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头颈部癌症的自适应放疗:前瞻性试验的初步临床结果。

Adaptive radiotherapy for head-and-neck cancer: initial clinical outcomes from a prospective trial.

机构信息

Department of Radiation Medicine, Hofstra North Shore-Long Island Jewish School of Medicine, New Hyde Park, NY 11040, USA.

出版信息

Int J Radiat Oncol Biol Phys. 2012 Jul 1;83(3):986-93. doi: 10.1016/j.ijrobp.2011.08.017. Epub 2011 Dec 2.

DOI:10.1016/j.ijrobp.2011.08.017
PMID:22138459
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4271827/
Abstract

PURPOSE

To present pilot toxicity and survival outcomes for a prospective trial investigating adaptive radiotherapy (ART) for oropharyngeal squamous cell carcinoma.

METHODS AND MATERIALS

A total of 24 patients were enrolled in an institutional review board-approved clinical trial; data for 22 of these patients were analyzed. Daily CT-guided setup and deformable image registration permitted serial mapping of clinical target volumes and avoidance structures for ART planning. Primary site was base of tongue in 15 patients, tonsil in 6 patient, and glossopharyngeal sulcus in 1 patient. Twenty patients (91%) had American Joint Committee on Cancer (AJCC) Stage IV disease. T stage distribution was 2 T1, 12 T2, 3 T3, 5 T4. N stage distribution was 1 N0, 2 N1, 5 N2a, 12 N2b, and 2 N2c. Of the patients, 21 (95%) received systemic therapy.

RESULTS

With a 31-month median follow-up (range, 13-45 months), there has been no primary site failure and 1 nodal relapse, yielding 100% local and 95% regional disease control at 2 years. Baseline tumor size correlated with absolute volumetric treatment response (p = 0.018). Parotid volumetric change correlated with duration of feeding tube placement (p = 0.025). Acute toxicity was comparable to that observed with conventional intensity-modulated radiotherapy (IMRT). Chronic toxicity and functional outcomes beyond 1 year were tabulated.

CONCLUSION

This is the first prospective evaluation of morbidity and survival outcomes in patients with locally advanced head-and-neck cancer treated with automated adaptive replanning. ART can provide dosimetric benefit with only one or two mid-treatment replanning events. Our preliminary clinical outcomes document functional recovery and preservation of disease control at 1-year follow-up and beyond.

摘要

目的

介绍一项前瞻性研究的初步毒性和生存结果,该研究旨在探讨适形调强放疗(ART)治疗口咽鳞癌。

方法与材料

这项经机构审查委员会批准的临床试验共纳入 24 例患者,对其中 22 例患者的数据进行了分析。每日 CT 引导下的摆位和形变图像配准,实现了临床靶区和避靶结构的连续勾画,以便进行 ART 计划。原发灶位于舌根 15 例,扁桃体 6 例,舌咽隐窝 1 例。20 例(91%)患者 AJCC 分期为 IV 期。T 分期分布为 T1 期 2 例,T2 期 12 例,T3 期 3 例,T4 期 5 例。N 分期分布为 N0 期 1 例,N1 期 2 例,N2a 期 5 例,N2b 期 12 例,N2c 期 2 例。其中 21 例(95%)患者接受了系统治疗。

结果

中位随访时间为 31 个月(范围 13-45 个月),无原发灶失败,1 例淋巴结复发,2 年时局部和区域疾病控制率分别为 100%和 95%。基线肿瘤大小与绝对肿瘤体积治疗反应相关(p=0.018)。腮腺体积变化与置管时间相关(p=0.025)。急性毒性与常规调强放疗(IMRT)相似。记录了 1 年以上的慢性毒性和功能结果。

结论

这是首次前瞻性评估局部晚期头颈部癌患者接受自动自适应再计划治疗后的发病率和生存结果。ART 仅需 1 次或 2 次治疗中再计划,即可提供剂量学优势。我们的初步临床结果显示,1 年随访及之后患者的功能恢复和疾病控制得到了保持。

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Adaptive replanning strategies accounting for shrinkage in head and neck IMRT.考虑头颈部调强放疗中组织收缩的自适应再计划策略。
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Pre-trial quality assurance processes for an intensity-modulated radiation therapy (IMRT) trial: PARSPORT, a UK multicentre Phase III trial comparing conventional radiotherapy and parotid-sparing IMRT for locally advanced head and neck cancer.调强放射治疗(IMRT)试验的审前质量保证流程:PARSPORT,一项英国多中心III期试验,比较传统放疗与腮腺保留IMRT治疗局部晚期头颈癌的疗效。
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A comprehensive assessment by tumor site of patient setup using daily MVCT imaging from more than 3,800 helical tomotherapy treatments.使用来自3800多次螺旋断层放射治疗的每日兆伏级计算机断层扫描成像,按肿瘤部位对患者摆位进行全面评估。
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Performance evaluation of automatic anatomy segmentation algorithm on repeat or four-dimensional computed tomography images using deformable image registration method.使用可变形图像配准方法对重复或四维计算机断层扫描图像上的自动解剖分割算法进行性能评估。
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Beam path toxicities to non-target structures during intensity-modulated radiation therapy for head and neck cancer.头颈部癌调强放射治疗期间非靶结构的射线路径毒性
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Parotid gland dose in intensity-modulated radiotherapy for head and neck cancer: is what you plan what you get?头颈部癌调强放射治疗中的腮腺剂量:计划的剂量与实际得到的剂量相符吗?
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