Evidence mapPaperPMID 42467205Full record

ArticleStrahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft ... [et al]2026

Clinical target volume radiomics from planning CT for pretreatment response prediction  in rectal cancer undergoing chemoradiotherapy.

Yen-Cho Huang, Shih-Ming Huang, Jih-Hsiang Yeh, Shu-Ju Tu

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Article in Strahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft ... [et al], 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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5 · Who and what money

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4 authors.

Yen-Cho HuangDepartment of Radiation Oncology, Keelung Chang Gung Memorial Hospital, 20445, Keelung, Taiwan.ORCID http://orcid.org/0009-0007-7905-4958
Shih-Ming HuangDepartment of Radiation Oncology, Keelung Chang Gung Memorial Hospital, 20445, Keelung, Taiwan.
Jih-Hsiang YehDepartment of Radiation Oncology, Keelung Chang Gung Memorial Hospital, 20445, Keelung, Taiwan.
Shu-Ju TuDepartment of Medical Imaging and Radiological Sciences, College of Medicine, Chang Gung University, 33302, Taoyuan, Taiwan. sjtu@mail.cgu.edu.tw.ORCID http://orcid.org/0000-0003-2545-1062

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeResponse to neoadjuvant chemoradiotherapy (nCRT) in rectal cancer remains heterogeneous. This exploratory study evaluated whether radiomics features extracted from the clinical target volume (CTV) on pretreatment non-contrast radiotherapy planning CT could provide additional information for pretreatment prediction of poor treatment response.

methodsThis retrospective single-center study included 60 patients with rectal cancer treated with nCRT between 2008 and 2024, including 50 good responders and 10 poor responders. A total of 1148 radiomics features were extracted from the original pretreatment treatment-planning CTV and combined with clinical variables, including age, sex, cT stage, cN stage, log-transformed carcinoembryonic antigen, and tumor-to-anal verge distance. Models were internally evaluated using repeated nested cross-validation with fold-wise ComBat harmonization. Performance was assessed from pooled repeated out-of-fold predictions, including discrimination, apparent calibration, exploratory threshold-based operating characteristics, and decision curve analysis.

resultsThe best-performing combined clinical-radiomics model was Extra Trees, with an area under the receiver operating characteristic curve of 0.754 (95% confidence interval [CI], 0.713-0.789), compared with 0.507 for the clinical-only model. At a post hoc sensitivity-prioritized operating threshold, the combined Extra Trees model achieved sensitivity of 0.94 (95% CI, 0.89-0.98), specificity of 0.47 (95% CI, 0.42-0.51), and negative predictive value of 0.98 in pooled repeated out-of-fold analysis. Decision curve analysis suggested potential net benefit across low-to-moderate threshold probabilities in internal analysis.

conclusionClinical target volume-based radiomics from routine pretreatment non-contrast planning CT may provide exploratory information for prediction of poor response to nCRT in rectal cancer. Because treatment-planning CTVs are routinely generated before radiotherapy, this workflow may be practical for radiotherapy-based research. The findings are hypothesis generating and require external validation before clinical use.

Indexed as

Clinical target volumeCT radiomicsDecision curve analysisMachine learningNeoadjuvant chemoradiotherapyRectal cancer

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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 Socratic graph.