Transarterial Chemoembolization (TACE) and Stereotactic Body Radiation (SBRT) in Patients With Hepatocellular Carcinoma (HCC) Prior to Liver Transplantation (TREASURE-Tx)
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.
調査の概要
状態
状態
条件
条件
介入・治療
介入・治療
詳細な説明
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.
研究の種類
研究の種類
入学 (推定)
入学
段階
段階
- 適用できない
連絡先と場所
研究連絡先
研究連絡先
- 名前:Ursula Ehmer, PD Dr. med.
- 電話番号:+49 (0) 89 4140-9324
- メール:ursula.ehmer@tum.de
研究連絡先のバックアップ
- 名前:Ulrike Bauer, Dr. med. univ. Dr. med.
- メール:Ulrike.Bauer@mri.tum.de
研究場所
-
-
-
München、ドイツ、81675
- 募集
- Klinik und Poliklinik für Innere Medizin II, TUM Klinikum, Rechts der Isar
-
コンタクト:
- Ursula Ehmer, PD Dr. med.
- 電話番号:+49 (0) 89 4140-9324
- メール:ursula.ehmer@mri.tum.de
-
-
参加基準
適格基準
適格基準
就学可能な年齢
健康ボランティアの受け入れ
受講資格のある性別
説明
Inclusion Criteria:
-
Written informed consent obtained from the subject prior to performing any protocol related procedures, including screening evaluations.
-
Age ≥ 18 years at time of study entry.
-
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.
-
Patients planned for liver transplantation after discussion within a multidisciplinary board.
-
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).
-
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).
-
At least one measurable site of disease with spiral CT scan or MRI according to mRECIST for HCC.
-
Sufficient liver function (< Child Pugh B8)
-
Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0 or 1.
-
Adequate blood count, liver enzymes and renal function:
- Hemoglobin ≥ 7 g/dL, absolute neutrophil count ≥ 1000 /µL, platelets ≥ 35000/µL
- Total bilirubin and serum albumin as part of Child Pugh requirement
- ALAT and ASAT ≤5 x ULN
-
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
-
Female patients with reproductive potential must have a negative urine or serum pregnancy test within 14 days prior to start of the study (randomization).
-
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.
-
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:
- Involvement in the planning and/or conduct of the study.
- Prior local tumor specific treatment of the same tumor nodule within the last 24 months.
- Histological proven fibrolamellar HCC or mixed HCC/cholangiocarcinoma.
- Other invasive malignancies within the past 2 years (except for non-melanoma skin cancer or non-invasive bladder cancer).
- Impaired liver function Child-Pugh Class B > 7.
- 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.
- Dementia or significantly altered mental status that would prohibit the understanding or rendering of information, consent, and compliance with the requirements of the protocol.
- Pregnancy and breastfeeding. Should a patient become pregnant, the treating physician has to be informed immediately.
- 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.
- Weight less than or equal to 30 kg.
- Prior radiotherapy to the upper abdomen
研究計画
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:ランダム化
- 介入モデル:並列代入
- マスキング:なし(オープンラベル)
アーム数
武器と介入
参加者グループ / アーム参加者グループ / アーム |
介入・治療介入・治療 |
|---|---|
|
アクティブコンパレータ: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) |
|
実験的: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 |
この研究は何を測定していますか?
主要な結果の測定
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Primary Endpoint: histopathological response (presence of vital tumor tissue) in explant histopathology after liver transplantation.
時間枠: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)
|
二次結果の測定
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Overall survival (OS)
時間枠: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)
時間枠: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)
時間枠: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)
時間枠: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
時間枠: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)
時間枠: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
時間枠: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
時間枠: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)
時間枠: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
時間枠:Up to 24 months after informed consent
|
Analysis of the effect on Child Pugh Score |
Up to 24 months after informed consent
|
協力者と研究者
研究記録日
主要日程の研究
研究開始 (実際)
研究開始
一次修了 (推定)
一次修了
研究の完了 (推定)
研究の完了
試験登録日
最初に提出
最初に提出
QC基準を満たした最初の提出物
QC基準を満たした最初の提出物
最初の投稿 (実際)
最初の投稿
学習記録の更新
投稿された最後の更新 (実際)
投稿された最後の更新
QC基準を満たした最後の更新が送信されました
QC基準を満たした最後の更新が送信されました
最終確認日
最終確認日
詳しくは
本研究に関する用語
追加の関連 MeSH 用語
その他の研究ID番号
その他の研究ID番号
- AIO-HEP-0124
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?
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
米国FDA規制機器製品の研究
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。