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TerminatedNCT01984866Updated Aug 11, 2020

CPR Prediction After Neoadjuvant Using Excisional Biopsy By Radiofrequency In Breast Cancer From II-III UICC Stages.

An observational study in Triple Negative, HER2+, Luminal B Breast Tumors (Stages II-III)in Female Patients, sponsored by Hospital General Universitario Gregorio Marañon. Terminated at 1 site in Spain. Open to female participants aged 18 Years to 75 Years. Per ClinicalTrials.gov, last updated 2020-08-11.

Sponsored by Hospital General Universitario Gregorio Marañon · Observational

Why this study was terminated
Recruitment was very low.
Study type
Observational
Model
Case-only
Time perspective
Prospective
Enrollment
13
Ages
18 Years to 75 Years
Sex
Female
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Study summary

This project aims to determine whether biopsy using radiofrequency is a procedure suitable for this patient selection. Findings from biopsy will be correlated with the conventional surgery ones. If the technique is validated to predict the presence or absence of residual tumor, breast surgery could be avoided in cases of absence of tumor.

Read the detailed description

Breast cancer is a set of at least 4 different diseases, currently known as intrinsic genomic subtypes. Two of them are the so-called HER2-enriched, characterized by the HER-2 oncogene amplification, and the basal-like, which correlates closely with some of the triple negative tumors (TNBC). These subtypes are very sensitive to the primary medical treatment (neoadjuvant or Presurgical). The use of modern medical treatments as initial treatment, can allow the complete disappearance of cancer in the breast and axilla (pathologic complete response, CPR) in 40% of patients with TNBC and around 60% of patients with HER2-positive tumors in stage II and III.

The need of local surgery in patients where the tumor disappeared completely (CPR) after primary medical treatment, is recently questioned, the improvement is not clear and radiotherapy could be sufficient to assure the locoregional disease control.

The use of conventional diagnostic techniques (MRI, ultrasound, mammography and PET) is not enough reliable to determine the pathological complete response, making difficult to adopt an attitude of surgical abstention. The existence of a minimally invasive technique that could reliably determine the absence of cancer after primary medical treatment surgery, could avoid the surgery in these cases.

Percutaneous biopsy guided by ultrasound radiofrequency is a technique that allows the complete resection of breast lesions up to 2 cm of diameter with minimal aggression to the mammary gland from the area of the initial tumor after the neoadjuvant treatment.

Several studies report the use of this technique in patients with breast cancer. Results show a good tolerability of the technique by the patients and suggest that it would not only reduce the need of the re-excision, but also reduce the rate of local recurrence due to radiation absence.

Biopsy using radiofrequency could be useful to confirm CPR in patients with triple-negative and HER2-positive tumors and several luminal B tumors and good response previously determined by conventional methods (MR in particular). Despite that, new prospective studies to analyse the reliability in patients selection with CPR and could avoid the traditional surgery are needed.

To confirm this hypothesis, a group of 100 treated patients with unicentered tumors in stages II or III and good response determined by MR after 6 cycles of treatment (less than 2 cm apparent residual injury) will be consecutively subjected to radiofrequency biopsy and the surgery previously established for each case (Tumorectomy or mastectomy). Before surgery, the sentinel node will be biopsied in order to define the surgical treatment on the axilla (none in case of negative sentinel node, axillary lymphadenectomy if positive).

The tumor samples obtained by percutaneous radiofrequency and mastectomy-Tumorectomy biopsy will be studied thoroughly to define the correlation between the two.

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Conditions studied

  • Triple Negative, HER2+, Luminal B Breast Tumors (Stages II-III)in Female Patients

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Keywords

  • CPR: Complete Pathological Response
03

In context

Breast Neoplasms

12,544 studies on the registry are indexed under Breast Neoplasms; 2,892 are open to participants now.

This study's enrollment of 13 is below the median of 184 across 2,642 observational studies indexed under Breast Neoplasms.

Browse Breast Neoplasms studies →

Lead sponsor

Hospital General Universitario Gregorio Marañon is the lead sponsor of 59 studies on the registry; 6 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 75 Years
Sexes eligible
Female
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Female patients with breast tumors sensitive to neoadjuvancy

Inclusion criteria

  • Informed consent Form signed
  • Adequate Performance status (ECOG 0-1)
  • Female patients with unifocal breast tumors (stages II-III, TN, HER2+ or Luminal B) very sensitive to neoadjuvant medical treatment (5 to 6 months in accordance with the current standard)
  • Patients who submit clinical-radiologic greater response to the treatment administered (equal to or less than 1.5 cm in NMR residual tumor)

Exclusion criteria

Exclusion Criteria:

  • Ki67\<14%
  • Excisional biopsy Contraindications
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Study design

Observational model
Case-only
Time perspective
Prospective
Enrollment
13 participants (actual)
Patient registry
No
Biospecimen retention
Samples with dna

Groups and cohorts

  • Breast tumors sensitive to neoadjuvant

    Treated patients as usual clinical practice with unicentered tumors in stages II or III and good response determined by MR after 6 cycles of treatment (less than 2 cm apparent residual injury) will be consecutively subjected to radiofrequency biopsy and the surgery previously established for each case (Tumorectomy or mastectomy). Before surgery, the sentinel node will be biopsied in order to define the surgical treatment on the axilla (none in case of negative sentinel node, axillary lymphadenectomy if positive). The tumor samples obtained by percutaneous radiofrequency and mastectomy-Tumorectomy biopsy will be studied thoroughly to define the correlation between the two.

06

What researchers measure

Primary outcomes

  1. determination of the negative predictive value (NPV) of the excisional biopsy technique

    Proportion of biopsies which PCR, are really PCR in the surgical specimen.

    Time frame: up to 15 months

Secondary outcomes

  1. Evaluation of sensitivity and specificity of the excisional biopsy by radiofrequency technique

    * Determine the sensitivity and specificity of excisional biopsy, radiofrequency technique, to classify correctly the stage of the tumor in the breast after neoadjuvant therapy. * Determine the positive predictive value (proportion of biopsies which are not CPR and actually have tumor in the surgical specimen). * Describe the side effects of the excisional biopsy technique by radiofrequency. * Describe the technical problems associated to excisional biopsy technique by radiofrequency. * Assess the concordance between the responses obtained in breast MRI and the previous reported in the anatomy-pathological study. * Determine the % of cases in which surgery could have been avoided within the group defined in the study. * Estimate the economic cost of excisional biopsy with standard therapy

    Time frame: up to 15 months

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Study locations

1 site
  • Hospital General Universitario Gregorio Marañón
    Madrid, 28032, Spain
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 11, 2020, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT01984866
Lead sponsor
Hospital General Universitario Gregorio Marañon
Responsible party
Sponsor
First posted
Nov 15, 2013
Start date
Jul 2013
Primary completion
Apr 2018
Completion
Aug 2018
Last update
Aug 11, 2020
View the source record on ClinicalTrials.gov ↗

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This study is terminated, as verified in Aug 2020. You cannot join it, but the record below documents what was studied.

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