首页> 外文期刊>Medical dosimetry: official journal of the American Association of Medical Dosimetrists >Comparative dosimetric and radiobiological assessment among a nonstandard RapidArc, standard RapidArc, classical intensity-modulated radiotherapy, and 3D brachytherapy for the treatment of the vaginal vault in patients affected by gynecologic cancer
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Comparative dosimetric and radiobiological assessment among a nonstandard RapidArc, standard RapidArc, classical intensity-modulated radiotherapy, and 3D brachytherapy for the treatment of the vaginal vault in patients affected by gynecologic cancer

机译:非标准RapidArc,标准RapidArc,经典强度调制放射疗法和3D近距离放射疗法对妇科癌症患者阴道穹ault的剂量和放射生物学评估

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摘要

To evaluate a nonstandard RapidArc (RA) modality as alternative to high-dose-rate brachytherapy (HDR-BRT) or IMRT treatments of the vaginal vault in patients with gynecological cancer (GC). Nonstandard (with vaginal applicator) and standard (without vaginal applicator) RapidArc plans for 27 women with GC were developed to compare with HDR-BRT and IMRT. Dosimetric and radiobiological comparison were performed by means of dose-volume histogram and equivalent uniform dose (EUD) for planning target volume (PTV) and organs at risk (OARs). In addition, the integral dose and the overall treatment times were evaluated. RA, as well as IMRT, results in a high uniform dose on PTV compared with HDR-BRT. However, the average of EUD for HDR-BRT was significantly higher than those with RA and IMRT. With respect to the OARs, standard RA was equivalent of IMRT but inferior to HDR-BRT. Furthermore, nonstandard RA was comparable with IMRT for bladder and sigmoid and better than HDR-BRT for the rectum because of a significant reduction of d 2cc, d 1cc, and d max (p 0.01). Integral doses were always higher than HDR-BRT, although the values were very low. Delivery times were about the same and more than double for HDR-BRT compared with IMRT and RA, respectively. In conclusion, the boost of dose on vaginal vault in patients affected by GC delivered by a nonstandard RA technique was a reasonable alternative to the conventional HDR-BRT because of a reduction of delivery time and rectal dose at substantial comparable doses for the bladder and sigmoid. However HDR-BRT provides better performance in terms of PTV coverage as evidenced by a greater EUD.
机译:评估非标准的RapidArc(RA)方式,以替代高剂量率近距离放射疗法(HDR-BRT)或IMRT对妇科癌症(GC)患者的阴道穹ault进行治疗。制定了针对27名患有GC的女性的非标准(带阴道涂抹器)和标准(不带阴道涂抹器)RapidArc计划,以与HDR-BRT和IMRT进行比较。通过剂量体积直方图和等效均匀剂量(EUD)进行剂量和放射生物学比较,以规划目标体积(PTV)和高危器官(OAR)。另外,评估了积分剂量和总治疗时间。与HDR-BRT相比,RA和IMRT在PTV上产生了较高的均匀剂量。但是,HDR-BRT的EUD平均值明显高于RA和IMRT。对于OAR,标准RA等同于IMRT,但不如HDR-BRT。此外,由于d 2cc,d 1cc和d max显着降低,因此非标准RA在膀胱和乙状结肠方面与IMRT相当,并且在直肠方面优于HDR-BRT(p <0.01)。积分剂量始终高于HDR-BRT,尽管该值非常低。与IMRT和RA相比,HDR-BRT的交付时间大约相同,并且是后者的两倍以上。总之,通过非标准RA技术输送的受GC影响的患者,阴道穹顶剂量的增加是常规HDR-BRT的合理替代方案,因为在与膀胱和乙状结肠相当的剂量下,输送时间和直肠剂量减少了。然而,HDR-BRT在PTV覆盖方面提供了更好的性能,这由更大的EUD所证明。

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