SEED01: ROLL Versus Magnetic Seed for Preoperative Localization of Non-palpable Breast Lesion: Comparison Between Techniques.

Sponsor
Istituti Clinici Scientifici Maugeri SpA (Other)
Overall Status
Recruiting
CT.gov ID
NCT05942092
Collaborator
(none)
1,400
1
65.2
21.5

Study Details

Study Description

Brief Summary

Nowadays, Breast Conservative Surgery (BCS) is the standard of care for patients affected by early breast lesions. Screening programmes led to an increase of impalpable breast lesion detection rates. These patients are often eligible for BCS and an accurate preoperative localization technique for the detection of the lesion is required in order to guarantee a safe surgical excision.

The primary goal of BCS is to obtain a complete resection of the tumor with disease-free surgical margins. The presence of tumor on surgical margins on postoperative histological examination of the specimen increases the risk of local recurrence and it requires a surgical re-excision. For all these reasons different techniques for localization of occult breast lesions have been developed over time. Since '70s, the wire guided localization (WGL) technique has represented the gold standard technique; however, it has several limitations such as wire migration or fracture and patient's referred discomfort related to wire placement. Other techniques have been proposed such as the ROLL and magnetic seeds.

The ROLL consists of the injection of a radioactive substance into the breast lesion and the localization during surgery is allowed by using a handheld gamma probe. Limitations of this technique are represented by the need of radioactive injection the day before surgery with subsequent longer hospitalizations and the possible spread of the radioactive substance into breast tissue leading to larger resections.

The latest technological evolution is represented by magnetic seeds, small devices deployed into the lesion even up to more than 30 days before surgery and identified with a specific magnetic probe during surgery.

Currently there are several studies of comparison between the WGL and the more modern techniques. All of these data claim the effectiveness of the new "wire-free" methodics ensuring a safe surgical resection with tumor-free margins and, in some cases, a better aesthetic result.

Studies of comparison between the modern techniques are limited. There is no scientific evidence of the superiority of magnetic seeds compared to ROLL.

The aim of this retrospective study is to compare ROLL with magnetic seed to assess their efficacy in the localization of non-palpable breast lesions.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Breast conserving surgery

Study Design

Study Type:
Observational
Anticipated Enrollment :
1400 participants
Observational Model:
Cohort
Time Perspective:
Retrospective
Official Title:
A Retrospective Multicentric Clinical Study Comparing Radioguided Occult Lesion Localization (ROLL) and Magnetic Seed in the Intraoperative Localization of Non-palpable Breast Lesions During Breast Conservative Surgery.
Actual Study Start Date :
Apr 26, 2023
Anticipated Primary Completion Date :
Sep 30, 2023
Anticipated Study Completion Date :
Sep 30, 2028

Arms and Interventions

Arm Intervention/Treatment
ROLL

Procedure: Breast conserving surgery
Breast conserving surgery after lesion's localization with ROLL or magnetic seed

SEED

Procedure: Breast conserving surgery
Breast conserving surgery after lesion's localization with ROLL or magnetic seed

Outcome Measures

Primary Outcome Measures

  1. Free-surgical margins [6 months]

    Number of surgical procedures in which surgical margins are tumor disease-free ("no ink on tumor" for invasive cancer and margin of 2 mm for in situ-carcinoma).

Secondary Outcome Measures

  1. Excess breast resection [6 months]

    Excess breast resection calculated by the "calculated resection ratio" (CRR=total resection volume/optimal resection volume)

  2. Surgery time [6 months]

    Surgery duration

  3. Hospitalization's days [6 months]

    Number of hospitalization's days

  4. Complications [6 months]

    Complications occurred after biopsy or surgery

  5. Reintervention [6 months]

    Reintervention rates

  6. Follow up [5 years after enrollment]

    5-years follow-up outcomes

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 85 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Female patients between 18 and 85 years who underwent to breast conservative surgery for non-palpable occult breast lesions;

  • Intraoperative localization of breast lesion with ROLL or magnetic seed;

  • Preoperative diagnosis on histology or cytology of borderline lesion (B3 or C3) or malignant lesion (B4-B5 or C4-C5).

Exclusion Criteria:
  • B2 or C2 at preoperative needle breast biopsy or fine needle breast aspiration.

  • Breast tumor localization with clip for neoadjuvant chemotherapy.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Istituti Clinici Scientifici Maugeri SpA Pavia Lombardia Italy 27100

Sponsors and Collaborators

  • Istituti Clinici Scientifici Maugeri SpA

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Fabio Corsi, Professor, Istituti Clinici Scientifici Maugeri SpA
ClinicalTrials.gov Identifier:
NCT05942092
Other Study ID Numbers:
  • 2755
First Posted:
Jul 12, 2023
Last Update Posted:
Jul 12, 2023
Last Verified:
Jul 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Fabio Corsi, Professor, Istituti Clinici Scientifici Maugeri SpA

Study Results

No Results Posted as of Jul 12, 2023