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Combination Therapy of HAIC and HLX10 and HLX04 in HCC With Major Portal Vein Tumor Thrombosis

24 giugno 2021 aggiornato da: Shanghai Zhongshan Hospital

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

This is a randomized, double-blinded, controlled, phase II study. The purpose is to evaluate efficacy and safety of the combination therapy of HAIC (Hepatic arterial infusion chemotherapy) with HLX10 (PD-1 antibody) and HLX04 (VEGF antibody) compared with HAIC and placebo in patients with hepatocellular carcinoma with major portal vein tumor thrombosis.

Panoramica dello studio

Tipo di studio

Interventistico

Iscrizione (Anticipato)

100

Fase

  • Fase 2

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

18 anni e precedenti (Adulto, Adulto più anziano)

Accetta volontari sani

No

Sessi ammissibili allo studio

Tutto

Descrizione

Inclusion Criteria:

  1. Willing to attend the study and having given the ICF
  2. Age ≥18
  3. Have a HCC diagnosis confirmed by radiology, histology, or cytology
  4. HCC is diagnosed at Barcelona Clinic Liver Cancer (BCLC) Stage C with major portal vein tumor thrombosis ( VP3~4, or Cheng's II~IV)
  5. Have not accepted any of systemic therapy for HCC such as systemic chemotherapy, molecular targeted drugs, immunotherapy.
  6. 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.
  7. Child-Pugh score ≤7
  8. Eastern Cooperative Oncology Group (ECOG) 0 or 1
  9. Expected life time is over 12 weeks.
  10. HBV-DNA < 2000 IU/mL
  11. 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:

  1. Known fibrolamellar HCC, sarcomatoid HCC, mixed cholangiocarcinoma and HCC
  2. History of hepatic encephalopathy
  3. History of GI bleeding within 6 months, or investigator defined with high risk of haemorrhage for esophageal varices
  4. With distant metastasis (hilar lymph nodes metastasis is allowed)
  5. Co-infection of HBV and HCV
  6. History of other malignancy within 5 years except for healed local tumor.
  7. History of or plan to accept allogenic organ transplantation
  8. Ascites requiring invasive intervention (e.g. paracentesis) to maintain symptomatic control (every month or more often)
  9. 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.
  10. New York Heart Association Grade ≥2 congestive heart failure or LVEF <50%
  11. Uncontrolled hypertension
  12. History of hypertensive crisis or hypertensive encephalopathy
  13. Active infection including but not limited to tuberculosis and HIV
  14. With interstitial lung disease, lung fibrosis, pneumoconiosis, radiation pneumonitis, drug-associated pneumonia and serious impairment in lung function
  15. Active autoimmune disorders except patients with substitutional treatment with thyroid hormone and type I diabetes under treatment with insulin.
  16. Receipt of live attenuated vaccine within 28 days prior to randomization
  17. Current or prior use of steroids (>10mg/d prednisone) or immunosuppressive medication within 14 days before randomization
  18. Significant traumatic injury or major surgical procedure within 28 days prior to randomization
  19. Receipt of checkpoint inhibitors or T cell costimulatory drugs
  20. Receipt of bevacizumab or its analogues
  21. Involved in another clinical trial less than 14 days before randomization
  22. Known allergy or hypersensitivity to any of the study drugs or any of the study drug excipients
  23. Female patients who are pregnant or breastfeeding or male or female patients of reproductive potential who are not willing to employ effective birth control
  24. Active bleeding, with history of ≥grade 3 bleeding within 6 months, or ≥grade 2 bleeding within 3 months
  25. Use of anti-thrombotics within 5 days prior to randomization
  26. In need of NSAIDs for long-term treatment.
  27. 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

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Quadruplicare

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: 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.
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.
Comparatore placebo: 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.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Objective response rate
Lasso di tempo: 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.

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Progression free survival
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: From date of randomization until 12-month time point
efficacy
From date of randomization until 12-month time point

Altre misure di risultato

Misura del risultato
Misura Descrizione
Lasso di tempo
Objective response rate according to iRECIST criteria
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Severe adverse events rate
Lasso di tempo: 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
Lasso di tempo: 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

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Anticipato)

1 agosto 2021

Completamento primario (Anticipato)

1 luglio 2024

Completamento dello studio (Anticipato)

1 luglio 2024

Date di iscrizione allo studio

Primo inviato

18 giugno 2021

Primo inviato che soddisfa i criteri di controllo qualità

24 giugno 2021

Primo Inserito (Effettivo)

1 luglio 2021

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

1 luglio 2021

Ultimo aggiornamento inviato che soddisfa i criteri QC

24 giugno 2021

Ultimo verificato

1 giugno 2021

Maggiori informazioni

Termini relativi a questo studio

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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