Department of Radiation Oncology, University Hospital Zurich, Rämistrasse 100, Zurich, Switzerland.
Strahlenther Onkol. 2010 Mar;186(3):135-42. doi: 10.1007/s00066-010-2048-y. Epub 2010 Feb 22.
To assess the efficacy and safety of using simultaneous integrated boost intensity-modulated radiotherapy (SIB-IMRT) to treat nasopharyngeal cancer (NPC) in a Caucasian cohort. Outcome was analyzed with respect to dose-volume histogram (DVH) values.
Between 03/2002 and 01/2008, 39 NPC patients underwent SIB-IMRT (37 Caucasians; 31 males; mean age 53 years [16-78 years]). 41% presented with WHO (World Health Organization) type 1 unfavorable histology, 85% with stage III/IV disease. 19 patients had total gross tumor volume (GTV) 16-70 cm3 (mean 36 cm3), while 16 had GTV > 70 cm3 (73-217 cm3; mean 115 cm3). All patients with stage II-IV disease received concomitant cisplatin. The prescribed SIB dose delivered to the planning target volume (PTV) was 70 Gy (2.00 Gy/fraction) in 17, 69.6 Gy (2.11 Gy/fraction) in 19, and 66 Gy (2.20 Gy/fraction) in three patients.
3-year local relapse-free, nodal relapse-free, distant metastases-free, disease-free rates and overall survival were 86%, 89%, 85%, 72%, and 85% (median follow-up 30 months [8-71 months]). Histology was a significant prognostic factor concerning overall survival, with worst prognosis in WHO type 1 compared to type 2/3 (75% vs. 93%; p = 0.03). There was a trend in favor of WHO type 2/3 regarding local control (74% vs. 94%; p = 0.052). The PTV DVHs showed a slight left shift compared to reported series. Three patients developed grade 3 late effects (xerostomia [n = 2], dysphagia [n = 1], hearing loss [n = 1]).
In comparison with predominantly Asian NPC IMRT series in the literature, chemo-IMRT in the own Caucasian cohort, characterized by less radio-responsive WHO type 1, was equally effective. Treatment tolerance was excellent.
评估在白种人群体中使用同步整合加量强度调节放射治疗(SIB-IMRT)治疗鼻咽癌(NPC)的疗效和安全性。通过剂量体积直方图(DVH)值分析结果。
2002 年 3 月至 2008 年 1 月期间,39 例 NPC 患者接受了 SIB-IMRT 治疗(37 例白种人;31 例男性;平均年龄 53 岁[16-78 岁])。41%的患者组织学类型为世界卫生组织(WHO)1 型预后不良,85%的患者分期为 III/IV 期。19 例患者的总肿瘤总体积(GTV)为 16-70cm3(平均 36cm3),而 16 例患者的 GTV >70cm3(73-217cm3;平均 115cm3)。所有 II-IV 期疾病患者均接受顺铂同期化疗。计划靶区(PTV)的 SIB 处方剂量为 70Gy(2.00Gy/次)17 例,69.6Gy(2.11Gy/次)19 例,66Gy(2.20Gy/次)3 例。
3 年局部无复发生存率、淋巴结无复发生存率、远处无转移生存率、无疾病生存率和总生存率分别为 86%、89%、85%、72%和 85%(中位随访时间 30 个月[8-71 个月])。组织学是影响总生存率的显著预后因素,与 WHO 1 型相比,2/3 型预后最差(75%比 93%;p=0.03)。2/3 型 WHO 组织学在局部控制方面有更好的趋势(74%比 94%;p=0.052)。与文献报道的亚洲 NPC 调强放疗系列相比,PTV 的 DVH 显示出轻微的左移。3 例患者发生 3 级晚期效应(口干[2 例]、吞咽困难[1 例]、听力损失[1 例])。
与文献中主要为亚洲人的 NPC 调强放疗系列相比,本高加索人群的化疗调强放疗,以较少的放射反应性 WHO 1 型为特征,同样有效。治疗耐受性极好。