Clinical Utility of Comprehensive Genomic Profiling in Patients with Unresectable Hepatocellular Carcinoma.
Shun IshidoKaoru TsuchiyaYoshihito KanoYutaka YasuiKenta TakauraNaoki UchiharaKeito SuzukiYuki TanakaHaruka MiyamotoMichiko YamadaHiroaki MatsumotoTsubasa NobusawaTaisei KeitokuShohei TanakaChiaki MaeyashikiNobuharu TamakiYuka TakahashiHiroyuki NakanishiUrara SakuraiYasuhiro AsahinaRyuichi OkamotoMasayuki KurosakiNamiki IzumiPublished in: Cancers (2023)
The molecular mechanism of hepatocellular carcinoma (HCC) is partially demonstrated. Moreover, in the patients receiving multiple molecular-targeted therapies, the gene alternations are still unknown. Six molecular-targeted therapies of unresectable HCC (uHCC) and comprehensive genomic profiling (CGP) have been approved in clinical practice. Hence, the utility of CGP in patients with uHCC treated with multiple molecular-targeted agents is investigated. The data of the patients with uHCC who received CGP tests were collected, retrospectively, between February 2021 and May 2022. Gene alterations detected by foundation testing, excluding variants of unknown significance, were reported in all nine patients. The samples for CGP were derived from liver tumor biopsy ( n = 2), surgical specimens of bone metastases ( n = 2), and blood ( n = 5). The median number of systemic therapies was four. Seven patients were candidates eligible for clinical trials. One patient with a high tumor mutation burden (TMB) could receive pembrolizumab after CGP. This study presented genomic alternations after receiving multiple molecular-targeted therapies. However, further investigation needs to be conducted to develop personalized therapies and invent newer agents for treating HCC.
Keyphrases
- copy number
- newly diagnosed
- clinical trial
- ejection fraction
- clinical practice
- prognostic factors
- dna methylation
- randomized controlled trial
- genome wide
- gene expression
- risk factors
- machine learning
- drug delivery
- mass spectrometry
- deep learning
- liver metastases
- study protocol
- transcription factor
- locally advanced
- advanced non small cell lung cancer
- double blind