity was 28%. Of the patients with 2 years with no evidence of disease (n = 20), only 1 patient was still feeding tube dependent and 2 patients had Grade 3 xerostomia.
According to our knowledge, this study is the first report of patients with primary OPC who received boosts by means of SBRT. Patients with OPC who are not suitable for the standard BTB can safely and effectively receive boosts by SBRT. With this radiation technique, an excellent outcome was achieved. Furthermore, the SBRT boost did not have a negative impact regarding acute and late side effects.
前瞻性评估无框架立体定向体部放射治疗(SBRT)作为治疗选择的结果和毒性,用于提升不适合标准近距离放疗(BTB)的原发性口咽癌(OPC)患者的肿瘤。
2005 年至 2010 年间,51 例经活检证实的 I 至 IV 期 OPC 患者因不适合 BTB 而接受 SBRT 增敏治疗(3 次 5.5Gy,处方至 80%等剂量线),此前已接受 46Gy 的调强放疗(IMRT)照射原发肿瘤和颈部(有指征时)。本研究的终点是局部控制(LC)、无病生存(DFS)、总生存(OS)和急性及迟发性毒性。
中位随访 18 个月(范围 6-65 个月)后,2 年的 LC、DFS 和 OS 的累积生存率分别为 86%、80%和 82%,3 年的累积生存率分别为 70%、66%和 54%。治疗耐受性良好,无治疗中断,无 1 例或以上 3-4 级急性或慢性毒性反应。总的 2 年迟发性毒性发生率≥2 级的累积发生率为 28%。在 2 年无疾病证据的患者(n=20)中,仅有 1 例仍依赖饲管,2 例有 3 级口干。
根据我们的知识,这是首次报告接受 SBRT 增敏治疗的原发性 OPC 患者。不适合标准 BTB 的 OPC 患者可以安全有效地接受 SBRT 增敏治疗。采用这种放射技术,获得了良好的结果。此外,SBRT 增敏治疗对急性和迟发性副作用没有负面影响。