Literature DB >> 28984520

Prediction of BRAF mutation status of craniopharyngioma using magnetic resonance imaging features.

Qi Yue1, Yang Yu2, Zhifeng Shi1, Yongfei Wang1, Wei Zhu1, Zunguo Du3, Zhenwei Yao2, Liang Chen1, Ying Mao1,4.   

Abstract

OBJECTIVE Treatment with a BRAF mutation inhibitor might shrink otherwise refractory craniopharyngiomas and is a promising preoperative treatment to facilitate tumor resection. The aim of this study was to investigate the noninvasive diagnosis of BRAF-mutated craniopharyngiomas based on MRI characteristics. METHODS Fifty-two patients with pathologically diagnosed craniopharyngioma were included in this study. Polymerase chain reaction was performed on tumor tissue specimens to detect BRAF and CTNNB1 mutations. MRI manifestations-including tumor location, size, shape, and composition; signal intensity of cysts; enhancement pattern; pituitary stalk morphology; and encasement of the internal carotid artery-were analyzed by 2 neuroradiologists blinded to patient identity and clinical characteristics, including BRAF mutation status. Results were compared between the BRAF-mutated and wild-type (WT) groups. Characteristics that were significantly more prevalent (p < 0.05) in the BRAF-mutated craniopharyngiomas were defined as diagnostic features. The minimum number of diagnostic features needed to make a diagnosis was determined by analyzing the receiver operating characteristic (ROC) curve. RESULTS Eight of the 52 patients had BRAF-mutated craniopharyngiomas, and the remaining 44 had BRAF WT tumors. The clinical characteristics did not differ significantly between the 2 groups. Interobserver agreement for MRI data analysis was relatively reliable, with values of Cohen κ ranging from 0.65 to 0.97 (p < 0.001). A comparison of findings in the 2 patient groups showed that BRAF-mutated craniopharyngiomas tended to be suprasellar (p < 0.001), spherical (p = 0.005), predominantly solid (p = 0.003), and homogeneously enhancing (p < 0.001), and that patients with these tumors tended to have a thickened pituitary stalk (p = 0.014). When at least 3 of these 5 features were present, a tumor might be identified as BRAF mutated with a sensitivity of 1.00 and a specificity of 0.91. The area under the ROC curve for the sum of all 5 diagnostic criteria was 0.989 (p < 0.001). CONCLUSIONS The BRAF mutation status of craniopharyngiomas might be predicted using certain MRI features with relatively high sensitivity and specificity, thus offering potential guidance for the preoperative administration of BRAF mutation inhibitors.

Entities:  

Keywords:  AUC = area under the curve; BRAF; FFPE = formalin-fixed and paraffin-embedded; ICA = internal carotid artery; ROC = receiver operating characteristic; WT = wild type; craniopharyngioma; diagnosis; magnetic resonance imaging; oncology

Mesh:

Substances:

Year:  2017        PMID: 28984520     DOI: 10.3171/2017.4.JNS163113

Source DB:  PubMed          Journal:  J Neurosurg        ISSN: 0022-3085            Impact factor:   5.115


  16 in total

1.  Targeted treatment of papillary craniopharyngiomas harboring BRAF V600E mutations.

Authors:  Tareq A Juratli; Pamela S Jones; Nancy Wang; Megha Subramanian; Simon J B Aylwin; Yazmin Odia; Elham Rostami; Olafur Gudjonsson; Brian L Shaw; Daniel P Cahill; Evanthia Galanis; Fred G Barker; Sandro Santagata; Priscilla K Brastianos
Journal:  Cancer       Date:  2019-07-17       Impact factor: 6.860

2.  Duct-like diverticulum at the base of third ventricle tumors: a morphological signature diagnostic of papillary craniopharyngioma.

Authors:  José María Pascual; Ruth Prieto; Rodrigo Carrasco; Laura Barrios
Journal:  Neurosurg Rev       Date:  2022-08-19       Impact factor: 2.800

3.  Duct-like Recess in the Infundibular Portion of Third Ventricle Craniopharyngiomas: An MRI Sign Identifying the Papillary Type.

Authors:  J M Pascual; R Carrasco; L Barrios; R Prieto
Journal:  AJNR Am J Neuroradiol       Date:  2022-08-11       Impact factor: 4.966

4.  Immunohistochemistry or Molecular Analysis: Which Method Is Better for Subtyping Craniopharyngioma?

Authors:  Noriaki Fukuhara; Takeo Iwata; Naoko Inoshita; Katsuhiko Yoshimoto; Masanobu Kitagawa; Hirokazu Fukuhara; Keita Tatsushima; Mitsuo Yamaguchi-Okada; Akira Takeshita; Junko Ito; Yasuhiro Takeuchi; Shozo Yamada; Hiroshi Nishioka
Journal:  Endocr Pathol       Date:  2020-09-23       Impact factor: 3.943

5.  BRAF V600E mutant papillary craniopharyngiomas: a single-institutional case series.

Authors:  Emanuele La Corte; Iyan Younus; Francesca Pivari; Adelina Selimi; Malte Ottenhausen; Jonathan A Forbes; David J Pisapia; Georgiana A Dobri; Vijay K Anand; Theodore H Schwartz
Journal:  Pituitary       Date:  2018-12       Impact factor: 4.107

6.  A suprasellar bronchogenic cyst: A case report.

Authors:  Bingyang Bian; Miao Yu; Shanshan Liu; Shu Li; Ying Wei; Bei Zhang
Journal:  Medicine (Baltimore)       Date:  2019-07       Impact factor: 1.817

7.  A rare case of giant cystic adamantinomatous craniopharyngioma in an adult.

Authors:  Si-Ping Luo; Han-Wen Zhang; Juan Yu; Juan Jiao; Ji-Hu Yang; Yi Lei; Fan Lin
Journal:  Radiol Case Rep       Date:  2020-04-30

8.  Subtype-dependent difference of glucose transporter 1 and hexokinase II expression in craniopharyngioma: an immunohistochemical study.

Authors:  Naoto Mukada; Masahiko Tosaka; Nozomi Matsumura; Rei Yamaguchi; Masanori Aihara; Koji Isoda; Tetsuya Higuchi; Yoshito Tsushima; Hideaki Yokoo; Yuhei Yoshimoto
Journal:  Sci Rep       Date:  2021-01-08       Impact factor: 4.379

9.  Non-Invasive Radiomics Approach Predict Invasiveness of Adamantinomatous Craniopharyngioma Before Surgery.

Authors:  Guofo Ma; Jie Kang; Ning Qiao; Bochao Zhang; Xuzhu Chen; Guilin Li; Zhixian Gao; Songbai Gui
Journal:  Front Oncol       Date:  2021-02-17       Impact factor: 6.244

10.  Aggressive Childhood-onset Papillary Craniopharyngioma Managed With Vemurafenib, a BRAF Inhibitor.

Authors:  Constance L Chik; Frank K H van Landeghem; Jacob C Easaw; Vivek Mehta
Journal:  J Endocr Soc       Date:  2021-03-16
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.