Evidence map›Paper›PMID 39726705›Full record

ArticleFrontiers in oncology2024

Developing a novel dosiomics model to predict treatment failures following lung stereotactic body radiation therapy.

Ashok Bhandari, Kurtis Johnson, Kyuhak Oh, Fang Yu, Linda M Huynh, Yu Lei, Sarah Wisnoskie, Sumin Zhou, Michael James Baine, Chi Lin and 2 more

Abstract read
In one paragraph

Article in Frontiers in oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Ashok BhandariDepartment of Radiation Oncology, University of Nebraska Medical Center, Omaha, NE, United States.
Kurtis JohnsonDepartment of Radiation Oncology, University of Nebraska Medical Center, Omaha, NE, United States.
Kyuhak OhDepartment of Radiation Oncology, University of Nebraska Medical Center, Omaha, NE, United States.
Fang YuDepartment of Biostatistics, University of Nebraska Medical Center, Omaha, NE, United States.
Linda M HuynhDepartment of Radiation Oncology, University of Nebraska Medical Center, Omaha, NE, United States.
Yu LeiDepartment of Radiation Oncology, University of Nebraska Medical Center, Omaha, NE, United States.
Sarah WisnoskieDepartment of Radiation Oncology, University of Nebraska Medical Center, Omaha, NE, United States.
Sumin ZhouDepartment of Radiation Oncology, University of Nebraska Medical Center, Omaha, NE, United States.
Michael James BaineDepartment of Radiation Oncology, University of Nebraska Medical Center, Omaha, NE, United States.
Chi LinDepartment of Radiation Oncology, University of Nebraska Medical Center, Omaha, NE, United States.
Chi ZhangDepartment of Radiation Oncology, University of Nebraska Medical Center, Omaha, NE, United States.
Shuo WangDepartment of Radiation Oncology, University of Nebraska Medical Center, Omaha, NE, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: The purpose of this study was to investigate the dosiomics features of the interplay between CT density and dose distribution in lung SBRT plans, and to develop a model to predict treatment failure following lung SBRT treatment. Methods: A retrospective study was conducted involving 179 lung cancer patients treated with SBRT at the University of Nebraska Medical Center (UNMC) between October 2007 and June 2022. Features from the CT image, Biological Effective Dose (BED) and five interaction matrices between CT and BED were extracted using radiomics mathematics. Our in-house feature selection pipeline was utilized to evaluate and rank features based on their importance and redundancy, with only the selected non-redundant features being used for predictive modeling. We randomly selected 151 cases and 28 cases as training and test datasets. Four different models were trained utilizing the Balanced Random Forest framework on the same training dataset to differentiate between failure and non-failure cases. These four models utilized the same number of selected features extracted from CT-only, BED-only, a combination of CT and BED, and a composite of CT and BED including their interaction matrices, respectively. Results: The cohort included 125 non-failure cases and 54 failure cases, with a median follow-up time of 34.4 months. We selected the top 17 important and non-redundant features (with the Pearsons's coefficient < 0.5) in each model. When evaluated on the same independent test set, the four models-CT features-only, BED features-only, a combination of CT and BED features, and a composite model including features from CT and BED that includes their interaction matrices-achieved AUC values of 0.56, 0.75, 0.73, and 0.82, respectively, with corresponding accuracies of 0.61, 0.79, 0.71, and 0.79. The composite model demonstrated the highest AUC and accuracy, indicating that incorporating interactions between CT and BED reveals more predictive capabilities in distinguishing between failure and non-failure cases. Conclusion: The dosiomics model integrating the interaction between CT and Dose can effectively predict treatment failure following lung SBRT treatment and may serve as a useful tool to proactively evaluate and select lung SBRT treatment plans to reduce treatment failure in the future.

Indexed as

CT-dose interactiondosiomicslung SBRTmodelingNon-Small Cell Lung Cancer (NSCLC)radiomicstreatment failure

Identifiers

PMID39726705
PMCPMC11669717

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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.