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Datasets/TCGA-STAD

Stomach Adenocarcinoma

MixedMachine-extracted
TCGAAvailable from GDC and IDC

The Cancer Genome Atlas-Stomach Adenoarcinoma (TCGA-STAD) data collection is part of a larger effort to enhance the TCGA data set with characterized radiological images. The Cancer Imaging Program (CIP) with the cooperation of several of the TCGA tissue-contributing institutions are working to archive a large portion of the radiological images of the genetically-analyzed STAD cases. Please see the TCGA-STAD page to learn more about the radiology images and to obtain any supporting metadata for this collection. Please see the DICOM converted Slide Microscopy images for the TCGA-STAD collection page to learn more about the histopathology images and to obtain any supporting metadata for this collection.

Can it answer your research question?

6 of 6 supported
  • Overall survival

    Supported

    Vital status and time are populated; median follow-up 1.2 years; 440 cases with follow-up; endpoints: overall survival, progression-free interval.API

  • Progression or recurrence

    Supported

    A time to event is derivable: progression-free interval; progression_or_recurrence is informative for 26% of cases.API

  • Treatment response

    Supported

    disease_response is populated for 92% of cases; criteria: complete response, partial response.API

  • Which drug was given

    Supported

    therapeutic_agents is recorded for 43% of cases.API

  • Stage-adjusted modelling

    Supported

    ajcc_pathologic_stage is informative for 94% of cases.API

  • Analysis by race or ethnicity

    Supported

    Race is informative for 86% 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
CasesAPI2
443
Measurement types
12
31,604 files, 324 TB
Follow-upAPI
13.9 months
for 440 of 443 cases; overall survival, progression-free interval
Treatment responseAPI
Recorded
complete response, partial response, progressive disease

SubjectCALC

Esophagus and stomach

As filed by the repository

Adenomas and AdenocarcinomasCystic, Mucinous and Serous NeoplasmsStomach

Who is in the cohortAPI

A usable value“Not reported” or “unknown”No value recorded
  • Sex285 male · 158 female
  • Race278 white · 89 asian · 13 black or african american · 1 1 other · 50 not reported · 12 unknown
  • Ethnicity318 not hispanic or latino · 5 hispanic or latino · 115 not reported · 5 unknown
  • Vital status268 alive · 175 dead

Age at diagnosis

Median 68, middle half 59–74, range 30–90 years across 433 cases.

What was measured, and on how many

12 measurement types, 5 covering the whole cohort.

  • Whole exome sequencing443 of 443 · 100%
  • SNP genotyping array (copy number, germline)443 of 443 · 100%
  • DNA methylation array443 of 443 · 100%
  • Clinical443 of 443 · 100%
  • DICOM medical imaging443 of 443 · 100%
  • microRNA sequencing436 of 443 · 98%
  • Whole genome sequencing436 of 443 · 98%
  • Somatic Structural Variation430 of 443 · 97%
  • Whole-slide diagnostic images416 of 443 · 94%
  • Bulk RNA sequencing415 of 443 · 94%
  • Reverse phase protein array357 of 443 · 81%
  • ATAC sequencing (chromatin accessibility)21 of 443 · 5%
Platform, files and data levels
AssayPlatformFilesLevels
Whole exome sequencingAPIillumina7,086-
SNP genotyping array (copy number, germline)APIillumina5,846-
DNA methylation arrayAPIillumina1,410-
ClinicalAPI2-906-
DICOM medical imagingAPI--DICOM series
microRNA sequencingAPIillumina1,473-
Whole genome sequencingAPI2illumina7,936-
Somatic Structural VariationAPI-1,789-
Whole-slide diagnostic imagesAPI2illumina442-
Bulk RNA sequencingAPIillumina4,032-
Reverse phase protein arrayAPIillumina357-
ATAC sequencing (chromatin accessibility)APIillumina21-
How complete all 29 clinical fields are - 16 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 statusAPI100%
  • Cause of deathAPI29%
  • Progression or recurrenceAPI0%
  • Last known disease statusAPI0%

Follow-up

  • Disease response at follow-up1:nAPI92%
  • Progression at follow-upAPI26%
  • ECOG performance statusAPI0%

Treatment

  • Prior treatment1:nAPI100%
  • Treatment type1:nAPI93%
  • Treatment given1:nAPI93%
  • Therapeutic agents1:nAPI43%
  • Treatment outcomeAPI37%
  • Regimen or line of therapyAPI<1%

Staging

  • AJCC pathologic stageAPI94%
  • AJCC clinical stageAPI0%

Diagnosis

  • Primary diagnosis1:nAPI100%
  • Tissue or organ of origin1:nAPI100%
  • Prior malignancyAPI100%
  • Synchronous malignancyAPI100%

Pathology

  • Morphology (ICD-O)1:nAPI100%
  • Tumor gradeAPI100%
  • Classification of tumor1:nAPI100%

Demographics

  • Sex at birthAPI100%
  • Country of residenceAPI100%
  • RaceAPI86%
  • EthnicityAPI73%
  • Population groupAPI0%

Exposure

  • Tobacco smoking statusAPI0%
  • Alcohol historyAPI0%

Access

MixedSome components are open; others need approval.API

Data Access Request through dbGaP using an eRA Commons account; institutional signing official approval required

Open components
11,791 open-access files
Controlled components
19,813 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
1,405
accession in the methods; 100% of a 27-article sample really cited it
Declared using it
143
named in a data availability statement
Cited the paper
5,063
attention to the publication, not reuse of the data
Against expectation
As expected or above
about 293 articles expected; index 2.26

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.

