Prediction of O(6)-methylguanine-DNA methyltransferase promoter methylation status in IDH-wildtype glioblastoma using MRI histogram analysis

被引:0
|
作者
Liu, Xianwang [1 ,2 ,3 ]
Han, Tao [1 ,2 ,3 ]
Wang, Yuzhu [3 ,4 ,5 ]
Liu, Hong [1 ,2 ,3 ]
Zhou, Junlin [1 ,2 ,3 ]
机构
[1] Lanzhou Univ, Hosp 2, Dept Radiol, Cuiyingmen 82, Lanzhou 730030, Peoples R China
[2] Gansu Int Sci & Technol Cooperat Base Med Imaging, Lanzhou, Peoples R China
[3] Key Lab Med Imaging Gansu Prov, Lanzhou, Peoples R China
[4] Gansu Prov Canc Hosp, Dept Nucl Med, 2 East Xiaoxihu St, Lanzhou 730050, Peoples R China
[5] Sun Yat sen Univ, Gansu Hosp, Canc Ctr, Dept Nucl Med, 2 East Xiaoxihu St, Lanzhou 730050, Peoples R China
基金
中国国家自然科学基金;
关键词
Glioblastoma; O(6)-methylguanine-DNA methyltransferase; Magnetic resonance imaging; Histogram analysis; TEMOZOLOMIDE; BIOMARKER; BENEFIT; TUMORS;
D O I
10.1007/s10143-024-02522-w
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
To evaluate the utility of magnetic resonance imaging (MRI) histogram parameters in predicting O(6)-methylguanine-DNA methyltransferase promoter (pMGMT) methylation status in IDH-wildtype glioblastoma (GBM). From November 2021 to July 2023, forty-six IDH-wildtype GBM patients with known pMGMT methylation status (25 unmethylated and 21 methylated) were enrolled in this retrospective study. Conventional MRI signs (including location, across the midline, margin, necrosis/cystic changes, hemorrhage, and enhancement pattern) were assessed and recorded. Histogram parameters were extracted and calculated by Firevoxel software based on contrast-enhanced T1-weighted images (CET1). Differences and diagnostic performance of conventional MRI signs and histogram parameters between the pMGMT-unmethylated and pMGMT-methylated groups were analyzed and compared. No differences were observed in the conventional MRI signs between pMGMT-unmethylated and pMGMT-methylated groups (all p > 0.05). Compared with the pMGMT-methylated group, pMGMT-unmethylated showed a higher minimum, mean, Perc.01, Perc.05, Perc.10, Perc.25, Perc.50, and coefficient of variation (CV) (all p < 0.05). Among all significant CET1 histogram parameters, minimum achieved the best distinguishing performance, with an area under the curve of 0.836. CET1 histogram parameters could provide additional value in predicting pMGMT methylation status in patients with IDH-wildtype GBM, with minimum being the most promising parameter.
引用
收藏
页数:9
相关论文
共 50 条
  • [21] Assessment of O(6)-Methylguanine-DNA Methyltransferase (MGMT) Promotor Methylation and Protein Expression in Pituitary Adenomas
    Lee, S. H.
    Ko, Y. S.
    Lee, M. J.
    Hwang, T. S.
    Kim, W. S.
    Han, H. S.
    Lim, S. D.
    LABORATORY INVESTIGATION, 2010, 90 : 377A - 377A
  • [22] IN VIVO EVALUATION OF O6-METHYLGUANINE-DNA-METHYLTRANSFERASE (MGMT) PROMOTER METHYLATION STATUS FOR DE NOVO GLIOBLASTOMA PATIENTS USING DEEP LEARNING FEATURES
    Rathore, Saima
    Nasrallah, MacLean
    Akbari, Hamed
    Shukla, Gaurav
    Bagley, Stephen
    Watt, Christopher
    Ha, Sung Min
    Mamourian, Elizabeth
    Sako, Chiharu
    Binder, Zev
    O'Rourke, Donald
    Davatzikos, Christos
    NEURO-ONCOLOGY, 2019, 21 : 271 - 272
  • [23] PROSPECTIVE EVALUATION OF THE METHYLATION OF THE O6-METHYLGUANINE-DNA-METHYLTRANSFERASE IN GLIOBLASTOMA MULTIFORME
    Maurice, Catherine
    Belanger, Karl
    Berthelet, France
    Weng, Xiaoduan
    NEURO-ONCOLOGY, 2012, 14 : 50 - 51
  • [24] O6-methylguanine-DNA methyltransferase (MGMT) promoter methylation status is a prognostic factor in anaplastic astrocytomas
    Tosoni, A.
