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repeat sentinel lymph node biopsy in patients with breast tumor recurrence

Not Applicable
Conditions
Neoplasms
Registration Number
KCT0005856
Lead Sponsor
Yonsei University Health System, Gangnam Severance Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot yet recruiting
Sex
Female
Target Recruitment
532
Inclusion Criteria

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

Exclusion Criteria

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

Study & Design

Study Type
Interventional Study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
5-year disease free survival
Secondary Outcome Measures
NameTimeMethod
identification rate of sentinel lymph node;5-year overall survival;5-year local recurrence free survival;5-year regional recurrence free survival;5-year distant metastasis free survival;survival analysis according to the adjuvant treatment after secondary surgery;survival analysis by tumor subtype;identification rate of sentinel lymph node according to the location of primary tumor(caudal/non-caudal);5-year DFS accoridng to the location of primary tumor (caudal/non-caudal)
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