Clinical trial · Observational
Eribulin Mesylate-based Therapy in Patients With Advanced HER2-negative Breast Cancer Previously Treated With ADC
Real-world Study of Eribulin Mesylate-based Therapy in Patients With Advanced HER2-negative Breast Cancer Previously Treated With Antibody-drug Conjugates
- 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)
This study is a real-world study. we collected patients with advanced HER2-negative breast cancer previously treated with antibody-drug conjugates, and received eribulin mesylate-based therapy post-ADC. We retrospectively collect the data on previous systemic treatment, and prospectively collect the treatment data of the therapeutic regimens based on eribulin mesylate.
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 |
|---|---|---|---|
| Treatment Efficacy | — | UNRESOLVED | — |
Interventions
Interventions (0)
Data not yet available
Design
Arms and outcomes
Arms (1)
- label
- advanced HER2-negative breast cancer patients previously treated with ADC
Primary outcomes (1)
- measure
- Progression-Free Survival (PFS)
- timeFrame
- From enrollment to the last patient experiences disease progression or completes the 24-month follow-up.
- description
- the period from the start of eribulin mesylate-based therapy treatment until the disease progress or death from any cause, whichever occurred first
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: 1. At least 18 years old; 2. Inoperable locally advanced or metastatic breast cancer; 3. Planning to use a single-agent or combination treatment regimen based on eribulin; 4. HER2 negative (IHC 0,+, or ++ but ISH negative); 5. Previously received ADC treatment at the local advanced or metastatic disease stage; 6. Previously received chemotherapy (including ADC) for local advanced or metastatic disease no more than 2 lines, where one treatment line is defined as completing at least one cycle of chemotherapy; 7. Eastern Cooperative Oncology Group (ECOG) performance status score (PS) 0-2; 8. The investigators have evaluated that the patient's organ and bone marrow functions are suitable for medication use and there are no relevant contraindications; 9. The subjects voluntarily join the study and sign the informed consent. Exclusion Criteria: 1. HER2-positive tumors 2. The hormone receptor status is unknown; 3. Patients who have received eribulin treatment before; 4. Those who have had other malignant tumors within the past 5 years (excluding the following situations: cured skin basal cell carcinoma, cervical carcinoma in situ, papillary thyroid carcinoma; second primary cancer that has been cured and has no recurrence within 5 years; subjects who have clearly identified the origin of the metastatic lesion as being from a certain primary tumor); 5. Mental illness or mental disorder, patients with poor compliance and inability to cooperate and describe treatment responses; 6. Pregnant or lactating women; 7. Other serious or uncontrollable diseases, or other conditions assessed by the researcher as not suitable for enrollment.
References
Publications (0)
Data not yet available