Novel MRI deformation-heterogeneity radiomic features are associated with molecular subgroups and overall survival in pediatric medulloblastoma: Preliminary findings from a multi-institutional study

被引:6
|
作者
Iyer, Sukanya [1 ]
Ismail, Marwa [2 ]
Tamrazi, Benita [3 ]
Salloum, Ralph [4 ]
de Blank, Peter [5 ]
Margol, Ashley [3 ]
Correa, Ramon [1 ]
Chen, Jonathan [1 ]
Bera, Kaustav [1 ]
Statsevych, Volodymyr [6 ]
Ho, Mai-Lan [7 ]
Vaidya, Pranjal [1 ]
Verma, Ruchika [1 ]
Hawes, Debra [3 ]
Judkins, Alexander [3 ]
Fu, Pingfu [1 ]
Madabhushi, Anant [8 ,9 ]
Tiwari, Pallavi [2 ]
机构
[1] Case Western Reserve Univ, Dept Populat & Quantitat Hlth Sci, Cleveland, OH USA
[2] Univ Wisconsin Madison, Dept Radiol, Madison, WI 53705 USA
[3] Childrens Hosp Los Angeles, Dept Pathol, Los Angeles, CA USA
[4] Nationwide Childrens Hosp, Div Hematol Oncol & Bone Marrow Transplant, Columbus, OH USA
[5] Cincinnati Childrens Hosp Med Ctr, Div Oncol, Cincinnati, OH USA
[6] Cleveland Clin, Imaging Inst, Dept Neuroradiol, Cleveland, OH USA
[7] Nationwide Childrens Hosp, Dept Radiol, Columbus, OH USA
[8] Georgia Inst Technol, Radiol & Imaging Sci, Biomed Informat BMI & Pathol, Atlanta, GA USA
[9] Emory Univ, Atlanta, GA USA
来源
FRONTIERS IN ONCOLOGY | 2022年 / 12卷
基金
美国国家卫生研究院;
关键词
medulloblastoma; deformation; molecular subgroups; survival; LASSO; PROGNOSIS; CHILDREN; THERAPY;
D O I
10.3389/fonc.2022.915143
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction: Medulloblastoma (MB) is a malignant, heterogenous brain tumor. Advances in molecular profiling have led to identifying four molecular subgroups of MB (WNT, SHH, Group 3, Group 4), each with distinct clinical behaviors. We hypothesize that (1) aggressive MB tumors, growing heterogeneously, induce pronounced local structural deformations in the surrounding parenchyma, and (b) these local deformations as captured on Gadolinium (Gd)-enhanced-T1w MRI are independently associated with molecular subgroups, as well as overall survival in MB patients. Methods: In this work, a total of 88 MB studies from 2 institutions were analyzed. Following tumor delineation, Gd-T-1w scan for every patient was registered to a normal age-specific T-1w-MRI template via deformable registration. Following patient-atlas registration, local structural deformations in the brain parenchyma were obtained for every patient by computing statistics from deformation magnitudes obtained from every 5mm annular region, 0 < d < 60 mm, where d is the distance from the tumor infiltrating edge. Results: Multi-class comparison via ANOVA yielded significant differences between deformation magnitudes obtained for Group 3, Group 4, and SHH molecular subgroups, observed up to 60-mm outside the tumor edge. Additionally, Kaplan-Meier survival analysis showed that the local deformation statistics, combined with the current clinical risk-stratification approaches (molecular subgroup information and Chang's classification), could identify significant differences between high-risk and low-risk survival groups, achieving better performance results than using any of these approaches individually. Discussion: These preliminary findings suggest there exists significant association of our tumor-induced deformation descriptor with overall survival in MB, and that there could be an added value in using the proposed radiomic descriptor along with the current risk classification approaches, towards more reliable risk assessment in pediatric MB.
引用
收藏
页数:16
相关论文
共 6 条
  • [1] Novel MRI deformation-heterogeneity radiomic features are associated with molecular subgroups and overall survival in pediatric medulloblastoma: Preliminary findings from a multi-institutional study (vol 12, 915143, 2022)
    Frontiers Production Office
    FRONTIERS IN ONCOLOGY, 2023, 13
  • [2] A Radiomic Approach for Evaluating Intra-Subgroup Heterogeneity in SHH and Group 4 Pediatric Medulloblastoma: A Preliminary Multi-Institutional Study
    Ismail, Marwa
    Um, Hyemin
    Salloum, Ralph
    Hollnagel, Fauzia
    Ahmed, Raheel
    de Blank, Peter
    Tiwari, Pallavi
    CANCERS, 2024, 16 (12)
  • [3] Radiomic features for prostate cancer detection on MRI differ between the transition and peripheral zones: Preliminary findings from a multi-institutional study
    Ginsburg, Shoshana B.
    Algohary, Ahmad
    Pahwa, Shivani
    Gulani, Vikas
    Ponsky, Lee
    Aronen, Hannu J.
    Bostrom, Peter J.
    Bohm, Maret
    Haynes, Anne-Maree
    Brenner, Phillip
    Delprado, Warick
    Thompson, James
    Pulbrock, Marley
    Taimen, Pekka
    Villani, Robert
    Stricker, Phillip
    Rastinehad, Ardeshir R.
    Jambor, Ivan
    Madabhushi, Anant
    JOURNAL OF MAGNETIC RESONANCE IMAGING, 2017, 46 (01) : 184 - 193
  • [4] Prognostic Modeling of Overall Survival in Glioblastoma Using Radiomic Features Derived from Intraoperative Ultrasound: A Multi-Institutional Study
    Cepeda, Santiago
    Esteban-Sinovas, Olga
    Singh, Vikas
    Moiyadi, Aliasgar
    Zemmoura, Ilyess
    Del Bene, Massimiliano
    Barbotti, Arianna
    Dimeco, Francesco
    West, Timothy Richard
    Nahed, Brian Vala
    Giammalva, Giuseppe Roberto
    Arrese, Ignacio
    Sarabia, Rosario
    CANCERS, 2025, 17 (02)
  • [5] Radiomic Features From Multi-Parameter MRI Combined With Clinical Parameters Predict Molecular Subgroups in Patients With Medulloblastoma
    Yan, Jing
    Liu, Lei
    Wang, Weiwei
    Zhao, Yuanshen
    Li, Kay Ka-Wai
    Li, Ke
    Wang, Li
    Yuan, Binke
    Geng, Haiyang
    Zhang, Shenghai
    Liu, Zhen
    Duan, Wenchao
    Zhan, Yunbo
    Pei, Dongling
    Zhao, Haibiao
    Sun, Tao
    Sun, Chen
    Wang, Wenqing
    Hong, Xuanke
    Wang, Xiangxiang
    Guo, Yu
    Li, Wencai
    Cheng, Jingliang
    Liu, Xianzhi
    Ng, Ho-Keung
    Li, Zhicheng
    Zhang, Zhenyu
    FRONTIERS IN ONCOLOGY, 2020, 10
  • [6] Stable and Discriminatory Radiomic Features from the Tumor and Its Habitat Associated with Progression-Free Survival in Glioblastoma: A Multi-Institutional Study
    Verma, R.
    Hill, V. B.
    Statsevych, V.
    Bera, K.
    Correa, R.
    Leo, P.
    Ahluwalia, M.
    Madabhushi, A.
    Tiwari, P.
    AMERICAN JOURNAL OF NEURORADIOLOGY, 2022, 43 (08) : 1115 - 1123