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Predicting Neoadjuvant Therapy Response of Rectal Cancer With MRI

Predicting Neoadjuvant Therapy Response of Rectal Cancer With MRI

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02640586
Enrollment
1614
Registered
2015-12-29
Start date
2016-01-10
Completion date
2023-12-31
Last updated
2023-06-22

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

Conditions

Rectal Neoplasms

Brief summary

The purpose of this study is to investigate if MRI scans performed after neoadjuvant radiotherapy can predict the therapeutic response of rectal cancer following preoperative chemo-radiotherapy. This will help doctors to better tailor treatments for rectal cancer in the future.

Detailed description

We proposed to constructed multi-parameter predictive model for predicting therapeutic response and pathological complete response(pCR) of patients with rectal cancer who received neoadjuvant chemoradiation. MR radiomics,convolutional neural networks, morphological parameters and quantitative functional parameters derived from diffusion-weighted MR images will be integrated for model construction.

Interventions

DEVICEthree MR examination

Three MR examinations: first MRI taken within 1 week before preoperative chemo-radiotherapy; second MRI taken between 14-16days after the initiation of radio-chemotherapy; third MRI taken 7-9 weeks after the completion of preoperative chemo-radiotherapy.

Sponsors

Sun Ying-Shi
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age \> 18 years * T3/4 or node positive biopsy-proved primary rectal cancer * Suitable for pre-operative chemoradiotherapy and surgical resection * No contraindication to MRI * Ability to understand and the willingness to sign a written informed consent document

Exclusion criteria

* History or concurrent of other cancer * Previous therapy to pelvis * Unable/unwilling to have MRI * Pacemaker or implanted defibrillator * Pregnancy, lactation or inadequate contraception * Patients with a history of psychological illness or condition such as to interfere with the patient's ability to understand requirements of the study * Unwilling or unable to give informed consent

Design outcomes

Primary

MeasureTime frameDescription
Predictive value of eary MRI (14-16 days MRI) for assessing pathological complete response(pCR) at surgery2 yearsA scoring system for predicting pCR will be developed based on MRI parameters and their changes between baseline and early MRI. No viable cancer cells seen in the resection specimen is regarded as pCR
Predictive value of preoperative MRI(7-9 weeks after the completion of preoperative chemo-radiotherapy) for assessing pCR2 yearsA scoring system for predicting pCR will be developed based on MRI parameters

Secondary

MeasureTime frameDescription
Predictive value of eary MRI (14-16 days after initiation of preoperative radio-chemotherapy) for assessing pathological response according to Tumour Regression Grade (TRG)2 yearsA scoring system for predicting pathological response will be developed based on MRI parameters and their changes between baseline and early MRI.TRG1 is regarded as responder, and TRG2/3 is regarded as non-responder.
Feasibility of conducting MRI scans at 7-9 weeks after preoperative radio-chemotherapy2 yearsThis will be assessed in terms of whether MR imaging at 7-9 weeks after preoperative radio-chemotherapy adds any additional predictive value to imaging performed 14-16 days after initiation of preoperative radio-chemotherapy.
MRI-predicted pCR and MRI-predicted response on long-term disease control and survival3 years3 years disease-free survival and overall survival will be assessed
Predictive value of preoperative MRI(7-9 weeks after the completion of preoperative chemo-radiotherapy) for assessing pathological response according to Tumour Regression Grade (TRG)2 yearsA scoring system for predicting pathological response will be developed based on MRI parameters and their changes between baseline and early MRI.TRG1 is regarded as responder, and TRG2/3 is regarded as non-responder.

Countries

China

Outcome results

None listed

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