  • Cited the paper5,063
  • Mentioned the dataset112
  • Accession found in text0
  • Declared using it143
  • Analyzed the data1,405

Against comparable datasets

1,405 articles analyzed these data. About 293 would be expected. The expectation comes from a model of size, age, breadth and access tier.

  • Analyzed it1,405
  • Expected~293
Reuse assessment
  • Reuse is within the expected range for comparable datasets (index +2.26).

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. 108 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, 10 of the 10 we could check had no author in common with the generating team, and 1 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 = "TCGA-STAD"
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": ["TCGA-STAD"]}}
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("TCGA-STAD_clinical.tsv", "w").write(tsv)
IDC: pull the DICOM collection with idc-indexpython

pip install idc-index. Images are public; the package uses s5cmd under the hood.

from idc_index import IDCClient

COLLECTION = "tcga_stad"
client = IDCClient()

series = client.index[client.index["collection_id"] == COLLECTION]   # one row per DICOM series
print(len(series), "series,", series["PatientID"].nunique(), "patients,",
      round(series["series_size_MB"].sum() / 1024, 1), "GB")
print(series["Modality"].value_counts().to_dict())

# Everything above is an index lookup and costs nothing. Uncomment to pull the pixels;
# the client refuses up front if the disk cannot hold them.
# client.download_from_selection(collection_id=COLLECTION, downloadDir="./tcga_stad")
This page as data: limitations firstbash
curl -s https://cd2s.vercel.app/data/datasets/gdc-tcga-stad.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/TCGA-STAD

    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

    11,791 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

    19,813 controlled-access files require an approved data access request. The request starts at dbGaP, not in the portal. The relevant study is phs000178.

    Requires: eRA Commons account, institutional signing official approval, dbGaP data access request for phs000178

    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=phs000178

    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":["TCGA-STAD"]}}' \
      --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 2013
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 data generation

  • U24CA180951Cloud Based Resource for Data Hosting, Visualization and Analysis Using UCSC CancDAVID H HAUSSLERFY2013-2017API
  • U24CA144025Harvard Genome Characterization CenterRaju S. KucherlapatiFY2009-2016API
  • U24CA143883Integrative Pipeline for Analysis & Translational Application of TCGA Data (GDAC)Rehan Akbani, GORDON B. MILLSFY2009-2016API
  • U24CA143882The USC-JHU Cancer Epigenome Characterization CenterSTEPHEN B. BAYLIN, Daniel Joseph WeisenbergerFY2009-2016API
  • U24CA143867Genome Characterization Center (GCC)Stacey Gabriel, Matthew L. MeyersonFY2009-2016API
  • U24CA143866Cancer transcriptome characterization using massively parallel DNA sequencingMarco Antonio MarraFY2009-2015API
  • U24CA143858UCSC-Buck Inst. Genome Data Analysis Center for TCGA Research Network (GDAC)Christopher Benz, DAVID H HAUSSLERFY2009-2016API
  • U24CA143848Gene Expression Patterns in Human Tumors Identified Using Transcript SequencingDavid N Hayes, CHARLES M PEROUFY2009-2016API
  • U24CA143845The Cancer Genome Atlas Data Analysis CenterLYNDA CHIN, GAD A GETZFY2009-2016API
  • U24CA143843The BCM Tumor Genome Characterization CenterRICHARD A GIBBS, David Andrew WheelerFY2009-2013API

and 8 more

Funded reuse of these data

  • R01CA265026Defining the role of histone H3K4 mono-methyltransferase dysfunction in urothelial carcinomaYu ChenFY2022-2025API
  • R01CA228216Epigenetic mechanisms of transcriptional activation of a novel oncogenic ALK variant in cancerPing ChiFY2018-2022API
  • R01CA208100Understanding the role of an aberrant hepatic nuclear transcription circuit in prostate cancer tumorigenesis and castration resistanceYu ChenFY2017-2021API
  • R01CA193837Role of ETS factors in specifying prostate luminal cell identity and androgen receptor dependenceCHARLES L. SAWYERSFY2015-2025API

Funded infrastructure or harmonization

  • U54CA224079Project 2: Reversing resistance caused by lineage plasticity through epigenetic therapyYu Chen, CHARLES L. SAWYERSFY2017-2021API
  • U01CA224044Patient-Derived Models of Prostate Cancer for Personalized MedicineYu Chen, PHILLIP ANDREW FUTREALFY2019-2023API
  • P50CA221745Biospecimen Repository CoreHikmat Al-Ahmadie, David B. SolitFY2018-2024API
  • P50CA217694Project 3: Identifying Targetable Epigenetic and Immuno-Oncologic Vulnerabilities in Synovial SarcomaMarc Ladanyi, SAMUEL SINGERFY2018-2025API
  • P50CA092629SPORE in Prostate CancerYu Chen, MICHAEL J MORRISFY2001-2026API
  • P30CA008748Antitumor AssessmentElisa de Stanchina, FRANCESCA M GANYFY1985-2026API

For softwarerecord JSON