Department of Radiation Oncology, University Cancer Institute, University of Pittsburgh School of Medicine, Pittsburgh, PA 15232, USA.
Am J Clin Oncol. 2010 Jun;33(3):286-93. doi: 10.1097/COC.0b013e3181aacba5.
The aim of this study was to assess the safety and outcome of stereotactic body radiotherapy (SBRT) in patients with recurrent previously irradiated squamous cell carcinoma of the head and neck (rSCCHN).
We reviewed our experience with 85 patients who received SBRT for rSCCHN between January 2003 and May 2008. The mean dose of SBRT was 35 Gy (range: 15-44 Gy). The following end points were evaluated: tumor response, time-to-progression, acute and late toxicities, local control (LC) rates and impact of tumor dose and tumor size on LC, and overall survival.
The median follow-up of all patients was 6 months (range: 1.3-39 months). For those patients who were alive at last follow-up (40%) the median follow-up was 17.6 months. The mean total dose of prior radiation to the primary site was 74 Gy (range: 32-170 Gy). Those patients who received SBRT <35 Gy had significantly lower LC than those with > or =35 Gy at 6 months the median follow-up time (P = 0.014). Tumor responses were 34% complete response, 34% partial response, 20% stable disease, and 12% progressive disease. Among those with an initial tumor response followed by progression (58 patients), there was a median interval of 5.5 months for time-to-progression. The 1-year and 2-year LC and overall survival rates for all patients were 51.2% and 30.7%, and 48.5% and 16.1%, respectively. Overall, the median survival for all patients was 11.5 months (range: 3-51). Treatment was well-tolerated with no grade 4 or 5 treatment-related toxicities.
SBRT is feasible and safe with minimal toxicities for treatment of rSCCHN patients with prior radiation therapy deemed to be poor candidates for re-irradiation by conventional means.
本研究旨在评估立体定向体放射治疗(SBRT)在复发性头颈部鳞癌(rSCCHN)患者中的安全性和疗效。
我们回顾性分析了 2003 年 1 月至 2008 年 5 月期间 85 例接受 SBRT 治疗 rSCCHN 的患者的资料。SBRT 的平均剂量为 35 Gy(范围:15-44 Gy)。评估了以下终点:肿瘤反应、无进展时间、急性和迟发性毒性、局部控制率(LC)以及肿瘤剂量和肿瘤大小对 LC 的影响,以及总生存率。
所有患者的中位随访时间为 6 个月(范围:1.3-39 个月)。在最后随访时存活的患者(40%)的中位随访时间为 17.6 个月。原发灶的总放疗剂量中位数为 74 Gy(范围:32-170 Gy)。在中位随访时间为 6 个月时,SBRT 剂量<35 Gy 的患者 LC 明显低于剂量≥35 Gy 的患者(P=0.014)。肿瘤反应率为完全缓解 34%,部分缓解 34%,疾病稳定 20%,疾病进展 12%。在最初有肿瘤反应后进展的 58 例患者中,无进展时间的中位数为 5.5 个月。所有患者的 1 年和 2 年 LC 率和总生存率分别为 51.2%和 30.7%,48.5%和 16.1%。总的来说,所有患者的中位生存时间为 11.5 个月(范围:3-51 个月)。治疗耐受性良好,无 4 级或 5 级与治疗相关的毒性。
对于因先前放疗而被认为不适合常规再放疗的复发性头颈部鳞癌患者,SBRT 是一种可行且安全的治疗方法,毒性较小。