Evidence map›Paper›PMID 38734989›Full record

ArticleMedical physics2024

A novel method for rapid estimation of active bone marrow dose for radiotherapy patients in epidemiological studies.

Yeon Soo Yeom, Lior Braunstein, Lindsay M Morton, Kelly L Bolton, Ji Won Choi, Hyeong Yun Choi, Natasha Greenstein, Choonsik Lee

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Article in Medical physics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1 · What the graph read from it

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3 · Its place in the literature

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Yeon Soo YeomDepartment of Radiation Convergence Engineering, Yonsei University, Wonju, Gangwon, Republic of Korea.
Lior BraunsteinDepartment of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Lindsay M MortonDivision of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Rockville, Maryland, USA.
Kelly L BoltonDepartment of Medicine, Washington University School of Medicine, St. Louis, Missouri, USA.
Ji Won ChoiDepartment of Radiation Convergence Engineering, Yonsei University, Wonju, Gangwon, Republic of Korea.
Hyeong Yun ChoiDivision of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Rockville, Maryland, USA.
Natasha GreensteinDepartment of Physics, Princeton University, Princeton, New Jersey, USA.
Choonsik LeeDivision of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Rockville, Maryland, USA.

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Impact of Oncologic Therapy on Clonal Hematopoiesis and Subsequent Risk of Therapy-Related LeukemiaK08CA241318 · NCI · WASHINGTON UNIVERSITY · PI BOLTON, KELLY LEIGH · 2019 to 2023
$1.2M
Korea Institute of Energy Technology Evaluation and Planning (KETEP) and the Ministry of Trade, Industry & Energy 20214000000070Ministry of Education 2022RIS-005National Research Foundation of Korea 2022R1C1C100809312NCI NIH HHS P30 CA008748NIH HHS
6 · The paper itself

Abstract

backgroundIn a dedicated effort to improve the assessment of clonal hematopoiesis (CH) and study leukemia risk following radiotherapy, we are developing a large-scale cohort study among cancer patients who received radiation. To that end, it will be critical to analyze dosimetric parameters of red bone marrow (ABM) exposure in relation to CH and its progression to myeloid neoplasms, requiring reconstruction method for ABM doses of a large-scale patients rapidly and accurately. PURPOSE: To support a large-scale cohort study on the assessment of clonal hematopoiesis and leukemia risk following radiotherapy, we present a new method for the rapid reconstruction of ABM doses of radiotherapy among cancer patients.

methodsThe key idea of the presented method is to segment patient bones rapidly and automatically by matching a whole-body computational human phantom, in which the skeletal system is divided into 34 bone sites, to patient CT images via 3D skeletal registration. The automatic approach was used to segment site-specific bones for 40 radiotherapy patients. Also, we segmented the bones manually. The bones segmented both manually and automatically were then combined with the patient dose matrix calculated by the treatment planning system (TPS) to derive patient ABM dose. We evaluated the performance of the automatic method in geometric and dosimetric accuracy by comparison with the manual approach.

resultsThe pelvis showed the best geometric performance [volume overlap fraction (VOF): 52% (mean) with 23% (σ) and average distance (AD): 0.8 cm (mean) with 0.5 cm (σ)]. The pelvis also showed the best dosimetry performance [absorbed dose difference (ADD): 0.7 Gy (mean) with 1.0 Gy (σ)]. Some bones showed unsatisfactory performances such as the cervical vertebrae [ADD: 5.2 Gy (mean) with 10.8 Gy (σ)]. This impact on the total ABM dose, however, was not significant. An excellent agreement for the total ABM dose was indeed observed [ADD: 0.4 Gy (mean) with 0.4 Gy (σ)]. The computation time required for dose calculation using our method was robust (about one minute per patient).

conclusionsWe confirmed that our method estimates ABM doses across treatment sites accurately, while providing high computational efficiency. The method will be used to reconstruct patient-specific ABM doses for dose-response assessment in a large cohort study. The method can also be applied to prospective dose calculation within a clinical TPS to support clinical decision making at the point of care.

Indexed as

Bone MarrowRadiotherapy DosageEpidemiologic StudiesHumansPhantoms, ImagingRadiation DosageRadiometryRadiotherapy Planning, Computer-AssistedTime FactorsTomography, X-Ray Computedactive bone marrow dosecomputational human phantomradiotherapy

Identifiers

PMID38734989
PMCPMC12167658

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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.