Evidence map›Paper›PMID 38125298›Full record

ArticleComputational and structural biotechnology journal2024

Cluster-based radiomics reveal spatial heterogeneity of bevacizumab response for treatment of radiotherapy-induced cerebral necrosis.

Hong Qi Tan, Jinhua Cai, Shi Hui Tay, Adelene Y L Sim, Luo Huang, Melvin L K Chua, Yamei Tang

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Article in Computational and structural biotechnology journal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

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6citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Hong Qi TanDivision of Radiation Oncology, National Cancer Centre Singapore, Singapore.
Jinhua CaiDepartment of Neurology, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, People's Republic of China.
Shi Hui TayDivision of Medical Sciences, National Cancer Centre Singapore, Singapore.
Adelene Y L SimDivision of Medical Sciences, National Cancer Centre Singapore, Singapore.
Luo HuangDepartment of Radiation Oncology, Chongqing University Cancer Hospital, People's Republic of China.
Melvin L K ChuaDivision of Radiation Oncology, National Cancer Centre Singapore, Singapore.
Yamei TangDepartment of Neurology, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Bevacizumab is used in the treatment of radiation necrosis (RN), which is a debilitating toxicity following head and neck radiotherapy. However, there is no biomarker to predict if a patient would respond to bevacizumab. Purpose: We aimed to develop a cluster-based radiomics approach to characterize the spatial heterogeneity of RN and map their responses to bevacizumab. Methods: 118 consecutive nasopharyngeal carcinoma patients diagnosed with RN were enrolled. We divided 152 lesions from the patients into 101 for training, and 51 for validation. We extracted voxel-level radiomics features from each lesion segmented on T1-weighted+contrast and T2 FLAIR sequences of pre- and post-bevacizumab magnetic resonance images, followed by a three-step analysis involving individual- and population-level clustering, before delta-radiomics to derive five radiomics clusters within the lesions. We tested the association of each cluster with response to bevacizumab and developed a clinico-radiomics model using clinical predictors and cluster-specific features. Results: 71 (70.3%) and 34 (66.7%) lesions had responded to bevacizumab in the training and validation datasets, respectively. Two radiomics clusters were spatially mapped to the edema region, and the volume changes were significantly associated with bevacizumab response ( Conclusion: Our radiomics approach yielded intralesional resolution, enabling a more refined feature selection for predicting bevacizumab efficacy in the treatment of RN.

Indexed as

BevacizumabClusteringRadiation necrosisRadiomicsSpatial heterogeneity

Identifiers

PMID38125298
PMCPMC10730953

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