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首页> 外文期刊>International Journal of Radiation Oncology, Biology, Physics >Parametrial boost using midline shielding results in an unpredictable dose to tumor and organs at risk in combined external beam radiotherapy and brachytherapy for locally advanced cervical cancer.
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Parametrial boost using midline shielding results in an unpredictable dose to tumor and organs at risk in combined external beam radiotherapy and brachytherapy for locally advanced cervical cancer.

机译:使用中线屏蔽进行子宫内膜增强术会导致局部晚期宫颈癌的联合外照射治疗和近距离放射治疗给处于危险中的肿瘤和器官带来不可预测的剂量。

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PURPOSE: Midline-blocked boost (MBB) fields are frequently used in the treatment of locally advanced cervical cancer. The purpose of this study was to evaluate the dose contribution from MBBs to tumor and organs at risk. METHODS AND MATERIALS: Six patients with locally advanced cervical cancer (IIB-IIIB) treated with definitive chemoradiotherapy and magnetic resonance imaging (MRI)-guided brachytherapy were analyzed. A three-phase plan was modeled: 45 Gy (1.8 Gy per fraction) four-field box, 9 Gy (1.8 Gy per fraction) MBB (midline-shielded anteroposterior/posteroanterior fields), and intracavitary MRI-guided brachytherapy boost of 28 Gy (7 Gy per fraction). Midline shields 3, 4, and 5 cm wide were simulated for each patient. Brachytherapy and MBB plans were volumetrically summed. The rectum, sigmoid, and bladder minimum dose in the most exposed 2 cm(3) of an organ at risk (D(2 cc)) and high-risk clinical target volume (HR-CTV) and intermediate-risk clinical target volume (IR-CTV) D90 and D100 were evaluated. The intended HR-CTV D90 was 85 Gy or greater, and the intended IR-CTV D90 was greater than 60 Gy. RESULTS: After a 4-cm MBB, HR-CTV D90 remained lower than 85 Gy in all cases (mean, 74 Gy; range, 64-82 Gy). High-risk clinical target volume (85 Gy) coverage increased slightly from 73% (range, 64-82%) to 78% (range, 69-88%). Mean IR-CTV D90 increased from 56 Gy (range, 53-64 Gy) to 62 Gy (range, 59-67 Gy). Intermediate-risk clinical target volume 60-Gy dose coverage increased from 81% (range, 72-96%) to 96% (range, 90-100%). The mean volume irradiated to 85 Gy increased by 14 cm(3) (range, 10-22 cm(3)), whereas the volume irradiated to 60 Gy increased from 276 cm(3) (range, 185-417 cm(3)) to 592 cm(3) (range, 385-807 cm(3)). Bladder, rectum, or sigmoid D(2 cc) increased by more than 50% of the boost dose in 4 of 6 patients. CONCLUSIONS: Midline-blocked boosts contribute substantial dose to rectum, sigmoid, and bladder D(2 cc). HR-CTV dose and 85-Gy coverage remain compromised in large tumors despite MBB. IR-CTV 60-Gy coverage improved at the expense of a considerable increase in volume of normal tissue irradiated to 60 Gy.
机译:目的:中线阻断增强(MBB)领域经常用于治疗局部晚期宫颈癌。这项研究的目的是评估MBB对有风险的肿瘤和器官的剂量贡献。方法和材料:分析了6例接受了明确放化疗和磁共振成像(MRI)引导的近距离放射治疗的局部晚期宫颈癌(IIB-IIIB)患者。建模了一个三阶段计划:45 Gy(每部分1.8 Gy)四视野盒,9 Gy(每部分1.8 Gy)MBB(中线屏蔽前后/后前视野)和腔内MRI引导的近距离放疗提高28 Gy (每部分7 Gy)。为每位患者模拟了3、4和5厘米宽的中线护罩。近距离治疗和MBB计划进行了体积汇总。处于风险的器官中最暴露的2 cm(3)中的直肠,乙状结肠和膀胱的最低剂量(D(2 cc))和高风险的临床目标体积(HR-CTV)和中等风险的临床目标体积(评估了IR-CTV D90和D100。预期的HR-CTV D90为85 Gy或更大,而预期的IR-CTV D90大于60 Gy。结果:在4 cm MBB之后,HR-CTV D90在所有情况下均保持低于85 Gy(平均74 Gy;范围64-82 Gy)。高风险临床目标量(85 Gy)覆盖率从73%(范围64-82%)略增至78%(范围69-88%)。平均IR-CTV D90从56 Gy(范围53-64 Gy)增加到62 Gy(范围59-67 Gy)。中度风险临床目标量60-Gy剂量覆盖率从81%(范围72-96%)增加到96%(范围90-100%)。辐照到85 Gy的平均体积增加了14 cm(3)(范围10-22 cm(3)),而辐照到60 Gy的平均体积从276 cm(3)(范围185-417 cm(3))增加了)至592 cm(3)(范围385-807 cm(3))。 6例患者中有4例的膀胱,直肠或乙状结肠D(2 cc)增加了增强剂量的50%以上。结论:中线受阻的助推器对直肠,乙状结肠和膀胱D(2 cc)的贡献很大。尽管有MBB,在大肿瘤中HR-CTV剂量和85-Gy覆盖率仍然受到损害。 IR-CTV 60-Gy的覆盖率得到改善,但以60 Gy照射的正常组织体积显着增加为代价。

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