Clinical trial

OPTImaL:Optimisation of Treatment for Patients With Low Stage Triple-negative Breast Cancer With High Stromal Tumor-infiltrating Lymphocytes

Name
M24OTI
Description
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 consulatiation with their treating physician, whether they choose to be treated with adjuvant chemotherapy or not.
Trial arms
Trial start
2024-09-15
Estimated PCD
2032-09-15
Trial end
2034-09-15
Status
Not yet recruiting
Treatment
Adjuvant chemotherapy
adjuvant chemotherapy according to local/ national guidelines
Arms:
Control cohort
Other names:
according to local/ national guidelines
No adjuvant chemotherapy
no adjuvant chemotherapy
Arms:
Optimisation cohort
Size
490
Primary endpoint
Disease recurrence Free Interval (DRFI) - optimalisation cohort
up to 96 months after inclusion of the last patient
Eligibility criteria
Inclusion Criteria: * 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 preoperative 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% (≥75% for patients \<40 years) 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; * 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). Exclusion Criteria: * Prior disease history of breast cancer, or ongoing treatment for breast cancer; * Multifocal, multicentric or bilateral breast cancer at the time of screening; * 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; * 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.
Protocol
{'studyType': 'OBSERVATIONAL', 'patientRegistry': False, 'designInfo': {'observationalModel': 'COHORT', 'timePerspective': 'PROSPECTIVE'}, 'bioSpec': {'retention': 'SAMPLES_WITH_DNA', 'description': 'ctDNA samples'}, 'enrollmentInfo': {'count': 490, 'type': 'ESTIMATED'}}
Updated at
2024-06-26

1 organization

1 product

2 indications