Spectrum of Findings Seen in Patients With
IDH1/2 mutation
cholangiocarcinoma
isocitrate dehydrogenase
ivosidenib
Journal
International journal of surgical pathology
ISSN: 1940-2465
Titre abrégé: Int J Surg Pathol
Pays: United States
ID NLM: 9314927
Informations de publication
Date de publication:
24 Sep 2024
24 Sep 2024
Historique:
medline:
24
9
2024
pubmed:
24
9
2024
entrez:
24
9
2024
Statut:
aheadofprint
Résumé
Cholangiocarcinoma-with a growing incidence rate and poor prognosis-is not an aggressive tumor that is not uncommon. Molecular profiling can reveal actionable aberrations in at least a third of the tumors. This is especially so in the case of intrahepatic cholangiocarcinoma (ICC), where mutations in the isocitrate dehydrogenase 1 and 2 genes ( We descriptively characterize the clinical, radiological, and histopathological findings of 12 such patients. Our findings indicate an increasing need to personalize an approach for these patients with specific molecular alterations. With the advent of the
Sections du résumé
BACKGROUND
BACKGROUND
Cholangiocarcinoma-with a growing incidence rate and poor prognosis-is not an aggressive tumor that is not uncommon. Molecular profiling can reveal actionable aberrations in at least a third of the tumors. This is especially so in the case of intrahepatic cholangiocarcinoma (ICC), where mutations in the isocitrate dehydrogenase 1 and 2 genes (
METHODS AND RESULTS
RESULTS
We descriptively characterize the clinical, radiological, and histopathological findings of 12 such patients.
CONCLUSION
CONCLUSIONS
Our findings indicate an increasing need to personalize an approach for these patients with specific molecular alterations. With the advent of the
Identifiants
pubmed: 39314068
doi: 10.1177/10668969241271397
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
10668969241271397Déclaration de conflit d'intérêts
Declaration of Conflicts of InterestThe authors declare the following financial interests/personal relationships which may be considered as potential competing interests: PMK reports grants paid to the institution by Merck, Agenus Bio, Novartis, Advanced Accelerator Applications, Tersera, and Boston Scientific; a consultancy and advisory board relationship with Elicio (scientific advisory board member/shares/stock ownership); cofounder of Precision BioSensors Inc.; consultancy/advisory board fees from Guardant Health, Natera, Foundation Medicine, Illumina, BostonGene, Merck/MSD Oncology, Tempus, Bayer, Lilly, Delcath Systems, IPBA, QED Therapeutics, Boston Healthcare Associates, Servier, Taiho Oncology, Exact Sciences, Daiichi Sankyo/AstraZeneca, Eisai, Saga Diagnostics, Neogenomics, Do More Diagnostics AS, and Seattle Genetics; consulting fees paid to the institution by Taiho Pharmaceutical and Ipsen; receiving travel support from AstraZeneca for presentation of an investigator-initiated trial. All other authors have no conflicts of interest to report.