NCT06476119Recruiting
OPTImaL:Optimisation of Treatment for Patients With Low Stage Triple-negative Breast Cancer With High Stromal Tumor-infiltrating Lymphocytes
Source: ClinicalTrials.gov · Last updated 23 Apr 2025 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
The aim of this study is to investigate whether subjects with breast cancer that have certain favorable features, after performing the surgery and radiation, the chemotherapy can be safely omitted in the treatment. In addition, the investigation looks at whether the omission of chemotherapy ensures a better quality of life. Participants decide, in consultation with their treating physician, whether they choose to be treated with adjuvant chemotherapy or not.
- Status (registry)
- Recruiting
- Study type
- Observational
- Enrollment
- 490 (estimated)
- First submitted
- 7 Jun 2024
- Start date
- 15 Apr 2025
- Primary completion date
- 15 Sept 2032
- Lead sponsor
- The Netherlands Cancer Institute
- Diseases
- Triple-negative breast cancer
- NCT number
- NCT06476119
What you commit to
- Study type: Observational
- Planned participants: 490
- From 15 Apr 2025 to the primary completion date, 15 Sept 2032
- 28 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
- Administration of neoadjuvant systemic therapy;
- Presence of lymphovascular invasion on the diagnostic biopsy and/or the surgical specimen;
- Other invasive malignancy within 5 years prior to inclusion, with the exception of ade-quately treated non-melanoma skin cancer, localized cervical cancer, localized and Gleason ≤6 prostate cancer;
Other illness
- Prior disease history of invasive and/or non-invasive breast cancer, or ongoing treatment for invasive and/or non-invasive breast cancer;
- Multifocal, multicentric or bilateral breast cancer at the time of screening;
- Uncontrolled severe illness or medical condition;
- Any psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol and follow-up schedule; those conditions should be assessed and discussed with the patient before the enrolment in the in the trial.
Who the study is looking for
- Female or male patients;
- \>=18 years;
- Written informed consent;
- TNBC (defined as: invasive carcinoma; ER/PR expression 0-9%; Human Epidermal Growth Factor Receptor 2 \[HER2\] negative \[0, 1+ or 2+ on immunohistochemistry, without HER2 amplification on in-situ hybridization\]) on the diagnostic biopsy and the surgical specimen;
- Pathological stage I TNBC (according to the TNM staging 8th edition):
- pT1a/b/c (≤2 cm), confirmed by an invasive component of ≤2 cm on the surgical specimen (microinvasive disease \[pT1mi, ≤1 mm) is not allowed);
- pN0, confirmed by absence of malignant cells in the sentinel lymph node or any other lymph node after surgery (isolated tumor cells \[N0(i+)\] are not allowed);
- No evidence of nodal or distant metastases (cN0M0) on pre and/or postoperative imaging examinations (performed following local/national guidelines, but must include an 18F-fluorodeoxyglucose positron emission tomography/computed tomography \[18F-FDG-PET/CT, at least from skull base to upper legs\] or computed tomography \[CT\] of neck/chest/abdomen/pelvis \[CT only if 18F-FDG-PET/CT would not be available; 18F-FDG-PET/CT mandatory in the Netherlands\]);
- sTIL score of ≥50% for patients ≥40 years at the time of TNBC diagnosis and ≥75% for patients \<40 years at the time of TNBC diagnosis on an H\&E FFPE tissue slide on the surgical specimen, according to International Immuno-Oncology Biomarker Working Group on Breast Cancer (formerly International TILs Working Group) guidelines, by local and central review
- Has undergone curative breast surgery (breast-conserving surgery or mastectomy and surgical axillary staging \[including at least sentinel lymph node procedure\]);
- Absence of recurrence between curative breast surgery and expression of patient preference;
- Eligible for radiotherapy (if indicated).
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (28)
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 | Not yet recruiting |
| Flevoziekenhuis Coordinator of this site? Confirm its status | Almere Stad | Netherlands | Not yet recruiting |
| Meander Medisch Centrum Coordinator of this site? Confirm its status | Amersfoort | Netherlands | Recruiting |
| Antoni van Leeuwenhoek Coordinator of this site? Confirm its status | Amsterdam | Netherlands | Recruiting |
| Onze Lieve Vrouwe Gasthuis (OLVG) Coordinator of this site? Confirm its status | Amsterdam | Netherlands | Recruiting |
| Rijnstate Coordinator of this site? Confirm its status | Arnhem | Netherlands | Recruiting |
| Amphia Ziekenhuis Coordinator of this site? Confirm its status | Breda | Netherlands | Recruiting |
| Deventer Ziekenhuis Coordinator of this site? Confirm its status | Deventer | Netherlands | Recruiting |
| Ziekenhuis Gelderse Vallei Coordinator of this site? Confirm its status | Ede | Netherlands | Recruiting |
| Jeroen Bosch ziekenhuis Coordinator of this site? Confirm its status | Eindhoven | Netherlands | Recruiting |
| Catharina Ziekenhuis Coordinator of this site? Confirm its status | Eindhoven | Netherlands | Recruiting |
| Medical Spectrum Twente Coordinator of this site? Confirm its status | Enschede | Netherlands | Recruiting |
| St.Jansdal Coordinator of this site? Confirm its status | Harderwijk | Netherlands | Recruiting |
| Ziekenhuisgroep Twente Coordinator of this site? Confirm its status | Hengelo | Netherlands | Recruiting |
| Tergooi Ziekenhuizen Coordinator of this site? Confirm its status | Hilversum | Netherlands | Recruiting |
| Spaarne Gasthuis Coordinator of this site? Confirm its status | Hoofddorp | Netherlands | Recruiting |
| Dijklander Ziekenhuis Coordinator of this site? Confirm its status | Hoorn | Netherlands | Not yet recruiting |
| MCL Coordinator of this site? Confirm its status | Leeuwarden | Netherlands | Not yet recruiting |
| LUMC Coordinator of this site? Confirm its status | Leiden | Netherlands | Not yet recruiting |
| MUMC+ Coordinator of this site? Confirm its status | Maastricht | Netherlands | Not yet recruiting |
| St. Antonius Ziekenhuis Coordinator of this site? Confirm its status | Nieuwegein | Netherlands | Recruiting |
| Radboud UMC Coordinator of this site? Confirm its status | Nijmegen | Netherlands | Not yet recruiting |
| Erasmus Medical Center Cancer Institute Coordinator of this site? Confirm its status | Rotterdam | Netherlands | Not yet recruiting |
| Franciscus Gasthuis & Vlietland Coordinator of this site? Confirm its status | Schiedam | Netherlands | Recruiting |
| Zuyderland Medisch Centrum Coordinator of this site? Confirm its status | Sittard-Geleen | Netherlands | Not yet recruiting |
| Haaglanden Medisch Centrum Coordinator of this site? Confirm its status | The Hague | Netherlands | Recruiting |
| VieCuri Medisch Centrum voor Noord-Limburg Coordinator of this site? Confirm its status | Venlo | Netherlands | Not yet recruiting |
| Isala Coordinator of this site? Confirm its status | Zwolle | Netherlands | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.