CClinicalTrials.gg
RecruitingNCT07773818Updated Aug 19, 2026

Establishment of a Multi-omics Prediction Model for Early Triple-negative Breast Cancer Based on UPGRADE-TNBC Study

An observational study in Triple -Negative Breast Cancertriple, Meta-Learning and Predictive Models, sponsored by Cancer Institute and Hospital, Chinese Academy of Medical Sciences. Recruiting at 1 site in China. Open to female participants aged 18 Years to 75 Years. Per ClinicalTrials.gov, last updated 2026-08-19.

Sponsored by Cancer Institute and Hospital, Chinese Academy of Medical Sciences · Observational

Study type
Observational
Model
Other
Time perspective
Prospective
Enrollment
32
Ages
18 Years to 75 Years
Sex
Female
01

Study summary

Based on the UPGRADE-TNBC study, a high-quality TNBC sample repository was established. By integrating multi-source data-including clinical information, radiomics, pathological images, and molecular sequencing-and innovatively incorporating a meta-learning strategy, a treatment response prediction model based on multimodal small-sample learning was developed. This approach aims to optimize drug combinations and precisely identify patient subgroups likely to benefit from treatment, thereby providing a new paradigm for personalized therapy in early-stage TNBC.

02

Conditions studied

  • Triple -Negative Breast Cancertriple
  • Meta-Learning
  • Predictive Models
  • Multimodal
03

Who can participate

Ages eligible
18 Years to 75 Years
Sexes eligible
Female
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

The participants in the UPGRADE-TNBC study were all patients with early-stage triple-negative breast cancer who received neoadjuvant therapy.

Inclusion criteria

  • The UPGRADE-TNBC Study Population

Exclusion criteria

Exclusion Criteria:

  • Populations outside the UPGRADE-TNBC study
04

Study design

Observational model
Other
Time perspective
Prospective
Enrollment
32 participants (estimated)
Target follow-up
2 Years
Patient registry
Yes
Biospecimen retention
Samples with dna

Groups and cohorts

  • The Population in the UPGRADE-TNBC Study(early-stage triple-negative breast cancer)

    Other: Collect data

Interventions

  • OtherCollect data

    Collect multi-source data from patients, including clinical information, radiomics, pathological images, and molecular sequencing

05

What researchers measure

Primary outcomes

  1. Model building

    A predictive model for neoadjuvant therapy in TNBC was successfully established

    Time frame: 2 years

06

Study locations

1 of 1 sites recruiting
  • Cancer Hospital, Chinese Academy of Medical Sciences
    Beijing, Beijing Municipality 100021, China
    Recruiting
07

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT07773818
Lead sponsor
Cancer Institute and Hospital, Chinese Academy of Medical Sciences
Responsible party
PENG YUAN (Professor, Cancer Institute and Hospital, Chinese Academy of Medical Sciences) — Principal investigator
First posted
Aug 19, 2026
Start date
Aug 6, 2026
Primary completion
Sep 1, 2028 (estimated)
Completion
Sep 1, 2029 (estimated)
Last update
Aug 19, 2026

Study contacts

Xue Wang
Contact
wxyxyuki@163.com
86-010-87787242

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Interested in this study?

Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.

Contact study team

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion