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PET/MR Radiomics for Breast Cancer Diagnosis

Use of PET/MR Radiomics to Evaluate the Clinical Phenotypes, Response Status of Neoadjuvant Chemotherapy and Long-term Prognosis of Breast Cancer: a Preliminary Study

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05466760
Enrollment
120
Registered
2022-07-20
Start date
2018-07-06
Completion date
2022-12-31
Last updated
2022-07-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Cancer

Keywords

Breast cancer, radiomics, hybrid PET/MRI

Brief summary

Breast cancer is the most common malignancy in women in our country (2013 cancer registry report, Health Promotion Administration). MRI is a more accurate imaging modality for breast lesion diagnosis, monitoring of treatment response, and local staging than compared with mammography and ultrasound. ¹⁸ F-FDG PET was reported to be used for breast cancer diagnosis, staging, and prediction of treatment response as well. We usually interpret the aforementioned imaging modalities by qualitative methods for decision-making. Radiomics is a process involving the conversion of images to quantitative data for subsequent data mining to improve decisional making for patient care, to adjust the patient management, that is so-called precision medicine. Our study is to use semantic and agnostic features of radiomics by hybrid PET/MR for 1. The pre-operative breast cancer patients (without neoadjuvant chemotherapy before operation). 2. The patients will receive neoadjuvant chemotherapy (NAC). The study intends to investigate the association of PET/MR radiomics data with the probability of metastasis or risk of recurrences and survival. We will also investigate if the BD and BPE (measured on MRI) are associated with molecular subtypes, histologic grade and clinical outcome, risk of metastases, and long-term survival of breast cancer patients for the study participants.

Detailed description

Purposes and background introduction: Breast cancer is the most common malignancy in women in our country (2013 cancer registry report, Health Promotion Administration). MRI is a more accurate imaging modality for breast lesion diagnosis, monitoring of treatment response, and local staging than compared with mammography and ultrasound. ¹⁸ F-FDG PET was reported to be used for breast cancer diagnosis, staging, and prediction of treatment response as well. We usually interpret the aforementioned imaging modalities by qualitative methods for decision-making. In recent years, the concept of Radiomics is emerging. Radiomics is a process involving the conversion of images (imaging phenotypes) to quantitative data for subsequent data mining to improve decisional making for patient care, to adjust the patient management, that is so-called precision medicine. Radiomics is applied for the diagnostic, prognostic, and predictive purposes of diseases. There are two main approaches to radiomics: First, the semantic approach, which uses the usual radiological lexicon derived from regions of interest; second, the agnostic approach is higher-order, mathematically computed data derived from images instead of the commonly used radiologists' lexicon. MRI and PET can be used in breast radiomics studies. Hybrid PET/MR is a machine that the PET and MRI can be performed on the same table at the same time slot, therefore, the imaging data of MRI and PET can be obtained at the same examination, with less radiation dosage, more reliable lesion mapping than separate examinations of PET/CT and MRI. Material and methods: There is a total of 120 patients would like to be included in the study. Our study is to use semantic and agnostic features of radiomics by hybrid PET/MR for: 1. The pre-operative breast cancer patients (without neoadjuvant chemotherapy before operation): to investigate the association of PET/MR imaging data with molecular subtypes, cell proliferation (Ki-67), tumor aggressiveness (by histologic grade). 2. The patients who will receive neoadjuvant chemotherapy (NAC): PET/MR study will be performed for 3 times: pre-MAC (study 1), PET/MR after 1st dose of NAC (study 2), and PET/MR after 3rd or 4th NAC (study 3). We will investigate the predictive ability of PET/MR imaging data for NAC response. And we will investigate which parameters at which series of examinations are more predictive of the final NAC response. Therefore, we can adjust the NAC regimen as early as possible. 3. The breast cancer patients mentioned above: we will investigate the association of PET/MR radiomics data with the probability of metastasis or risk of recurrences and survival. 4. We will also investigate if the BD and BPE (measured on MRI) are associated with molecular subtypes, histologic grade and clinical outcome, risk of metastases, and long-term survival of breast cancer patients for the study participants. Data analysis: 1. For the breast cancer patients who will go directly to surgical treatment: We will analyze the association of MRI and PET semantic radiomics features (including DCE MRI, DWI/ADC, CEST, MRS and SUVmax, MTV, TLG) and agnostic radiomics ( texture) features with molecular subtypes, proliferation index (Ki-67), histology type and grades, and tumor size, lymph node status. And we will also investigate whether the semantic or agnostic/ texture analysis, or combination of both can be predictive of the factors associated with clinical outcome (that is, molecular subtype, Ki-67, histology type and grade, size, LN status). 2. For the patients who will receive NAC: As stated previously, each participant is designed to undergo three examinations: Study 1- pre-NAC PET/MR; Study 2- first follow-up PET/MR is performed after first dose of NAC; Study 3, second follow-up PET/MR is performed after third or fourth dose of the NAC. The NAC protocol is mainly antracycline-based followed by taxane-based regimen for a total of 6- 8 cycles. 3. For long-term follow-up:The 5-year survival of each study participant will be obtained, and we will investigate the association of all aforementioned PET or MRI-related radiomics parameters with overall survival, disease-free survival by Cox proportional hazards model. Kaplan-Meier analysis for survival curves and comparison of survival by log-rank test will also be estimated. 4. The association of BPE and breast density (BD) with long term outcome: 5. The Statistical analysis will be performed by Stata 13 (Stata Corp., College Station, Texas, USA) and SAS 9.3 (SAS Institute Inc., Cary, NC, USA). A P value \<0.05 will be regarded as statistical significance.

