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Initial clinical experience with scanned proton beams at the Italian National Center for Hadrontherapy (CNAO)

机译:意大利国家强子疗法中心(CNAO)扫描质子束的初步临床经验

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摘要

We report the initial toxicity data with scanned proton beams at the Italian National Center for Hadrontherapy (CNAO). In September 2011, CNAO commenced patient treatment with scanned proton beams within two prospective Phase II protocols approved by the Italian Health Ministry. Patients with chondrosarcoma or chordoma of the skull base or spine were eligible. By October 2012, 21 patients had completed treatment. Immobilization was performed using rigid non-perforated thermoplastic-masks and customized headrests or body-pillows as indicated. Non-contrast CT scans with immobilization devices in place and MRI scans in supine position were performed for treatment-planning. For chordoma, the prescribed doses were 74 cobalt grey equivalent (CGE) and 54 CGE to planning target volume 1 (PTV1) and PTV2, respectively. For chondrosarcoma, the prescribed doses were 70 CGE and 54 CGE to PTV1 and PTV2, respectively. Treatment was delivered five days a week in 35–37 fractions. Prior to treatment, the patients' positions were verified using an optical tracking system and orthogonal X-ray images. Proton beams were delivered using fixed-horizontal portals on a robotic couch. Weekly MRI incorporating diffusion-weighted-imaging was performed during the course of proton therapy. Patients were reviewed once weekly and acute toxicities were graded with the Common Terminology Criteria for Adverse Events (CTCAE). Median age of patients = 50 years (range, 21–74). All 21 patients completed the proton therapy without major toxicities and without treatment interruption. Median dose delivered was 74 CGE (range, 70–74). The maximum toxicity recorded was CTCAE Grade 2 in four patients. Our preliminary data demonstrates the clinical feasibility of scanned proton beams in Italy.
机译:我们在意大利国家强子疗法中心(CNAO)报告了使用扫描质子束的初步毒性数据。 2011年9月,CNAO在意大利卫生部批准的两个前瞻性II期方案中开始使用扫描质子束进行患者治疗。有软骨肉瘤或颅底或脊柱脊索瘤的患者符合条件。截至2012年10月,已有21名患者完成了治疗。如所示,使用刚性的无孔热塑性口罩和定制的头枕或身体枕进行固定。进行固定装置的非对比CT扫描和仰卧位MRI扫描以制定治疗计划。对于脊索瘤,处方剂量分别为计划目标体积1(PTV1)和PTV2的74钴灰色当量(CGE)和54 CGE。对于软骨肉瘤,PTV1和PTV2的处方剂量分别为70 CGE和54 CGE。每周5天以35-37的比例进行治疗。在治疗之前,使用光学跟踪系统和正交X射线图像验证患者的位置。质子束通过机器人卧榻上的水平固定入口传送。在质子治疗过程中,每周进行MRI结合扩散加权成像。每周对患者进行一次检查,并按照《不良事件通用术语标准》(CTCAE)对急性毒性进行分级。患者的中位年龄= 50岁(范围21-74)。所有21例患者均完成了质子治疗,无重大毒性反应,也没有中断治疗。中位剂量为74 CGE(范围70-74)。记录的最大毒性为四名患者的CTCAE 2级。我们的初步数据证明了意大利扫描质子束的临床可行性。

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