Pituitary tumor

disease
On this page

Also known as neoplasm of pituitaryneoplasm of pituitary glandneoplasm of the pituitaryneoplasm of the pituitary glandpituitary gland neoplasmpituitary gland tumorpituitary gland tumourpituitary neoplasmtumor of pituitarytumor of pituitary glandtumor of the pituitarytumor of the pituitary glandtumour of pituitarytumour of pituitary glandtumour of the pituitarytumour of the pituitary gland

Summary

Pituitary tumor (MONDO:0017611) is a cancer (an umbrella term covering 9 Mondo subtypes) and 75 clinical trials. Top therapeutic interventions include cabergoline, bromocriptine, and corticorelin ovine triflutate. A subtype of endocrine gland neoplasm — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • Classification: Cancer
  • Umbrella term: 9 Mondo subtypes
  • Clinical trials: 75

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical namepituitary tumor
Mondo IDMONDO:0017611
Orphanet304055
NCITC3330
SNOMED CT127024001
UMLSC0032019
MedGen19326
GARD0021253
Anatomy (UBERON)UBERON:0000007
Is cancer (heuristic)yes

Also known as: neoplasm of pituitary · neoplasm of pituitary gland · neoplasm of the pituitary · neoplasm of the pituitary gland · pituitary gland neoplasm · pituitary gland tumor · pituitary gland tumour · pituitary neoplasm · pituitary tumor · tumor of pituitary · tumor of pituitary gland · tumor of the pituitary · tumor of the pituitary gland · tumour of pituitary · tumour of pituitary gland · tumour of the pituitary · tumour of the pituitary gland

Disease family

This is a subtype of endocrine gland neoplasm. 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 etiologic mechanism › cancer or benign tumorneoplastic disease or syndromeneoplasmendocrine gland neoplasmpituitary tumor

Related subtypes (13): benign endocrine neoplasm, thymus neoplasm, granulosa cell tumor, thyroid tumor, familial tumoral calcinosis, neuroendocrine neoplasm, malignant endocrine neoplasm, non-functioning endocrine neoplasm, functioning endocrine neoplasm, adrenal gland neoplasm, pineal body neoplasm, tumor of parathyroid gland, liver and intrahepatic bile duct neoplasm

Subtypes (9): pituitary cancer, posterior pituitary gland neoplasm, prolactin producing pituitary tumor, non-functioning pituitary gland neoplasm, functioning pituitary gland neoplasm, pituitary gland adenoma, growth hormone-producing pituitary gland neoplasm, benign neoplasm of pituitary gland, ACTH-producing pituitary gland neoplasm

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: 75.

Phase distribution (across all retrieved trials)

