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调强放疗治疗妇科癌症后para-aortic 淋巴结时,十二指肠毒性的剂量学预测因子。

Dosimetric predictors of duodenal toxicity after intensity modulated radiation therapy for treatment of the para-aortic nodes in gynecologic cancer.

机构信息

Department of Radiation Oncology, University of Miami Miller School of Medicine, Miami, Florida.

Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

出版信息

Int J Radiat Oncol Biol Phys. 2014 Feb 1;88(2):357-62. doi: 10.1016/j.ijrobp.2013.09.053.

Abstract

PURPOSE

To determine the incidence of duodenal toxicity in patients receiving intensity modulated radiation therapy (IMRT) for treatment of para-aortic nodes and to identify dosimetric parameters predictive of late duodenal toxicity.

METHODS AND MATERIALS

We identified 105 eligible patients with gynecologic malignancies who were treated with IMRT for gross metastatic disease in the para-aortic nodes from January 1, 2005, through December 31, 2009. Patients were treated to a nodal clinical target volume to 45 to 50.4 Gy with a boost to 60 to 66 Gy. The duodenum was contoured, and dosimetric data were exported for analysis. Duodenal toxicity was scored according to Radiation Therapy Oncology Group criteria. Univariate Cox proportional hazards analysis and recursive partitioning analysis were used to determine associations between dosimetric variables and time to toxicity and to identify the optimal threshold that separated patients according to risk of toxicity.

RESULTS

Nine of the 105 patients experienced grade 2 to grade 5 duodenal toxicity, confirmed by endoscopy in all cases. The 3-year actuarial rate of any duodenal toxicity was 11.7%. A larger volume of the duodenum receiving 55 Gy (V55) was associated with higher rates of duodenal toxicity. The 3-year actuarial rates of duodenal toxicity with V55 above and below 15 cm(3) were 48.6% and 7.4%, respectively (P<.01). In Cox univariate analysis of dosimetric variables, V55 was associated with duodenal toxicity (P=.029). In recursive partitioning analysis, V55 less than 13.94% segregated all patients with duodenal toxicity.

CONCLUSIONS

Dose-escalated IMRT can safely and effectively treat para-aortic nodal disease in gynecologic malignancies, provided that care is taken to limit the dose to the duodenum to reduce the risk of late duodenal toxicity. Limiting V55 to below 15 cm(3) may reduce the risk of duodenal complications. In cases where the treatment cannot be delivered within these constraints, consideration should be given to other treatment approaches such as resection or initial chemotherapy.

摘要

目的

确定接受调强放疗(IMRT)治疗腹主动脉旁淋巴结的患者发生十二指肠毒性的发生率,并确定预测晚期十二指肠毒性的剂量学参数。

方法和材料

我们从 2005 年 1 月 1 日至 2009 年 12 月 31 日,共确定了 105 名患有妇科恶性肿瘤的合格患者,这些患者因腹主动脉旁淋巴结的广泛转移性疾病接受了 IMRT 治疗。患者接受了淋巴结临床靶区 45 至 50.4 Gy 的照射,并对 60 至 66 Gy 进行了加量照射。对十二指肠进行了轮廓勾画,并导出剂量学数据进行分析。根据放射治疗肿瘤学组( Radiation Therapy Oncology Group )的标准对十二指肠毒性进行评分。使用单变量 Cox 比例风险分析和递归分区分析来确定剂量学变量与毒性时间之间的关联,并确定根据毒性风险对患者进行分类的最佳阈值。

结果

105 名患者中有 9 名(8.6%)经内镜证实发生了 2 至 5 级的十二指肠毒性。3 年的任何十二指肠毒性发生率为 11.7%。十二指肠接受 55 Gy(V55)的体积越大,发生十二指肠毒性的几率越高。V55 大于和小于 15 cm3 的 3 年十二指肠毒性发生率分别为 48.6%和 7.4%(P<.01)。在剂量学变量的单变量 Cox 分析中,V55 与十二指肠毒性相关(P=.029)。在递归分区分析中,V55 小于 13.94% 可将所有发生十二指肠毒性的患者分开。

结论

剂量递增的 IMRT 可以安全有效地治疗妇科恶性肿瘤的腹主动脉旁淋巴结疾病,前提是要注意将十二指肠的剂量限制在可降低晚期十二指肠毒性风险的范围内。将 V55 限制在 15 cm3 以下可能会降低十二指肠并发症的风险。在无法在这些限制范围内进行治疗的情况下,应考虑其他治疗方法,如切除术或初始化疗。

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