Fluorouracil-labeled Nascent RNA Technology for Evaluating the Effects of Different Hyperthermic Intraperitoneal Chemotherapy Regimens on the Transcriptome of Pseudomyxoma Peritonei

Status: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The main objective of this study is to combine HIPEC regimens with Flura-seq to detect the effects of different HIPEC regimens (cisplatin vs. cisplatin+ docetaxel) on the nascent transcriptome of PMP tumors, so as to quantitatively assess the efficacy of different HIPEC regimens in the early stage, and to lay the foundation for optimizing the HIPEC regimens and exploring new therapeutic targets.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 75
Healthy Volunteers: f
View:

• Age 18-75 years old, regardless of gender and race;

• Pathologically confirmed as pseudomyxoma peritonei; acceptable for CRS+HIPEC treatment;

• KPS score ≥ 60, with expected survival time more than 12 months;

• The functions of important organs are basically normal, with no significant abnormalities in liver or kidney function;

• No history of allergy to biological products;

• No serious bacterial or viral infection;

• Non-pregnancy and lactation;

• The patient or his/her delegate understands and cooperates with the treatment and signs the informed consent for the treatment.

Locations
Other Locations
China
Beijing Tsinghua Changgung Hospital
RECRUITING
Beijing
Contact Information
Primary
Yan Li, PhD
lya03816@btch.edu.cn
+86 18612709123
Backup
Basnet Harihar, PhD
mapy21@mails.tsinghua.edu.cn
+86 13661370360
Time Frame
Start Date: 2025-02-17
Estimated Completion Date: 2027-02-17
Participants
Target number of participants: 36
Treatments
Experimental: Cisplatin Group
After completing CRS, the patient will undergo cisplatin HIPEC treatment. Add 120 mg of cisplatin to 3000 ml of physiological saline, heat to 43 ℃, perfuse at a flow rate of 400 ml/min, and perfuse for 60 minutes.
Active_comparator: Cisplatin + Docetaxel Group
After completing CRS, the patient will undergo HIPEC treatment with cisplatin and docetaxel. Add 120 mg of docetaxel and 120 mg of cisplatin to 3000 ml of physiological saline, heat to 43 ℃, perfuse at a flow rate of 400 ml/min, and perfuse for 60 minutes.
Related Therapeutic Areas
Sponsors
Leads: Beijing Tsinghua Chang Gung Hospital
Collaborators: Tsinghua University

This content was sourced from clinicaltrials.gov