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Dosimetric evaluation of accelerated partial breast irradiation (APBI) using volumetric modulated arc therapy (VMAT) technique 使用体积调制电弧治疗(VMAT)技术的加速部分乳房照射(APBI)的剂量学评价
Pub Date : 2023-09-20 DOI: 10.15406/ijrrt.2023.10.00363
Jean L Peng, Daniel G McDonald, Lisa M Warwick, Jennifer L Harper
Purpose: Five-fraction radiation therapy treatment regimens for accelerated partial breast irradiation (APBI) using intensity modulated radiotherapy (IMRT) have become increasingly used after several phase three trials demonstrated similar or reduced toxicity compared with whole breast irradiation. Improving the treatment efficiency of this technique could significantly improve delivery accuracy and tolerability, especially for treatment plans utilizing deep inspiration breath hold (DIBH) technique. The aim of this study was to determine the optimal technique for APBI, with a focus on volumetric modulated arc therapy technique (VMAT) and flattening-filter free (FFF) delivery. Methods: Ten APBI cases, five cases each left and right breast, were randomly selected. Each case was contoured following guidelines included in the APBI-IMRT-Florence Trial and planned to use both non-coplanar static-field IMRT with standard flattened-filter (FF) beam and VMAT techniques with both FF and FFF beam. For each VMAT plan, two partial arcs were used with patient-specific start and stop angles. Arc extents emulated opposed tangential fields and were chosen based on target and organ at risk (OAR) locations. Evaluated OARs included the heart, ipsilateral and contralateral lung, and normal breast. All plans were generated using the Eclipse treatment planning system (Version 15.6). A prescription dose of 30Gy delivered in 5 fractions was used for all cases. Plans were compared and evaluated using several dose metrics as well as treatment time. Results: For targets, VMAT exhibited similar coverage (V95%) but higher Dmax compared to IMRT (105% (IMRT) v.s .111% (VMAT), p=0.002. VMAT provided similar OAR avoidance compared to IMRT for the heart (Dmean, V3Gy, V0.5Gy), ipsilateral lung (V10Gy), contralateral lung (V5Gy) and contralateral breast Dmax within 10cGy/2% (p~0.005). VMAT contributed slightly lower dose outside the target in the ipsilateral breast, with an average difference in V15Gy of approximately 8% (37% (IMRT) v.s. 29% (VMAT)). Finally, because IMRT delivery is non-coplanar, and typically requires at least 5 treatment fields, co-planar VMAT reduced the total treatment significantly. VMAT with FF beam energies also used fewer monitor unites compared to IMRT with FF beam energies. The utilization of FFF beam energies for VMAT further improved delivery time compared to IMRT. Overall, VMAT with FFF beam energies reduced treatment time by approximately 20% compared to IMRT with FF beam. Conclusions: Co-planar partial-arc FFF VMAT technique produced equivalent target coverage, improved efficiency, better normal tissue sparing, and shorter delivery time compared to non-coplanar IMRT technique. Shorter delivery time also assists in the reduction of patient motion associated with breath hold. VMAT technique with FFF delivery is a suitable replacement for IMRT in APBI.
