ID

45822

Beschreibung

Principal Investigator: MeSH: Neoplasms,Sarcoma,Sarcoma, Ewing,Rhabdomyosarcoma,Wilms Tumor,Desmoplastic Small Round Cell Tumor,Carcinoma, Transitional Cell,Rhabdoid Tumor,Sarcoma, Synovial,Neuroblastoma,Neuroendocrine tumors https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs001052 The Center for Cancer Research (CCR), of the intramural NCI undertook a multidimensional clinical genomics study of children and adolescent young adults with relapsed and refractory cancers who were enrolled on other therapeutic trials to determine the feasibility of a genome guided precision therapy protocol in these patients.

Link

dbGaP study=phs001052

Stichworte

  1. 09.07.23 09.07.23 - Simon Heim
Rechteinhaber

dbGAP

Hochgeladen am

9. Juli 2023

DOI

Für eine Beantragung loggen Sie sich ein.

Lizenz

Creative Commons BY 4.0

Modell Kommentare :

Hier können Sie das Modell kommentieren. Über die Sprechblasen an den Itemgruppen und Items können Sie diese spezifisch kommentieren.

Itemgroup Kommentare für :

Item Kommentare für :


Keine Kommentare

Um Formulare herunterzuladen müssen Sie angemeldet sein. Bitte loggen Sie sich ein oder registrieren Sie sich kostenlos.

dbGaP phs001052 Multi-Dimensional ClinOmics for Precision Therapy

Eligibility Criteria

Inclusion and exclusion criteria
Beschreibung

Inclusion and exclusion criteria

Alias
UMLS CUI [1,1]
C1512693
UMLS CUI [1,2]
C0680251
The study was comprised of a unique cohort of 59 pediatric patients with solid tumors outside of the central nervous system (CNS) who presented to the National Institutes of Health (NIH) from 2010 to December 2014. Patients had to have matched tumor/normal DNA and RNA available for analysis to qualify for the study.
Beschreibung

The study was comprised of a unique cohort of 59 pediatric patients with solid tumors outside of the central nervous system (CNS) who presented to the National Institutes of Health (NIH) from 2010 to December 2014. Patients had to have matched tumor/normal DNA and RNA available for analysis to qualify for the study.

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1709709
UMLS CUI [1,2]
C1521725
UMLS CUI [1,3]
C0280100
UMLS CUI [1,4]
C0205101
UMLS CUI [1,5]
C3714787
UMLS CUI [1,6]
C0027468
UMLS CUI [1,7]
C0332168
UMLS CUI [1,8]
C0150103
UMLS CUI [1,9]
C4331441
UMLS CUI [1,10]
C4331443
UMLS CUI [1,11]
C0035668
UMLS CUI [1,12]
C0012854
UMLS CUI [1,13]
C0871309
UMLS CUI [1,14]
C0936012

Ähnliche Modelle

Eligibility Criteria

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
Inclusion and exclusion criteria
C1512693 (UMLS CUI [1,1])
C0680251 (UMLS CUI [1,2])
The study was comprised of a unique cohort of 59 pediatric patients with solid tumors outside of the central nervous system (CNS) who presented to the National Institutes of Health (NIH) from 2010 to December 2014. Patients had to have matched tumor/normal DNA and RNA available for analysis to qualify for the study.
Item
The study was comprised of a unique cohort of 59 pediatric patients with solid tumors outside of the central nervous system (CNS) who presented to the National Institutes of Health (NIH) from 2010 to December 2014. Patients had to have matched tumor/normal DNA and RNA available for analysis to qualify for the study.
boolean
C1709709 (UMLS CUI [1,1])
C1521725 (UMLS CUI [1,2])
C0280100 (UMLS CUI [1,3])
C0205101 (UMLS CUI [1,4])
C3714787 (UMLS CUI [1,5])
C0027468 (UMLS CUI [1,6])
C0332168 (UMLS CUI [1,7])
C0150103 (UMLS CUI [1,8])
C4331441 (UMLS CUI [1,9])
C4331443 (UMLS CUI [1,10])
C0035668 (UMLS CUI [1,11])
C0012854 (UMLS CUI [1,12])
C0871309 (UMLS CUI [1,13])
C0936012 (UMLS CUI [1,14])

Benutzen Sie dieses Formular für Rückmeldungen, Fragen und Verbesserungsvorschläge.

Mit * gekennzeichnete Felder sind notwendig.

Benötigen Sie Hilfe bei der Suche? Um mehr Details zu erfahren und die Suche effektiver nutzen zu können schauen Sie sich doch das entsprechende Video auf unserer Tutorial Seite an.

Zum Video