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Spots Global Cancer Trial Database for Post-Neoadjuvant Treatment MRI Based AI System to Predict pCR for Rectal Cancer

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Trial Identification

Brief Title: Post-Neoadjuvant Treatment MRI Based AI System to Predict pCR for Rectal Cancer

Official Title: A Post-Neoadjuvant Treatment MRI Based AI System to Predict Pathologic Complete Response for Patients With Rectal Cancer: A Multicenter, Prospective Clinical Study

Study ID: NCT04278274

Conditions

Rectal Cancer

Study Description

Brief Summary: In this study, investigators seek for a better way to identify the potential pathologic complete response (pCR) patients form non-pCR patients with locally advanced rectal cancer (LARC), based on their post-neoadjuvant treatment Magnetic Resonance Imaging (MRI) data. Previously, a post neoadjuvant treatment MRI based radiomics AI model had been constructed and trained. Here, the predictive power of this artificial intelligence system and expert radiologist to identify pCR patients from non-pCR LARC patients will be compared in this prospective, multicenter, back-to-back clinical study

Detailed Description: This is a multicenter, prospective, observational clinical study for seeking out a better way to predict the pathologic complete response (pCR) in patients with locally advanced rectal cancer (LARC) based on the post-neoadjuvant treatment Magnetic Resonance Imaging (MRI) data. Patients who have been pathologically diagnosed as rectal adenocarcinoma and defined as clinical II-III stage will be enrolled from the Sixth Affiliated Hospital of Sun Yat-sen University, Sir Run Run Shaw Hospital and the Third Affiliated Hospital of Kunming Medical College. All participants should follow a standard treatment protocol, including neoadjuvant treatment, total mesorectum excision (TME) surgery. Patients with LARC who received neoadjuvant treatment will be enrolled and their post-neoadjuvant treatment MRI images will be used to predict their pathologic response (pCR vs. non-pCR). The artificial intelligence prediction system and the expert radiologist will define the pathologic response as pCR or non-pCR, respectively. The pathologist will provide the final pathology report of TME surgery specimen (pCR or non-pCR) as a standard. The predictive efficacy of these two back-to-back approaches generated will be compared in this multicenter, prospective clinical study.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

the Sixth Affiliated Hospital of Sun Yat-sen University, Guangzhou, Guangdong, China

The Third Affiliated Hospital of Kunming Medical College, Kunming, Yunnan, China

Sir Run Run Shaw Hospital, Hangzhou, Zhejiang, China

Contact Details

Name: Xiangbo Wan, MD, PhD

Affiliation: Sixth Affiliated Hospital, Sun Yat-sen University

Role: STUDY_CHAIR

Name: Weidong Han, MD, PhD

Affiliation: Sir Run Run Shaw Hospital

Role: PRINCIPAL_INVESTIGATOR

Name: Zhenhui Li, MD

Affiliation: The Third Affiliated Hospital of Kunming Medical College.

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

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