Association of 18F-FDG PET/CT textural features with immunohistochemical characteristics in invasive ductal breast cancer

被引:0
作者
Onner, Hasan [1 ]
Coskun, Nazim [2 ]
Erol, Mustafa [1 ]
Karanis, Meryem Ilkay Eren [1 ]
机构
[1] Konya City Hosp, Konya, Turkey
[2] Ankara City Hosp, Ankara, Turkey
来源
REVISTA ESPANOLA DE MEDICINA NUCLEAR E IMAGEN MOLECULAR | 2022年 / 41卷 / 01期
关键词
Breast cancer; Fluoride-18; fluorodeoxyglucose; Positron emission tomography/Computed; tomography; Textural features; Tumor heterogeneity; STANDARDIZED UPTAKE VALUES; METABOLIC TUMOR VOLUME; PROGNOSTIC-FACTORS; HETEROGENEITY; EVOLUTION; SUBTYPES; IMAGES;
D O I
10.1016/j.remn.2020.10.009
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Objectives: This study investigates whether textural features (TFs) extracted from 18F-FDG positron emission tomography/computed tomography (PET/CT) are associated with i 1111111.1 no hi s toc hemica 1 characteristics (IHCs) of invasive ductal breast carcinoma (IDBC). Materials and methods: The relationship of TFs with IHCs [estrogen receptor (ER), progesterone receptor (PR), human epidermal growth factor receptor-2 (HER-2), Ki-67 proliferation index, and histological grades] from solely excised primary tumors were evaluated for a more accurate assessment. Therefore patients with early -stage IDBC who underwent pre -operative 18F-FDG PET/CT scan for staging were included in this retrospective study. The clinical staging was performed according to the 8th edition of the American joint Committee on Cancer. Maximum standardized uptake value (SUVmax) and 37 TFs of the primary tumor were extracted from 18F-FDG PET/CT. Spearman's rank correlation test was used to evaluate the correlation between TFs and SUVmax. Receiver operating characteristic curves were generated to define the diagnostic performance of each parameter. Among these parameters, those with the highest diagnostic performance were included in the multivariate logistic regression model to identify the independent predictors of histopathological characteristics. Results: A total of 124 patients were included. Histogram-uniformity, grey-level co -occurrence matrix (GLCM), GLCM-energy, and GLCM-homogeneity showed a strong negative correlation with SUVmax, while grey-level run-length matrix (GLRLM), GLRLM-SRHGE, grey-level zone length matrix (GLZLM), GLZLM-HGZE, GLRLM-HGRE, GLCM-entropy, GLCM-contrast, histogram-entropy, and GLCMdissimilarity showed a strong positive correlation. Some of the TFs were independently associated with ER-negativity, PR-negativity, HER-2 -positivity, and increased Ki-67 proliferation index (GLCM-contrast, GLZLM-GLNU, histogram-uniformity, and shape -sphericity respectively). While SUVmax had an independent association with high-grade and triple -negativity, GLZLM-SZLGE, a high-order TF that shows the distribution of the short homogeneous zones with low grey-levels, had an independent association with axillary lymph node metastasis. Conclusions: ER-negative, PR-negative, HER-2 -positive, triple -negative, high-grade, highly proliferative, and high-stage tumors were found to be more glycolytic and metabolically heterogeneous. These findings suggest that the use of TFs in addition to SUVmax may improve the prognostic value of 18F-FDG PET/CT in IDBC, as certain TFs were independently associated with many IHCs and predicted axillary lymph node involvement. 0 2020 Sociedad Espanola de Medicina Nuclear e Imagen Molecular. Published by Elsevier Espana, S.L.U. All rights reserved.
引用
收藏
页码:11 / 16
页数:6
相关论文
共 29 条
[1]   Comparison of the volumetric and radiomics findings of 18F-FDG PET/CT images with immunohistochemical prognostic factors in local/locally advanced breast cancer [J].
Acar, Emine ;
Turgut, Bulent ;
Yigit, Seyran ;
Kaya, GamzeCapa .
NUCLEAR MEDICINE COMMUNICATIONS, 2019, 40 (07) :764-772
[2]  
Amin MB, 2017, AJCC Cancer Staging Manual, V8th
[3]   The Implications of Clonal Genome Evolution for Cancer Medicine [J].
Aparicio, Samuel ;
Caldas, Carlos .
NEW ENGLAND JOURNAL OF MEDICINE, 2013, 368 (09) :842-851
[4]  
Bera Kaustav, 2018, Am Soc Clin Oncol Educ Book, V38, P1008, DOI 10.1200/EDBK_199747
[5]   Quantifying tumour heterogeneity in 18F-FDG PET/CT imaging by texture analysis [J].
Chicklore, Sugama ;
Goh, Vicky ;
Siddique, Musib ;
Roy, Arunabha ;
Marsden, Paul K. ;
Cook, Gary J. R. .
EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING, 2013, 40 (01) :133-140
[6]   Are Pretreatment 18F-FDG PET Tumor Textural Features in Non-Small Cell Lung Cancer Associated with Response and Survival After Chemoradiotherapy? [J].
Cook, Gary J. R. ;
Yip, Connie ;
Siddique, Muhammad ;
Goh, Vicky ;
Chicklore, Sugama ;
Roy, Arunabha ;
Marsden, Paul ;
Ahmad, Shahreen ;
Landau, David .
JOURNAL OF NUCLEAR MEDICINE, 2013, 54 (01) :19-26
[7]   PATHOLOGICAL PROGNOSTIC FACTORS IN BREAST-CANCER .1. THE VALUE OF HISTOLOGICAL GRADE IN BREAST-CANCER - EXPERIENCE FROM A LARGE STUDY WITH LONG-TERM FOLLOW-UP [J].
ELSTON, CW ;
ELLIS, IO .
HISTOPATHOLOGY, 1991, 19 (05) :403-410
[8]   Cancer heterogeneity: implications for targeted therapeutics [J].
Fisher, R. ;
Pusztai, L. ;
Swanton, C. .
BRITISH JOURNAL OF CANCER, 2013, 108 (03) :479-485
[9]   Intratumor Heterogeneity and Branched Evolution Revealed by Multiregion Sequencing [J].
Gerlinger, Marco ;
Rowan, Andrew J. ;
Horswell, Stuart ;
Larkin, James ;
Endesfelder, David ;
Gronroos, Eva ;
Martinez, Pierre ;
Matthews, Nicholas ;
Stewart, Aengus ;
Tarpey, Patrick ;
Varela, Ignacio ;
Phillimore, Benjamin ;
Begum, Sharmin ;
McDonald, Neil Q. ;
Butler, Adam ;
Jones, David ;
Raine, Keiran ;
Latimer, Calli ;
Santos, Claudio R. ;
Nohadani, Mahrokh ;
Eklund, Aron C. ;
Spencer-Dene, Bradley ;
Clark, Graham ;
Pickering, Lisa ;
Stamp, Gordon ;
Gore, Martin ;
Szallasi, Zoltan ;
Downward, Julian ;
Futreal, P. Andrew ;
Swanton, Charles .
NEW ENGLAND JOURNAL OF MEDICINE, 2012, 366 (10) :883-892
[10]   Strategies for subtypes-dealing with the diversity of breast cancer: highlights of the St Gallen International Expert Consensus on the Primary Therapy of Early Breast Cancer 2011 [J].
Goldhirsch, A. ;
Wood, W. C. ;
Coates, A. S. ;
Gelber, R. D. ;
Thuerlimann, B. ;
Senn, H. -J. .
ANNALS OF ONCOLOGY, 2011, 22 (08) :1736-1747