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Completed

NCT Number: NCT04882371

Comparison of MRI With PET / CT in the Evaluation of Response to Neoadjuvant Therapy Based on the Molecular Subtypes of Breast Cancer

The current study aims to determine the diagnostic accuracy of Magnetic Resonance Imaging (MRI) and Positron Emission Tomography- Computed Tomography (PET-CT) in predicting a pathological response of molecular subtypes of breast cancer to neoadjuvant chemotherapy (NAC).

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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Observational

Primary location

Istanbul Medeniyet University Goztepe City Hospital

Istanbul, Kadikoy, 34100, Turkey (Türkiye)

About this study

Eighty-eight patients with breast cancer who had undergone surgery after NAC were retrospectively analyzed between January 2018 and May 2020, at the general surgery clinic of Istanbul Medeniyet University Göztepe Training and Research Hospital. Demographic data, clinical findings, tumor markers, radiologic findings and pathology data were documented. With the use of MRI and / or PET-CT obtained before and after NAC, tumor staging was performed, and tumor size and the presence of metastatic lymph nodes and radiological response to NAC were evaluated. The response to NAC was evaluated according to the Response Evaluation Criteria in Solid Tumors (RECIST) and contrast enhancement patterns described by Tozaki et al. on MRI, and the classification PET Response Criteria in Solid Tumors (PERCIST) on PET-CT. The postoperative pathology study reported the followings: the size and histopathologic type of the tumor, its hormone receptor status, staining intensities (Allred score), HER-2 positivity, Ki-67 proliferation percentages, and the molecular subtypes; the presence and number of metastatic lymph nodes, the response of the tumor and, the metastatic lymph node, if any, to NAC according to the Sataloff classification. Patients with a Sataloff score of "A" were considered to have a pCR, those with the scores of "B" or "C" were considered to have a partial response. When examining the Sataloff scores, the presence of pCR in both the primary tumor and axilla was evaluated and compared with the presence of radiological complete response on MRI and / or PET-CT. In addition, the sensitivities of MRI and PET-CT in predicting pCR in patients undergoing NAC were statistically compared based on the molecular subtypes. Patients whose MRI and PET-CT findings were consistent with histopathologic data were included in the "Radiology-Pathology agreement " group. The sensitivity of imaging methods was determined by examining the rates of agreement in the molecular subgroups. The Statistical Package for Social Sciences software for Windows version 20 (SPSS Inc.; Chicago, IL, USA) was used for all analyses. Normality was assessed by the Shapiro-Wilk test. Categorical variables were compared using chi-square or, where appropriate, Fisher's exact test. The Mc-Nemar test was used for paired categorical data. Trends in tables larger than 2x2 were examined with the linear-by-linear association test. Kruskal-Wallis test was used to compare non-normal distributed variables in three groups. Cohen's kappa (κ) was calculated to test the agreement between the classifications of radiology and pathology.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Older than 18
  • Breast cancer patients
  • Had neoadjuvant chemotherapy before surgery
  • Had undergone surgery after chemotherapy

Exclusion criteria

  • Younger than 18
  • History of surgery for breast cancer

Treatment and study plan

Chemotherapy

Drug

Neoadjuvant Chemotherapy for Breast Cancer

Magnetic Resonance Imaging (MRI)

Diagnostic Test

Performed contrasted MRI for evaluate response of neoadjuvant chemotherapy

Positron emission tomography - Copmputer Tomography (PET-CT)

Diagnostic Test

Performed contrasted PET-CT for evaluate response of neoadjuvant chemotherapy

Primary outcomes

  1. Radiological evaluation of response to neoadjuvant chemotheraphy for breast cancer

    Time frame: 2 months

    All patient had neoadjuvant chemotherapy, then a group of patient evaluated with MRI and the other group of patient with PET-CT

Secondary outcomes

  1. Pathological evaluation of response to neoadjuvant chemotheraphy for breast cancer

    Time frame: 2 months

    Surgery was performed for all patient after neoadjuvant chemotherapy. Pathological datas were analyzed

Sponsors and collaborators

Lead sponsor

Cem Ilgin Erol

Other

Registry information

Important dates

Study start
2018
Primary completion
2020
Study completion
2020
First posted
May 11, 2021
Registry last updated
May 11, 2021

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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