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Combination Therapy of HAIC and HLX10 and HLX04 in HCC With Major Portal Vein Tumor Thrombosis
A Randomized, Double-blinded, Controlled Phase II Study of Combination Therapy of HAIC (Hepatic Arterial Infusion Chemotherapy), HLX10 (PD-1 Antibody) and HLX04 (VEGF Antibody) Compared With HAIC and Placebo in Hepatocellular Carcinoma With Major Portal Vein Tumor Thrombosis
Studie Overzicht
Toestand
Studietype
Inschrijving (Verwacht)
Fase
- Fase 2
Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
Accepteert gezonde vrijwilligers
Geslachten die in aanmerking komen voor studie
Beschrijving
Inclusion Criteria:
- Willing to attend the study and having given the ICF
- Age ≥18
- Have a HCC diagnosis confirmed by radiology, histology, or cytology
- HCC is diagnosed at Barcelona Clinic Liver Cancer (BCLC) Stage C with major portal vein tumor thrombosis ( VP3~4, or Cheng's II~IV)
- Have not accepted any of systemic therapy for HCC such as systemic chemotherapy, molecular targeted drugs, immunotherapy.
- At least 1 measurable intrahepatic lesion suitable for repeat assessments according to RECISTv1.1 criteria and it has not undergone surgery, radiology and/or other regional therapy (including but not limited to radiofrequency ablation, percutaneous ethanol injection, freezing therapy, high intensity focused ultrasound, transcatheter arterial chemoembolization, transcatheter arterial embolization). But if it progressed after the regional therapy, it could be selected as a target lesion. The local regional therapy must be done 4 weeks before randomization and the related AEs must recover to ≤ CTCAE grade 1.
- Child-Pugh score ≤7
- Eastern Cooperative Oncology Group (ECOG) 0 or 1
- Expected life time is over 12 weeks.
- HBV-DNA < 2000 IU/mL
- Organs function:
Platelet count ≥75×109/L Absolute neutrophil count (ANC) ≥1.5×109 /L White blood cell count ≥3.0×109 /L Haemoglobin ≥9.0 g/dL Serum total bilirubin ≤1.5×ULN ALT ≤5×ULN, and AST ≤5×ULN(ALT ≤3×ULN, and AST ≤3×ULN, if HCV-RNA is detectable) Albumin ≥28 g/L INR ≤1.5×ULN PT ≤1.5×ULN APTT ≤1.5×ULN Creatinine clearance (CL) >50 mL/min or serum creatinine ≤1.5×ULN Urine protein ≤1+ or ≤1.0g/24h 12. Patient is not fertile or willing and able to obey effective contraception.
Exclusion Criteria:
- Known fibrolamellar HCC, sarcomatoid HCC, mixed cholangiocarcinoma and HCC
- History of hepatic encephalopathy
- History of GI bleeding within 6 months, or investigator defined with high risk of haemorrhage for esophageal varices
- With distant metastasis (hilar lymph nodes metastasis is allowed)
- Co-infection of HBV and HCV
- History of other malignancy within 5 years except for healed local tumor.
- History of or plan to accept allogenic organ transplantation
- Ascites requiring invasive intervention (e.g. paracentesis) to maintain symptomatic control (every month or more often)
- History of myocardial infarction or unstable angina or uncontrolled arrythmia or stroke or cerebral hemorrhage within 6 months prior to randomization. QTcF value ≥450ms(male)or ≥470ms(female) detected by 12-lead electrocardiogram.
- New York Heart Association Grade ≥2 congestive heart failure or LVEF <50%
- Uncontrolled hypertension
- History of hypertensive crisis or hypertensive encephalopathy
- Active infection including but not limited to tuberculosis and HIV
- With interstitial lung disease, lung fibrosis, pneumoconiosis, radiation pneumonitis, drug-associated pneumonia and serious impairment in lung function
- Active autoimmune disorders except patients with substitutional treatment with thyroid hormone and type I diabetes under treatment with insulin.
