Gastrin-producing neuroendocrine tumor

disease
On this page

Also known as G cell tumorG cell tumourG-cell gastrin producing tumorG-cell gastrin producing tumourG-cell tumorG-cell tumourgastrin cell tumorgastrin secreting tumorgastrin secreting tumourgastrin-producing NETgastrinomamalignant gastrinoma

Summary

Gastrin-producing neuroendocrine tumor (MONDO:0003523) is a cancer and 17 clinical trials. Top therapeutic interventions include edotreotide gallium ga-68, esomeprazole, and gefitinib. A subtype of digestive system neuroendocrine tumor, grade 1/2 — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • Classification: Cancer
  • Clinical trials: 17

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical namegastrin-producing neuroendocrine tumor
Mondo IDMONDO:0003523
DOIDDOID:5577
ICD-111333125891
NCITC3050
UMLSC0017150
MedGen6551
GARD0023546
Is cancer (heuristic)yes

Also known as: G cell tumor · G cell tumour · G-cell gastrin producing tumor · G-cell gastrin producing tumour · G-cell tumor · G-cell tumour · gastrin cell tumor · gastrin secreting tumor · gastrin secreting tumour · gastrin-producing NET · gastrin-producing neuroendocrine tumor · gastrinoma · malignant gastrinoma

Disease family

This is a subtype of digestive system neuroendocrine tumor, grade 1/2. Genetic, therapeutic, and trial evidence is largely curated at the broader-term level — see the parent page for the associated-gene cohort and molecular evidence.

Classification path: disease › human disease › disease by body system or component › digestive system disorderdigestive system neuroendocrine neoplasmdigestive system neuroendocrine tumor, grade 1/2gastrin-producing neuroendocrine tumor

Related subtypes (9): small intestine neuroendocrine tumor, well differentiated, low or intermediate grade, esophageal neuroendocrine tumor, L-cell glucagon-like peptide-producing neuroendocrine tumor, gastric neuroendocrine tumor, well differentiated, low or intermediate grade, neuroendocrine tumor of the colon, well differentiated, low or intermediate grade tumor, rectal neuroendocrine tumor, gallbladder neuroendocrine tumor, grade 1/2, pancreatic neuroendocrine tumor, intestinal neuroendocrine tumor G1

Subtypes (3): gastric gastrin-producing neuroendocrine tumor, pancreatic gastrin-producing neuroendocrine tumor, duodenal gastrin-producing neuroendocrine tumor

Genetics & variants

GWAS landscape

No GWAS associations recorded — common-variant (GWAS) studies don’t cover this disease (typical for Mendelian / rare diseases). See the curated gene cohort and Mendelian overlap below.

Variant details and genetic-evidence tiers

No tiered GWAS variants or ClinVar records for this disease.

Genes & proteins

No associated-gene cohort resolved for this disease. Atlas builds the molecular and therapeutic sections — associated genes, protein families, druggability, pathways, interactions, and drug associations — by aggregating over a disease’s associated genes (resolved via GWAS / GenCC / ClinVar / CIViC), and none resolved here. This is expected for antibody-mediated, autoimmune, or otherwise non-gene-defined conditions; the curated evidence for this disease is its clinical features, GWAS susceptibility, and clinical trials (above).

Function

No pathway enrichment — requires an associated-gene cohort.

Therapeutics

No druggable-target or therapeutic data for this disease’s cohort.

Clinical trials & evidence

Clinical trials

Clinical trials: 17.

Phase distribution (across all retrieved trials)

PhaseTrials
PHASE212
PHASE13
Not specified2

Top trials by phase / activity

NCTPhaseStatusTitle
NCT01824875PHASE2ACTIVE_NOT_RECRUITINGTemozolomide With or Without Capecitabine in Treating Patients With Advanced Pancreatic Neuroendocrine Tumors
NCT00001191PHASE2COMPLETEDThe Use of Oral Omeprazole and Intravenous Pantoprazole in Patients With Hypersecretion of Gastric Acid
NCT00075439PHASE2COMPLETEDGefitinib in Treating Patients With Progressive Metastatic Neuroendocrine Tumors
NCT00084461PHASE2TERMINATEDRomidepsin in Treating Patients With Locally Advanced or Metastatic Neuroendocrine Tumors
NCT00131911PHASE2COMPLETEDSorafenib Tosylate in Treating Patients With Progressive Metastatic Neuroendocrine Tumors
NCT00454363PHASE2COMPLETEDPazopanib Hydrochloride in Treating Patients With Advanced Neuroendocrine Cancer
NCT01525082PHASE2COMPLETEDCapecitabine, Temozolomide, and Bevacizumab for Metastatic or Unresectable Pancreatic Neuroendocrine Tumors
NCT02031536PHASE2TERMINATEDEverolimus in Patients With Pancreatic Neuroendocrine Tumors Metastatic to the Liver Previously Treated With Surgery
NCT02108782PHASE2WITHDRAWNDovitinib Lactate in Treating Patients With Pancreatic Neuroendocrine Tumors
NCT02259725PHASE2COMPLETEDRegorafenib in Treating Patients With Advanced or Metastatic Neuroendocrine Tumors
NCT02273752PHASE2TERMINATEDPharmacokinetically Guided Everolimus in Patients With Breast Cancer, Pancreatic Neuroendocrine Tumors, or Kidney Cancer
NCT04915144PHASE2WITHDRAWN177Lu-DOTATOC for the Treatment of Patients With Somatostatin Receptor Positive NETs
NCT00004074PHASE1COMPLETEDInterleukin-12 and Trastuzumab in Treating Patients With Cancer That Has High Levels of HER2/Neu
NCT00655655PHASE1COMPLETEDEverolimus and Vatalanib in Treating Patients With Advanced Solid Tumors
NCT01204476PHASE1COMPLETEDCixutumumab, Everolimus, and Octreotide Acetate in Treating Patients With Advanced Low to Intermediate Grade Neuroendocrine Carcinoma
NCT03583528Not specifiedACTIVE_NOT_RECRUITINGDOTATOC PET/CT for Imaging NET Patients
NCT00001240Not specifiedCOMPLETEDEvaluating Patients With Abnormal Levels of Gastric Acid

Drugs tested across these trials (top 30)

MoleculeMax phaseTrials referencing
EDOTREOTIDE GALLIUM GA-6841
ESOMEPRAZOLE41
GEFITINIB41
OCTREOTIDE ACETATE41
OMEPRAZOLE41
PANTOPRAZOLE41
PAZOPANIB HYDROCHLORIDE41
REGORAFENIB41
ROMIDEPSIN41
SORAFENIB41
VATALANIB32
CIXUTUMUMAB21
DOVITINIB LACTATE21
EDODEKIN ALFA21
LUTETIUM LU177 EDOTREOTIDE21
CHEMBL406646501