Interventions

RADIATIONPET/MR

Study 1- pre-NAC PET/MR; Study 2- first follow-up PET/MR is performed after first dose of NAC; Study 3, second follow-up PET/MR is performed after third or fourth dose of the NAC. The NAC protocol is mainly antracycline-based followed by taxane-based regimen for a total of 6-8 cycles.

Sponsors

Taipei Veterans General Hospital, Taiwan
Lead SponsorOTHER_GOV

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
25 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* 1\. Women aged 25-75 years old. * 2\. Women with recently diagnosed breast cancer.

Exclusion criteria

* 1\. Estimated GFR (eGFR) \< 60 mL/min/1.73 m2 and blood glucose \> 135 mg/dl; Past/ present history of acute renal failure, renal dialysis, DM. * 2\. Women with metallic fixation, coronary artery stent in recent 3 months; or women with mechanical valve replacement not compatible with MR magnet; or women with aneurysmal clips, pacemakers. * 3\. Past history of claustrophobia. * 4\. Women who are pregnant or who are planning to be pregnant, or who are lactating * 5\. Past history of breast cancer within recent 5 years * 6\. Women undergoing chemotherapy for other disease entity in recent 1 year. * 7\. Women who cannot cooperate with the examinations.

Design outcomes

Primary

MeasureTime frameDescription
Diagnostic performance of PET/MR imaging metrics in prediction of treatment response to chemotherapy40 weeksDetermination of the sensitivity, specificity of PET/MR imaging metrics to predict treatment response to neoadjuvant chemotherapy. The treatment response will be determined by RCB (residual cancer burden) index at surgical pathology after completion of neoadjuvant chemotherapy and further categorized as group 1: RCB 0 or I; group 2: RCB II or III. The logistic regression will be performed with the groups (1 or 2) as dependent variable and the different PET/MR imaging metrics as independent variables, the ROC analysis and sensitivity, specificity of the PET/MR imaging metrics will be inferred from the regression models.

Secondary

MeasureTime frameDescription
Comparison of PET/MR imaging metrics among patients with different histologic grades2 weeksThe histologic grades will be categorized as grade I, II, III. The difference of PET/MR imaging metrics among patients of non-high grade (grades I, II) and high grade (grade III) will be compared by Mann-Whitney U test.
Comparison of PET/MR imaging metrics among patients with different molecular subtypes.2 weeksThe molecular subtypes will be categorized as luminal, HER2-enriched, triple negative breast cancers (TNBC). The difference of PET/MR imaging metrics among patients of different subtypes will be compared by Kruskal-Wallis test.
Performance of PET/MR imaging metrics to predict the recurrence status.5 yearsDetermination of the of PET/MR imaging metrics to predict recurrence status at 5 years after breast cancer diagnosis. The Cox proportional hazards regression model will be performed with the recurrence status (recurrence or not) as dependent variable and the different PET/MR imaging metrics as independent variables, the hazards ratios from the different PET/MR imaging metrics estimated from the models will be compared.

Countries

Taiwan

Contacts

Primary ContactJane Wang, PhD
jwang2@vghtpe.gov.tw+886-2-28712121

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026