Clinical trial · Observational
Feasibility of Serial Multisite Image-guided Biopsy to Study Breast Cancer Evolution
Feasibility of Serial Multisite Image-Guided Biopsy To Study Breast Cancer Evolution
- 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)
FORTITUDE is a translational research study that aims to collect serial multi-site needle biopsy samples of tumour tissue and blood from metastatic breast cancer patients. Cancer biopsies are generally performed when cancer is diagnosed and are sometimes repeated when the cancer is suspected to have spread but this is not mandatory. However, studies have shown that cancers change with time and evolve to become resistant to therapy. The purpose of this study is to assess the feasibility of biopsies of multiple cancer sites across different time points during treatment and understand how cancers evolve and change throughout treatment. The findings of this study could pave the way for using cancer biopsies more frequently in the clinic to pick up changes in cancer behaviour that could influence treatment choice. The samples collected from this study will be used for molecular and genetic research to increase our understanding of how metastatic breast cancer changes during treatment and will enable us to develop new cancer treatments and new ways of monitoring response to cancer therapies.
Conditions
Conditions (3)
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 |
| Metastatic Breast Cancer | Malignant Breast Neoplasm | CURATED_BROADER | 0.78 |
| Triple Negative Breast Cancer | Triple-Negative Breast Carcinoma | ALIAS | 0.90 |
Interventions
Interventions (0)
Data not yet available
Design
Arms and outcomes
Arms (0)
[]Primary outcomes (3)
- measure
- Proportion of patients having two or more tumour sites sampled in one procedural sitting when technically feasible
- timeFrame
- Through study completion, 15 years
- measure
- Proportion of patients having longitudinal sampling in those progressing on treatment
- timeFrame
- Through study completion, 15 years
- measure
- Proportion of patients willing to undergo multisite sampling again in the future if clinically required
- timeFrame
- Through study completion, 15 years
Secondary outcomes (9)
- measure
- Quantification of procedural complication rates
- timeFrame
- Through study completion, 15 years
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: 1. Histologically confirmed locally advanced, inoperable breast cancer or metastatic breast cancer OR radiological evidence of metastatic disease with a high index of suspicion that this is a recurrence of a previously diagnosed breast cancer. 2. Be aged 18 years and over. 3. Have given written informed consent to participate. Exclusion Criteria: 1. Metastatic disease limited to bones, without a soft tissue component. 2. Any bleeding disorders or anticoagulation that cannot be corrected and that would render the risk of biopsy unacceptable. 3. If the consultant physician involved in the care of the patient assesses and decides the risk of the biopsy procedures is significant, defined as greater than 1% risk of significant complication. 4. Eastern Cooperative Oncology Group performance status of 3 and higher. 5. Known chronic infectious disease (Hepatitis B and C, HIV) that may impact patient safety. 6. Presence of any psychological, familial or sociological condition potentially hampering compliance with the study protocol and follow-up schedule.
References
Publications (0)
Data not yet available