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Trial Title:
Predictive Model of Axillary Nodal Status After Neoadjuvant Chemotherapy in Breast Cancer Patients
NCT ID:
NCT05798806
Condition:
Breast Cancer
Conditions: Official terms:
Breast Neoplasms
Study type:
Observational
Overall status:
Active, not recruiting
Study design:
Time perspective:
Retrospective
Summary:
The management of patients diagnosed with breast cancer (BC) with axillary nodal
involvement is still a controversial topic. These patients' treatment usually involves
the administration of a neoadjuvant chemotherapy (NAC) in order to improve survival rates
and increase local disease control. Depending on the tumor subtype, an axillary
pathologic complete response (pCR) is achieved in 40-70% of initially axillary
node-positive patients (cN+). Concerning patients with an axillary pCR, thus a clinically
negative node status (cN0), axillary lymphadenectomy (ALND) might be replaced by less
invasive surgical approaches and sentinel lymph node biopsy (SLNB) is considered, in
these cases, an effective alternative treatment.
However, the relatively high false negative rates, reported in several validation trials,
points out the complexity concerning these patients' treatment. Moreover, histological
findings' predictive and prognostic value, after SLNB, of micrometastases and isolated
tumor cells (ITCs) is still unclear.
Currently, dual-tracer-guided lymph node biopsy and the surgical removal of ≥ 3 sentinel
lymph nodes are known as effective strategies aimed to reduce the false negative rates.
There are several ongoing clinical trials to understand and define the best approach for
these patients.
Nowadays, there's great interest in potential prognostic role of systemic inflammation's
biochemical markers such as neutrophil-to-lymphocyte ratio (NLR). Systemic inflammation's
markers may be nodal pCR's predictors after NAC in node-positive breast cancer patients.
The aim of the study is to develop and validate a pre-operative model, able to predict
pCR after NAC to select the patients suitable for a surgery de-escalation strategy.
Detailed description:
This is a retrospective, observational, multicentric and no profit study. The study
involves patients with diagnosis of cN+ breast cancer who underwent neoadjuvant treatment
and then treated with lymph node biopsy or axillary lymphadenectomy, referring to the
participating centers.
For each patient the following clinical-anamnestic information will be collected: age,
pre-NAC blood cell count, tumor dimension, clinical staging (cT, cN), histological
information (tumor subtype, grading, receptors' status, Ki-67 value), neoadjuvant
treatment regimen, clinical and radiological local response after NAC, clinical and
radiological nodal response after NAC, type of surgery, number of examined lymph nodes,
number of positive lymph nodes, pathological staging after surgery (ypT, ypN).
Criteria for eligibility:
Study pop:
The study involves patients with diagnosis of cN+ breast cancer who underwent neoadjuvant
chemotherapy and afterwards treated with lymph node biopsy or axillary lymphadenectomy,
referring to the participating centers.
Sampling method:
Probability Sample
Criteria:
Inclusion Criteria:
- Diagnosis of breast cancer confirmed by histological examination
- Patients who underwent neoadjuvant chemotherapy
- Axillary lymph nodes involvement at diagnosis (cN≥1), identified by clinical
examination and/or imaging techniques and/or axillary lymph node cytology aspirate
positive for breast cancer cells.
Exclusion Criteria:
- Patients with M+ at diagnosis
- Contraindications for neoadjuvant chemotherapy
Gender:
Female
Gender based:
Yes
Gender description:
Breast cancer is gender based
Minimum age:
18 Years
Maximum age:
90 Years
Healthy volunteers:
No
Locations:
Facility:
Name:
Istituti Clinici Scientifici Maugeri SpA
Address:
City:
Pavia
Zip:
27100
Country:
Italy
Start date:
February 4, 2020
Completion date:
January 31, 2025
Lead sponsor:
Agency:
Istituti Clinici Scientifici Maugeri SpA
Agency class:
Other
Source:
Istituti Clinici Scientifici Maugeri SpA
Record processing date:
ClinicalTrials.gov processed this data on November 12, 2024
Source: ClinicalTrials.gov page:
https://clinicaltrials.gov/ct2/show/NCT05798806