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Safety and Efficacy of Folic Acid Combined With Atezolizumab and Bevacizumab as First-Line Therapy for Unresectable Hepatocellular Carcinoma

22. září 2026 aktualizováno: Hong Wu, West China Hospital

Safety and Efficacy of Folic Acid Combined With Atezolizumab and Bevacizumab as First-Line Therapy for Unresectable Hepatocellular Carcinoma: A Prospective, Open-Label, Single-Arm, Phase Ib/II Clinical Trial

This study is evaluating the safety and potential effectiveness of adding folic acid to atezolizumab plus bevacizumab as first-line treatment for adults with unresectable hepatocellular carcinoma (HCC).

The main questions this study aims to answer are:

Is daily folic acid safe and well tolerated when given together with atezolizumab and bevacizumab? What dose of folic acid should be recommended for further study? Does the combination show sufficient antitumor activity to support further clinical testing?

This is an open-label, single-arm phase Ib/II study. All participants will receive folic acid together with atezolizumab and bevacizumab. There is no placebo or separate control group.

Participants will:

Take folic acid by mouth once daily, starting 7 days before the first dose of atezolizumab and bevacizumab.

Receive atezolizumab and bevacizumab by intravenous infusion every 3 weeks. Attend regular clinic visits for physical examinations, blood tests, safety assessments, and tumor imaging.

Have tumor imaging every 6 weeks during the first 24 weeks and every 9 weeks thereafter.

Provide blood samples for exploratory biomarker studies. An additional tumor biopsy during treatment may be offered but is optional.

Treatment will continue until disease progression, unacceptable side effects, withdrawal of consent, or another protocol-defined reason for stopping treatment. Immunotherapy may be continued for up to 24 months.

Přehled studie

Postavení

Zatím nenabíráme

Typ studie

Intervenční

Zápis (Odhadovaný)

78

Fáze

  • Fáze 2
  • Fáze 1

Kritéria účasti

Výzkumníci hledají lidi, kteří odpovídají určitému popisu, kterému se říká kritéria způsobilosti. Některé příklady těchto kritérií jsou celkový zdravotní stav osoby nebo předchozí léčba.

Kritéria způsobilosti

Věk způsobilý ke studiu

18 let až 75 let (Dospělý, Starší dospělý)

Přijímá zdravé dobrovolníky

Ne

Pohlaví způsobilá ke studiu

Všechno

Popis

Inclusion Criteria:

  • Age 18 to 75 years, male or female, and willing to provide written informed consent.
  • Hepatocellular carcinoma (HCC) confirmed by histologic/cytologic examination or diagnosed according to accepted guideline-based clinical criteria.
  • Unresectable HCC as determined by multidisciplinary evaluation; BCLC stage B disease that is unsuitable for, declined, or has progressed after locoregional treatment, or BCLC stage C disease; candidate for first-line systemic therapy.
  • No prior systemic anticancer therapy for unresectable HCC. Prior locoregional treatment must have been completed at least 4 weeks before the first study treatment, with treatment-related toxicities recovered to Grade ≤1 or baseline.
  • At least one measurable lesion according to RECIST version 1.1. The measurable lesion must not have received prior locoregional treatment unless unequivocal radiologic progression has subsequently occurred.
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1 and life expectancy of at least 12 weeks.
  • Child-Pugh class A (score 5-6), without clinically decompensated ascites or hepatic encephalopathy.
  • Adequate bone marrow function: absolute neutrophil count ≥1.5 × 10^9/L, platelet count ≥75 × 10^9/L, and hemoglobin ≥90 g/L.
  • Adequate hepatic and renal function: total bilirubin ≤3 × upper limit of normal (ULN); AST and ALT ≤5 × ULN; albumin ≥28 g/L; INR ≤1.5; serum creatinine ≤1.5 × ULN or creatinine clearance ≥50 mL/min.
  • Urine protein dipstick ≤1+. If urine protein is ≥2+, 24-hour urinary protein must be <1 g. Blood pressure must be adequately controlled at ≤150/90 mmHg.
  • Upper gastrointestinal endoscopic evaluation within 6 months before the first study treatment. Intermediate- or high-risk gastroesophageal varices must have been appropriately managed and considered to have an acceptable bleeding risk by the investigator.
  • Participants with positive HBsAg or detectable HBV DNA must receive appropriate antiviral therapy and have HBV DNA <500 IU/mL before the first study treatment. HCV infection must be clinically stable.
  • Serum vitamin B12 at or above the institutional lower limit of normal, with no uncorrected megaloblastic anemia or progressive unexplained neurologic symptoms.
  • Participants of reproductive potential must agree to use highly effective contraception according to protocol requirements.

