Multi‐collimator proton minibeam radiotherapy with joint dose and PVDR optimization

剂量学 放射治疗 准直器 医学物理学 接头(建筑物) 质子疗法 医学影像学 核医学 质子 辐射剂量 医学 物理 放射科 光学 核物理学 工程类 建筑工程
作者
Weijie Zhang,Hong Xue,Wei Wu,Chao Wang,Daniel E. Johnson,Gregory N. Gan,Yuting Lin,Hao Gao
出处
期刊:Medical Physics [Wiley]
卷期号:52 (2): 1182-1192
标识
DOI:10.1002/mp.17548
摘要

The clinical translation of proton minibeam radiation therapy (pMBRT) presents significant challenges, particularly in developing an optimal treatment planning technique. A uniform target dose is crucial for maximizing anti-tumor efficacy and facilitating the clinical acceptance of pMBRT. However, achieving a high peak-to-valley dose ratio (PVDR) in organs-at-risk (OAR) is essential for sparing normal tissue. This balance becomes particularly difficult when OARs are located distal to the beam entrance or require patient-specific collimators. This work proposes a novel pMBRT treatment planning method that can achieve high PVDR at OAR and uniform dose at target simultaneously, via multi-collimator pMBRT (MC-pMBRT) treatment planning method with joint dose and PVDR optimization (JDPO). MC-pMBRT utilizes a set of generic and premade multi-slit collimators with different center-to-center distances and does not need patient-specific collimators. The collimator selection per field is OAR-specific and tailored to maximize PVDR in OARs while preserving target dose uniformity. Then, the inverse optimization method JDPO is utilized to jointly optimize target dose uniformity, PVDR, and other dose-volume-histogram based dose objectives, which is solved by iterative convex relaxation optimization algorithm and alternating direction method of multipliers. The need and efficacy of MC-pMBRT is demonstrated by comparing the single-collimator (SC) approach with the multi-collimator (MC) approach. While SC degraded either PVDR for OAR or dose uniformity for the target, MC provided a good balance of PVDR and target dose uniformity. The proposed JDPO method is validated in comparison with the dose-only optimization (DO) method for MC-pMBRT, in reference to the conventional (CONV) proton RT (no pMBRT). Compared to CONV, MC-pMBRT (DO and JDPO) preserved target dose uniformity and plan quality, while providing unique PVDR in OAR. Compared to DO, JDPO further improved PVDR via PVDR optimization during treatment planning. A novel pMBRT treatment planning method called MC-pMBRT is proposed that utilizes a set of generic and premade collimators with joint dose and PVDR optimization algorithm to optimize OAR-specific PVDR and target dose uniformity simultaneously.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
PDF的下载单位、IP信息已删除 (2025-6-4)

科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
wei发布了新的文献求助10
1秒前
Fqdgest完成签到,获得积分10
2秒前
3秒前
叮叮车完成签到,获得积分10
3秒前
完美世界应助明杰采纳,获得10
3秒前
善学以致用应助牛牛眉目采纳,获得10
5秒前
希望天下0贩的0应助Cynicism采纳,获得10
5秒前
6秒前
J33发布了新的文献求助10
8秒前
xr发布了新的文献求助10
9秒前
10秒前
11秒前
11秒前
张航发布了新的文献求助10
12秒前
Lucas应助科研鸟采纳,获得10
12秒前
可爱的函函应助叮叮车采纳,获得10
12秒前
12秒前
12秒前
14秒前
14秒前
15秒前
15秒前
优雅的化蛹完成签到,获得积分10
16秒前
16秒前
Whisper发布了新的文献求助10
17秒前
fanli发布了新的文献求助10
17秒前
17秒前
健忘飞风完成签到,获得积分10
20秒前
Cynicism发布了新的文献求助10
21秒前
明杰完成签到,获得积分10
21秒前
Aries完成签到 ,获得积分10
21秒前
houcheng发布了新的文献求助10
21秒前
21秒前
张航完成签到,获得积分10
25秒前
干饭大王应助2023204306324采纳,获得10
25秒前
J33完成签到,获得积分10
26秒前
ding应助houcheng采纳,获得10
28秒前
28秒前
29秒前
wei完成签到,获得积分10
29秒前
高分求助中
A new approach to the extrapolation of accelerated life test data 1000
Cognitive Neuroscience: The Biology of the Mind 1000
Technical Brochure TB 814: LPIT applications in HV gas insulated switchgear 1000
Immigrant Incorporation in East Asian Democracies 500
Nucleophilic substitution in azasydnone-modified dinitroanisoles 500
不知道标题是什么 500
A Preliminary Study on Correlation Between Independent Components of Facial Thermal Images and Subjective Assessment of Chronic Stress 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 生物化学 物理 内科学 纳米技术 计算机科学 化学工程 复合材料 遗传学 基因 物理化学 催化作用 冶金 细胞生物学 免疫学
热门帖子
关注 科研通微信公众号,转发送积分 3966370
求助须知:如何正确求助?哪些是违规求助? 3511789
关于积分的说明 11159900
捐赠科研通 3246400
什么是DOI,文献DOI怎么找? 1793416
邀请新用户注册赠送积分活动 874427
科研通“疑难数据库(出版商)”最低求助积分说明 804388