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Datasets/TARGET-ALL-P1

Acute Lymphoblastic Leukemia - Phase I

MixedMachine-extracted
TARGETAvailable from GDC

Can it answer your research question?

3 of 6 supported
  • Overall survival

    Supported

    Vital status and time are populated; median follow-up 4.1 years; 23 cases with follow-up; endpoint: overall survival.API

  • Progression or recurrence

    Supported

    progression_or_recurrence is informative for 63% of cases.API

  • Treatment response

    Not supported

    treatment_outcome is populated for no case in the harmonized records.API

  • Which drug was given

    Not supported

    therapeutic_agents is recorded for no case in the harmonized records.API

  • Stage-adjusted modelling

    Not supported

    ajcc_pathologic_stage is informative for no case in the harmonized records.API

  • Analysis by race or ethnicity

    Supported

    Ethnicity is informative for 96% of cases.API

Judged from the repository’s own field completeness (thresholds). “Not measured” means we have not probed that field for this record, not that the data lack it.

At a glance

Every percentage is the repository’s own record of what is filled in
CasesAPI
24
Measurement types
5
109 files, 1016 GB
Follow-upAPI
4.1 years
for 23 of 24 cases; overall survival
Treatment responseAPI
Not recorded

SubjectCALC

Lymphoid

As filed by the repository

Lymphoid LeukemiasHematopoietic and reticuloendothelial systems

Who is in the cohortAPI

A usable value“Not reported” or “unknown”No value recorded
  • 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

Median 13, middle half 6–14, range 1–18 years across 23 cases.

What was measured, and on how many

5 measurement types, 1 covering the whole cohort.

  • 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%
Platform, files and data levels
AssayPlatformFilesLevels
Bulk RNA sequencingAPIillumina84-
Whole genome sequencingAPIillumina20-
ClinicalAPI-4-
Copy Number VariationAPI-2-
Somatic Structural VariationAPI-2-
How complete all 29 clinical fields are - 9 informative for at least 80% of cases

A field counts as informative only when it holds a real value. “Not reported” blocks an analysis just as a missing field does. Fields marked 1:n can hold several records per case, so they show the share of cases with any record.

Informative - a usable valuePresent but uninformative - “not reported” or “unknown”Absent - no value recorded

Outcome

  • Vital statusAPI96%
  • Cause of deathAPI0%
  • Progression or recurrenceAPI0%
  • Last known disease statusAPI0%

Follow-up

  • Progression at follow-upAPI63%
  • Disease response at follow-upAPI0%
  • ECOG performance statusAPI0%

Treatment

  • Treatment givenAPI96%
  • Prior treatmentAPI0%
  • Treatment typeAPI0%
  • Therapeutic agentsAPI0%
  • Treatment outcomeAPI0%
  • Regimen or line of therapyAPI0%

Staging

  • AJCC pathologic stageAPI0%
  • AJCC clinical stageAPI0%

Diagnosis

  • Primary diagnosisAPI100%
  • Tissue or organ of originAPI100%
  • Prior malignancyAPI0%
  • Synchronous malignancyAPI0%

Pathology

  • Morphology (ICD-O)API100%
  • Classification of tumorAPI100%
  • Tumor gradeAPI0%

Demographics

  • Sex at birthAPI96%
  • EthnicityAPI96%
  • RaceAPI88%
  • Population groupAPI0%
  • Country of residenceAPI0%

Exposure

  • Tobacco smoking statusAPI0%
  • Alcohol historyAPI0%

Access

MixedSome components are open; others need approval.

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.

Analyzed the dataCALC2
14
accession in the methods section
Declared using it
6
named in a data availability statement
Cited the paper
-
attention to the publication, not reuse of the data
Against expectation
Somewhat below
about 15 articles expected; index -0.07

What articles did with it

Only the last row counts as reuse. Where the accession appears in an article tells us what the authors did with the data.

  • Mentioned the dataset0
  • Accession found in text14
  • Declared using it6
  • Analyzed the data14

Against comparable datasets

14 articles analyzed these data. About 15 would be expected. The expectation comes from a model of size, age, breadth and access tier.

  • Analyzed it14
  • Expected~15
Reuse assessment
  • Reuse is within the expected range for comparable datasets (index -0.07).

Compared against 132 datasets in this corpus with a citable accession and sufficient metadata. See Methods for the model.

Articles that analyzed the data

Examples, not the full list. 23 articles matching this dataset's accession search were retrieved and graded individually; these are the strongest of those.

Deep-review sample: author overlap and funding were checked only for the 10 articles listed here, not for every article examined. Of the 10 that analyzed the data, author overlap with the generating team could not be checked for any of them, and 8 of the 10 we could check were themselves NCI-funded. These are sample counts, not population estimates.

Community examples

Share your example

Analyses 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

Open-access files need no account. Controlled files need an approved dbGaP request and a token passed to gdc-client.

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.txt
GDC: 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

  1. 1
    Open the project in the GDC Data PortalFor people5 minutes

    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

    Generated from repository policy. Check the linked policy before downloading.