    Franceschi, E.
    Ermani, M.
    Poggi, R.
    La Torre, L.
    Tomasello, C.
    Marucci, G.
    Maestri, A.
    Bartolini, S.
    Brandes, A. A.
    EJC SUPPLEMENTS, 2009, 7 (02): : 500 - 500
  • [25] Analysis of O6-methylguanine-DNA methyltransferase methylation status in sporadic colon polyps
    Kycler, Witold
    Szarzynska, Bronislawa
    Lozinski, Cezary
    Korski, Konstanty
    Lamperska, Katarzyna
    REPORTS OF PRACTICAL ONCOLOGY AND RADIOTHERAPY, 2012, 17 (01) : 13 - 18
  • [26] Combined analysis of O6-methylguanine-DNA methyltransferase protein expression and promoter methylation provides optimized prognostication of glioblastoma outcome
    Lalezari, Shadi
    Chou, Arthur P.
    Tran, Anh
    Solis, Orestes E.
    Khanlou, Negar
    Chen, Weidong
    Li, Sichen
    Carrillo, Jose A.
    Chowdhury, Reshmi
    Selfridge, Julia
    Sanchez, Desiree E.
    Wilson, Ryan W.
    Zurayk, Mira
    Lalezari, Jonathan
    Lou, Jerry J.
    Ormiston, Laurel
    Ancheta, Karen
    Hanna, Robert
    Miller, Paul
    Piccioni, David
    Ellingson, Benjamin M.
    Buchanan, Colin
    Mischel, Paul S.
    Nghiemphu, Phioanh L.
    Green, Richard
    Wang, He-Jing
    Pope, Whitney B.
    Liau, Linda M.
    Elashoff, Robert M.
    Cloughesy, Timothy F.
    Yong, William H.
    Lai, Albert
    NEURO-ONCOLOGY, 2013, 15 (03) : 370 - 381
  • [27] O6-methylguanine DNA methyltransferase status determined by promoter methylation and immunohistochemistry in gliosarcoma and their clinical implications
    Kang, Shin-Hyuk
    Park, Kyung-Jae
    Kim, Chae-Yong
    Yu, Mi Ok
    Park, Chul-Kee
    Park, Sung-Hye
    Chung, Yong-Gu
    JOURNAL OF NEURO-ONCOLOGY, 2011, 101 (03) : 477 - 486
  • [28] O6-METHYLGUANINE DNA METHYLTRANSFERASE STATUS DETERMINED BY PROMOTER METHYLATION AND IMMUNOHISTOCHEMISTRY IN GLIOSARCOMA AND THEIR CLINICAL IMPLICATIONS
    Kang, Shin-Hyuk
    Park, Kyung-Jae
    Kim, Chae-Yong
    Yu, Mi Ok
    Park, Chul-Kee
    Park, Sung-Hye
    Chung, Yong-Gu
    NEURO-ONCOLOGY, 2010, 12 : 48 - 48
  • [29] Methylation status of MGMT (O6-methylguanine DNA methyltransferase) promoter in high-grade gliomas
    Choe, G. -Y.
    Moon, S. -Y.
    VIRCHOWS ARCHIV, 2010, 457 (02) : 236 - 236
  • [30] O6-methylguanine DNA methyltransferase status determined by promoter methylation and immunohistochemistry in gliosarcoma and their clinical implications
    Shin-Hyuk Kang
    Kyung-Jae Park
    Chae-Yong Kim
    Mi Ok Yu
    Chul-Kee Park
    Sung-Hye Park
    Yong-Gu Chung
    Journal of Neuro-Oncology, 2011, 101 : 477 - 486