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Efficacy, safety, and treatment modalities of Attilizumab in combination with bevacizumab in the treatment of unresectable primary liver cancer: a multicenter real-world study

Efficacy, safety, and treatment modalities of Attilizumab in combination with bevacizumab in the treatment of unresectable primary liver cancer: a multicenter real-world study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300076835
Enrollment
Unknown
Registered
2023-10-20
Start date
2023-10-20
Completion date
Unknown
Last updated
2023-10-22

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

Conditions

liver cancer cannot be resected

Interventions

Atrilizumab combined with bevacizumab:NA

Sponsors

the First Affiliated Hospital of Army Medical University,PLA
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1.18-75 years old, gender unlimited; 2. Histologically, pathologically, or clinically confirmed inoperable primary liver cancer with at least one measurable lesion; 3. Treatment with Atrilizumab combined with bevacizumab; 4. Patients with an ECOG score of 0-1 were included in the evaluation according to the activity status scale developed by the Eastern Cooperative Oncology Group (ECOG). 5, Child-Pugh liver function A or B grade.

Exclusion criteria

Exclusion criteria: (1) Complicated with other serious diseases, including serious cardiovascular and cerebrovascular diseases, serious liver function injury (bilirubin is 2 times higher than the reference value, transaminase is 5 times higher than the reference value), serious renal function injury (eGFR<45 ml/min), and blood diseases; 2. Combined with other malignant tumors, except cured cervical carcinoma in situ, non-melanoma skin cancer and superficial bladder tumors [Ta (non-invasive tumor), Tis (cancer in situ) and T1 (tumor infiltrating basal membrane)]; 3, combined with active infectious diseases, such as acute viral hepatitis; Have any active autoimmune disease or a history of autoimmune disease; 4. Pregnant or lactating women; 5. Incomplete data, including baseline data, follow-up data or outcome data, could not satisfy the data analysis of this study.

Design outcomes

Primary

MeasureTime frame
progression-free survival;

Secondary

MeasureTime frame
Overall Surivial;time to progress;Disease control rate;

Countries

China

Contacts

Public ContactZhang Hui

the First Affiliated Hospital of Army Medical University,PLA

13637912611@163.com+86 136 3791 2611

Outcome results

None listed

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