Clinical Trials Directory

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UnknownNCT05766605

Applicability of PDOX in Patients With Primary Liver Cancer: A Randomized Controlled Trial

Applicability of Patient Derived Orthotopic Xenograft (PDOX) in Patients With Primary Liver Cancer: A Randomized Controlled Trial

Status
Unknown
Phase
Phase 3
Study type
Interventional
Enrollment
90 (estimated)
Sponsor
Zhujiang Hospital · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

This Randomized Controlled Trial was to clarity the clinical feasibility of PDOX results in guiding the drug use of interventional chemotherapy after primary liver cancer surgery.

Detailed description

Data of Patients who received PDOX after primary liver cancer radical reaction and received Transarterial Chemoembolization #will be collected #excluding incomplete data. The primary endpoint was the one-year disease-free survival(DFS) rate #Secondary endpoint was the adverse event.

Conditions

Interventions

TypeNameDescription
DRUGOxaliplatin130 mg per square body surface area for a total of four transcatheter hepatic artery infusions per month.
DRUGDoxorubicin20 mg per square body surface area for a total of four transcatheter hepatic artery infusions per month.
DRUGLobaplatin50 mg per square body surface area for a total of four transcatheter hepatic artery infusions per month.
DRUGCisplatin50 mg per square body surface area was used for monthly transhepatic arterial infusions.
DRUGOxaliplatin, Leucovorin, fluorouracilOxaliplatin(130 mg per square body surface area), Leucovorin(400 mg per square body surface area), and fluorouracil(2800 mg per square body surface area) were used for monthly transhepatic arterial. infusions
DRUGLobaplatin, RaltitrexedLobaplatin(50 mg per square body surface area) and Raltitrexed(3 mg per square body surface area) were used for monthly transhepatic arterial infusions.

Timeline

Start date
2023-01-01
Primary completion
2026-01-01
Completion
2026-01-30
First posted
2023-03-13
Last updated
2023-03-13

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT05766605. Inclusion in this directory is not an endorsement.