  2. 2
    Download the open files without an accountFor peopleminutes to hours, by cohort size

    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.

    gdc-client download -m gdc_manifest.txt
    https://gdc.cancer.gov/access-data/gdc-data-transfer-tool

    Generated from repository policy. Check the linked policy before downloading.

  3. 3
    Request controlled access through dbGaPFor peopledays to a few weeks after signing official approval

    91 controlled-access files require an approved data access request. The request starts at dbGaP, not in the portal. The relevant study is phs000463.

    Requires: eRA Commons account, institutional signing official approval, dbGaP data access request for phs000463

    https://gdc.cancer.gov/access-data/obtaining-access-controlled-data

    Generated from repository policy. Check the linked policy before downloading.

  4. 4
    Download controlled files with your tokenFor people

    An approved request yields a token. The same manifest fetches nothing controlled without it.

    Requires: approved dbGaP request, GDC authentication token

    gdc-client download -m gdc_manifest.txt -t gdc-user-token.txt
    https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000463

    Generated from repository policy. Check the linked policy before downloading.

  5. 5
    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.

    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'
    https://docs.gdc.cancer.gov/API/Users_Guide/Getting_Started/

    Generated from repository policy. Check the linked policy before downloading.

  6. 6
    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.

    Requires: GDC authentication token

    curl -H "X-Auth-Token: $GDC_TOKEN" https://api.gdc.cancer.gov/data/<file_id>
    https://docs.gdc.cancer.gov/API/Users_Guide/Getting_Started/

    Generated from repository policy. Check the linked policy before downloading.

Provenance

All of it, and more, is in this record’s JSON.

Identifiers

Versions and verification

Released
1 Jan 2016
Metadata retrieved
18 Sept 2026
Review status
Machine-extracted
Data generation funding
Funded data generation

Funding

Awards resolved through NIH RePORTER. Awards that paid to generate these data are listed apart from awards that paid to reuse them. Both are returns on NCI investment, but different ones.

Funded reuse of these data

  • R37CA036401PHARMACOGENOMICS OF CHILDHOOD LEUKEMIA (ALL)WILLIAM E EVANSFY1987-2014API
  • R01CA036401Pharmacogenomics of Childhood Leukemia ALLWILLIAM E EVANSFY1985-2019API
  • R50CA211461Open Software and Resource Development Leveraging Next-gen Sequencing Data to Facilitate Computational Analysis of Cancer BiologyBrian HaasFY2016-2020API
  • K08CA273527Pathogenic role of human papillomavirus (HPV) DNA Integration and clonal expansion in cervical tumorigenesisAnne Van ArsdaleFY2022-2026API
  • R35CA210065Molecular pathways and targeted therapies in human leukemiaAdolfo A. FerrandoFY2017-2021API
  • R01CA196604Direct coregulation of Notch1 by Zmiz1 in T-cell leukemiaMARK Y CHIANGFY2015-2019API
  • K08CA208013Oncogenic programs driven by notch signaling in B-cell lymphomaRUSSELL James Hubbard RYANFY2016-2020API
  • F30CA228228Exploiting the Context-Dependence of Notch to Develop Safer T-ALL therapyAnna Catherine McCarterFY2018-2020API
  • T32CA009056Tumor Cell Biology Training ProgramGay M Crooks, David A. NathansonFY1985-2026API
  • K12CA076931Physician Scientist Training in Clinical OncologySTEPHEN Patrick HUNGER, LYNN M. SCHUCHTERFY1997-2026API

and 1 more

Funded infrastructure or harmonization

  • U10CA098543Children's Oncology Group Chair's GrantPETER C. ADAMSON, GREGORY H REAMANFY2003-2013API
  • P30CA021765Cancer Biology (CBP)Douglas R. Green, Michael A DyerFY1985-2026API
  • U24CA196172ECOG-ACRIN Biospecimen Bank to Support NCTNSTANLEY R. HAMILTON, Scott D JewellFY2015-2026API
  • U24CA196171The Alliance NCTN Biorepository and Biospecimen ResourceMine Cicek, Wendy FrankelFY2015-2026API
  • U24CA114766Support for Human Specimen Banking in NCI-Sponsored Clinical Trials-(CGB)Nilsa Del Carmen Ramirez Milan, GREGORY H REAMANFY2005-2014API
  • U24CA114737ECOG Specimen BankingROBERT L COMISFY2005-2014API
  • U10CA180899Children's Oncology Group Statistics and Data CenterTODD A ALONZO, Meenakshi DevidasFY2014-2026API
  • U10CA180861ITSC for Leukemia: Novel Molecular Strategies for NCTN: "Individualized" TherapieCLARA D BLOOMFIELD, GUIDO MARCUCCIFY2014-2018API
  • U10CA180850OSU as Network Lead Academic Participating Site for the NCI NCTNKRISTIE A BLUM, ARNAB CHAKRAVARTIFY2014-2018API
  • U10CA180827ECOG-ACRIN INTEGRATED LEUKEMIA TRANSLATIONAL RESEARCH CENTERRoss L Levine, ARI M. MELNICKFY2014-2018API

and 10 more

For softwarerecord JSON