Acute Lymphoblastic Leukemia - Phase I
Can it answer your research question?
3 of 6 supportedOverall survival
SupportedVital status and time are populated; median follow-up 4.1 years; 23 cases with follow-up; endpoint: overall survival.API
Progression or recurrence
Supportedprogression_or_recurrenceis informative for 63% of cases.APITreatment response
Not supportedtreatment_outcomeis populated for no case in the harmonized records.APIWhich drug was given
Not supportedtherapeutic_agentsis recorded for no case in the harmonized records.APIStage-adjusted modelling
Not supportedajcc_pathologic_stageis informative for no case in the harmonized records.APIAnalysis by race or ethnicity
SupportedEthnicity is informative for 96% of cases.API
At a glance
Every percentage is the repository’s own record of what is filled inSubjectCALC
As filed by the repository
Who is in the cohortAPI
- Sex14 male · 9 female · 1 unknown
- Race18 white · 2 asian · 1 black or african american · 2 unknown · 1 not reported
- Ethnicity13 hispanic or latino · 10 not hispanic or latino · 1 not reported
- Vital status14 dead · 9 alive · 1 not reported
Age at diagnosis
What was measured, and on how many
- Bulk RNA sequencing12 of 24 · 50%
- Whole genome sequencing10 of 24 · 42%
- Clinical24 of 24 · 100%
- Copy Number Variation1 of 24 · 4%
- Somatic Structural Variation1 of 24 · 4%
How complete all 29 clinical fields are - 9 informative for at least 80% of cases
Outcome
Follow-up
Treatment
Diagnosis
Demographics
Access
Data Access Request through dbGaP using an eRA Commons account; institutional signing official approval required
- Open components
- 18 open-access files
- Controlled components
- 91 controlled-access files
- Typical turnaround
- days to a few weeks after signing official approval
- License
- NIH Genomic Data Sharing Policy terms
- Citation requirement
- Cite the dataset accession and the program's publication guidelines; see the GDC publication policy.
What it is good for
Written and checked by a reviewer, not generated from metadata.
No reviewed research questions yet. The measurements and field completeness above are machine-extracted and still useful for judging fit.
What it cannot tell you
Written by a reviewer against the source, not inferred from what is missing.
No reviewed limitations yet. Check the field completeness chart above before committing to an analysis. Low coverage on an endpoint you need is the most common blocker.
Who has used it
Articles that analyzed these data, counted separately from articles that only cited the paper. Only the first counts as reuse.
What articles did with it
- Mentioned the dataset0
- Accession found in text14
- Declared using it6
- Analyzed the data14
Against comparable datasets
- Analyzed it14
- Expected~15
- Reuse is within the expected range for comparable datasets (index -0.07).
Articles that analyzed the data
Community examples
Share your exampleAnalyses someone ran on these data end to end, each with a receipt recording when it ran, against which packages and for how long.
Nobody has shared an analysis of this dataset yet. The examples on other datasets cover the common patterns and can be adapted - and if you adapt one, it belongs here.
Start here
Starter code generated from this record’s own identifiers, then the access steps.
Get the data in code
GDC: list open files and download thempython
import json, requests
PROJECT = "TARGET-ALL-P1"
filters = {"op": "and", "content": [
{"op": "in", "content": {"field": "cases.project.project_id", "value": [PROJECT]}},
{"op": "in", "content": {"field": "access", "value": ["open"]}},
]}
params = {"filters": json.dumps(filters),
"fields": "file_id,file_name,data_category,data_type,file_size",
"size": "10000", "format": "JSON"}
files = requests.get("https://api.gdc.cancer.gov/files", params=params, timeout=60).json()["data"]["hits"]
print(len(files), "open files")
# Write a manifest and fetch with the GDC client (https://gdc.cancer.gov/access-data/gdc-data-transfer-tool)
with open("manifest.txt", "w") as fh:
fh.write("id\n" + "\n".join(f["file_id"] for f in files))
# $ gdc-client download -m manifest.txtGDC: clinical table for every casepython
import json, requests
filters = {"op": "in", "content": {"field": "project.project_id", "value": ["TARGET-ALL-P1"]}}
params = {"filters": json.dumps(filters), "size": "5000", "format": "TSV",
"fields": ",".join([
"submitter_id", "demographic.vital_status", "demographic.days_to_death",
"diagnoses.days_to_last_follow_up", "diagnoses.ajcc_pathologic_stage",
"diagnoses.treatments.treatment_type", "diagnoses.treatments.treatment_outcome"])}
tsv = requests.get("https://api.gdc.cancer.gov/cases", params=params, timeout=60).text
open("TARGET-ALL-P1_clinical.tsv", "w").write(tsv)This page as data: limitations firstbash
curl -s https://cd2s.vercel.app/data/datasets/gdc-target-all-p1.json | python3 -c '
import json, sys
r = json.load(sys.stdin)
for l in r["limitations"]:
print(l["severity"].upper(), "-", l["statement"][:120])
print("survival endpoint:", r["longitudinal"]["has_survival_endpoint"], "| treatment response:", r["longitudinal"]["has_treatment_response"])'Access steps
- Open the project in the GDC Data PortalFor people
Check the portal's current case and file counts before requesting anything; the cohort can change after this record was built.