Exclusion Criteria:

  • Prior treatment with PD-1, PD-L1, CTLA-4, or other immune checkpoint inhibitors, or prior bevacizumab treatment for HCC.
  • Eligible for curative resection, ablation, or liver transplantation and willing to undergo such treatment.
  • Active or recent clinically significant bleeding, including gastrointestinal bleeding, hemoptysis, or other Grade ≥2 bleeding within 6 months before the first study treatment, or untreated high-risk varices.
  • Arterial thromboembolism, myocardial infarction, unstable angina, stroke/transient ischemic attack, severe arrhythmia, or NYHA class >II heart failure within 6 months before the first study treatment.
  • Tumor invasion of major blood vessels considered by the investigator to confer a significant near-term risk of fatal bleeding, or clinically significant risk of tumor rupture.
  • Uncontrolled hypertension, clinically significant proteinuria, active peptic ulcer disease, high risk of gastrointestinal perforation or fistula, unhealed wound, or major surgery within 28 days before the first study treatment.
  • Active autoimmune disease requiring systemic treatment, or systemic corticosteroid therapy equivalent to prednisone >10 mg/day or other immunosuppressive therapy within 14 days before the first study treatment, except physiologic replacement therapy.
  • Prior solid-organ transplantation or allogeneic hematopoietic stem-cell transplantation.
  • Active severe infection, including uncontrolled HBV or HCV infection, active tuberculosis, or HIV infection associated with clinically significant immunodeficiency.
  • Symptomatic, untreated, or unstable central nervous system metastases.
  • Vitamin B12 deficiency, pernicious anemia, folic acid hypersensitivity, or continuous use of folic acid >0.4 mg/day within 14 days before screening that cannot be discontinued.
  • Current use of methotrexate or other antifolate drugs, or use of phenytoin, phenobarbital, or primidone that cannot be replaced or appropriately monitored.
  • Pregnancy or breastfeeding; serious concurrent disease, psychiatric or cognitive disorder, or compliance issue that could interfere with study participation.
  • Participation in another interventional clinical study within 4 weeks before the first study treatment, or any other condition considered by the investigator to make the participant unsuitable for enrollment.

Studijní plán

Tato část poskytuje podrobnosti o studijním plánu, včetně toho, jak je studie navržena a co studie měří.

Jak je studie koncipována?

Detaily designu

  • Primární účel: Léčba
  • Přidělení: N/A
  • Intervenční model: Přiřazení jedné skupiny
  • Maskování: Žádné (otevřený štítek)

Zbraně a zásahy

Skupina účastníků / Arm
Intervence / Léčba
Experimentální: Folic Acid Plus Atezolizumab and Bevacizumab

All participants will receive folic acid in combination with atezolizumab and bevacizumab. During the phase Ib dose-finding portion, sequential cohorts will receive folic acid 1 mg once daily or 5 mg once daily, starting 7 days before the first administration of atezolizumab and bevacizumab, to determine the recommended phase II dose (RP2D). In the phase II expansion, participants will receive folic acid at the selected RP2D. Atezolizumab 1200 mg and bevacizumab 15 mg/kg will be administered intravenously on Day 1 of each 3-week cycle.

Folic acid will be administered orally once daily, beginning 7 days before the first administration of atezolizumab and bevacizumab. During phase Ib, sequential dose levels of 1 mg once daily and 5 mg once daily will be evaluated to determine the recommended phase II dose (RP2D). In the phase II expansion, participants will receive folic acid at the selected RP2D.

Atezolizumab 1200 mg and bevacizumab 15 mg/kg will be administered by intravenous infusion on Day 1 of each 3-week treatment cycle.

Co je měření studie?

Primární výstupní opatření

Měření výsledku
Popis opatření
Časové okno
Incidence of Dose-Limiting Toxicities (DLTs) During Phase Ib
Časové okno: From the first folic acid dose on Day -7 through Cycle 1 Day 21 (28 days)

The number and proportion of participants experiencing a protocol-defined dose-limiting toxicity (DLT). DLTs will be graded according to NCI CTCAE version 6.0 and adjudicated according to protocol-defined attribution criteria.

From the first folic acid dose on Day -7 through Cycle 1 Day 21 (28 days)
Recommended Phase II Dose (RP2D) of Folic Acid
Časové okno: At completion of the Phase Ib dose-finding portion, approximately up to 10 months after study initiation

The recommended phase II dose of folic acid will be selected based on the integrated assessment of dose-limiting toxicities, overall safety and tolerability, treatment adherence, serum folate exposure, and pharmacodynamic findings during the phase Ib dose-finding portion.

At completion of the Phase Ib dose-finding portion, approximately up to 10 months after study initiation
Objective Response Rate (ORR) by Blinded Independent Central Review per RECIST Version 1.1
Časové okno: From the first study treatment until documented disease progression or initiation of new anticancer therapy, up to 24 months

The proportion of participants treated at the recommended phase II dose whose best overall response is a confirmed complete response (CR) or partial response (PR), as assessed by blinded independent central review (BICR) according to RECIST version 1.1. A response must be confirmed by a subsequent assessment at least 4 weeks later.

