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Transarterial Chemoembolization (TACE) and Stereotactic Body Radiation (SBRT) in Patients With Hepatocellular Carcinoma (HCC) Prior to Liver Transplantation (TREASURE-Tx)

3 novembre 2026 aggiornato da: AIO-Studien-gGmbH

Transarterial Chemoembolization (TACE) and Stereotactic Body Radiation (SBRT) in Patients With Hepatocellular Carcinoma (HCC) Prior to Liver Transplantation A Randomized, 2-arm Phase II Study Comparing the Combination of Transarterial Chemoembolization (TACE) and Stereotactic Body Radiation (SBRT) Versus TACE Alone in Patients With Hepatocellular Carcinoma as Bridging to Liver Transplantation With Regard to Explant Histopathology

In this randomised study it should be investigated, whether and to what extent standard TACE treatment combined with additional stereotactic body radiotherapy (SBRT) leads to improved outcomes for patients with HCC when used as a bridging therapy prior to liver transplantation.

Panoramica dello studio

Stato

Reclutamento

Condizioni

Intervento / Trattamento

Descrizione dettagliata

Hepatocellular carcinoma (HCC) is one of the most frequent malignancies worldwide and is characterized by a rising incidence. A first line curative treatment option is surgical resection. As most patients with HCC suffer from liver cirrhosis, resection is often constrained due to limited liver function. In patients with tumors within Milan criteria, liver transplantation remains a curative therapeutic option even if liver resection is not feasible. Due to organ shortage, there are long waiting periods and waitlist withdrawal because of tumor progression remains an eminent risk. Hence, bridging therapies are used to halt tumor growth. Transarterial chemoembolization (TACE) is one of the most commonly used bridging therapies. Other possible bridging therapies are local ablation and stereotactic body radiation therapy (SBRT). Importantly, there are several studies showing a potential benefit of the combination of TACE and SBRT in the treatment of HCC. Recently, we were able to show a high rate of complete histopathological response in patients who were treated with a combination of TACE and SBRT as bridging to liver transplant, suggesting a potential benefit of combining both therapies in a pre-transplant setting.

Tipo di studio

Interventistico

Iscrizione (Stimato)

44

Fase

  • Non applicabile

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

  • Nome: Ursula Ehmer, PD Dr. med.
  • Numero di telefono: +49 (0) 89 4140-9324
  • Email: ursula.ehmer@tum.de

Backup dei contatti dello studio

Luoghi di studio

      • München, Germania, 81675
        • Reclutamento
        • Klinik und Poliklinik für Innere Medizin II, TUM Klinikum, Rechts der Isar
        • Contatto:

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. Written informed consent obtained from the subject prior to performing any protocol related procedures, including screening evaluations.

  2. Age ≥ 18 years at time of study entry.

  3. HCC diagnosed by histopathology and/or according to EASL or AASLD criteria at an early stage (BCLC A or UNOS T2), without any curative treatment option (resection or ablation) other than liver transplantation as determined by tumor board decision of at least one tumor lesion. Guidance: Patients with prior HCC who had surgery or locoregional treatment and had a complete remission for over 2 years and develop denovo HCC at a location different from previously treated HCC lesion(s) are eligible to participate.

  4. Patients planned for liver transplantation after discussion within a multidisciplinary board.

  5. Patients eligible to receive a matchReMELD-Na (SE-ReMELD-Na) - Score for hepatocellular carcinoma according to German transplant regulations. Guidance: All listing assessments must be completed before first on-study radiologic tumor assessment (first radiologic tumor assessment in treatment follow-up).

  6. Treatment of all lesions by SBRT is feasible as determined by the local physician. The central review board recommendation process has been initiated (i.e. image upload by site).

  7. At least one measurable site of disease with spiral CT scan or MRI according to mRECIST for HCC.

  8. Sufficient liver function (< Child Pugh B8)

  9. Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0 or 1.

  10. Adequate blood count, liver enzymes and renal function:

    1. Hemoglobin ≥ 7 g/dL, absolute neutrophil count ≥ 1000 /µL, platelets ≥ 35000/µL
    2. Total bilirubin and serum albumin as part of Child Pugh requirement
    3. ALAT and ASAT ≤5 x ULN
  11. Patients with active HIV Infection must show a CD4 cell count above 200/µL and no detectable HIV RNA for at least three months prior to the study

  12. Female patients with reproductive potential must have a negative urine or serum pregnancy test within 14 days prior to start of the study (randomization).

  13. Patients of childbearing potential who are sexually active must use an adequate contraceptive method with a failure rate less than 1 % per year. Enrolled patients must agree to use adequate contraception for the duration of study treatment and up to 6 months after the end of the treatment (depending on treatment received), manufactures recommendation (TACE) and local guidelines.

  14. Subject is willing and able to comply with the protocol for the duration of the study including undergoing treatment and scheduled visits and examinations including follow up.

