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NCT Number: NCT04741737

Repeat Sentinel Lymph Node Biopsy in Ipsilateral Breast Tumor Recurrence

According to the standard treatment guidelines established until recently, in the case of ipsilateral breast tumor recurrence without systemic metastasis, salvage mastectomy or lumpectomy can be performed when either partial or whole breast radiation therapy is possible. On the other hand, there are currently no standard treatment guidelines for axillary treatment, and the evidence for this is limited. Axillary lymph node metastasis was reported to occur in about 26% of breast cancer patients who had negative sentinel lymph nodes from previous surgery for primary breast cancer and only local recurrence occurred. It is still important in the decision of treatment or adjuvant radiation therapy. However, it is known that most of the patients with ipsilateral breast recurrence do not have axillary lymph node metastasis. Therefore, performing axillary axillary surgery in all of these patients does not help the patient's survival in many cases, but rather can lead to complications such as lymphedema and seroma and postoperative wound infection. A question about the implementation of axillary lymph node resection has been raised and for this reason, it is necessary to study whether surveillance lymph node biopsy is still effective in patients with recurrence in the ipsilateral breast.

Most of the studies on ipsilateral breast tumor recurrence without systemic metastasis reported to date are case reports or small retrospective studies. In addition, the combined meta-analysis also has limitations in that the study design is not uniform, and there are many cases in which primary breast cancer surgery performed total mastectomy or axillary lymph node dissection. This study is a multicenter prospective study designed to validate the clinical effectiveness of repeat-SLNB conducted in patients with ipsilateral breast tumor recurrence among patients who previously underwent breast conservation and sentinel lymph node biopsy for unilateral primary breast cancer.

Recruiting

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Key information

Age range

19 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Gangnam Severance Hospital, Yonsei University College of Medicine

Seoul, 06273, South Korea

Location status: Recruiting

Location contact

Soong June Bae, M.D.

CONTACT

[email protected]

82-2-2019-4401

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age over 19 years old
  • Patients who are expected to undergo surgery under the diagnosis of ipsilateral breast tumor recurrence(histologically confirmed in situ disease or invasive disease)
  • Patients who had partial mastectomy and sentinel lymph node biopsy for prior operation for the initially diagnosed breast cancer
  • Patients considered to be axillary lymph node negative from clinical findings
  • Patients who understand and willingly participate in the study

Exclusion criteria

  • Patients with recurrence in other regions. (e.g. ipsilateral axillary lymph node, supraclavicular lymph node, internal mammary lymph node, etc.)
  • Patients who are not eligible to perform SLNB
  • Patients who received mastectomy or axillary lymph node dissection for prior operation
  • Patients who experienced recurrence within a year from the primary operation
  • Patientes who are known to have axillary lymph node metastasis before the secondary operation, histologically confirmed from tissue biopsy or cytology
  • Patients with systemic recurrence
  • Patients with inflammatory breast cancer
  • Pregnant and lactating patients

Treatment and study plan

reSLNB arm

Procedure

Radioisotope, blue dye, dual mapping methods are all allowed for re-SLNB mapping. Positive finding in re-SLNB is defined according to AJCC 8th edition, as micrometastasis or macrometastasis. Isolated tumor cell is considered negative. When sentinel lymph node is not identified, axillary operation is via physician's choice. When re-SLNB finding is negative, no further axillary lymph node dissection is performed. If there is node metastasis from re-SLNB, axillary lymph node dissection or radiation therapy can be performed as in physician's choice.

Primary outcomes

  1. 5 year disease free survival

    Time frame: 5 years after surgery (re-SLNB)

    To prove non-inferiority of re-SLNB compared to ALND regarding disease free survival

Secondary outcomes

  1. identification rate of sentinel lymph node

    Time frame: 5 years after surgery

    identification rate of sentinel lymph node

  2. 5-year overall survival

    Time frame: 5 years after surgery

    5-year overall survival

  3. 5-year local recurrence free survival

    Time frame: 5 years after surgery

    5-year local recurrence free survival

  4. 5-year regional recurrence free survival

    Time frame: 5 years after surgery

    5-year regional recurrence free survival

  5. 5-year distant metastasis free survival

    Time frame: 5 years after surgery

    5-year distant metastasis free survival

  6. survival by adjuvant treatment

    Time frame: 5 years after surgery

    survival analysis according to the adjuvant treatment after secondary surgery

  7. survival by tumor subtype

    Time frame: 5 years after surgery

    survival analysis by tumor subtype

  8. identification rate of sentinel lymph node by tumor location

    Time frame: 5 years after surgery

    identification rate of sentinel lymph node according to the location of primary tumor(caudal/non-caudal)

  9. 5-year DFS by tumor location

    Time frame: 5 years after surgery

    5-year DFS accoridng to the location of primary tumor (caudal/non-caudal)

Study contacts

Contact information is provided by the study sponsor or research team.

Soong June Bae, M.D.

CONTACT

[email protected]

82-2-2019-4401

Sponsors and collaborators

Lead sponsor

Gangnam Severance Hospital

Other

Registry information

Official study title

Repeat Sentinel Lymph Node Biopsy in Ipsilateral Breast Tumor Recurrence Without Distant Metastasis: A Single-arm, Multicenter, Prospective Study

Important dates

Study start
2020
Primary completion
2024
Study completion
2029
First posted
Feb 5, 2021
Registry last updated
Oct 11, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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