同时综合增强的加速低分割乳腺放疗:可行性研究。

IF 1.8 Q3 ONCOLOGY Radiation Oncology Journal Pub Date : 2022-06-01 Epub Date: 2022-06-20 DOI:10.3857/roj.2021.01053
Budhi Singh Yadav, Shipra Gupta, Divya Dahiya, Ankita Gupta, Arun Singh Oinam
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引用次数: 1

摘要

目的:探讨同步综合增强加速低分割放疗(SIB)治疗乳腺癌的可行性。材料与方法:本研究共纳入27例保乳术后患者。患者在四维计算机断层扫描上进行计划,并根据RTOG指南完成轮廓。乳腺剂量为34 Gy/10#/2周,肿瘤床剂量为40 Gy/10#/2周,采用体积调制电弧技术。主要终点是2级急性皮肤毒性。计算了对处于危险中的器官的剂量。分别采用RTOG/LENT/SOMA和HARVARD/NSABP/RTOG分级量表评估毒性和美容效果。采用Kaplan-Meier曲线计算无病生存期(DFS)和总生存期(OS)。结果:患者平均年龄42岁。左、右乳腺癌患者分别为17例(63%)和10例(37%)。同侧肺V16和对侧肺V5的平均值分别为16.01%和3.74%。左乳房和右乳房的平均心脏剂量分别为7.25 Gy和4.37 Gy。对侧乳房、食道和臂丛Dmax的平均剂量分别为2.64 Gy、3.69 Gy和26.95 Gy。甲状腺V25平均值为19.69%。1级和2级急性皮肤毒性分别为9例(33%)和5例(18.5%)。2级色素沉着、水肿和硬结分别为1例(3.7%)、2例(7.4%)和4例(14.8%)。1例(3.4%)患者报告轻度乳房疼痛和手臂/肩部不适。中位随访时间为51个月(12至61个月)。4年时,1例(3.7%)患者出现乳房硬化、水肿和纤维化。美容效果优良21例(78%),良好6例(22%)。局部复发1例(3.7%),远处转移2例(7.4%)。4年DFS和OS分别为88%和92%。结论:采用该放疗方案,急性和晚期毒性均可接受,无不良美容。本地控制、DFS和OS都很好。
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Accelerated hypofractionated breast radiotherapy with simultaneous integrated boost: a feasibility study.

Purpose: To assess the feasibility of accelerated hypofractionated radiotherapy with simultaneous integrated boost (SIB) in patients with breast cancer.

Materials and methods: A total of 27 patients after breast-conserving surgery were included in this study. Patients were planned on a four-dimensional computerized tomogram, and contouring was done using RTOG guidelines. The dose was 34 Gy/10#/2 week to the breast and 40 Gy/10#/2 week to the tumor bed as SIB with volumetric modulated arc technique. The primary endpoint was grade 2 acute skin toxicity. Doses to the organs-at-risk were calculated. Toxicities and cosmesis were assessed using RTOG/LENT/SOMA and HARVARD/NSABP/RTOG grading scales, respectively. Disease-free survival (DFS) and overall survival (OS) were calculated with Kaplan-Meier curves.

Results: The mean age of the patients was 42 years. Left and right breast cancers were seen in 17 (63%) and 10 (37%) patients, respectively. The mean values of ipsilateral lung V16 and contralateral lung V5 were 16.01% and 3.74%, respectively. The mean heart doses from the left and right breast were 7.25 Gy and 4.37 Gy, respectively. The mean doses to the contralateral breast, oesophagus, and Dmax to brachial plexus were 2.64 Gy, 3.69 Gy, and 26.95 Gy, respectively. The mean value of thyroid V25 was 19.69%. Grade 1 and 2 acute skin toxicities were observed in 9 (33%) and 5 (18.5%) patients, respectively. Grade 2 hyperpigmentation, edema, and induration were observed in 1 (3.7%), 2 (7.4%), and 4 (14.8%) patients, respectively. Mild breast pain and arm/shoulder discomfort were reported by 1 (3.4%) patient. The median follow-up was 51 months (range, 12 to 61 months). At four years, breast induration, edema, and fibrosis were observed in 1 (3.7%) patient. Cosmesis was excellent and good in 21 (78%) and 6 (22%) patients, respectively. Local recurrence and distant metastases occurred in 1 (3.7%) and 2 (7.4%) patients, respectively. DFS and OS at four years were 88% and 92%, respectively.

Conclusion: With this radiotherapy schedule, acute and late toxicity rates were acceptable with no adverse cosmesis. Local control, DFS, and OS were good.

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