- Receipt of live attenuated vaccine within 28 days prior to randomization
- Current or prior use of steroids (>10mg/d prednisone) or immunosuppressive medication within 14 days before randomization
- Significant traumatic injury or major surgical procedure within 28 days prior to randomization
- Receipt of checkpoint inhibitors or T cell costimulatory drugs
- Receipt of bevacizumab or its analogues
- Involved in another clinical trial less than 14 days before randomization
- Known allergy or hypersensitivity to any of the study drugs or any of the study drug excipients
- Female patients who are pregnant or breastfeeding or male or female patients of reproductive potential who are not willing to employ effective birth control
- Active bleeding, with history of ≥grade 3 bleeding within 6 months, or ≥grade 2 bleeding within 3 months
- Use of anti-thrombotics within 5 days prior to randomization
- In need of NSAIDs for long-term treatment.
- With one of the following diseases within 6 months before randomization:
(1) Digestive fistula, perforation and abscess (2) Gastrointestinal obstruction (3) Abdominal infection or inflammation (4) Major vascular disease 28. With severe and green wound, active ulcer or untreated fracture 29. History of drug abuse 30. Judgment by the Investigator that the patient should not participate in the study if the patient is unlikely to screen for the study
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
- Toewijzing: Gerandomiseerd
- Interventioneel model: Parallelle opdracht
- Masker: Verviervoudigen
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
|---|---|
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Experimenteel: HAIC + HLX10 + HLX04
HAIC: FOLFOX, q3w, up to 8 times; HLX10: 4.5mg/kg, iv, q3w, up to 2 years; HLX04: 15.0mg/kg, iv, q3w, up to 2 years.
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For the HAIC procedure, a 5F catheter was introduced using the Seldinger technique through the femoral artery or the radial artery.
Then, angiographic surveys of the celiac trunk and superior mesenteric artery were performed.
According to tumor size, location, and arterial supply, the catheter or a 2.7F microcatheter was advanced into the hepatic artery at the level of selective segmental, lobar, or whole liver.
The catheter or microcatheter was connected to an external infusion pump.
The following regimen of modified FOLFOX was administered: oxaliplatin, 85mg/m2 for 2 hours; leucovorin, 400mg/m2; and 5-fluorouracil, 2400mg/m2 for 44-46 hours.
After HAIC treatment, the catheter or microcatheter, and the sheath were removed.
PD-1 antibody with proven efficacy in advanced hepatocellular carcinoma
Combination of PD-1 antibody and VEGF antibody might promote the efficacy of HAIC in hepatocellular carcinoma with major portal vein thrombosis.
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Placebo-vergelijker: HAIC + Placebo
HAIC: FOLFOX, q3w, up to 8 times; Placebo1: saline, iv, q3w, up to 2 years; Placebo2: saline, iv, q3w, up to 2 years.
|
Placebo
For the HAIC procedure, a 5F catheter was introduced using the Seldinger technique through the femoral artery or the radial artery.
Then, angiographic surveys of the celiac trunk and superior mesenteric artery were performed.
According to tumor size, location, and arterial supply, the catheter or a 2.7F microcatheter was advanced into the hepatic artery at the level of selective segmental, lobar, or whole liver.
The catheter or microcatheter was connected to an external infusion pump.
The following regimen of modified FOLFOX was administered: oxaliplatin, 85mg/m2 for 2 hours; leucovorin, 400mg/m2; and 5-fluorouracil, 2400mg/m2 for 44-46 hours.
After HAIC treatment, the catheter or microcatheter, and the sheath were removed.
