Lenvatinib Plus Sintilimab in Patients With Immune Checkpoint Inhibitor Previously Treated Advanced Liver Cancer
Study Details
Study Description
Brief Summary
The objective of this study is to evaluate the efficacy and safety of Lenvatinib plus Sintilimab in patients with advanced liver cancer progressed after treatment with immune checkpoint inhibitors.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
| Phase 2 |
Detailed Description
There is a need for options to address progressed liver cancer after the treatment of immune checkpoint inhibitors (ICIs). Sintilimab and lenvatinib are active as monotherapies liver cancer; Therefore, our aim was to evaluate the efficacy of lenvatinib combined with sintilimab in the treatment of these patients.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Lenvatinib plus Sintilimab
|
Drug: Sintilimab
Sintilimab will be administered at 200 mg i.v. every 3 weeks until documented disease progression, development of unacceptable toxicity, participant request, or withdrawal of consent.
Drug: Lenvatinib
Lenvatinib will be administered (bodyweight ≥ 60 kg, 12 mg; < 60 kg, 8 mg) orally daily every 3 weeks until documented disease progression, development of unacceptable toxicity, participant request, or withdrawal of consent.
|
Outcome Measures
Primary Outcome Measures
- Objective Response Rate (ORR) [max 24 months]
ORR according to RECIST 1.1
Secondary Outcome Measures
- DoR [max 24 months]
Duration of Response
- PFS [max 24 months]
Progression-free survival
- OS [max 42 months]
Overall Survival
- DCR [max 24 months]
disease control rate
- Adverse Events [max 42 months]
Adverse event (AE)、Treatment emergent adverse event(TEAE)、Serious adverse event (SAE).
Eligibility Criteria
Criteria
Inclusion Criteria:
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Written informed consent obtained.
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Age ≥ 18 years at time of study entry.
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Participants must have unresectable or metastatic histologically or cytologically confirmed hepatocellular carcinoma or intrahepatic cholangiocarcinoma
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Participants must have disease progression with an anti-PD-1 or anti-PD-L1 based regimen.
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At least one measurable site of disease as defined by RECIST 1.1 criteria with spiral CT scan or MRI.
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Performance status (PS) ≤ 2 (ECOG scale).
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Life expectancy of at least 12 weeks.
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Adequate blood count, liver-enzymes, and renal function: absolute neutrophil count ≥ 1,500/L, platelets ≥75 x103/L; Total bilirubin ≤ 3x upper normal limit; Aspartate Aminotransferase (SGOT), Alanine aminotransferase (SGPT) ≤ 5 x upper normal limit (ULN); International normalized ratio (INR) ≤1.25; Albumin ≥ 31 g/dL; Serum Creatinine ≤ 1.5 x institutional ULN or creatinine clearance (CrCl) ≥ 30 mL/min (if using the Cockcroft-Gault formula )
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Female patients with reproductive potential must have a negative urine or serum pregnancy test within 7 days prior to start of trial.
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Subject is willing and able to comply with the protocol for the duration of the study including undergoing treatment, adherence to contraceptive measures, scheduled visits and examinations including follow up.
Exclusion Criteria:
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History of cardiac disease, including clinically significant gastrointestinal bleeding within 4 weeks prior to start of study treatment
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Thrombotic or embolic events such as cerebrovascular accident (including transient ischemic attacks), deep vein thrombosis or pulmonary embolism within the 6 months Prior to the first dose of study drug with the exception of thrombosis of a segmental portal vein.
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Prior treatment with Lenvatinib or other targeted therapy.
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RFA and resection administered less then 4 weeks prior to study treatment start.
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Radiotherapy administered less then 4 weeks prior to study treatment start.
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Major surgery within 4 weeks of starting the study treatment OR subjects who have not recovered from effects of major surgery.
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Patients with second primary cancer, except adequately treated basal skin cancer or carcinoma in-situ of the cervix.
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Immunocompromised patients, e.g. patients who are known to be serologically positive for human immunodeficiency virus (HIV).
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Participation in another clinical study with an investigational product during the last 30 days before inclusion or 7 half-lifes of previously used trial medication, whichever is longer.
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Any condition or comorbidity that, in the opinion of the investigator, would interfere with evaluation of study Treatment or interpretation of patient safety or study results, including but not limited to:
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history of interstitial lung disease
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known acute or chronic pancreatitis
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active tuberculosis
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any other active infection (viral, fungal or bacterial) requiring systemic therapy
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history of allogeneic tissue/solid organ transplant
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diagnosis of immunodeficiency or patient is receiving chronic systemic steroid therapy or any other form of immunosuppressive therapy within 7 days prior to the first dose of nivolumab-monotherapy treatment.
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Has an active autoimmune disease requiring systemic treatment within the past 3 months or a documented history of clinically severe autoimmune disease, or a syndrome that requires systemic steroids or immunosuppressive agents. Exceptions: Subjects with vitiligo, hypothyroidism, diabetes mellitus type I or resolved childhood asthma/atopy are an exception to this rule. Subjects that require intermittent use of bronchodilators or local steroid injections would not be excluded from the study. Subjects with Hashimoto thyroiditis, hypothyroidism stable on hormone replacement or psoriasis not requiring treatment are not excluded from the study.
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Live vaccine within 30 days prior to the first dose of nivolumab-monotherapy treatment or during study treatment.
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History or clinical evidence of Central Nervous System (CNS) metastases Exceptions are: Subjects who have completed local therapy and who meet both of the following criteria: I. are asymptomatic and II. have no requirement for steroids 6 weeks prior to start of nivolumab-monotherapy treatment. Screening with CNS imaging (CT or MRI) is required only if clinically indicated or if the subject has a history of CNS
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Medication that is known to interfere with any of the agents applied in the trial.
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Any other efficacious cancer treatment except protocol specified treatment at study start.
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Patient has received any other investigational product within 28 days of study entry.
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Female subjects who are pregnant, breast-feeding or male/female patients of reproductive potential who are not employing an effective method of birth control (failure rate of less than 1% per year). [Acceptable methods of contraception are: implants, injectable contraceptives, combined oral contraceptives, intrauterine pessars (only hormonal devices), sexual abstinence or vasectomy of the partner]. Women of childbearing potential must have a negative pregnancy test (serum β-HCG) at screening.
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Patient with any significant history of non-compliance to medical regimens or with inability to grant reliable informed consent.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Fudan University Shanghai Cancer Center | Shanghai | Shanghai | China | 200032 |
Sponsors and Collaborators
- Fudan University
Investigators
- Principal Investigator: Peng Wang, MD, Fudan University
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- MIT-015