Clinical trial · Observational
Measuring the Impact of MammaPrint on Adjuvant and Neoadjuvant Treatment in Breast Cancer Patients: A Prospective Registry
NCT02670577CI-TRIAL-00033469IMPACtcompletedClinicalTrials.gov clinicaltrialsProvenance
- 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)
The scope of this study is to measure the impact of MammaPrint on treatment in Hormone Receptor (HR)-positive HER2-negative breast cancer patients. In addition, the impact of MammaPrint on treatment in patients with T1a/T1b and pN0/pN1 (up to 1 node), Triple Negative or HER2-positive tumors will be assessed.
Conditions
Conditions (1)
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 |
Interventions
Interventions (0)
Data not yet available
No intervention recorded.
Design
Arms and outcomes
Arms (4)
- label
- stage I or II HR-positive, HER2-negative
- description
- Histologically proven invasive stage I and II breast cancer and Hormone Receptor positive \& HER2 negative \& Axillary lymph node status: 0-3 involved
- label
- HER2+
- description
- Histologically proven invasive T1a or T1b breast cancer \& Hormone receptor negative or positive \& HER2 positive \& Axillary lymph node status: 0-1 involved
- label
- Triple Negative
- description
- Histologically proven invasive T1a or T1b breast cancer \& Hormone receptor negative \& HER2 negative \& Axillary lymph node status: 0-1 involved
- label
- Neoadjuvant
- description
- Stage I or II patients receiving neoadjuvant therapy.
Primary outcomes (1)
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * Eligible to receive chemotherapy and endocrine therapy as defined by a good Karnofsky index (≥80) and no hematologic, cardiologic or hepatic contraindications, nor any impeding comorbidity * Informed consent form signed on the same day or before enrollment * ≥ 18 years of age at time of consent Per study arm * Histologically proven invasive stage I and II breast cancer and Hormone Receptor positive (ER+ PR-, ER- PR+ or ER+ PR+) according to local standards \& HER2 negative: IHC 0-1+, or FISH or other ISH non-amplified (locally assessed) IMPACt study; version 1 2015 September 1 Page 10 Axillary lymph node status: 0-3 involved (macro metastases i.e. \>2mm OR micro metastases i.e. \>0.2-2mm) OR Histologically proven invasive T1a or T1b breast cancer \& Hormone receptor negative (ER- and PR-) according to local standards \& HER2 negative: IHC 0-1+, or FISH or other ISH non-amplified (locally assessed) \& Axillary lymph node status: 0-1 involved (macro metastases i.e. \>2mm OR micro metastases i.e. \>0.2-2mm) OR Histologically proven invasive T1a or T1b breast cancer \& Hormone receptor negative or positive (ER-PR-, ER+PR-, ER-PR+, ER+PR+) according to local standards \& HER2 positive: IHC 3+, or FISH or other ISH amplified (locally assessed) \& Axillary lymph node status: 0-1 involved (macro metastases i.e. \>2mm OR micro metastases i.e. \>0.2-2mm) Exclusion Criteria: * Previous diagnosis of breast malignancy unless disease free for 10 years * Metastatic disease * Tumor sample shipped to Agendia with ≤ 30% tumor cells or that fails QA or QC criteria * Women who have started or completed adjuvant chemotherapy or neo-adjuvant chemotherapy for current breast cancer
References
Publications (1)
- DERIVEDSoliman H, Shah V, Srkalovic G, Mahtani R, Levine E, Mavromatis B, Srinivasiah J, Kassar M, Gabordi R, Qamar R, Untch S, Kling HM, Treece T, Audeh W. MammaPrint guides treatment decisions in breast Cancer: results of the IMPACt trial. BMC Cancer. 2020 Jan 31;20(1):81. doi: 10.1186/s12885-020-6534-z. PMID 32005181