pleuropulmonary blastoma (Cancer)
Information
- Disease name
- pleuropulmonary blastoma
- Disease ID
- DOID:4769
- Description
- "A pulmonary blastoma that derives_from the lung or pleural cavity." [url:https\://www.ncbi.nlm.nih.gov/pubmed/30480950]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
| NCT ID | Status | Phase | Summary | Start date | Completion date |
|---|---|---|---|---|---|
| NCT01464606 | Active, not recruiting | N/A | International Pleuropulmonary Blastoma (PPB) Treatment and Biology Registry | December 22, 2009 | December 2024 |
| NCT01353300 | Completed | Gene Mutation in Samples From Young Patients With Pleuropulmonary Blastoma Syndrome at Risk for Developing Cancer | May 2011 | ||
| NCT00565903 | Completed | Elucidating the Genetic Basis of the Pleuropulmonary Blastoma (PPB) Familial Cancer Syndrome | March 2005 | December 31, 2022 | |
| NCT02452554 | Completed | Phase 2 | Lorvotuzumab Mertansine in Treating Younger Patients With Relapsed or Refractory Wilms Tumor, Rhabdomyosarcoma, Neuroblastoma, Pleuropulmonary Blastoma, Malignant Peripheral Nerve Sheath Tumor, or Synovial Sarcoma | October 12, 2015 | September 30, 2021 |
| NCT03044834 | Completed | Review of the Paediatric Pleuropulmonary Blastoma French Series | January 9, 2017 | July 9, 2018 | |
| NCT03044769 | Recruiting | Congenital Lung Anomalies (CLA) Swiss Database | April 1, 2016 | April 1, 2026 | |
| NCT01247597 | Recruiting | DICER1-related Pleuropulmonary Blastoma Cancer Predisposition Syndrome: A Natural History Study | February 13, 2011 | ||
| NCT03382158 | Recruiting | International PPB/DICER1 Registry | December 6, 2016 | December 6, 2035 |
- Disase is a (Disease Ontology)
- DOID:4765
- Cross Reference ID (Disease Ontology)
- GARD:8757
- Cross Reference ID (Disease Ontology)
- ICDO:8973/3
- Cross Reference ID (Disease Ontology)
- MESH:C537516
- Cross Reference ID (Disease Ontology)
- NCI:C5669
- Cross Reference ID (Disease Ontology)
- ORDO:64742
- Cross Reference ID (Disease Ontology)
- SNOMEDCT_US_2023_03_01:707670009
- Cross Reference ID (Disease Ontology)
- UMLS_CUI:C1266144
- HPO Human Phenotype ID (Human Phenotype Ontology)
- HP:0100528