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Safety and Efficacy of Camrelizumab (Anti-PD-1 Antibody) in Recurrent HCC After Liver Transplantation

Primary Purpose

Hepatocellular Carcinoma, Liver Transplantation

Status
Recruiting
Phase
Phase 1
Locations
China
Study Type
Interventional
Intervention
Camrelizumab treatment
Sponsored by
Third Affiliated Hospital, Sun Yat-Sen University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hepatocellular Carcinoma

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Age 18-65 years old, male or female;
  2. Pathologically confirmed hepatocellular carcinoma after liver transplantation;
  3. Tumor recurrence or metastasis is confirmed by CT and/or MRI examination, and neither intrahepatic recurrence nor extrahepatic metastasis is suitable for surgical resection;
  4. At least one measurable recurrent or metastatic tumor lesion;
  5. Tumor progression (mRECIST) or intolerance to treatment was assessed at least 1 month after oral administration of sorafenib or lenvatinib;
  6. The expected survival time is more than 3 months;
  7. Child-Pugh grade A or B (≤7 points);
  8. Other vital organs' function: The absolute count of neutrophils ≥1.5×10E9/L; Platelet ≥50×10E9/L; Hemoglobin ≥9g/dL; Serum albumin ≥2.8g/dL; Thyroid stimulating hormone (TSH) ≤1 times ULN (If TSH is abnormal, T3 and T4 levels should be examined at the same time. Then, if both T3 and T4 levels are normal, patient could be enrolled); Bilirubin ≤1.5 times ULN; ALT and AST ≤3 times ULN; Serum creatinine ≤1.5 times ULN;
  9. ECOG score 0-2 points;
  10. Patients have sufficient understanding and voluntarily sign the informed consent, and are willing and able to comply with the visit, treatment plan, laboratory examination and other requirements of the study schedule.

Exclusion Criteria:

  1. Positive PD-L1 expression in liver biopsy by immunohistochemistry (either liver parenchyma or non-parenchymal cells);
  2. Be Allergic to Camrelizumab;
  3. ≥ Grade II myocardial ischemia or myocardial infarction;
  4. With hypertension that can't be controlled to normal level with medication (SBP >140mmHg, DBP >90mmHg);
  5. With abnormal coagulation function (PT>16s, APTT>43s, TT>21s, Fbg<2g/L), and with a history of gastrointestinal bleeding within 6 months;
  6. With high risk of bleeding or is receiving thrombolysis or anticoagulant therapy;
  7. With autoimmune diseases including systemic lupus erythematosus, rheumatoid arthritis, psoriasis, etc;
  8. The primary liver disease for liver transplantation was autoimmune hepatitis, primary biliary cirrhosis, or primary sclerosing cholangitis;
  9. With pulmonary diseases such as interstitial pneumonia and poor lung function;
  10. Participating in clinical trials of other experimental drugs within four weeks;
  11. With infections requiring systemic treatment;
  12. With positive infection of human immunodeficiency virus (HIV);
  13. Special groups that not recommended in the instructions of Camrelizumab: with moderate or severe insufficiency of liver and renal function;
  14. With MDM2/4 amplification, EGFR mutation, or JAK mutation by NGS sequencing;
  15. With other factors that may influence the safety or compliance;
  16. During the treatment of acute rejection or within 1 month after treatment;
  17. Poor compliance.

Sites / Locations

  • Third Affiliated Hospital, Sun Yat-sen UniversityRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Camrelizumab treatment

Arm Description

Camrelizumab (SHR-1210), 200mg, I.V., Q3W

Outcomes

Primary Outcome Measures

Objective Response Rate (ORR)
Objective Response Rate after Camrelizumab treatment according to the mRECIST

Secondary Outcome Measures

Overall Survival (OS)
Time from the initiation of Camrelizumab treatment to the patient death from any cause
Progression-free Survival (PFS)
Time from the initiation of Camrelizumab treatment to radiological tumor progression or death from any cause
Time to Progression (TTP)
Time from the initiation of Camrelizumab treatment to radiological tumor progression
Serious Adverse Event (SAE)
The incidence of serious adverse event caused by Camrelizumab treatment
Graft Rejection (GR)
The incidence of graft rejection during the Camrelizumab treatment

Full Information

First Posted
September 21, 2020
Last Updated
April 29, 2022
Sponsor
Third Affiliated Hospital, Sun Yat-Sen University
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1. Study Identification

Unique Protocol Identification Number
NCT04564313
Brief Title
Safety and Efficacy of Camrelizumab (Anti-PD-1 Antibody) in Recurrent HCC After Liver Transplantation
Official Title
Clinical Study of Anti-PD-1 Antibody Camrelizumab in the Treatment of Recurrent Hepatocellular Carcinoma After Liver Transplantation
Study Type
Interventional

