ID

45423

Description

Principal Investigator: Mary V. Relling, PharmD, St. Jude Children Research Hospital, Memphis, TN, USA MeSH: Precursor Cell Lymphoblastic Leukemia-Lymphoma https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000638 Using risk-directed therapy for childhood acute lymphoblastic leukemia (ALL), outcome has improved dramatically in the last 40 years. However, a substantial portion of patients experience relapse, many of whom have no known risk factors. Taking a genome-wide approach, we sought to evaluate the relationships between germline SNP genotypes and the risk of relapse in 2,535 children with newly diagnosed ALL after adjusting for genetic ancestry and treatment regimen. We examine prognostic value of selected SNPs in the context of known relapse risk factors (molecular subtypes, minimal residual disease, age and leukocyte count at diagnosis). Associations of relapse-related SNPs with pharmacokinetic and pharmacodynamics of antileukemic drugs offer plausible mechanism by which they are linked to treatment outcome. Finally, we aim to identify SNPs that are related to both genetic ancestry and relapse which are likely to contribute to racial disparities in ALL survival.

Lien

dbGaP-study=phs000638

Mots-clés

  1. 25/11/2022 25/11/2022 - Chiara Middel
Détendeur de droits

Mary V. Relling, PharmD, St. Jude Children Research Hospital, Memphis, TN, USA

Téléchargé le

25 novembre 2022

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

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dbGaP phs000638 Genome-Wide Association Study of Relapse of Childhood Acute Lymphoblastic Leukemia

Eligibility Criteria

Inclusion and exclusion criteria
Description

Inclusion and exclusion criteria

Alias
UMLS CUI [1,1]
C1512693
UMLS CUI [1,2]
C0680251
Inclusion/exclusion was based on enrollment on the clinical trials of ALL at St. Jude Children Research Hospital and the Children Oncology Group, informed consent following OPRR guidelines, availability of germline DNA, and data quality in subsequent genotyping experiments.
Description

Elig.phs000638.v1.p1.1

Type de données

boolean

Alias
UMLS CUI [1,1]
C1516879
UMLS CUI [1,2]
C0008976
UMLS CUI [1,3]
C0023449
UMLS CUI [1,4]
C1519168
UMLS CUI [1,5]
C1516477
UMLS CUI [2,1]
C0021430
UMLS CUI [2,2]
C0162791
UMLS CUI [3,1]
C0470187
UMLS CUI [3,2]
C2986526
UMLS CUI [4,1]
C0242483
UMLS CUI [4,2]
C1285573
UMLS CUI [4,3]
C0681814

Similar models

Eligibility Criteria

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
Inclusion and exclusion criteria
C1512693 (UMLS CUI [1,1])
C0680251 (UMLS CUI [1,2])
Elig.phs000638.v1.p1.1
Item
Inclusion/exclusion was based on enrollment on the clinical trials of ALL at St. Jude Children Research Hospital and the Children Oncology Group, informed consent following OPRR guidelines, availability of germline DNA, and data quality in subsequent genotyping experiments.
boolean
C1516879 (UMLS CUI [1,1])
C0008976 (UMLS CUI [1,2])
C0023449 (UMLS CUI [1,3])
C1519168 (UMLS CUI [1,4])
C1516477 (UMLS CUI [1,5])
C0021430 (UMLS CUI [2,1])
C0162791 (UMLS CUI [2,2])
C0470187 (UMLS CUI [3,1])
C2986526 (UMLS CUI [3,2])
C0242483 (UMLS CUI [4,1])
C1285573 (UMLS CUI [4,2])
C0681814 (UMLS CUI [4,3])

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