Omission of Surgery in Clinically Low-risk HER2positive Breast Cancer With High HER2 Addiction and a Complete Response Following Standard Anti-HER2-based Neoadjuvant Therapy

HER2-positive Breast Cancer Clinical Trial

— ELPIS  

Official title:

Omission of Surgery and Sentinel Lymph Node Dissection in Clinically Low-risk HER2positive Breast Cancer With High HER2 Addiction and a Complete Response Following Standard Anti-HER2-based Neoadjuvant Therapy

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04578106
• Other study ID #: HCB-ONC001 (ML41519)
• Status: Recruiting
• Phase: Phase 2
• Start date: September 23, 2020
• Est. completion date: December 2026

Study information

• Verified date: January 2022
• Source: Fundacio Clinic Barcelona
• Contact: Laia Arenas
• Phone: 93 2275400
• Email: ELPIS[@]clinic.cat
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a prospective, single arm, open-label, unicenter, exploratory study in women with primary operable HER2-positive, HER2-enriched/ERBB2-high breast cancer according to PAM50 intrinsic subtype and a ERBB2 pre-defined cutoff (high vs low ERBB2 expression), to evaluate the omission of surgery and sentinel lymph node dissection in patients with HER2-E and ERBB2 high breast cancer who achieving a complete response following standard anti-HER2-based neoadjuvant therapy with paclitaxel/trastuzumab/pertuzumab. The primary trial objective is to estimate the loco-regional invasive disease-free survival at 3-year of patients who achieve a complete response based on imaging (i.e. Magnetic resonance imaging) and a stereotactic-guided vacuum-assisted breast biopsy, and omit loco-regional surgery.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 17
• Est. completion date: December 2026
• Est. primary completion date: December 2023
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 40 Years and older

Eligibility

Inclusion Criteria:

1. Female participants who are at least 40 years of age on the day of signing the informed consent form with histologically confirmed diagnosis of breast cancer.

2. A participant is eligible to participate if she is not pregnant, not breastfeeding.

3. The participant (or legally acceptable representative if applicable) provides written informed consent for the trial.

4. Histologically confirmed invasive adenocarcinoma of the breast, with all of the

following characteristics:

• HER2-positive status by local determination according to 2018 ASCO/CAP guidelines.
• PAM50 HER2-enriched subtype and ERBB2-high as predefined cutoff as per central determination.
• Unifocal invasive carcinoma: only 1 invasive focus can be observed (the tumor focus containing or not containing an in situ component)
• Tumor largest diameter =4 cm as defined by breast MRI.
• No nodal involvement (i.e. cN0). Any suspicious axillary node by ultrasound must be biopsied. If the biopsy or the FNA is negative of tumor cells, patient is eligible.
• No evidence of distant metastasis (M0) by routine clinical assessment.

5. Patient must have known ER and PR status locally determined prior to study entry.

6. Eligible for taxane therapy.

7. Willingness of the patient to omit surgery if all criteria are met following neoadjuvant therapy.

8. Estimated life expectancy of at least 5 years irrespective of the diagnosis of breast cancer.

9. Breast cancer eligible for primary surgery

10. Have provided archival tumor tissue sample or newly obtained core. Formalin-fixed,paraffin embedded (FFPE) tissue blocks are mandatory. Available pre-treatment FFPE core biopsy evaluable for PAM50 or possibility to obtain one.

11. Have an Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 1.

12. Ability and willingness to comply with study visits, treatment, testing and to comply with the protocol.

13. Have adequate organ function.

Exclusion Criteria:

1. Has received prior anti-cancer therapy, including investigational agents, or treatment for primary invasive breast cancer.

2. Known hypersensitivity to any of the excipients of trastuzumab, pertuzumab, TDM1 or paclitaxel.

3. Clinical stage II, III or IV.

4. History of radiotherapy in the ipsilateral breast or axilla.

5. History of surgery of the ipsilateral axilla.

6. Bilateral invasive breast cancer.

7. Infiltrating lobular carcinoma.

8. Multicentric or multifocal breast cancer, defined as the presence of two or more foci of cancer in the same or different quadrants of the same breast.

9. Patients who have undergone sentinel lymph node biopsy prior to study treatment.

10. Patient has active cardiac disease or a history of cardiac dysfunction

11. Has an active infection requiring systemic therapy.

13. Patients with a history of previous breast cancer are excluded.

Related Conditions & MeSH terms

• Breast Neoplasms
• HER2-positive Breast Cancer
• Stage I Breast Cancer

Intervention

Biological:
• Trastuzumab and pertuzumab Subcutaneous Fixed-Dose Combination
After 13 weeks of neoadjuvant treatment, a breast MRI will be performed. If a complete response is observed on breast MRI, patients will undergo a stereotactic-guided VAB of the marker area to obtain 12 cylinders of breast parenchyma, which is equivalent to 2 grams of tissue. If no invasive tumor cells and no in situ disease are identified in the stereotactic-guided VAB, patients will be eligible to omit loco-regional surgery.

Locations

Country	Name	City	State
Spain	Hospital Clinic de Barcelona	Barcelona

Sponsors (3)

Lead Sponsor	Collaborator
Fundacio Clinic Barcelona	Roche Pharma AG, SOLTI Breast Cancer Research Group

Country where clinical trial is conducted

Spain, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	To evaluate the possibility of omission of surgery and sentinel lymph node dissection in clinically low-risk HER2-positive breast cancer with high HER2 addiction and a complete response following standard neoadjuvant chemotherapy and dual HER2 blockade.	To estimate the loco-regional invasive disease-free survival (LR-IDFS) at 3-year of patients who achieve a complete response based on imaging and a stereotactic-guided vacuum-assisted breast biopsy, and omit loco-regional surgery.	3 years