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Radiomics of Mp-MRI Assessing NAC Outcome in Breast Cancer

Radiomics of Multiparametric MRI for Neoadjuvant Chemotherapy Outcomes Assessment in Breast Cancer

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03592004
Enrollment
500
Registered
2018-07-19
Start date
2018-07-18
Completion date
2022-06-01
Last updated
2018-07-19

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

Conditions

Breast Cancer, Multi-parametric MRI, Neoadjuvant Chemotherapy, Radiomics

Brief summary

This is a single-arm, multicentre study that aims to assess whether Radiomics combining multiparametric MRI and clinical data could be a good predictor of the responses to neoadjuvant chemotherapy in Breast Cancer.

Detailed description

Patients undergo multiparametric MRI (including T2WI, DWI and DCE-MRI) at baseline, after 2 courses of neoadjuvant chemotherapy, and prior to the surgery at least 8 weeks after the treatment procedure. Patients undergo biopsy test in one week after the baseline MRI scan to detect the biomarkers including ER, PR, Her-2 and Ki-67, which can be used to select the treatment plan referring to the NCCN clinical guidelines. After the surgery, responses to neoadjuvant chemotherapy are determined according to the histopathologically examination of the surgically resected specimens. After completion of treatment procedure, patients are followed up for 5 years.

Interventions

OTHERneoadjuvant chemotherapy

neoadjuvant chemotherapy

Sponsors

Guangdong Provincial People's Hospital
CollaboratorOTHER
Cancer Institute and Hospital, Chinese Academy of Medical Sciences
CollaboratorOTHER
Beijing Friendship Hospital
CollaboratorOTHER
Yunnan Cancer Hospital
CollaboratorOTHER
Liaoning Cancer Hospital & Institute
CollaboratorOTHER
First Hospital of China Medical University
CollaboratorOTHER
Affiliated Hospital of Hebei University
CollaboratorOTHER
Chinese Academy of Sciences
Lead SponsorOTHER_GOV

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Healthy volunteers
No

Inclusion criteria

* biopsy-proven invasive breast cancer; * received complete neoadjuvant chemotherapy and no treatment has been done before; * surgery was performed after completion of neoadjuvant chemotherapy, after which pCR was confirmed by postoperative pathological examination; * pretreatment MRI data within a month before the start of the treatment was eligible, including T2WI, DWI and DCE-MRI.

Exclusion criteria

* not completing neoadjuvant chemoradiotherapy; * not undergoing surgery at our hospital, or pCR was not assessed; * lack of T2WI, or DWI or DCE-MRI data; * insufficient MRI quality to obtain measurements (e.g., owing to motion artifacts); * had unilateral multifocal cancers, and the correlation between the tumor in MR images and postoperative pathological examination was uncertain.

Design outcomes

Primary

MeasureTime frameDescription
predicting pathological complete response (pCR) or no response (NR)20 weeksThe value of Radiomics of multiparametric MRI in predicting responses to neoadjuvant chemotherapy, including pathological complete response (pCR) and no response (NR).
5 years for Disease free survival5 yearsThe association between Radiomics of multiparametric MRI and disease free survival (DFS), which defined as the time from the beginning of neoadjuvant chemotherapy to the confirmed time of recurrence or metastatic disease, or death due to any other cause.
5 years for Overall survival5 yearsThe association between Radiomics of multiparametric MRI and overall survival (OS), which defined as the time from the beginning of neoadjuvant chemotherapy to the death with any causes.

Countries

China

Contacts

Primary ContactZhenyu Liu, Doctor
zhenyu.liu@ia.ac.cn8613466358609

Outcome results

None listed

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