Trans-Artery/Intra-Tumor Infusion of Checkpoint Inhibitors Plus Chemodrug for Immunotherapy of Advanced Solid Tumors

Trial statusRecruiting
Trial phasePhase 2, Phase 3
Trial typeInterventional
Biological sexAll
Age18+
SponsorSecond Affiliated Hospital of Guangzhou Medical University

About this trial

This trial was designed to investigate the safety, response rates and survival outcomes of patients with advanced solid tumors by trans-artery/intra-tumor infusion of PD1/PDL1 antibody and/or CTLA4 antibody ipilimumab plus chemotherapeutic drug and to compare their differences.

Eligibility criteria

Qualifiers

Cytohistological confirmation is required for diagnosis of cancer.

Signed informed consent before recruiting.

Age above 18 years with estimated survival over 3 months.

Child-Pugh class A or B/Child score > 7; ECOG score < 2

Disqualifiers

Patients participated in clinical trials of equipment or drugs (signed informed consent) within 4 weeks;

Patients accompany by ascites, hepatic encephalopathy and esophageal and gastric varices bleeding;

Any serious accompanying disease, which is expected to have an unknown, impact on the prognosis, include heart disease, inadequately controlled diabetes and psychiatric disorders;

Patients accompanied with other tumors or past medical history of malignancy;

Trial design

Treatments tested in this trial

  • Checkpoint inhibitor (CPI) such as Pembrolizumab plus chemotherapy

Treatment groups

200 Participants
are divided into 2 treatment groups