目的:使用调强放疗(IMRT)加速部分乳房照射(APBI)的五段式放疗治疗方案已被越来越多地使用,因为几项三期试验表明与全乳房照射相比毒性相似或更低。提高该技术的治疗效率可以显著提高输送精度和耐受性,特别是对于使用深度吸气屏气(DIBH)技术的治疗方案。本研究的目的是确定APBI的最佳技术,重点是体积调制电弧治疗技术(VMAT)和无平坦滤波器(FFF)输送。方法:随机选取10例APBI患者,左、右乳腺各5例。每个病例都按照APBI-IMRT-Florence试验中的指导方针进行轮廓,并计划使用标准平坦滤波(FF)光束的非共面静场IMRT和FF和FFF光束的VMAT技术。对于每个VMAT计划,使用两个具有特定患者起始和停止角度的部分弧线。弧度模拟对切场,并根据靶和危险器官(OAR)的位置选择。评估的OARs包括心脏、同侧和对侧肺以及正常乳房。所有计划都是使用Eclipse治疗计划系统(Version 15.6)生成的。所有病例均采用处方剂量30Gy分5次给药。使用几种剂量指标和治疗时间对计划进行比较和评估。结果:对于靶标,VMAT与IMRT相比具有相似的覆盖率(V95%),但Dmax更高(105% (IMRT) vs .111% (VMAT), p=0.002。与IMRT相比,VMAT对心脏(Dmean, V3Gy, V0.5Gy)、同侧肺(V10Gy)、对侧肺(V5Gy)和对侧乳房的Dmax均在10cGy/2%以内(p~0.005)。VMAT对同侧乳房靶区外的剂量贡献略低,V15Gy的平均差异约为8% (IMRT为37%,VMAT为29%)。最后,由于IMRT递送是非共面的,通常需要至少5个治疗场,共面VMAT显著减少了总治疗。与具有FF束能量的IMRT相比,具有FF束能量的VMAT使用的监测单元也更少。与IMRT相比,FFF束流能量在VMAT中的利用进一步提高了传输时间。总的来说,与FF束的IMRT相比,FFF束能量的VMAT减少了大约20%的治疗时间。结论:与非共面IMRT技术相比,共面部分弧FFF VMAT技术具有相同的靶覆盖范围,提高了效率,更好地保留了正常组织,并且缩短了递送时间。更短的分娩时间也有助于减少与屏气相关的患者运动。VMAT技术与FFF交付是APBI中IMRT的合适替代。
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引用次数: 0
Stereotactic ablative radiotherapy for stage I lung cancer: a retrospective single institution report in Western Australia 立体定向消融放疗治疗I期肺癌:西澳大利亚单一机构的回顾性报告
Pub Date : 2023-05-02 DOI: 10.15406/ijrrt.2023.10.00352
Caris Chong, Hendrick Tan, Cherie Vaz, Susan Mincham, Eugene Leong, Max Hoffman, Tee Lim
Objectives: Stereotactic ablative radiotherapy (SABR) is now standard management of stage I non-small cell lung cancer in patients who are not medically operable. The purpose of this study was to assess clinical outcomes in our single institution to review comparability with worldwide outcomes. Methods: The institutional database was screened for all patients with Stage I NSCLC treated in between September 2010 to November 2018 with SABR. Local control was defined on PET/CT or CT imaging and survival status retrieved from electronic medical records. Overall survival and local control were calculated using Kaplan-Meier method. Results: 93 patients were treated with SBRT for stage I NSCLC. Median follow up time was 30 months (range 1-99 months). Overall survival was 67% and local control was 91% at 3 years respectively. Toxicity included grade 1-2 pneumonitis (16.5%), chest wall pain (3.3%) and rib fracture (2.1%) Conclusion: In our local institution SABR for Stage I NSCLC is a safe and effective form of management of medically inoperable patients.
目的:立体定向消融放疗(SABR)是目前不能手术治疗的I期非小细胞肺癌患者的标准治疗方法。本研究的目的是评估我们单一机构的临床结果,以审查与全球结果的可比性。方法:筛选2010年9月至2018年11月期间接受SABR治疗的所有I期NSCLC患者的机构数据库。通过PET/CT或CT成像确定局部控制,并从电子病历中检索生存状态。采用Kaplan-Meier法计算总生存率和局部控制率。结果:93例I期NSCLC患者接受SBRT治疗。中位随访时间为30个月(范围1-99个月)。3年总生存率为67%,局部控制率为91%。毒性包括1-2级肺炎(16.5%)、胸壁疼痛(3.3%)和肋骨骨折(2.1%)。结论:在我们当地机构,SABR治疗I期非小细胞肺癌是一种安全有效的治疗方法。
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引用次数: 0
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International journal of radiology & radiation therapy
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