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

NCT ID: NCT04882371

Last Updated: 2021-05-11

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

88 participants

Study Classification

OBSERVATIONAL

Study Start Date

2018-01-01

Study Completion Date

2020-08-01

Brief Summary

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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).

Detailed Description

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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.

Conditions

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Breast Cancer Chemotherapy Effect

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Study Groups

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MRI RECIST

Radiological responses were evaluated according to the Response Evaluation Criteria in Solid Tumors (RECIST) and changes in contrast enhancement patterns on MRI

Chemotherapy

Intervention Type DRUG

Neoadjuvant Chemotherapy for Breast Cancer

Magnetic Resonance Imaging (MRI)

Intervention Type DIAGNOSTIC_TEST

Performed contrasted MRI for evaluate response of neoadjuvant chemotherapy

PET-CT PERCIST

Radiological responses were evaluated according to the classification of PET Response Criteria in Solid Tumors (PERCIST) on PET-CT.

Chemotherapy

Intervention Type DRUG

Neoadjuvant Chemotherapy for Breast Cancer

Positron emission tomography - Copmputer Tomography (PET-CT)

Intervention Type DIAGNOSTIC_TEST

Performed contrasted PET-CT for evaluate response of neoadjuvant chemotherapy

Interventions

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Chemotherapy

Neoadjuvant Chemotherapy for Breast Cancer

Intervention Type DRUG

Magnetic Resonance Imaging (MRI)

Performed contrasted MRI for evaluate response of neoadjuvant chemotherapy

Intervention Type DIAGNOSTIC_TEST

Positron emission tomography - Copmputer Tomography (PET-CT)

Performed contrasted PET-CT for evaluate response of neoadjuvant chemotherapy

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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Cem Ilgin Erol

OTHER

Sponsor Role lead

Responsible Party

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Cem Ilgin Erol

MD

Responsibility Role SPONSOR_INVESTIGATOR

Locations

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Istanbul Medeniyet University Goztepe City Hospital

Istanbul, Kadikoy, Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

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Other Identifiers

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2020-0327

Identifier Type: -

Identifier Source: org_study_id

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