A Real-world Study of Camrelizumab Combined With Apatinib Mesylate in Unresectable Hepatocellular Carcinoma

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

To evaluate the efficacy and safety of camrelizumab combined with apatinib mesylate in the treatment of unresectable hepatocellular carcinoma.

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

• Age: 18 years old ≤ age ≤ 75 years old, both male and female;

• Strictly meet the clinical diagnostic criteria of the Guidelines for the Diagnosis and Treatment of Primary Liver Cancer (2022 Edition) or hepatocellular carcinoma patients diagnosed by histopathological or cytological examinations , and at least one measurable lesion (according to the mRECIST1.1 standard, the long diameter of the measurable lesion on spiral CT scan is ≥10mm or the short diameter of the malignant lymph node is ≥15mm);

• Not previously accepted Patients with hepatocellular carcinoma who have progressed/intolerable and unresectable after systemic therapy or first-line systemic therapy;

• CNLC stage IIb-IIIb;

• Child-Pugh liver function grade A or B (5- 7 points);

• ECOG PS score 0-1 points;

• Expected survival period ≥ 12 weeks;

• If the patient has active hepatitis B virus (HBV) infection: if HBV-DNA ≤ 2000, you can start directly Treatment; if HBV-DNA\>2000, antiviral treatment should be given for one week before starting treatment;

• The subjects volunteered to join the study, had good compliance, and cooperated with follow-up.

Locations
Other Locations
China
Mengchao Hepatobiliary Hospital, Fujian Medical University
RECRUITING
Fuzhou
Contact Information
Primary
Yong yi Zeng
lamp197311@126.com
13805083802
Time Frame
Start Date: 2022-08-20
Estimated Completion Date: 2026-03-01
Participants
Target number of participants: 300
Related Therapeutic Areas
Sponsors
Collaborators: Suzhou Suncadia Biopharmaceuticals Co., Ltd.
Leads: Meng Chao Hepatobiliary Hospital of Fujian Medical University

This content was sourced from clinicaltrials.gov