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Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Objective response rate
Tijdsspanne: The proportion of patients with complete response or partial response, through study completion, an average of 3 years.
|
efficacy
|
The proportion of patients with complete response or partial response, through study completion, an average of 3 years.
|
Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Progression free survival
Tijdsspanne: From date of randomization until the date of the first documented progression or date of death from any cause, whichever comes first, up to 48 months
|
efficacy
|
From date of randomization until the date of the first documented progression or date of death from any cause, whichever comes first, up to 48 months
|
|
Duration of response
Tijdsspanne: From date of randomization until the date of first documented progression, up to 48 months
|
efficacy
|
From date of randomization until the date of first documented progression, up to 48 months
|
|
Time to response
Tijdsspanne: From date of randomization until the date of first documented response, up to 48 months
|
efficacy
|
From date of randomization until the date of first documented response, up to 48 months
|
|
Time to progression
Tijdsspanne: From date of randomization until the date of first documented progression, up to 48 months
|
efficacy
|
From date of randomization until the date of first documented progression, up to 48 months
|
|
Overall survival
Tijdsspanne: From date of randomization until death from any cause, up to 48 months
|
efficacy
|
From date of randomization until death from any cause, up to 48 months
|
|
Progression free survival rate at 12-month time point
Tijdsspanne: From date of randomization until 12-month time point
|
efficacy
|
From date of randomization until 12-month time point
|
|
Overall survival rate at 12-month time point
Tijdsspanne: From date of randomization until 12-month time point
|
efficacy
|
From date of randomization until 12-month time point
|
Andere uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Objective response rate according to iRECIST criteria
Tijdsspanne: The proportion of patients with complete response or partial response according to iRECIST criteria, through study completion, an average of 3 years.
|
efficacy
|
The proportion of patients with complete response or partial response according to iRECIST criteria, through study completion, an average of 3 years.
|
|
Progression free survival according to iRECIST criteria
Tijdsspanne: From date of randomization until date of confirmed progression according to iRECIST criteria, up to 48 months
|
efficacy
|
From date of randomization until date of confirmed progression according to iRECIST criteria, up to 48 months
|
|
Duration of response according to iRECIST criteria
Tijdsspanne: From date of randomization until date of confirmed progression according to iRECIST criteria, up to 48 months
|
efficacy
|
From date of randomization until date of confirmed progression according to iRECIST criteria, up to 48 months
|
|
Time to response according to iRECIST criteria
Tijdsspanne: From date of randomization until date of the first documented response according to iRECIST criteria, up to 48 months
|
efficacy
|
From date of randomization until date of the first documented response according to iRECIST criteria, up to 48 months
|
|
Time to progression according to iRECIST criteria
Tijdsspanne: From date of randomization until date of confirmed progression according to iRECIST criteria, up to 48 months.
|
efficacy
|
From date of randomization until date of confirmed progression according to iRECIST criteria, up to 48 months.
|
|
Adverse events rate
Tijdsspanne: From date of randomization until 30 days after the last treatment or beginning of new anti-cancer therapy, whichever comes first, up to 48 months
|
Safety
|
From date of randomization until 30 days after the last treatment or beginning of new anti-cancer therapy, whichever comes first, up to 48 months
|
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Severe adverse events rate
Tijdsspanne: From date of randomization until 90 days after the last treatment, up to 48 months
|
Safety
|
From date of randomization until 90 days after the last treatment, up to 48 months
|
|
Discontinuation rate due to any adverse events
Tijdsspanne: From date of randomization until the last treatment, up to 48 months
|
Safety
|
From date of randomization until the last treatment, up to 48 months
|
Medewerkers en onderzoekers
Sponsor
Medewerkers
Studie record data
Bestudeer belangrijke data
Studie start (Verwacht)
Primaire voltooiing (Verwacht)
Studie voltooiing (Verwacht)
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Werkelijk)
Updates van studierecords
Laatste update geplaatst (Werkelijk)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Aanvullende relevante MeSH-voorwaarden
- Ziekten van het spijsverteringsstelsel
- Hart-en vaatziekten
- Vaatziekten
- Neoplasmata per histologisch type
- Neoplasmata
- Neoplasmata per site
- Adenocarcinoom
- Neoplasmata, glandulair en epitheel
- Neoplasmata van het spijsverteringsstelsel
- Lever Ziekten
- Embolie en trombose
- Lever neoplasmata
- Carcinoom
- Carcinoom, hepatocellulair
- Trombose
- Fysiologische effecten van medicijnen
- Immunologische factoren
- Antilichamen
- Immunoglobulinen
Andere studie-ID-nummers
- HHH
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
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