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

2026年9月22日 更新者: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.

調査の概要

状態

まだ募集していません

研究の種類

介入

入学 (推定)

78

段階

  • フェーズ2
  • フェーズ 1

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

18年~75年 (大人、高齢者)

健康ボランティアの受け入れ

いいえ

受講資格のある性別

全て

説明

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.

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:処理
  • 割り当て:なし
  • 介入モデル:単一グループの割り当て
  • マスキング:なし(オープンラベル)

武器と介入

参加者グループ / アーム
介入・治療
実験的: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.

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Incidence of Dose-Limiting Toxicities (DLTs) During Phase Ib
時間枠: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
時間枠: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
時間枠: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

二次結果の測定

結果測定
メジャーの説明
時間枠
Objective Response Rate per mRECIST
時間枠: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
時間枠: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)
時間枠: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)
時間枠: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)
時間枠: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)
時間枠: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
時間枠: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)
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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

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ここでは、この調査に関係する人々や組織を見つけることができます。

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研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (推定)

2026年10月1日

一次修了 (推定)

2029年10月1日

研究の完了 (推定)

2029年10月1日

試験登録日

最初に提出

2026年9月10日

QC基準を満たした最初の提出物

2026年9月22日

最初の投稿 (実際)

2026年9月23日

学習記録の更新

投稿された最後の更新 (実際)

2026年9月23日

QC基準を満たした最後の更新が送信されました

2026年9月22日

最終確認日

2026年9月1日

詳しくは

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個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

いいえ

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米国FDA規制医薬品の研究

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米国FDA規制機器製品の研究

いいえ

米国で製造され、米国から輸出された製品。

いいえ

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