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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01669265
Other study ID # SOLTI-1113
Secondary ID
Status Completed
Phase N/A
First received May 24, 2012
Last updated November 17, 2014
Start date June 2012
Est. completion date August 2012

Study information

Verified date November 2014
Source SOLTI Breast Cancer Research Group
Contact n/a
Is FDA regulated No
Health authority Spain: Comité Ético de Investigación Clínica
Study type Observational

Clinical Trial Summary

This is a retrospective, multicentric cohort study of patient cases with cT1-3, N0 early breast cancer, who previously had intraoperative sentinel lymph node (SLN) evaluation by one-step nucleic acid amplification (OSNA) assay with a complete axillary dissection.

The aim of the present study is to assess the intraoperative positive SLN total tumor load (TTL) obtained from the OSNA assay and to determine whether this TTL predicts non-SLN metastasis in patients with clinically node-negative early-stage breast cancer.


Recruitment information / eligibility

Status Completed
Enrollment 701
Est. completion date August 2012
Est. primary completion date June 2012
Accepts healthy volunteers No
Gender Female
Age group N/A and older
Eligibility Inclusion Criteria:

- Pathologically confirmed invasive breast carcinoma

- Stage T1-3,N0 evaluated by physical exam or imaging according to AJCC v.7 and best clinical local practices

- Intraoperative evaluation of sentinel lymph node (SLN) by OSNA

- Complete dissection of axillary lymph nodes after the evaluation of the SLNs by OSNA

- Pathology report of the tumor and dissected lymph nodes that includes the following information:

- primary tumor size (mm), tumor grade (Scarff-Bloom Richardson), estrogen receptor status

- progesterone receptor status

- HER2 status (ASCO/CAP guidelines)

- Ki67 index

- presence/absence of lymphovascular invasion

- total number of sentinel and non-sentinel lymph nodes dissected during surgery

- total number of positive and negative sentinel and non-sentinel lymph nodes, *size of the metastasis in both sentinel and non-sentinel lymph nodes

- total tumoral load in each sentinel lymph node, expressed as number of CK19 mRNA copies per microliter.

Exclusion Criteria:

- Patients who underwent neoadjuvant chemotherapy

- CK19-negative breast tumor

- ALND with <10 lymph nodes

- In situ carcinoma only

- Metastatic breast cancer at time of diagnosis

Study Design

Observational Model: Cohort, Time Perspective: Retrospective


Related Conditions & MeSH terms


Locations

Country Name City State
Spain Hospital Universitario de Bellvitge Barcelona
Spain Vall d´Hebron University Hospital Barcelona
Spain Hospital Clínico Universitario de Santiago de Compostela La Coruña
Spain Hospital Universitario de Gran Canaria Doctor Negrin Las Palmas
Spain Hospital Universitario Arnau de Vilanova Lleida
Spain Hospital Universitario 12 de Octubre Madrid
Spain Hospital Universitario de Salamanca Salamanca
Spain Hospital Universitario Virgen Del Rocio Seville
Spain Instituto Valenciano de Oncología Valencia

Sponsors (2)

Lead Sponsor Collaborator
SOLTI Breast Cancer Research Group Sysmex America, Inc.

Country where clinical trial is conducted

Spain, 

References & Publications (2)

Peg V, Espinosa-Bravo M, Vieites B, Vilardell F, Antúnez JJ, Salas MS, Sansano I, Delgado Sánchez JJ, Pinto W, Gozalbo F, Petit A, Rubio I. Intraoperative molecular analysis of sentinel lymph node as a new predictor of axillary status in early breast canc

Peg V, Espinosa-Bravo M, Vieites B, Vilardell F, Antúnez JR, de Salas MS, Delgado-Sánchez JJ, Pinto W, Gozalbo F, Petit A, Sansano I, Del Mar Téllez M, Rubio IT. Intraoperative molecular analysis of total tumor load in sentinel lymph node: a new predictor — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Estimate the negative predictive value of the technique OSNA. Estimate the negative predictive value of the technique OSNA for the cutoff point that maximizes (tentatively, 10,000 to 15,000 copies / uL) of axillary lymph node involvement in breast cancer early N0. At time of surgery No
Secondary ROC curve that describes the assay ROC curve (Receiver Operating Characteristic) from the true and false positives and negatives of OSNA test for different cutoffs At time of surgery No
Secondary Sensitivity of the assay Probability that OSNA in sentinel lymph nodes (SLN) is positive given that there is involvement of non-sentinel lymph nodes (NSLN) At time of surgery No
Secondary Specificity of the assay Probability that OSNA in SLN is negative because there is no involvement of NSLN At time of surgery No
Secondary Likelihood ratio for the cutoff of 10,000-15,000 copies/uL Likelihood ratio of positive and negative results At time of surgery No
Secondary Positive predictive value at the cutoff of 10.000-15.000 copies/µL. At time of surgery No
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