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Clinical Trial Summary

The study evaluates the associations between peak and valley concentrations of SN-38 with the efficacy and adverse effects of advanced rectal cancer patients carrying genotype (TA) 6 /(TA) 6 or (TA) 6 /(TA) 7 after neoadjuvant chemoradiotherapy with CPT-11.All participants will be scheduled to receive surgery 6-8 weeks after the completion of CRT. The primary end point are toxicity and pCR rate.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03824899
Study type Interventional
Source Fudan University
Contact Ji Zhu, PhD
Phone +86-2164175590
Email leo.zhu@126.com
Status Recruiting
Phase N/A
Start date October 10, 2018
Completion date May 2020

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