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E-Poster Display

1178P - Impact of comprehensive genomics profiling on treatment management of patients with advanced neuroendocrine neoplasms

Date

17 Sep 2020

Session

E-Poster Display

Topics

Tumour Site

Neuroendocrine Neoplasms

Presenters

Alejandro Garcia-Alvarez

Citation

Annals of Oncology (2020) 31 (suppl_4): S711-S724. 10.1016/annonc/annonc281

Authors

A. Garcia-Alvarez1, J. Hernando2, A. Vivancos3, S. Landolfi4, A. Casteras5, M. Simo6, A. Garcia Burillo6, L. Blanco7, L. Trejo8, M. Diez Garcia9, D.A. Acosta Eyzaguirre9, J. Capdevila10

Author affiliations

  • 1 Medical Oncology, Vall d'Hebron University Hospital, 8035 - Barcelona/ES
  • 2 Medical Oncology Department, Vall d'Hebron University Hospital, 8035 - Barcelona/ES
  • 3 Genomics, Vall d'Hebron University Hospital, 08035 - Barcelona/ES
  • 4 Pathology, Vall d'Hebron University Hospital, 8035 - Barcelona/ES
  • 5 Endocrinology Department, Vall d'Hebron University Hospital, 8035 - Barcelona/ES
  • 6 Nuclear Medicine Department, Vall d'Hebron University Hospital, 8035 - Barcelona/ES
  • 7 General Surgery Department, Vall d'Hebron University Hospital, 8035 - Barcelona/ES
  • 8 Medical Oncology, Vall d'Hebron Institute of Oncology (VHIO)-Cellex Center, 08035 - Barcelona/ES
  • 9 Medical Oncology Department, Vall d'Hebron University Hospital, 08035 - Barcelona/ES
  • 10 Gastrointestinal And Endocrine Tumor Dept., Vall d`Hebron University Hospital Institut d'Oncologia, 8035 - Barcelona/ES

Resources

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Abstract 1178P

Background

Molecular genomic analyses are widely used in oncology but experience in advanced neuroendocrine neoplasms (NENs) is still limited. We have analyzed the sensibility to detect genomic aberrations in advanced NENs and the potential impact in the treatment decision process.

Methods

We selected the last correlative 100 patients with advanced NENs in which next-generation sequencing (NGS) analyses were performed. Two different NGS techniques were used on formalin fixed paraffin embedded archival tumor samples: amplicon-seq for detection of DNA mutations and nanostring n-counter for fusions and copy number alterations.

Results

We analyzed 37 G1/2 gastroenteropancreatic (GEP) neuroendocrine tumors (NETs), 30 G3 GEP NENs, 21 medullary thyroid cancers (MTC) and 12 G1/G2 NETs of other locations. Genomic alterations were identified in 81.5% of G3 NENs including potentially targetable mutations in KRAS (50%), BRAF (27%), FGFR1 (7%), AKT1/2 (6%), BRCA2 (3%) and ERBB3 (3%). Mutations in RET were detected in 48% of MTC. However, few genomic mutations were identified in G1/G2 NETs (GEP & others) suitable to be treated with targeted agents, including KRAS (6%), FGFR3 (4%), and 1 reported mutation (2%) in each of the following genes of particular interest: FGFR2, ERBB2, PIK3CA and NRAS.

Conclusions

NGS analyses may open new treatment options in advanced G3 NENs and are also mandatory upfront in advanced MTC to guide treatment with selective RET inhibitors in current development. However, the rentability of NGS in G1/G2 NETs is clearly lower and should be used in refractory setting or for investigational purposes.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

The authors.

Funding

Has not received any funding.

Disclosure

J. Hernando: Speaker Bureau/Expert testimony: Eisai, Ipsen, Roche, Novartis, AAA, Angelini. J. Capdevila: Advisory/Consultancy: Novartis, Pfizer, Ipsen, Exelixis, Bayer, Eisai, Advanced Accelerator Applications, Amgen, Sanofi and Merck Serono.; Research grant/Funding (self), Research grant/Funding (institution): Novartis, Ipsen, Pfizer, AstraZeneca, Advanced Accelerator Applications and Eisai.; Non-remunerated activity/ies, Investigator initiated studies supported: Eisai, AstraZeneca and Advanced Accelerator Applications. All other authors have declared no conflicts of interest.

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