Neoadjuvant Anti-PD1 in HCC

Phase 2

Completed

• Conditions: Hepatocellular Carcinoma; HCC; Liver Cancer
• Interventions: Drug: Nivolumab; Procedure: Hepatectomy

• Registration Number: NCT05471674
• Lead Sponsor: Dr Tan-to CHEUNG

Brief Summary

This is a phase 2, single-arm trial designed to assess the clinical benefit of treatment with nivolumab administered in patients with untreated, borderline resectable HCC.

Detailed Description

Not available

Study Timeline

• Study Start: 2020-07-03
• Study First Submitted: 2022-07-04
• Study First Submitted QC: 2022-07-20
• Study First Posted: 2022-07-25
• Primary Completion: 2022-12-31
• Study Completion: 2022-12-31
• Status Verified: 2023-01
• Last Update Submitted: 2023-01-31
• Last Update Posted: 2023-02-01

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 20

Inclusion Criteria

1. Signed written informed consent form prior to the screening procedures.
2. Age ≥ 18 years.
3. Histological proof of HCC.
4. Willingness to undergo a pre-dosing fresh tumour biopsy. Patients for whom fresh biopsy may not be feasible will be ineligible for enrollment.
5. Intermediate or locally-advanced HCC (according to HKLC tumour status categorization) with the option of resection for potential cure as assessed by surgeon.
6. Child-Pugh score ≤ 7 with no symptomatic ascites or ascites requiring therapeutic paracentesis.
7. ECOG performance status ≤ 1.
8. Life expectancy of ≥ 12 weeks.
9. Adequate organ function (blood transfusion or use of biologic response modifiers is not permitted).
10. Measurable disease according to RECIST v1.1.
11. Women of childbearing potential (WOCBP) must agree to follow instructions for method(s) of contraception.
12. Males who are sexually active with WOCBP must agree to follow instructions for method(s) of contraception.
13. Able and willing to meet all protocol-required treatments, investigations and visits.

Exclusion Criteria

1. Patients who have history of organ transplantation.
2. History of allergy or hypersensitivity to study drug components.
3. Patients who have active, known or suspected autoimmune disease. Patients are permitted to enroll if they have vitiligo, type I diabetes mellitus, residual hypothyroidism due to autoimmune condition adequately treated with hormonal replacement, skin disorders (such as vitiligo, psoriasis, or alopecia) not requiring systemic treatment, or conditions not expected to recur in the absence of an external trigger or deemed by the investigator not to affect safety assessment.
4. Patients with a condition requiring systemic treatment with either corticosteroids (> 10 mg daily prednisone equivalent) or other immunosuppressive medications within 14 days prior to start of study treatment. Inhaled or topical steroids, and adrenal replacement steroid doses > 10 mg daily prednisone equivalent, are permitted in the absence of active autoimmune disease.
5. Patients who have received prior therapy with an anti-PD-1, anti-PD-L1, anti-PDL-2, or anti-CTLA-4 antibody (or any other antibody targeting T cell co-regulatory pathways).
6. Receipt of any cancer therapy in the pre-operative period.
7. Treatment with botanical preparations (e.g., herbal supplements or traditional Chinese medicine) intended for general health support or to treat the disease under study within 2 weeks prior to treatment.
8. Active, acute, or chronic clinically significant infections requiring therapy with the exception of hepatitis B or C virus infection. Patients with chronic HBV infection must be on antiviral therapy and have HBV DNA < 500 IU/ml. Active or chronic co-infection with hepatitis B and C, or hepatitis B and D is not allowed.
9. Known history of positive test for human immunodeficiency virus (HIV) or known acquired immunodeficiency syndrome (AIDS).
10. Symptomatic congestive heart failure, defined as ≥ Class II of the New York Heart Association functional classification system or known LVEF < 50% at baseline.
11. Active angina pectoris or recent myocardial infarction (within 6 months).
12. Chronic atrial fibrillation or QTcF > 470 msec.
13. History of other previous cancer that would interfere with the determination of safety or efficacy of nivolumab with respect to HCC.
14. Women who are pregnant or breast-feeding.
15. Substance abuse, medical, psychological or social conditions that may interfere with the patient's participation in the study or evaluation of study results.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Treatment	Hepatectomy	-
Treatment	Nivolumab	-

Primary Outcome Measures

Name	Time	Method
Pathological tumour response rate	After surgery (normally 6 weeks after the start of nivolumab)	Proportion of patients with resected tumours having ≥30% necrosis

Secondary Outcome Measures

Name	Time	Method
Recurrence-free survival	At least 3 months after surgery	The time from resection to disease recurrence or death from any cause
Overall survival	At least 3 months after surgery	The time from start of treatment to the date of death from any cause or last follow-up date
Short-term surgery outcomes	2 weeks after surgery	Operation time, blood loss during surgery, transfusion requirement during surgery, and complication rate within 2 weeks following surgery
Safety and tolerability of nivolumab	6 months	The incidence, severity as graded by NCI CTCAE v5.0, seriousness and relationship to study medication of adverse events (AEs)

Trial Locations

Locations (1)

Queen Mary Hospital; 🇭🇰 Hong Kong, Hong Kong