ID

45497

Description

Principal Investigator: David Solit, MD, Memorial Sloan-Kettering Cancer Center, New York, NY, USA MeSH: Urinary Bladder Neoplasms https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000535 One primary bladder cancer and paired peripheral blood sample were subjected to whole genome sequencing on an Illumina HiSeq 2000 platform. This technology was utilized to investigate the genetic basis of a durable remission of metastatic bladder cancer in a patient treated with everolimus, a drug that inhibits the mTOR (mammalian target of rapamycin) signaling pathway. Among the somatic mutations found was a loss-of-function mutation in TSC1 (Tuberous Sclerosis Complex 1), a regulator of mTOR pathway activation. Targeted sequencing using an exon capture and sequencing assay was performed on 13 tumors derived from patients on the same everolimus trial as the index patient and the sequencing data from these tumors is included. TSC1 mutation status was correlated with response to everolimus. The index patient responder tumor and peripheral blood DNA were also subjected to exon capture and sequencing.

Link

dbGap study = phs000535

Keywords

  1. 11/7/22 11/7/22 - Simon Heim
  2. 12/13/22 12/13/22 - Kristina Keller
Copyright Holder

David Solit, MD, Memorial Sloan-Kettering Cancer Center, New York, NY, USA

Uploaded on

December 13, 2022

DOI

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License

Creative Commons BY 4.0

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dbGaP phs000535 Genome and Targeted Sequencing of Bladder Cancer

Eligibility Criteria

Inclusion and exclusion criteria
Description

Inclusion and exclusion criteria

Alias
UMLS CUI [1,1]
C1512693
UMLS CUI [1,2]
C0680251
All cases were derived from patients on a phase II study of everolimus performed at Memorial Sloan-Kettering Cancer Center (ClinicalTrials.gov number NCT00805129). Patients were analyzed for which adequate tumor and normal tissue was available for sequencing. DNA was extracted from tumor tissue and from peripheral blood or adjacent normal urothelial tissue.
Description

All cases were derived from patients on a phase II study of everolimus performed at Memorial Sloan-Kettering Cancer Center (ClinicalTrials.gov number NCT00805129). Patients were analyzed for which adequate tumor and normal tissue was available for sequencing. DNA was extracted from tumor tissue and from peripheral blood or adjacent normal urothelial tissue.

Data type

boolean

Alias
UMLS CUI [1,1]
C1706256
UMLS CUI [1,2]
C0282460
UMLS CUI [1,3]
C0541315
UMLS CUI [1,4]
C1513120
UMLS CUI [2,1]
C0475358
UMLS CUI [2,2]
C3640076
UMLS CUI [2,3]
C0040300
UMLS CUI [3,1]
C3839098
UMLS CUI [3,2]
C0475358
UMLS CUI [3,3]
C0229664
UMLS CUI [3,4]
C0205307
UMLS CUI [3,5]
C0227598

Similar models

Eligibility Criteria

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Inclusion and exclusion criteria
C1512693 (UMLS CUI [1,1])
C0680251 (UMLS CUI [1,2])
All cases were derived from patients on a phase II study of everolimus performed at Memorial Sloan-Kettering Cancer Center (ClinicalTrials.gov number NCT00805129). Patients were analyzed for which adequate tumor and normal tissue was available for sequencing. DNA was extracted from tumor tissue and from peripheral blood or adjacent normal urothelial tissue.
Item
All cases were derived from patients on a phase II study of everolimus performed at Memorial Sloan-Kettering Cancer Center (ClinicalTrials.gov number NCT00805129). Patients were analyzed for which adequate tumor and normal tissue was available for sequencing. DNA was extracted from tumor tissue and from peripheral blood or adjacent normal urothelial tissue.
boolean
C1706256 (UMLS CUI [1,1])
C0282460 (UMLS CUI [1,2])
C0541315 (UMLS CUI [1,3])
C1513120 (UMLS CUI [1,4])
C0475358 (UMLS CUI [2,1])
C3640076 (UMLS CUI [2,2])
C0040300 (UMLS CUI [2,3])
C3839098 (UMLS CUI [3,1])
C0475358 (UMLS CUI [3,2])
C0229664 (UMLS CUI [3,3])
C0205307 (UMLS CUI [3,4])
C0227598 (UMLS CUI [3,5])

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