Comparative Genomic Analysis of Intrahepatic Cholangiocarcinoma: Biopsy Type, Ancestry, and Testing Patterns.

Bile duct neoplasms Comparative genomics Intrahepatic cholangiocarcinoma Liquid biopsy

Journal

The oncologist
ISSN: 1549-490X
Titre abrégé: Oncologist
Pays: England
ID NLM: 9607837

Informations de publication

Date de publication:
09 2021
Historique:
received: 14 01 2021
accepted: 19 05 2021
pubmed: 4 6 2021
medline: 29 9 2021
entrez: 3 6 2021
Statut: ppublish

Résumé

At diagnosis, the majority of patients with intrahepatic cholangiocarcinoma (IHCC) present with advanced disease and a poor prognosis. Comprehensive genomic profiling (CGP) early in the disease course may increase access to targeted therapies and clinical trials; however, unresolved issues remain surrounding the optimal biopsy type to submit for CGP. Mutational frequencies between primary tumor biopsies (Pbx), metastatic biopsies (Mbx), and liquid biopsies (Lbx) in 1,632 patients with IHCC were compared. Potentially actionable alterations were found in 52%, 34%, and 35% of patients in the Pbx, Mbx, and Lbx cohorts, respectively. In Pbx, Mbx, and Lbx, FGFR2 rearrangements were found in 9%, 6%, and 4%, and IDH1 mutations were identified in 16%, 5%, and 9% patients, respectively. Moreover, alterations in FGFR2 and IDH1 were significantly associated with distinct ancestries, including 2.1-fold enrichment for FGFR2 rearrangements in patients with African ancestry and 1.5-fold enrichment for IDH1 mutations in patients with admixed American (Hispanic) ancestry. Finally, the publication of biomarker-driven clinical trials in IHCC correlated with changing CGP testing patterns. Significant correlations between patient characteristics and IHCC trial disclosures were observed, including a significant decrease from time between biopsy and CGP testing, and more frequent testing of primary versus metastatic samples. Overall, because of the high likelihood of identifying actionable genomic alterations, CGP should be considered for the majority of patients with inoperable IHCC, and Lbx and Mbx can be considered as part of the diagnostic suite. Comprehensive genomic profiling (CGP) should be considered for all patients with intrahepatic cholangiocarcinoma (IHCC) or suspected IHCC, as actionable alterations were commonly found in multiple genes and a wide variety of FGFR2 fusion partners were identified. The disclosure of IHCC trial data correlated with increased use of CGP, an encouraging trend that moves new therapeutic options forward for rare cancers with a rare biomarker. Although tissue from the primary lesion may identify actionable alterations at higher rates, CGP of a liquid biopsy or metastatic site can be considered, particularly if the primary tissue block is exhausted.

Sections du résumé

BACKGROUND
At diagnosis, the majority of patients with intrahepatic cholangiocarcinoma (IHCC) present with advanced disease and a poor prognosis. Comprehensive genomic profiling (CGP) early in the disease course may increase access to targeted therapies and clinical trials; however, unresolved issues remain surrounding the optimal biopsy type to submit for CGP.
PATIENTS AND METHODS
Mutational frequencies between primary tumor biopsies (Pbx), metastatic biopsies (Mbx), and liquid biopsies (Lbx) in 1,632 patients with IHCC were compared.
RESULTS
Potentially actionable alterations were found in 52%, 34%, and 35% of patients in the Pbx, Mbx, and Lbx cohorts, respectively. In Pbx, Mbx, and Lbx, FGFR2 rearrangements were found in 9%, 6%, and 4%, and IDH1 mutations were identified in 16%, 5%, and 9% patients, respectively. Moreover, alterations in FGFR2 and IDH1 were significantly associated with distinct ancestries, including 2.1-fold enrichment for FGFR2 rearrangements in patients with African ancestry and 1.5-fold enrichment for IDH1 mutations in patients with admixed American (Hispanic) ancestry. Finally, the publication of biomarker-driven clinical trials in IHCC correlated with changing CGP testing patterns. Significant correlations between patient characteristics and IHCC trial disclosures were observed, including a significant decrease from time between biopsy and CGP testing, and more frequent testing of primary versus metastatic samples.
CONCLUSION
Overall, because of the high likelihood of identifying actionable genomic alterations, CGP should be considered for the majority of patients with inoperable IHCC, and Lbx and Mbx can be considered as part of the diagnostic suite.
IMPLICATIONS FOR PRACTICE
Comprehensive genomic profiling (CGP) should be considered for all patients with intrahepatic cholangiocarcinoma (IHCC) or suspected IHCC, as actionable alterations were commonly found in multiple genes and a wide variety of FGFR2 fusion partners were identified. The disclosure of IHCC trial data correlated with increased use of CGP, an encouraging trend that moves new therapeutic options forward for rare cancers with a rare biomarker. Although tissue from the primary lesion may identify actionable alterations at higher rates, CGP of a liquid biopsy or metastatic site can be considered, particularly if the primary tissue block is exhausted.

Identifiants

pubmed: 34080753
doi: 10.1002/onco.13844
pmc: PMC8417854
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

787-796

Informations de copyright

© 2021 AlphaMed Press.

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Auteurs

Mason A Israel (MA)

Foundation Medicine Inc., Cambridge, Massachusetts, USA.

Natalie Danziger (N)

Foundation Medicine Inc., Cambridge, Massachusetts, USA.

Kimberly A McGregor (KA)

Foundation Medicine Inc., Cambridge, Massachusetts, USA.

Karthikeyan Murugesan (K)

Foundation Medicine Inc., Cambridge, Massachusetts, USA.

Ole Gjoerup (O)

Foundation Medicine Inc., Cambridge, Massachusetts, USA.

Ethan S Sokol (ES)

Foundation Medicine Inc., Cambridge, Massachusetts, USA.

Hanna Tukachinsky (H)

Foundation Medicine Inc., Cambridge, Massachusetts, USA.

Razelle Kurzrock (R)

Center for Personalized Cancer Therapy and Division of Hematology and Oncology, Department of Medicine, University of California, San Diego Moores Cancer Center, La Jolla, California, USA.
Department of Medicine, Division of Hematology and Oncology, University of California, San Diego, San Diego, California, USA.

Shumei Kato (S)

Center for Personalized Cancer Therapy and Division of Hematology and Oncology, Department of Medicine, University of California, San Diego Moores Cancer Center, La Jolla, California, USA.
Department of Medicine, Division of Hematology and Oncology, University of California, San Diego, San Diego, California, USA.

Jason K Sicklick (JK)

Center for Personalized Cancer Therapy and Division of Hematology and Oncology, Department of Medicine, University of California, San Diego Moores Cancer Center, La Jolla, California, USA.
Department of Surgery, Division of Surgical Oncology, University of California, San Diego, San Diego, California, USA.

Halla S Nimeiri (HS)

Foundation Medicine Inc., Cambridge, Massachusetts, USA.

Geoffrey R Oxnard (GR)

Foundation Medicine Inc., Cambridge, Massachusetts, USA.

Jeffrey S Ross (JS)

Foundation Medicine Inc., Cambridge, Massachusetts, USA.
Departments of Urology and Pathology, SUNY Upstate Medical University, Syracuse, New York, USA.

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