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Detecting Somatic Mutations for Well-Differentiated Pancreatic Neuroendocrine Tumors in Endoscopic Ultrasound-Guided Fine Needle Aspiration with Next-Generation Sequencing.
Ghabi, Elie M; Habib, Joseph R; Shoucair, Sami; Javed, Ammar A; Sham, Jonathan; Burns, William R; Cameron, John L; Ali, Syed Z; Shin, Eun Ji; Arcidiacono, Paolo Giorgio; Doglioni, Claudio; Falconi, Massimo; Yu, Jun; Partelli, Stefano; He, Jin.
Afiliação
  • Ghabi EM; Department of Surgery, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
  • Habib JR; Department of Surgery, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
  • Shoucair S; Department of Surgery, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
  • Javed AA; Department of Surgery, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
  • Sham J; Department of Surgery, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
  • Burns WR; Department of Surgery, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
  • Cameron JL; Department of Surgery, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
  • Ali SZ; Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
  • Shin EJ; Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
  • Arcidiacono PG; Pancreato-Biliary Endoscopy and Endosonography Division, Pancreas Translational and Clinical Research Center, San Raffaele Scientific Institute IRCCS, Vita Salute San Raffaele University, Milan, Italy.
  • Doglioni C; Pathology Unit, Pancreas Translational and Clinical Research Center, IRCCS Ospedale San Raffaele, ENETS Center of Excellence, Milan, Italy.
  • Falconi M; Pancreatic and Transplant Surgery Unit, Pancreas Translational and Clinical Research Center, IRCCS Ospedale San Raffaele, ENETS Center of Excellence, Milan, Italy.
  • Yu J; Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
  • Partelli S; Pancreatic and Transplant Surgery Unit, Pancreas Translational and Clinical Research Center, IRCCS Ospedale San Raffaele, ENETS Center of Excellence, Milan, Italy.
  • He J; Department of Surgery, Johns Hopkins University School of Medicine, Baltimore, MD, USA. jhe11@jhmi.edu.
Ann Surg Oncol ; 30(12): 7720-7730, 2023 Nov.
Article em En | MEDLINE | ID: mdl-37488390
ABSTRACT

BACKGROUND:

Pancreatic neuroendocrine tumors (PanNETs) exhibit heterogenous behavior, whereby some small tumors are aggressive with a propensity for metastasis. Detection of somatic mutations associated with aggressive biology may help with patient stratification and surgical decision-making in patients with well-differentiated PanNETs. Using next-generation sequencing (NGS), we investigated the feasibility of detecting somatic mutations in endoscopic ultrasound-guided, fine-needle aspiration (EUS-FNA) specimens and determining the mutational concordance between the EUS-FNA specimens and the primary tumors.

METHODS:

Thirty-eight patients with well-differentiated, nonfunctioning PanNETs were obtained from two tertiary referral centers. Patient demographic characteristics and tumor, clinicopathologic features were collected. Tissue from both the EUS-FNA specimen and the primary tumor was extracted from archival tissue blocks. NGS using a panel of ten genes was performed on both samples.

RESULTS:

In our series, the median age was 61.1 years. Tumors were predominantly left-sided (60.5%) and unifocal (94.7%). The median tumor size was 2.2 cm. NGS detected somatic mutations in 29% of primary tumors and 36.8% of EUS-FNA specimens. In primary tumors, DAXX/ATRX mutations were predominantly detected (63.6%). In EUS-FNA specimens, MEN1 mutations were predominantly detected (64.3%). Among non-wild-type specimens, mutational concordance was achieved in 31.6% of cases. In 11 patients with a detectable mutation in the primary tumor, a mutation was detected in the EUS-FNA specimen in 45.5% of cases, with a mutational concordance of 54.5%.

CONCLUSIONS:

NGS can detect somatic mutations in EUS-FNA specimens of well-differentiated PanNETs. Efforts to improve detection sensitivity and mutational concordance are required to overcome current technical limitations.

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2023 Tipo de documento: Article