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A novel risk stratification model based on the Children's Hepatic Tumours International Collaboration-Hepatoblastoma Stratification and deoxyribonucleic acid methylation analysis for hepatoblastoma

Authors :
Kondo, Takafumi
1000090588089
Honda, Shohei
Suzuki, Hiromu
1000010334236
Ito, Yoichi M.
Kawakita, Issei
Okumura, Kazuyoshi
1000030741219
Ara, Momoko
Minato, Masashi
Kitagawa, Norihiko
Tanaka, Yukichi
Tanaka, Mio
Shinkai, Masato
Hishiki, Tomoro
Watanabe, Kenichiro
Ida, Kohmei
Takatori, Atsushi
Hiyama, Eiso
1000070363364
Taketomi, Akinobu
Kondo, Takafumi
1000090588089
Honda, Shohei
Suzuki, Hiromu
1000010334236
Ito, Yoichi M.
Kawakita, Issei
Okumura, Kazuyoshi
1000030741219
Ara, Momoko
Minato, Masashi
Kitagawa, Norihiko
Tanaka, Yukichi
Tanaka, Mio
Shinkai, Masato
Hishiki, Tomoro
Watanabe, Kenichiro
Ida, Kohmei
Takatori, Atsushi
Hiyama, Eiso
1000070363364
Taketomi, Akinobu
Publication Year :
2022

Abstract

Introduction: Hepatoblastoma (HB) is the most common paediatric liver tumour, and epigenetic aberrations may be important in HB development. Recently, the Children's He-patic Tumors International Collaboration-Hepatoblastoma Stratification (CHIC-HS) devel-oped risk stratification based on clinicopathological factors. This study aimed to construct a more accurate model by integrating CHIC-HS with molecular factors based on DNA methylation. Methods: HB tumour specimens (N = 132) from patients treated with the Japanese Pediatric Liver Tumors Group-2 protocol were collected and subjected to methylation analysis by bisul-fite pyrosequencing. Associations between methylation status and clinicopathological factors, overall survival (OS), and event-free survival (EFS) were retrospectively analysed. We inves-tigated the effectiveness of the evaluation of methylation status in each CHIC-HS risk group and generated a new risk stratification model. Results: Most specimens (82%) were from post-chemotherapy tissue. Hypermethylation in > 2 of the four genes (RASSF1A, PARP6, OCIAD2, and MST1R) was significantly associated with poorer OS and EFS. Multivariate analysis indicated that > 2 methylated genes was an in-dependent prognostic factor (hazard ratios of 6.014 and 3.684 for OS and EFS, respectively). Two or more methylated genes was also associated with poorer OS in the CHIC-very low (VL)-/low (L)-risk and CHIC-intermediate (I) risk groups (3-year OS rates were 83% vs. 98% and 50% vs. 95%, respectively). The 3-year OS rates of the VL/L, I, and high-risk groups in the new stratification model were 98%, 90%, and 62% (vs. CHIC-HS [96%, 82%, and 65%, respectively]), optimising CHIC-HS. Conclusions: Our proposed stratification system considers individual risk in HB and may improve patient clinical management. (C) 2022 Elsevier Ltd. All rights reserved.

Details

Database :
OAIster
Notes :
application/pdf, application/vnd.openxmlformats-officedocument.presentationml.presentation, application/vnd.openxmlformats-officedocument.wordprocessingml.document, English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1409766609
Document Type :
Electronic Resource