Clinical trial · Observational
Metabolomics Explores Biomarkers for Metastatic Breast Cancer
Clinical Study of Metabolomics-based Approach Explore Biomarkers for Metastatic Breast Cancer
NCT04302415CI-TRIAL-00043920unknownClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
RATIONALE: Studying samples of plasm by metabolomics-based approach from women with metastasis breast cancer may help doctors understand the biomarker of visceral metastasis. PURPOSE: This clinical trial is studying the biomarker of visceral metastasis by metabolomics approach in metastasis breast cancer undergoing treatment.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Breast Cancer | Malignant Breast Neoplasm | CURATED_EXACT | 0.92 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| There is no other intervention, only clinical treatment. | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (5)
- label
- only liver metastasis
- description
- There is no other intervention, only clinical treatment.
- interventionNames
- Drug: There is no other intervention, only clinical treatment.
- label
- only lung metastasis
- description
- There is no other intervention, only clinical treatment.
- interventionNames
- Drug: There is no other intervention, only clinical treatment.
- label
- only brain
- description
- There is no other intervention, only clinical treatment.
- label
- No distant metastasis
- description
- There is no other intervention, only clinical treatment.
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 18 Years
- Maximum age
- 70 Years
Show eligibility criteria text
Inclusion Criteria: * Age: 18-70 yrs. * Any menopausal status. * Any hormone receptor status. * Patients must have histologically or imaging confirmed breast cancer with visceral metastatic. * Patients must have measurable disease, per RECIST criteria v1.1.21. * Estimated life expectancy of ≥ 12 weeks. * Ability to swallow oral medications. * Participants must have adequate organ function as defined by: 1. ANC ≥1.5 x 109/L, platelet count ≥100 x 109/L, haemoglobin ≥ 10 g/dL. 2. creatinine \< 1.5 x UNL (upper normal limit). 3. Total bilirubin \< 1.5x UNL. 4. ALT \& AST \< 2.5xUNL; alkaline phosphatase \< 2.5xUNL. 5. Creatine phosphokinase (CPK) ≤ 2.5 x UNL. * Patients with CNS metastatic disease are allowed if the disease is controlled and stable for at least 3 months by CT or MRI. Exclusion Criteria: * Current severe, uncontrolled systemic disease (e.g. pulmonary, or metabolic disease; wound healing disorders; ulcers; or bone fractures). * History of other malignancies. * No measureable lesion is present, as defined by RECIST 1.1. * Patients who suffer from a medical or psychiatric condition that, in the opinion of the principal investigator, would impair their ability to participate in the study. * Concurrent interventional studies.
References
Publications (0)
Data not yet available
No reference posted for this study.