Ultrasound-assisted CNSs Mapping Versus Dual-tracer-guided Sentinel Lymph Node Biopsy (UltraCars)

Guangdong Provincial People's Hospital (Guangdong Provincial Academy of Medical Sciences)

Status and phase

Completed

Phase 3

Conditions

Breast Cancer

Treatments

Procedure: UC group: ultrasound-assisted CNSs guided

Procedure: GC group: CNSs plus ICG dual-tracer-guided

Study type

Interventional

Funder types

Other

Identifiers

NCT04951245

20190511

Details and patient eligibility

About

The investigators suggested ultrasound-assisted Carbon nanoparticle suspensions (CNSs) mapping had great clinical value in clinical application and might serve as a useful alternative to the dual-tracer-guided SLNB. The investigators designed this prospective, randomized controlled phase 3 trial, to compare the feasibility and diagnostic performance of ultrasound-assisted carbon nanoparticle suspensions mapping versus dual-tracer-guided sentinel lymph node biopsy in patients with early breast cancer.

Full description

The study was a single-center, open-label, randomized controlled, non-inferiority, phase 3 trial. Eligible participants were 18 year's of age or older and had histologically confirmed primary invasive breast cancer, or ductal carcinoma in situ scheduled for mastectomy, without clinical or radiological nodal involvement (cN0) or with clinical positive lymph nodes (cN1) that were downstaged to cN0 following neoadjuvant chemotherapy (NCT); and had an Eastern Cooperative Oncology Group (ECOG) performance status score of 0 or 1. Participants were randomly assigned (1:1) using a permuted block randomization scheme to receive either ultrasound-assisted CNSs (UC group) or CNSs plus ICG dual-tracer-guided (GC group) SLN mapping.

Enrollment

330 patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

The participants must be female and 18 years of age or older.
Resectable invasive adenocarcinoma of the breast, confirmed histologically.
Ductal carcinoma in situ confirmed histologically.
The participants must be a preoperative clinical Tis, T1, T2, T3 as well as clinical M0 breast cancer.
Without clinical or radiological nodal involvement (cN0): No positive ipsilateral axillary lymph nodes; No prior removal of ipsilateral axillary lymph nodes; No suspicious palpable nodes in the contralateral axilla or palpable supraclavicular or infraclavicular nodes, unless proven nonmalignant by biopsy.
With clinical positive lymph nodes (cN1) (including any abnormal or enlarged clinically palpable lymph nodes or core biopsy/surgical biopsy/FNA evidence of malignant cell within any lymph nodes) that was downstaged to cN0 following neoadjuvant therapy.
The participants must have an ECOG performance status of Grade 0-1.
The participants must provide written informed consent before participating in the study.

Exclusion criteria

The breast has ulceration, erythema, infiltration of the skin or underlying chest wall (complete fixation), peau d'orange, or skin edema of any magnitude. Tethering or dimpling of the skin or nipple inversion allowed.
The participants has a known hypersensitivity to tracers planned for use during SLNB.
Other prior breast malignancy except lobular carcinoma in situ.
The participants has had prior breast implants.
The participants has had prior breast reduction surgery.
The participants has had other prior surgery in the upper, outer quadrant, areola, or axilla to the indicated breast.
The participants has a positive pregnancy test or is lactating.
The participants has participated in another investigational drug study during the 30 days prior to signing informed consent.