From the first study treatment until documented disease progression or initiation of new anticancer therapy, up to 24 months

Sekundární výstupní opatření

Měření výsledku
Popis opatření
Časové okno
Objective Response Rate per mRECIST
Časové okno: Up to 24 months

Proportion of participants with a confirmed complete response (CR) or partial response (PR) according to modified RECIST criteria for hepatocellular carcinoma.

Up to 24 months
Investigator-Assessed Objective Response Rate per RECIST 1.1
Časové okno: Up to 24 months

Proportion of participants with a confirmed CR or PR according to investigator assessment using RECIST version 1.1.

Up to 24 months
Disease Control Rate (DCR)
Časové okno: Up to 24 months

Proportion of participants achieving CR, PR, or stable disease according to RECIST version 1.1.

Up to 24 months
Duration of Response (DOR)
Časové okno: Up to approximately 36 months

Time from the first documented CR or PR to disease progression or death from any cause.

Up to approximately 36 months
Time to Response (TTR)
Časové okno: Up to 24 months

Time from the first study treatment to the first documented CR or PR.

Up to 24 months
Progression-Free Survival (PFS)
Časové okno: Up to approximately 36 months

Time from the first study treatment to disease progression according to RECIST version 1.1 or death from any cause, whichever occurs first.

Up to approximately 36 months
Progression-Free Survival Rates at 6 and 12 Months
Časové okno: 6 months and 12 months

Proportion of participants alive without disease progression at 6 months and 12 months after initiation of study treatment.

6 months and 12 months
Overall Survival (OS)
Časové okno: Up to approximately 36 months

Time from the first study treatment to death from any cause.

Up to approximately 36 months
Overall Survival Rates at 12 and 24 Months
Časové okno: 12 months and 24 months

Proportion of participants alive at 12 months and 24 months after initiation of study treatment.

12 months and 24 months
AFP Response Rate
Časové okno: Up to 24 months

Proportion of evaluable participants with a decrease in serum alpha-fetoprotein (AFP) of at least 20% from baseline.

Up to 24 months
Conversion to Curative Surgical Resection
Časové okno: Up to 24 months

Proportion of participants who become eligible for and undergo protocol-defined R0 surgical resection after multidisciplinary evaluation.

Up to 24 months
Incidence of Adverse Events
Časové okno: From informed consent through protocol-defined safety follow-up; immune-related adverse events monitored for at least 90 days after the last dose of atezolizumab

Incidence and severity of adverse events, serious adverse events, treatment-related adverse events, immune-related adverse events, and adverse events leading to treatment interruption or discontinuation, graded according to NCI CTCAE version 6.0.

From informed consent through protocol-defined safety follow-up; immune-related adverse events monitored for at least 90 days after the last dose of atezolizumab

Spolupracovníci a vyšetřovatelé

Zde najdete lidi a organizace zapojené do této studie.

Termíny studijních záznamů

Tato data sledují průběh záznamů studie a předkládání souhrnných výsledků na ClinicalTrials.gov. Záznamy ze studií a hlášené výsledky jsou před zveřejněním na veřejné webové stránce přezkoumány Národní lékařskou knihovnou (NLM), aby se ujistily, že splňují specifické standardy kontroly kvality.

Hlavní termíny studia

Začátek studia (Odhadovaný)

1. října 2026

Primární dokončení (Odhadovaný)

1. října 2029

Dokončení studie (Odhadovaný)

1. října 2029

Termíny zápisu do studia

První předloženo

10. září 2026

První předloženo, které splnilo kritéria kontroly kvality

22. září 2026

První zveřejněno (Aktuální)

23. září 2026

Aktualizace studijních záznamů

Poslední zveřejněná aktualizace (Aktuální)

23. září 2026

Odeslaná poslední aktualizace, která splnila kritéria kontroly kvality

22. září 2026

Naposledy ověřeno

1. září 2026

Více informací

Termíny související s touto studií

Plán pro data jednotlivých účastníků (IPD)

Plánujete sdílet data jednotlivých účastníků (IPD)?

NE

Informace o lécích a zařízeních, studijní dokumenty

Studuje lékový produkt regulovaný americkým FDA

Ne

Studuje produkt zařízení regulovaný americkým úřadem FDA

Ne

produkt vyrobený a vyvážený z USA

Ne

Tyto informace byly beze změn načteny přímo z webu clinicaltrials.gov. Máte-li jakékoli požadavky na změnu, odstranění nebo aktualizaci podrobností studie, kontaktujte prosím register@clinicaltrials.gov. Jakmile bude změna implementována na clinicaltrials.gov, bude automaticky aktualizována i na našem webu .

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