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방사선 치료, Atezolizumab 및 Bevacizumab을 받고 있는 간세포암종 환자의 과분극 13C-MRI

2026년 9월 26일 업데이트: Cheng-En Hsieh, Chang Gung Memorial Hospital

방사선 치료, Atezolizumab 및 Bevacizumab을 받고 있는 간세포 암종 환자의 면역 반응 예측을 위한 과분극 13C-MRI, 대사체학 및 방사선학

Increased pyruvate-to-lactate conversion is a hallmark of HCC metabolism. In parallel, activation of pro-inflammatory immune cells triggers a metabolic switch towards anaerobic glycolysis. Hyperpolarized carbon-13 (13C) pyruvate MRI is a state-of-the-art non-invasive imaging method that offers real-time insights into tissue metabolism. Recent studies have demonstrated its promising potential in predicting responses to radiotherapy and immunotherapy in solid tumors, given the significance of pyruvate as a downstream metabolite in glycolysis. However, its application in assessing treatment response in hepatocellular carcinoma (HCC) patients remains unclear. The establishment of quantitative imaging biomarkers for predicting responses to radio-immunotherapy is an unmet need in the management of HCC patients.

While radiotherapy (RT) effectively controls localized tumors through the induction of unrepairable DNA double-stranded breaks (DSBs) and cell death, its therapeutic efficacy on distal, non-irradiated tumor cells is limited, with out-of-field recurrence being a common pattern of failure in HCC patients treated with high-dose irradiation. Atezolizumab (anti-programmed death-ligand 1; anti-PD-L1) in conjunction with bevacizumab (anti-vascular endothelial growth factor; anti-VEGF) has recently emerged as the standard first-line systemic treatment for unresectable hepatocellular carcinoma (HCC). Despite an objective response rate (ORR) of only 27%, the majority of patients succumb to HCC progression and liver failure. Our preclinical study (Hsieh et al., Science Immunology 2022) uncovered that RT, when combined with PD-L1/PD-1 blockade, induces immunogenic cell death and tumor antigen cross-presentation in antigen-presenting cells, enhancing systemic antitumor T cell responses in murine tumor models. Recent retrospective cohorts suggest that RT targeting all hepatic tumors combined with PD-L1/programmed death-1 (PD-1) blockade is associated with an improved ORR and median progression-free survival (PFS) in patients with unresectable HCC, demonstrating a favorable safety profile. The synergistic antitumor effects of this combination therapy with RT, atezolizumab, and bevacizumab have led to its increasing adoption in routine clinical practice.

This phase II non-randomized trial aims to prospectively investigate the predictive value of hyperpolarized 13C-MRI, along with comprehensive metabolomics and radiomics analyses, for immune response assessment including tumor control outcomes and toxicity in patients with HCC undergoing radiotherapy, atezolizumab, and bevacizumab.

연구 개요

상태

모병

정황

개입 / 치료

연구 유형

중재적

등록 (추정된)

45

단계

  • 2 단계

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 연락처

  • 이름: Rodney Cheng-En Hsieh, MD, PhD
  • 전화번호: 7000 +886-3-328-1200
  • 이메일: chsieh@cgmh.org.tw

연구 장소

    • Taiwan
      • Taoyuan City, Taiwan, 대만, 333
        • 모병
        • Chang Gung Memorial Hospital at Linkou
        • 연락하다:
          • Rodney Cheng-En Hsieh, MD, PhD
          • 전화번호: 7000 +886-3-328-1200
          • 이메일: rodney445@gmail.com
        • 수석 연구원:
          • Rodney Cheng En HSIEH, MD, PhD

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

18년 이상 (성인, 고령자)

건강한 자원 봉사자를 받아들입니다

아니

연구 대상 성별

모두

설명

Inclusion Criteria:

  1. Participants must have diagnosis of HCC that is deemed unsuitable for surgical resection or transplant and will undergo radiotherapy, atezolizumab, and bevacizumab. Participants may have multiple lesions with a total maximal tumor dimension of < 20 cm, and no one lesion > 15 cm. Diagnosis should be confirmed by at least 1 criteria listed below:

    • Histologically or cytologically proven diagnosis of HCC.
    • Typical arterial enhancement and delayed washout on multiphasic CT or MRI.
  2. Age ≥18 years at the time of signing informed consent document.

  3. ECOG performance status 0-1.

  4. Barcelona Clinic Liver Cancer (BCLC) stages Intermediate (B) or Advanced (C).

  5. Child-Pugh score 5-6 liver function within 28 days of study registration.

  6. Documented virology status of hepatitis B virus (HBV), as confirmed by screening HBV serology test.

  7. Documented virology status of hepatitis C virus (HCV), as confirmed by screening HCV serology test.

  8. Ability to understand and the willingness to sign a written informed consent document

  9. Adequate bone marrow, liver, and renal function within 4 weeks before study registration

    • Hemoglobin ≥ 9.0 g/dL
    • Absolute neutrophil count (ANC) ≥ 1,000/mm3
    • Platelet count ≥ 50,000/μL
    • Total bilirubin < 2.5 mg/dL
    • Serum albumin >2.8 g/dL
    • Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤ 3 × upper limit of normal (ULN)
    • Prothrombin time ≤ 6 seconds prolonged
    • Serum creatinine ≤ 1.5 mg/dL
  10. The medical team, experienced in liver cancer treatment, has evaluated and confirmed that the benefits outweigh the risks for participants receiving proton or photon radiation therapy combined with atezolizumab and bevacizumab.