PhaseTrials
Not specified57
PHASE27
PHASE45
PHASE13
EARLY_PHASE12
PHASE31

Top trials by phase / activity

NCTPhaseStatusTitle
NCT01794793PHASE4COMPLETEDStudy to Allow Access to Pasireotide for Patients Benefiting From Pasireotide Treatment in Novartis-sponsored Studies
NCT02190994PHASE4UNKNOWNEffect of Perioperative Glucocorticoid Replacement on Prognosis of Surgical Patients With Sellar Lesions
NCT02351700PHASE4COMPLETEDAnalgesia Regimens Following Trans-sphenoidal Surgery for Pituitary Tumors
NCT02549768PHASE4UNKNOWNEffect of Dexmedetomidine on Plasmatic Cortisol Response in Transsphenoidal Surgery
NCT03132259PHASE4UNKNOWNComparative Low and High Dose of Dexmedethomidine in Pituitary Tumor Removal by Transphenoid Approach
NCT02288962PHASE3ACTIVE_NOT_RECRUITINGDopamine Agonist Treatment of Non-functioning Pituitary Adenomas
NCT04042753PHASE2ACTIVE_NOT_RECRUITINGNivolumab and Ipilimumab in People With Aggressive Pituitary Tumors
NCT00001860PHASE2COMPLETEDSandostatin LAR Depot vs. Surgery for Treating Acromegaly
NCT00003514PHASE2WITHDRAWNAntineoplaston Therapy in Treating Patients With Neuroendocrine Tumor That Is Metastatic or Unlikely to Respond to Surgery or Radiation Therapy
NCT00958841PHASE2TERMINATEDStudy of Pasireotide in Patients With Rare Tumors of Neuroendocrine Origin
NCT01689727PHASE2COMPLETEDSafety and Efficacy of FolateScan (Technetium Tc 99m EC20) in Subjects With Pituitary Tumors
NCT02749227PHASE2TERMINATEDPasireotide LAR Therapy of Silent Corticotroph Pituitary Tumors
NCT04863339PHASE2WITHDRAWNTranexamic Acid for Blood Loss Minimization in Endoscopic Pituitary Surgery
NCT01088763PHASE1TERMINATEDGamma-Secretase Inhibitor RO4929097 in Treating Young Patients With Relapsed or Refractory Solid Tumors, CNS Tumors, Lymphoma, or T-Cell Leukemia
NCT02629549PHASE1TERMINATEDIntraoperative Imaging of Pituitary Adenomas by OTL
NCT04212793PHASE1COMPLETEDDetection of PitNET Tissue During TSS Using Bevacizumab-800CW
NCT07254104EARLY_PHASE1ENROLLING_BY_INVITATIONClinical Evaluation of [68Ga]Ga-NOTA-RF PET Imaging Targeting RFVT3 in Patients With Pituitary Tumors
NCT01459237EARLY_PHASE1COMPLETEDEffects of Hormone Stimulation on Brain Scans for Cushing s Disease
NCT00599092Not specifiedRECRUITINGPituitary Tumor Surveillance: Pathogenic Correlation
NCT03665064Not specifiedACTIVE_NOT_RECRUITINGLong Term Outcome Study in Patients With Pituitary Disorders
NCT03678389Not specifiedRECRUITINGFeasibility of Endosphenoidal Coil Placement for Imaging of the Sella During Transsphenoidal Surgery
NCT04087902Not specifiedACTIVE_NOT_RECRUITINGLong-Term Longitudinal QoL in Patients Undergoing EEA
NCT05139277Not specifiedRECRUITINGEvaluation of the CONVIVO System
NCT05659524Not specifiedRECRUITINGNasal Outcomes Using Saline Irrigations After Endonasal Pituitary Surgery
NCT06266949Not specifiedNOT_YET_RECRUITINGPerimetry Based on Eye-movements in Patients With (Supra)Sellar Tumors
NCT06282224Not specifiedRECRUITINGApplication of Augmented Reality Neuronavigation in Transnasal Endoscopic Skull Base Surgery
NCT06472505Not specifiedRECRUITINGUsing Polyglycolic Acid Mesh Prevents Cerebrospinal Fluid Leakage
NCT06523582Not specifiedRECRUITINGGenetic Bases of Neuroendocrine Neoplasms in Mexican Patients
NCT06556186Not specifiedNOT_YET_RECRUITINGSurgical and Pharmacological Efficacy of Knosp Grade 0-2 Prolactinoma
NCT06705036Not specifiedRECRUITINGDifferential Study of Invasive Pituitary Adenomas in the Sellar and Cavernous Sinus Regions
NCT06936813Not specifiedACTIVE_NOT_RECRUITINGThe PROMISE Survey
NCT07594262Not specifiedRECRUITINGNET-TIME: Inflammatory Tumor Microenvironment in Pituitary Neoplasm
NCT00001171Not specifiedCOMPLETEDEvaluation of Factors in Human Brain Tumors
NCT00001981Not specifiedCOMPLETEDThe Treatment and Natural History of Acromegaly
NCT00005664Not specifiedTERMINATEDEvaluation of Patients With Endocrine-Related Conditions
NCT00462475Not specifiedCOMPLETEDEffect of 5 Years of GH Replacement on Atherosclerosis
NCT00565903Not specifiedCOMPLETEDElucidating the Genetic Basis of the Pleuropulmonary Blastoma (PPB) Familial Cancer Syndrome
NCT00598949Not specifiedUNKNOWNPrevalence of Pituitary Incidentaloma in Relatives of Patients With Pituitary Adenoma
NCT00646308Not specifiedTERMINATEDAssessment of Cardiovascular Risk Markers in Growth Hormone Deficient Patients With Nonsecreting Pituitary Adenomas
NCT00852501Not specifiedUNKNOWNCharacterization of Receptors in Non-functioning Pituitary Macroadenomas

Drugs tested across these trials (top 30)

MoleculeMax phaseTrials referencing
CABERGOLINE43
BROMOCRIPTINE41
CORTICORELIN OVINE TRIFLUTATE41
HYDROCORTISONE41
PAFOLACIANINE41
PASIREOTIDE41
PREDNISONE41
ANTINEOPLASTON A1031
CHEMBL459310503
CHEMBL519247003
CHEMBL1572001