FGFR Inhibitor Toxicity and Efficacy in Cholangiocarcinoma: Multicenter Single-Institution Cohort Experience.


Journal

JCO precision oncology
ISSN: 2473-4284
Titre abrégé: JCO Precis Oncol
Pays: United States
ID NLM: 101705370

Informations de publication

Date de publication:
2021
Historique:
received: 12 02 2021
revised: 08 06 2021
accepted: 07 07 2021
entrez: 15 11 2021
pubmed: 16 11 2021
medline: 16 11 2021
Statut: epublish

Résumé

Cholangiocarcinomas (CCA) are a group of heterogeneous tumors arising from the biliary epithelia. Significant sequencing efforts have provided further insights into the molecular mechanisms of this disease including fibroblast growth factor receptor ( This is a retrospective study of patients with CCA and known Our group identified 61 patients with advanced or metastatic CCA, 19 males (31%) and 42 females (69%), harboring FGFRi are well tolerated with clinical efficacy. With the recent approval of FGFRi by the US Food and Drug Administration and ongoing clinical trials for new FGFRi, understanding outcomes and toxicity associated with these medications is important for precision oncology.

Identifiants

pubmed: 34778691
doi: 10.1200/PO.21.00064
pii: PO.21.00064
pmc: PMC8575436
pii:
doi:

Types de publication

Journal Article Multicenter Study Research Support, N.I.H., Extramural

Langues

eng

Subventions

Organisme : NCI NIH HHS
ID : P30 CA015083
Pays : United States

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Informations de copyright

© 2021 by American Society of Clinical Oncology.

Déclaration de conflit d'intérêts

Nguyen H. Tran Honoraria: QED Therapeutics Consulting or Advisory Role: QED Therapeutics No other potential conflicts of interest were reported. Nguyen H. Tran Honoraria: QED Therapeutics Consulting or Advisory Role: QED Therapeutics No other potential conflicts of interest were reported.

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Auteurs

Jennifer J Gile (JJ)

Department of Internal Medicine, Mayo Clinic, Rochester, MN.

Fang-Shu Ou (FS)

Department of Health Sciences Research, Mayo Clinic, Rochester, MN.

Amit Mahipal (A)

Division of Oncology, Department of Medicine, Mayo Clinic, Rochester, MN.

Joseph J Larson (JJ)

Department of Health Sciences Research, Mayo Clinic, Rochester, MN.

Kabir Mody (K)

Division of Oncology, Department of Medicine, Mayo Clinic, FL USA.

Zhaohui Jin (Z)

Division of Oncology, Department of Medicine, Mayo Clinic, Rochester, MN.

Joleen Hubbard (J)

Division of Oncology, Department of Medicine, Mayo Clinic, Rochester, MN.

Thorvardur Halfdanarson (T)

Division of Oncology, Department of Medicine, Mayo Clinic, Rochester, MN.

Steven R Alberts (SR)

Division of Oncology, Department of Medicine, Mayo Clinic, Rochester, MN.

Aminah Jatoi (A)

Division of Oncology, Department of Medicine, Mayo Clinic, Rochester, MN.

Robert R McWilliams (RR)

Division of Oncology, Department of Medicine, Mayo Clinic, Rochester, MN.

Wen Wee Ma (WW)

Division of Oncology, Department of Medicine, Mayo Clinic, Rochester, MN.

Sumera Ilyas (S)

Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN.

Rory Smoot (R)

Department of Surgery, Mayo Clinic, Rochester, MN.

Lewis Roberts (L)

Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN.

Gregory Gores (G)

Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN.

Mitesh Borad (M)

Division of Oncology, Department of Medicine, Mayo Clinic, Scottsdale, AZ.

Tanios S Bekaii-Saab (TS)

Division of Oncology, Department of Medicine, Mayo Clinic, Scottsdale, AZ.

Nguyen H Tran (NH)

Division of Oncology, Department of Medicine, Mayo Clinic, Rochester, MN.

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