Exclusion Criteria:

  1. Prior invasive malignancy unless disease free for a minimum of 2 years

  2. Prior radiotherapy to the region of the liver that would result in overlap of radiation therapy fields

  3. Prior selective internal radiotherapy/hepatic arterial yttrium therapy, at any time

  4. Untreated active hepatitis B or hepatitis C

  5. Moderate to severe or intractable ascites

  6. Presence of distant metastases

  7. Untreated or incomplete treated esophageal or gastric varices

  8. Severe, active co-morbidity, defined as follows:

    • Unstable angina and/or congestive heart failure requiring hospitalization within the last 6 months prior to registration
    • Myocardial infarction within the last 6 months prior to study entry
    • Acute bacterial or fungal infection requiring intravenous antibiotics within 28 days prior to study entry
    • A bleeding episode within 6 months prior to study entry due to any cause.
    • Thrombolytic therapy within 28 days prior to study entry.
    • Known bleeding or clotting disorder.
    • Uncontrolled psychotic disorder
  9. Pregnancy or women of childbearing potential and men who are sexually active and not willing/able to use medically acceptable forms of contraception

  10. Prior solid organ transplantation.

  11. Prior or active autoimmune disease (AID) including autoimmune hepatitis, inflammatory bowel disease, myasthenia gravis, systemic lupus erythematosus, rheumatoid arthritis, antiphospholipid antibody syndrome, Wegener granulomatosis, Sjogren's syndrome, Guillain-Barre syndrome, and multiple sclerosis.

  12. Prior or active thrombotic or bleeding disorders, hemoptysis, cerebral vascular accident, significant cardiac disease (ischemic or congestive heart failure), or gastrointestinal perforation.

  13. Inability to treat all sites of disease by proton radiotherapy (such as extrahepatic metastases or massive liver tumors whereby the liver constraints cannot be met for covering all sites of liver tumors using radiotherapy.)

  14. Known HIV infection.

  15. Conditions not suitable for magnetic resonance imaging (MRI) include the presence of strongly magnetic arterial clips in the brain, cardiac pacemakers, cochlear implants, and claustrophobia.

  16. Concurrent medical conditions that may impact patients during MRI examination include active infections, symptomatic congestive heart failure, uncontrollable angina, arrhythmias, mental disorders, difficulty breathing, or diarrhea.

  17. An endoscopy report within the past six months indicates a high risk for upper gastrointestinal bleeding, and the patient has not received complete treatment for its prevention.

  18. Individuals who are allergic to hyperpolarized 13C pyruvate, atezolizumab, bevacizumab, or any ingredients contained in these medications.

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 특수 증상
  • 할당: 해당 없음
  • 중재 모델: 단일 그룹 할당
  • 마스킹: 없음(오픈 라벨)

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: Hyperpolarized 13C pyruvate MRI

Hyperpolarized 13C pyruvate MRI before and 2-5 weeks after radiotherapy combined with atezolizumab and bevacizumab

The subject enrolled in this trial will receive DNP-MRI scanning for two times through hyperpolarized [1-13C]pyruvate injection (~250 mM, 0.43 mL/Kg) before and 2-5 weeks after radiotherapy.

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Dynamic Nuclear Polarization (DNP)
기간: 4 months

Dynamic Nuclear Polarization (DNP) conversion flux (pyruvate-to-lactate conversion rate [Kpl] and area under the curve [AUC]) before radiotherapy combined with atezolizumab and bevacizumab

4 months
Dynamic Nuclear Polarization (DNP)
기간: 4 month

Dynamic Nuclear Polarization (DNP) conversion flux (pyruvate-to-lactate conversion rate [Kpl] and area under the curve [AUC]) 2-5 weeks after radiotherapy combined with atezolizumab and bevacizumab

4 month

2차 결과 측정

결과 측정
측정값 설명
기간
Overall survival (OS)
기간: 12 months

OS is defined as the time from signing the informed consent to death from any cause.

12 months
Incidence and severity of adverse events
기간: 12 months

Adverse events will be graded using CTCAE v5

12 months
Progression free survival (PFS) by RECIST1.1
기간: 12 months

PFS is defined as the time from signing the informed consent to the first occurrence of disease progression or death from any cause (whichever occurs first) according to RECIST1.1

12 months
Local control (LC) by RECIST1.1
기간: 12 months

LC is defined as the time from signing the informed consent to the first occurrence of disease progression in the irradiated field according to RECIST1.1

12 months
Time to progression (TTP) by RECIST1.1
기간: 12 months

TTP is defined as the time from signing the informed consent to the first occurrence of disease progression according to RECIST1.1

12 months
Overall Response Rate (ORR) by RECIST1.1
기간: 12 months

ORR is defined as a complete or partial response according to RECIST1.1

12 months

기타 결과 측정

결과 측정
측정값 설명
기간
Change in myeloid-derived suppressor cell (MDSC) level in peripheral blood
기간: 4 months

We will measure the level of Lin- HLA-DR- CD11b+ MDSCs in peripheral blood using flow cytometry before and 2-5 weeks after radiotherapy.

4 months

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

스폰서

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (실제)

2025년 5월 1일

기본 완료 (추정된)

2029년 6월 30일

연구 완료 (추정된)

2031년 9월 30일

연구 등록 날짜

최초 제출

2024년 9월 18일

QC 기준을 충족하는 최초 제출

2024년 9월 18일

처음 게시됨 (실제)

2024년 9월 20일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 9월 29일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 9월 26일

마지막으로 확인됨

2026년 9월 1일

추가 정보

이 연구와 관련된 용어

기타 연구 ID 번호

  • 2401190005

개별 참가자 데이터(IPD) 계획

개별 참가자 데이터(IPD)를 공유할 계획입니까?

미정

IPD 계획 설명

The sharing of individual participant data (IPD) requires IRB approval.

약물 및 장치 정보, 연구 문서

미국 FDA 규제 의약품 연구

아니

미국 FDA 규제 기기 제품 연구

아니

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .