Fact CheckerSign in

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
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

Full criteria on ClinicalTrials.gov

Sites (28)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Noordwest Ziekenhuisgroep
Coordinator of this site? Confirm its status
AlkmaarNetherlandsNot yet recruiting
Flevoziekenhuis
Coordinator of this site? Confirm its status
Almere StadNetherlandsNot yet recruiting
Meander Medisch Centrum
Coordinator of this site? Confirm its status
AmersfoortNetherlandsRecruiting
Antoni van Leeuwenhoek
Coordinator of this site? Confirm its status
AmsterdamNetherlandsRecruiting
Onze Lieve Vrouwe Gasthuis (OLVG)
Coordinator of this site? Confirm its status
AmsterdamNetherlandsRecruiting
Rijnstate
Coordinator of this site? Confirm its status
ArnhemNetherlandsRecruiting
Amphia Ziekenhuis
Coordinator of this site? Confirm its status
BredaNetherlandsRecruiting
Deventer Ziekenhuis
Coordinator of this site? Confirm its status
DeventerNetherlandsRecruiting
Ziekenhuis Gelderse Vallei
Coordinator of this site? Confirm its status
EdeNetherlandsRecruiting
Jeroen Bosch ziekenhuis
Coordinator of this site? Confirm its status
EindhovenNetherlandsRecruiting
Catharina Ziekenhuis
Coordinator of this site? Confirm its status
EindhovenNetherlandsRecruiting
Medical Spectrum Twente
Coordinator of this site? Confirm its status
EnschedeNetherlandsRecruiting
St.Jansdal
Coordinator of this site? Confirm its status
HarderwijkNetherlandsRecruiting
Ziekenhuisgroep Twente
Coordinator of this site? Confirm its status
HengeloNetherlandsRecruiting
Tergooi Ziekenhuizen
Coordinator of this site? Confirm its status
HilversumNetherlandsRecruiting
Spaarne Gasthuis
Coordinator of this site? Confirm its status
HoofddorpNetherlandsRecruiting
Dijklander Ziekenhuis
Coordinator of this site? Confirm its status
HoornNetherlandsNot yet recruiting
MCL
Coordinator of this site? Confirm its status
LeeuwardenNetherlandsNot yet recruiting
LUMC
Coordinator of this site? Confirm its status
LeidenNetherlandsNot yet recruiting
MUMC+
Coordinator of this site? Confirm its status
MaastrichtNetherlandsNot yet recruiting
St. Antonius Ziekenhuis
Coordinator of this site? Confirm its status
NieuwegeinNetherlandsRecruiting
Radboud UMC
Coordinator of this site? Confirm its status
NijmegenNetherlandsNot yet recruiting
Erasmus Medical Center Cancer Institute
Coordinator of this site? Confirm its status
RotterdamNetherlandsNot yet recruiting
Franciscus Gasthuis & Vlietland
Coordinator of this site? Confirm its status
SchiedamNetherlandsRecruiting
Zuyderland Medisch Centrum
Coordinator of this site? Confirm its status
Sittard-GeleenNetherlandsNot yet recruiting
Haaglanden Medisch Centrum
Coordinator of this site? Confirm its status
The HagueNetherlandsRecruiting
VieCuri Medisch Centrum voor Noord-Limburg
Coordinator of this site? Confirm its status
VenloNetherlandsNot yet recruiting
Isala
Coordinator of this site? Confirm its status
ZwolleNetherlandsRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.