Evidence map›Paper›PMID 42358281›Full record

ArticlePrecision radiation oncology2026

Dosimetric comparison of lattice radiotherapy across three modern linear accelerator platforms.

Shijun Li, Qingliang Pang, Bo Li, Jun Lv, Zhuxin Wei, Dawei Zhang, Wen Qin

Abstract read
In one paragraph

Article in Precision radiation oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Shijun LiDepartment of Radiation Oncology The First Affiliated Hospital of Guangxi Medical University Nanning Guangxi China.ORCID https://orcid.org/0009-0001-5887-7775
Qingliang PangHengzhou People's Hospital Nanning Guangxi China.
Bo LiDepartment of Radiation Oncology The First Affiliated Hospital of Guangxi Medical University Nanning Guangxi China.
Jun LvDepartment of Radiation Oncology The First Affiliated Hospital of Guangxi Medical University Nanning Guangxi China.
Zhuxin WeiDepartment of Radiation Oncology The First Affiliated Hospital of Guangxi Medical University Nanning Guangxi China.
Dawei ZhangDepartment of Radiation Oncology The First Affiliated Hospital of Guangxi Medical University Nanning Guangxi China.
Wen QinDepartment of Radiation Oncology The First Affiliated Hospital of Guangxi Medical University Nanning Guangxi China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: This study aimed to compare the dosimetric characteristics of lattice radiotherapy across different linear accelerator platforms (Versa HD, Halcyon, and NeuRT Aurora) and to evaluate the feasibility of its clinical application. Methods: This study included ten patients with bulky tumors who were eligible for spatially fractionated radiotherapy, including five pelvic cases and five abdominal cases. For each patient, high-dose vertices were contoured within the gross tumor volume using a standardized method, followed by three independently designed treatment plans on the Versa HD, Halcyon, and NeuRT Aurora platforms. The prescribed dose was 2400 cGy in three fractions. Dosimetric evaluation of the target volume included vertex coverage, maximum dose, and the peak-to-valley dose ratio. In addition, a vertex-specific dose analysis was performed to quantify the number of vertices with a D95 of less than 2400 cGy. For organs at risk, the following dosimetric parameters were evaluated: the mean dose to the intra-lattice margin volume, the maximum dose to tissues located more than 2 cm from the vertices, and standard dosimetric parameters for the spinal cord, small bowel, colon, liver, stomach, lungs, and kidneys. Results: All plans demonstrated the characteristic dosimetric features of lattice radiotherapy by establishing alternating high-dose peaks and low-dose valleys within the target volume, while achieving effective protection of surrounding normal tissues without compromising target coverage. Among the three platforms, NeuRT Aurora demonstrated superior performance in dose gradient control and normal tissue protection. The mean peak-to-valley ratios were 6.4, 6.9, and 8.9 for the Versa HD, Halcyon, and NeuRT Aurora platforms, respectively. The maximum dose to tissues located more than 2 cm from the vertices was significantly lower in the NeuRT Aurora plans (1158.6 cGy) than in the Versa HD plans (1280.6 cGy) and Halcyon plans (1257.8 cGy). Consistent with this trend, the NeuRT Aurora plans were also associated with a lower mean dose to the intra-lattice margin volume (792.4 cGy) than the Versa HD (831.4 cGy) and Halcyon (845.7 cGy) plans. For all specific organs at risk, the evaluated dosimetric parameters remained within clinical tolerance limits across the three treatment platforms. Conclusions: This study systematically evaluated lattice radiotherapy plans across three accelerator platforms. Although differences were observed in peak-to-valley ratios and organ-at-risk sparing, all plans met clinical requirements, confirming the overall feasibility of each platform.

Indexed as

dosimetrylattice radiotherapyspatially fractionated radiotherapy

Identifiers

PMID42358281
PMCPMC13292149

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.