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Clinical Trials/NCT06780735
NCT06780735RecruitingNot Applicable

Surgical Outcome of Breast Conserving Surgery Using Indocyanine Green Fluorescence in Breast Cancer Patients After Preoperative Chemotherapy: a Prospective Study

National Cancer Center, Korea1 site in 1 country128 target enrollmentStarted: July 6, 2023Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
128
Locations
1
Primary Endpoint
Margin-positive rate in final pathological report

Study Overview

Brief Summary

Neoadjuvant chemotherapy for advanced breast cancer has led to an increased rate of breast-conserving surgery (BCS) in these patients. As the demand for preoperative localization methods grows among surgeons performing BCS, traditional localization techniques have shown limitations. For non-palpable breast lesions, preoperative localization has commonly been achieved using ultrasound-guided skin markings or needle localization. However, these methods present challenges, including difficulty in depth localization for patients with large breasts and limitations in real-time re-verification during surgery due to air artifacts after incision. Needle localization, although commonly used, is invasive and poses risks such as displacement or detachment of the needle.

Indocyanine green (ICG), a fluorescent dye that appears green to the naked eye and is detectable by near-infrared (NIR) cameras, has been widely and safely used in clinical practice via intravenous or subcutaneous administration. Recently, ICG combined with NIR imaging has been adopted for sentinel lymph node biopsy in breast cancer and melanoma surgeries and is increasingly used as a localization method for various tumors, replacing conventional techniques.

A preliminary study (IRB No. NCC2016-0071) conducted at the institution evaluated ICG injection and NIR fluorescence imaging for tumor localization in early breast cancer patients undergoing BCS. The study demonstrated the efficacy of ICG-based localization in reducing the rate of positive surgical margins.

The objective of this study is to evaluate the effectiveness of ICG-guided tumor localization with NIR fluorescence imaging in patients with advanced breast cancer treated with neoadjuvant chemotherapy. It is hypothesized that this technique will allow for more accurate tumor excision compared to conventional methods, ultimately improving surgical outcomes.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
Female
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •The Patient with locally advanced breast cancer who is eligible for breast-conserving surgery after receiving neoadjuvant chemotherapy
  • •Aged over 18 years old
  • •ECOG performance status: 0 or 1
  • •The patients with written informed consent

Exclusion Criteria

  • •The patient who requires total mastectomy after receiving neoadjuvant chemotherapy
  • •The patient with no residual mass on ultrasonography or only with microcalcifications
  • •Pregnant or lactating patient
  • •The patient with a disability to understand and provide consent
  • •The patient with severe allergic history to indocyanine green
  • •Iodine-sensitive patient

Arms & Interventions

ICG-F

Experimental

Localization of breast cancer using indocyanine green fluorescence (ICG-F)

Intervention: The margin-positive rate using the localization technique (Procedure)

Outcomes

Primary Outcomes

Margin-positive rate in final pathological report

Time Frame: 10~35 days after surgery (the date when the pathological reports are available)

Collection of data for margin-positive rate from final pathological report after surgery

Secondary Outcomes

  • Localization rate(The day of surgery)
  • Centralization(10~35 days after surgery (the date when the pathological reports are available))
  • Margin-positive rate in frozen section(The day of surgery)
  • Additional resection rate(The day of surgery)
  • Re-excision rate(10~35 days after surgery (the date when the pathological reports are available))
  • Adverse event rate(10~35 days after surgery (the date of follow-up after surgery))

Investigators

Sponsor Class
Other Gov
Responsible Party
Principal Investigator
Principal Investigator

Seeyoun Lee

Doctor, M.D., head of center for breast cancer

National Cancer Center, Korea

Study Sites (1)

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