https://portal.gdc.cancer.gov/projects/TARGET-ALL-P1 - Download the open files without an accountFor people
18 open-access files are marked open access. Add them to a portal cart, export a manifest, and fetch it with the GDC Data Transfer Tool.
https://gdc.cancer.gov/access-data/gdc-data-transfer-toolgdc-client download -m gdc_manifest.txt - Request controlled access through dbGaPFor people
91 controlled-access files require an approved data access request. The request starts at dbGaP, not in the portal. The relevant study is phs000463.
https://gdc.cancer.gov/access-data/obtaining-access-controlled-data - Download controlled files with your tokenFor people
An approved request yields a token. The same manifest fetches nothing controlled without it.
https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000463gdc-client download -m gdc_manifest.txt -t gdc-user-token.txt - Query the project from code, with no credentialsFor agents
The file index is public even where files are not, so an agent can size the cohort before anyone requests access.
https://docs.gdc.cancer.gov/API/Users_Guide/Getting_Started/curl -s 'https://api.gdc.cancer.gov/files' --get \ --data-urlencode 'filters={"op":"in","content":{"field":"cases.project.project_id","value":["TARGET-ALL-P1"]}}' \ --data-urlencode 'fields=file_id,file_name,data_type' \ --data-urlencode 'size=10000' --data-urlencode 'format=TSV' - Pass the token when the agent needs controlled filesFor agents
Without a token, an API query may return only the open subset. Compare returned counts with the record before treating them as the whole cohort.
https://docs.gdc.cancer.gov/API/Users_Guide/Getting_Started/curl -H "X-Auth-Token: $GDC_TOKEN" https://api.gdc.cancer.gov/data/<file_id>
Provenance
All of it, and more, is in this record’s JSON.
Identifiers
- GDC projectTARGET-ALL-P1API
- GDC programAPI
- dbGaP studyphs000463API
Versions and verification
- Released
- 1 Jan 2016
- Metadata retrieved
- 18 Sept 2026
- Review status
- Machine-extracted
- Data generation funding
- Funded data generation
Funding
Funded reuse of these data
- R37CA036401PHARMACOGENOMICS OF CHILDHOOD LEUKEMIA (ALL)WILLIAM E EVANSAPI
- R01CA036401Pharmacogenomics of Childhood Leukemia ALLWILLIAM E EVANSAPI
- R50CA211461Open Software and Resource Development Leveraging Next-gen Sequencing Data to Facilitate Computational Analysis of Cancer BiologyBrian HaasAPI
- K08CA273527Pathogenic role of human papillomavirus (HPV) DNA Integration and clonal expansion in cervical tumorigenesisAnne Van ArsdaleAPI
- R35CA210065Molecular pathways and targeted therapies in human leukemiaAdolfo A. FerrandoAPI
- R01CA196604Direct coregulation of Notch1 by Zmiz1 in T-cell leukemiaMARK Y CHIANGAPI
- K08CA208013Oncogenic programs driven by notch signaling in B-cell lymphomaRUSSELL James Hubbard RYANAPI
- F30CA228228Exploiting the Context-Dependence of Notch to Develop Safer T-ALL therapyAnna Catherine McCarterAPI
- T32CA009056Tumor Cell Biology Training ProgramGay M Crooks, David A. NathansonAPI
- K12CA076931Physician Scientist Training in Clinical OncologySTEPHEN Patrick HUNGER, LYNN M. SCHUCHTERAPI
Funded infrastructure or harmonization
- U10CA098543Children's Oncology Group Chair's GrantPETER C. ADAMSON, GREGORY H REAMANAPI
- P30CA021765Cancer Biology (CBP)Douglas R. Green, Michael A DyerAPI
- U24CA196172ECOG-ACRIN Biospecimen Bank to Support NCTNSTANLEY R. HAMILTON, Scott D JewellAPI
- U24CA196171The Alliance NCTN Biorepository and Biospecimen ResourceMine Cicek, Wendy FrankelAPI
- U24CA114766Support for Human Specimen Banking in NCI-Sponsored Clinical Trials-(CGB)Nilsa Del Carmen Ramirez Milan, GREGORY H REAMANAPI
- U24CA114737ECOG Specimen BankingROBERT L COMISAPI
- U10CA180899Children's Oncology Group Statistics and Data CenterTODD A ALONZO, Meenakshi DevidasAPI
- U10CA180861ITSC for Leukemia: Novel Molecular Strategies for NCTN: "Individualized" TherapieCLARA D BLOOMFIELD, GUIDO MARCUCCIAPI
- U10CA180850OSU as Network Lead Academic Participating Site for the NCI NCTNKRISTIE A BLUM, ARNAB CHAKRAVARTIAPI
- U10CA180827ECOG-ACRIN INTEGRATED LEUKEMIA TRANSLATIONAL RESEARCH CENTERRoss L Levine, ARI M. MELNICKAPI