2. Study Status

Record Verification Date
April 2022
Overall Recruitment Status
Recruiting
Study Start Date
September 21, 2020 (Actual)
Primary Completion Date
September 2022 (Anticipated)
Study Completion Date
July 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Third Affiliated Hospital, Sun Yat-Sen University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
This is a prospective clinical study to investigate the safety and efficacy of anti-PD-1 immunotherapy (Camrelizumab) in patients with recurrent hepatocellular carcinoma (HCC) after liver transplantation. All of the enrolled patients have a background of liver transplantation for HCC. Due to the tumor recurrence, patients are not suitable for curative surgical resection, and targeted therapy provides poor therapeutic effect, leading to tumor progression or intolerance. Before immunotherapy, the PD-L1 expression was confirmed negative in the graft liver by immunohistochemistry, and patients continued targeted therapy as part of a combined antitumor regimen. In addition, the immunosuppression schedule is also reduced to a low level.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hepatocellular Carcinoma, Liver Transplantation

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
20 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Camrelizumab treatment
Arm Type
Experimental
Arm Description
Camrelizumab (SHR-1210), 200mg, I.V., Q3W
Intervention Type
Drug
Intervention Name(s)
Camrelizumab treatment
Intervention Description
Camrelizumab (SHR-1210), 200mg, I.V., Q3W
Primary Outcome Measure Information:
Title
Objective Response Rate (ORR)
Description
Objective Response Rate after Camrelizumab treatment according to the mRECIST
Time Frame
2 years
Secondary Outcome Measure Information:
Title
Overall Survival (OS)
Description
Time from the initiation of Camrelizumab treatment to the patient death from any cause
Time Frame
2 years
Title
Progression-free Survival (PFS)
Description
Time from the initiation of Camrelizumab treatment to radiological tumor progression or death from any cause
Time Frame
2 years
Title
Time to Progression (TTP)
Description
Time from the initiation of Camrelizumab treatment to radiological tumor progression
Time Frame
2 years
Title
Serious Adverse Event (SAE)
Description
The incidence of serious adverse event caused by Camrelizumab treatment
Time Frame
2 years
Title
Graft Rejection (GR)
Description
The incidence of graft rejection during the Camrelizumab treatment
Time Frame
2 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 18-65 years old, male or female; Pathologically confirmed hepatocellular carcinoma after liver transplantation; Tumor recurrence or metastasis is confirmed by CT and/or MRI examination, and neither intrahepatic recurrence nor extrahepatic metastasis is suitable for surgical resection; At least one measurable recurrent or metastatic tumor lesion; Tumor progression (mRECIST) or intolerance to treatment was assessed at least 1 month after oral administration of sorafenib or lenvatinib; The expected survival time is more than 3 months; Child-Pugh grade A or B (≤7 points); Other vital organs' function: The absolute count of neutrophils ≥1.5×10E9/L; Platelet ≥50×10E9/L; Hemoglobin ≥9g/dL; Serum albumin ≥2.8g/dL; Thyroid stimulating hormone (TSH) ≤1 times ULN (If TSH is abnormal, T3 and T4 levels should be examined at the same time. Then, if both T3 and T4 levels are normal, patient could be enrolled); Bilirubin ≤1.5 times ULN; ALT and AST ≤3 times ULN; Serum creatinine ≤1.5 times ULN; ECOG score 0-2 points; Patients have sufficient understanding and voluntarily sign the informed consent, and are willing and able to comply with the visit, treatment plan, laboratory examination and other requirements of the study schedule. Exclusion Criteria: Positive PD-L1 expression in liver biopsy by immunohistochemistry (either liver parenchyma or non-parenchymal cells); Be Allergic to Camrelizumab; ≥ Grade II myocardial ischemia or myocardial infarction; With hypertension that can't be controlled to normal level with medication (SBP >140mmHg, DBP >90mmHg); With abnormal coagulation function (PT>16s, APTT>43s, TT>21s, Fbg<2g/L), and with a history of gastrointestinal bleeding within 6 months; With high risk of bleeding or is receiving thrombolysis or anticoagulant therapy; With autoimmune diseases including systemic lupus erythematosus, rheumatoid arthritis, psoriasis, etc; The primary liver disease for liver transplantation was autoimmune hepatitis, primary biliary cirrhosis, or primary sclerosing cholangitis; With pulmonary diseases such as interstitial pneumonia and poor lung function; Participating in clinical trials of other experimental drugs within four weeks; With infections requiring systemic treatment; With positive infection of human immunodeficiency virus (HIV); Special groups that not recommended in the instructions of Camrelizumab: with moderate or severe insufficiency of liver and renal function; With MDM2/4 amplification, EGFR mutation, or JAK mutation by NGS sequencing; With other factors that may influence the safety or compliance; During the treatment of acute rejection or within 1 month after treatment; Poor compliance.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Guoying Wang, M.D.
Phone
+86-13632407313
Email
wanggy3@126.com
Facility Information:
Facility Name
Third Affiliated Hospital, Sun Yat-sen University
City
Guangzhou
State/Province
Guangdong
ZIP/Postal Code
510630
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Wang Guoying, M.D.
Phone
086-13632407313
Email
wanggy3@126.com

12. IPD Sharing Statement

Learn more about this trial

Safety and Efficacy of Camrelizumab (Anti-PD-1 Antibody) in Recurrent HCC After Liver Transplantation

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