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口腔和口咽癌术后选择性颈部放疗的应用:一项前瞻性临床研究。

Selective use of postoperative neck radiotherapy in oral cavity and oropharynx cancer: a prospective clinical study.

机构信息

Department of Radiation Oncology, Virgen de las Nieves University Hospital, Avda, Fuerzas Armadas 4, Granada 18014, Spain.

出版信息

Radiat Oncol. 2013 Apr 28;8:103. doi: 10.1186/1748-717X-8-103.

Abstract

BACKGROUND

In cervical postoperative radiotherapy, the target volume is usually the same as the extension of the previous dissection. We evaluated a protocol of selective irradiation according to the risk estimated for each dissected lymph node level.

METHODS

Eighty patients with oral/oropharyngeal cancer were included in this prospective clinical study between 2005 and 2008. Patients underwent surgery of the primary tumor and cervical dissection, with identification of positive nodal levels, followed by selective postoperative radiotherapy. Three types of selective nodal clinical target volume (CTV) were defined: CTV0, CTV1, and CTV2, with a subclinical disease risk of <10%, 10-25%, and 25% and a prescribed radiation dose of <35 Gy, 50 Gy, and 66-70 Gy, respectively. The localization of node failure was categorized as field, marginal, or outside the irradiated field.

RESULTS

A consistent pattern of cervical infiltration was observed in 97% of positive dissections. Lymph node failure occurred within a high-risk irradiated area (CTV1-CTV2) in 12 patients, marginal area (CTV1/CTVO) in 1 patient, and non-irradiated low-risk area (CTV0) in 2 patients. The volume of selective lymph node irradiation was below the standard radiation volume in 33 patients (mean of 118.6 cc per patient). This decrease in irradiated volume was associated with greater treatment compliance and reduced secondary toxicity. The three-year actuarial nodal control rate was 80%.

CONCLUSION

This selective postoperative neck irradiation protocol was associated with a similar failure pattern to that observed after standard neck irradiation and achieved a significant reduction in target volume and secondary toxicity.

摘要

背景

在宫颈癌术后放疗中,靶区通常与先前解剖的扩展范围相同。我们根据每个解剖淋巴结水平的风险评估,评估了一种选择性照射方案。

方法

本前瞻性临床研究纳入了 2005 年至 2008 年间 80 例口腔/口咽癌患者。患者接受原发灶和颈清扫术,识别阳性淋巴结水平,然后进行选择性术后放疗。定义了三种类型的选择性淋巴结临床靶区(CTV):CTV0、CTV1 和 CTV2,亚临床疾病风险分别为<10%、10-25%和 25%,照射剂量分别为<35 Gy、50 Gy 和 66-70 Gy。淋巴结失败的定位分为野内、边缘和照射野外。

结果

97%的阳性清扫术显示出一致的颈内浸润模式。12 例患者的淋巴结失败发生在高风险照射区域(CTV1-CTV2),1 例患者发生在边缘区域(CTV1/CTV0),2 例患者发生在未照射低风险区域(CTV0)。33 例患者的选择性淋巴结照射体积低于标准照射体积(每位患者平均 118.6 cc)。照射体积的减少与更高的治疗依从性和降低的二次毒性相关。三年无瘤生存率为 80%。

结论

这种选择性术后颈部照射方案与标准颈部照射后的失败模式相似,显著减少了靶区体积和二次毒性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46db/3653704/2fca2111d7d8/1748-717X-8-103-1.jpg

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