Predicting the Efficacy and Prognosis of Rectal Cancer Patients Based on ctDNA-MRD Technology

UnknownOBSERVATIONAL
Enrollment

50

Participants

Timeline

Start Date

June 21, 2023

Primary Completion Date

June 30, 2024

Study Completion Date

August 31, 2024

Conditions
Rectal AdenocarcinomaCirculating Tumor DNAMinimal Residual DiseaseNeoadjuvant Chemoradiotherapy
Interventions
DIAGNOSTIC_TEST

MRD detection

Peripheral blood samples were collected for MRD detection before neoadjuvant chemoradiotherapy, during neoadjuvant chemoradiotherapy, and 3-4 weeks after radical surgery. For patients who achieved cCR after neoadjuvant therapy and adopted the W \& W strategy, the sampling time point was 3 months after the start of watching and waiting.

Trial Locations (1)

510060

RECRUITING

WeiWei Xiao, Guangzhou

Sponsors
All Listed Sponsors
collaborator

Haplox Biotechnology Co., Ltd.

INDUSTRY

lead

WeiWei Xiao

OTHER

NCT05969938 - Predicting the Efficacy and Prognosis of Rectal Cancer Patients Based on ctDNA-MRD Technology | Biotech Hunter | Biotech Hunter