Skip to content

Application of CalliSpheres drug-loaded microspheres combined with PD-1 inhibitors and antiangiogenic drugs in advanced liver cancer

Application of CalliSpheres drug-loaded microspheres combined with PD-1 inhibitors and antiangiogenic drugs in advanced liver cancer

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100053624
Enrollment
Unknown
Registered
2021-11-25
Start date
2022-01-01
Completion date
Unknown
Last updated
2022-10-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Liver cancer

Interventions

Experimental group:D-TACE+PD-1 inhibitors + antiangiogenic drugs

Sponsors

Zhejiang Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Patients with HCC who strictly meet the clinical diagnostic criteria of The Code for The Diagnosis and Treatment of Primary Liver Cancer (2019 edition) or who have been confirmed by histopathological or cytological examination are unable to undergo surgical treatment or unwilling to undergo surgical treatment; 2.Complete preoperative laboratory examination and liver enhanced CT and/or MRI image data; 3.STAGE C of BCLC or Stage B unsuitable for radical surgery; 4.Child-Pugh liver function rating: GRADE A or better grade B (= 18 years, male or female; 6.ECOG PS score: 0-2; 7.The main organs function normally, that is, they meet the following criteria: (1)Blood routine examination :(no blood transfusion, no G-CSF, no drug correction within 14 days before screening) HB >= 90 G/L;The ANC acuity 1.5x10^9/L;PLT 50x10^9/L or higher; (2)Biochemical examination:(no ALB infusion within 14 days) ALB >= 30g/L, ALT and AST < 5 ULN; TBIL < =2 ULN; Creatinine <= 1.5 ULN; 8.Subjects voluntarily joined the study and signed informed consent with good compliance and follow-up.

Exclusion criteria

Exclusion criteria: 1.Hepatobiliary duct cell carcinoma and mixed cell carcinoma; 2.Patients who have received systematic treatment in the past; 3.CT or MRI imaging suggested the existence of obvious arteriovenous fistula; 4.Recent (<= 3 months) gastrointestinal bleeding (hematemesis or melena); 5.With severe infection such as liver abscess; 6.Patients with other uneffectively controlled malignant tumors; 7.Patients combined with HIV infection; 8.The investigator determines other conditions that may affect the conduct of the clinical study and the determination of the study results.

Design outcomes

Primary

MeasureTime frame
Progression-free survival;

Secondary

MeasureTime frame
Overall survival;Disease control rate;Objective remission rate;

Countries

China

Contacts

Public ContactZeng Hui

Zhejiang Cancer Hospital

zenghuiray@aliyun.com+86 13989898089

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026