NCT05301881RecruitingPhase 2
COntinue the SaMe Systemic Therapy After Local Ablative Therapy for Oligo Progression in Metastatic Breast Cancer - the COSMO Study
Source: ClinicalTrials.gov · Last updated 11 Sept 2026
Brief summary (registry, in English)
Patients with oligoprogression of metastatic breast cancer during palliative treatment that is amenable to local therapy will be included. The local ablative therapy (LAT) may consist of stereotactic ablative radiotherapy (SABR), also known as stereotactic body radiation therapy, surgery or percutaneous ablation.
- Status (registry)
- Recruiting
- Phase (registry)
- Phase 2
- Study type
- Interventional
- Enrollment
- 56 (estimated)
- First submitted
- 21 Mar 2022
- Start date
- 17 Apr 2023
- Primary completion date
- 1 Apr 2035
- Lead sponsor
- The Netherlands Cancer Institute
- Diseases
- Metastatic breast cancer
- NCT number
- NCT05301881
What you commit to
- Study type: Interventional · Phase 2
- Planned participants: 56
- From 17 Apr 2023 to the primary completion date, 1 Apr 2035
- 7 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Having received more than two lines of systemic therapy for MBC If a treatment regimen has been de-escalated without adding other therapies, this is seen as one line of therapy. For example: Pertuzumab/trastuzumab+docetaxel followed by pertuzumab/trastuzumab will be viewed as one line of systemic therapy.
Other illness
- Presence of any medical condition that would place the patient at unusual risk, up to the discretion of the clinician
- Presence of any psychological, familial, sociological, or geographical condition potentially hampering compliance with the study protocol and follow-up schedule
Age
- Other malignancy except carcinoma in situ and basal-cell and squamous cell carcinoma of the skin, unless the other malignancy was treated ≥5 years ago with curative intent without the use of chemotherapy or radiation therapy
Other
- Current pregnancy or breastfeeding. Women of childbearing potential must use adequate contraceptive protection
Who the study is looking for
- Histologically confirmed invasive breast cancer
- Metastatic breast cancer
- o Oligoprogression is defined as an increase of ≥20% in size or, in case of FDG-PET-CT, metabolic activity (≥20% in SUVmax) involving a maximum of two lesions. These lesions may consist of: 1 or 2 distant metastatic lesions limited to 1 organ, the primary tumor or locoregional lymph nodes.
- Systemic treatment can be either endocrine, targeted, chemotherapy or immune-checkpoint blockade
- Patients should be on systemic therapy for at least six months. Status should be stable disease or partial or complete response for at least 6 months.
- Oligoprogression has to be detected with radiological imaging comparing the lesion on the same type of imaging modality as has been used at the start of systemic therapy.
- Lesion(s) must be amenable to resection, radiotherapy or percutaneous ablation with the intent of local obliteration.
- The radiological imaging that shows progression must be performed within 70 days prior to LAT.
- Bone metastases are classified as progressive if the lytic component of the lesion increases by ≥20% or the FDG-uptake increases by ≥20% on FDG-PET-CT
- Lymph nodes should be larger than 15 mm upon first detection of oligoprogression to be classified as progressive.
- Oligo-progression has to be confirmed with a FDG-PET-CT-scan 5-7 weeks after the initial scan that showed oligoprogression.
- Age ≥18
- World Health Organization (WHO) Performance Status 0 or 1
- Signed written informed consent before patient registration according to ICH/GCP, and national/local regulations
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (7)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Noordwest Ziekenhuisgroep Coordinator of this site? Confirm its status | Alkmaar | Netherlands | Recruiting |
| Antoni van Leeuwenhoek Coordinator of this site? Confirm its status | Amsterdam | Netherlands | Recruiting |
| Rijnstate Coordinator of this site? Confirm its status | Arnhem | Netherlands | Recruiting |
| Deventer Ziekenhuis Coordinator of this site? Confirm its status | Deventer | Netherlands | Recruiting |
| ADRZ Coordinator of this site? Confirm its status | Goes | Netherlands | Recruiting |
| Martini Ziekenhuis Coordinator of this site? Confirm its status | Groningen | Netherlands | Recruiting |
| Antonius Ziekenhuis Coordinator of this site? Confirm its status | Utrecht | Netherlands | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.