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
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

10668969241271397

Déclaration 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.

Auteurs

Andrea Siobhan Kierans (AS)

Department of Radiology, Weill Cornell Medicine, New York, NY, USA.

Areeb Lutfi (A)

Division of Hematology and Oncology, Department of Medicine, Weill Cornell Medicine, New York, NY, USA.

Maaz Khan Afghan (MK)

Division of Hematology and Oncology, Department of Medicine, Weill Cornell Medicine, New York, NY, USA.

Sahrish Khan (S)

Division of Hematology and Oncology, Department of Medicine, Weill Cornell Medicine, New York, NY, USA.

Sana Javaid (S)

Division of Hematology and Oncology, Department of Medicine, Weill Cornell Medicine, New York, NY, USA.

Brian Michael Currie (BM)

Department of Vascular and Interventional Radiology, Weill Cornell Medicine, New York, NY, USA.

Juan Rocca (J)

Division of Liver Transplantation and Hepatobiliary Surgery, Department of Surgery, Weill Cornell Medicine, New York, NY, USA.

Benjamin Samstein (B)

Division of Liver Transplantation and Hepatobiliary Surgery, Department of Surgery, Weill Cornell Medicine, New York, NY, USA.

Encouse Golden (E)

Department of Radiation Oncology, Weill Cornell Medicine, New York, NY, USA.

Elizabeta Popa (E)

Division of Hematology and Oncology, Department of Medicine, Weill Cornell Medicine, New York, NY, USA.

Erika Hissong (E)

Department of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, NY, USA.

Pashtoon Murtaza Kasi (PM)

Division of Hematology and Oncology, Department of Medicine, Weill Cornell Medicine, New York, NY, USA.

Classifications MeSH