Exclusion Criteria:

  1. Involvement in the planning and/or conduct of the study.
  2. Prior local tumor specific treatment of the same tumor nodule within the last 24 months.
  3. Histological proven fibrolamellar HCC or mixed HCC/cholangiocarcinoma.
  4. Other invasive malignancies within the past 2 years (except for non-melanoma skin cancer or non-invasive bladder cancer).
  5. Impaired liver function Child-Pugh Class B > 7.
  6. Ongoing or active systemic infection or psychiatric illness/social situations that would limit compliance with study requirements. Uncontrolled intercurrent illness, including but not limited to, ongoing or active infection, or psychiatric illness/social situations that would limit compliance with study requirement, substantially increase risk of incurring AEs, or compromise the ability of the patient to give written informed consent.
  7. Dementia or significantly altered mental status that would prohibit the understanding or rendering of information, consent, and compliance with the requirements of the protocol.
  8. Pregnancy and breastfeeding. Should a patient become pregnant, the treating physician has to be informed immediately.
  9. Any condition, comorbidity or circumstance that, in the opinion of the investigator, would interfere with evaluation of study treatment or affect patient safety or study results.
  10. Weight less than or equal to 30 kg.
  11. Prior radiotherapy to the upper abdomen

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: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Comparatore attivo: The patients will receive two procedures of TACE prior to liver transplantation

Standard arm: The patients will receive two procedures of TACE prior to liver transplantation

The patients will receive two procedures of TACE prior to liver transplantation as bridging therapy (standard of care)

Sperimentale: The patients will receive two procedures of TACE followed by SBRT prior to liver transplantation

Experimental arm: The patients will receive two procedures of TACE followed by SBRT prior to liver transplantation

The patients will receive a stereotactic body radiation therapy (SBRT) in addition to two procedures of TACE prior to liver transplantation

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Primary Endpoint: histopathological response (presence of vital tumor tissue) in explant histopathology after liver transplantation.
Lasso di tempo: After liver transplantation (at least 24 months after randomization)

The percentage of vital tumor tissue is defined as the maximum percentage of vital tumor tissue per surface area per patient.

After liver transplantation (at least 24 months after randomization)

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Overall survival (OS)
Lasso di tempo: 24 months after randomization

Overall survival (OS) is defined as time from randomization to death from any cause. Overall survival-rate at 24 months is defined as the (estimated) proportion of patients who are still alive 24 months after randomization.

24 months after randomization
Objective response rate (ORR)
Lasso di tempo: up to 24 months after randomization

The objective response rate (ORR) is defined as the proportion of all randomized patients in whom a CR or PR was observed

up to 24 months after randomization
Complete response rate (CRR)
Lasso di tempo: up to 24 months after randomization

The complete response rate (CRR) is defined as the proportion of all randomized patients in whom a CR was observed

up to 24 months after randomization
Progression-free survival (PFS)
Lasso di tempo: up to 24 months after randomization

Progression-free survival (PFS) is defined as time from randomization to objective tumor progression or death from any cause

up to 24 months after randomization
Recurrence Rate
Lasso di tempo: up to 24 months after transplantation

Recurrence Rate is defined as the percentage of patients in whom cancer recurs after transplantation within 24 months. The recurrence is determined by regular standard of care follow-up examinations, which include imaging procedures (CT, MRI, ultrasound) and blood tests (e.g. alpha-fetoprotein). A division is made between local recurrence in the transplanted liver and distant metastases.

up to 24 months after transplantation
Recurrence free survival (RFS)
Lasso di tempo: up to 24 months after transplantation

Recurrence free survival (RFS) is defined as time from transplantation to tumor recurrence or death from HCC. Death from any other cause will be used as a censoring event.

up to 24 months after transplantation
Quality of Life Assessments
Lasso di tempo: up to 24 months after randomization

Quality of Life evaluated with EQ-5D-5L

up to 24 months after randomization
Safety reporting - treatment-emergent adverse events
Lasso di tempo: Up to 24 months after informed consent

Type, incidence, causal relationship, and severity of treatment-emergent adverse events

Up to 24 months after informed consent
Safety reporting - albumin-bilirubin score (ALBI Score)
Lasso di tempo: Up to 24 months after informed consent

Analysis of the effect on albumin-bilirubin score (ALBI Score)

Up to 24 months after informed consent
Safety reporting - Child Pugh Score
Lasso di tempo: Up to 24 months after informed consent

Analysis of the effect on Child Pugh Score

Up to 24 months after informed consent

Collaboratori e investigatori

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

Sponsor

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 (Effettivo)

28 luglio 2026

Completamento primario (Stimato)

1 gennaio 2031

Completamento dello studio (Stimato)

1 marzo 2031

Date di iscrizione allo studio

Primo inviato

16 settembre 2026

Primo inviato che soddisfa i criteri di controllo qualità

3 novembre 2026

Primo Inserito (Effettivo)

9 novembre 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

9 novembre 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

3 novembre 2026

Ultimo verificato

1 novembre 2026

Maggiori informazioni

Termini relativi a questo studio

Parole chiave

Altri numeri di identificazione dello studio

  • AIO-HEP-0124

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

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 .