PROMETHEUS-01: Carbon Ion Radiotherapy for Hepatocellular Carcinoma
Study Details
Study Description
Brief Summary
Treatment options for patients with advanced hepatocellular carcinoma (HCC) are often limited. In most cases, they are not amenable to local therapies including surgery or radiofrequency ablation. The multi-kinase inhibitor sorafenib has shown to increase overall survival in this patient group for about 3 months.
Radiation therapy is a treatment alternative, however, high local doses are required for long-term local control. However, due to the relatively low radiation tolerance of liver normal tissue, even using stereotactic techniques, delivery of sufficient doses for successful local tumor control has not be achieved to date.
Carbon ions offer physical and biological characteristics. Due to their inverted dose profile and the high local dose deposition within the Bragg peak precise dose application and sparing of normal tissue is possible. Moreover, in comparison to photons, carbon ions offer an increased relative biological effectiveness (RBE), which can be calculated between 2 and 3 depending on the HCC cell line as well as the endpoint analyzed.
Japanese Data on the evaluation of carbon ion radiation therapy showed promising results for patients with HCC.
In the current Phase I-PROMETHEUS-01-Study, carbon ion radiotherapy will be evaluated for patients with advanced HCC. The study will be performed as a dose-escalation study evaluating the optimal carbon ion dose with respect to toxicity and tumor control.
Primary endpoint is toxicity, secondary endpoint is progression-free survival and response.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
N/A |
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Carbon Ion Radiotherapy Increasing Dose of Carbon Ion Radiotherapy 4 x 10 Gy E to 4 x 14 Gy E |
Radiation: Carbon Ion Radiotherapy
Increasing Dose of Carbon Ion Radiotherapy 4 x 10 Gy E to 4 x 14 Gy E
|
Outcome Measures
Primary Outcome Measures
- Maximum Tolerated Dose (MTD) [3 months]
Determination the maximum tolerated dose (MTD) and dose limiting toxicities (DLTs) of carbon ion radiotherapy
Secondary Outcome Measures
- Progression-free Survival [Follow-up until progression up to 12 months]
Eligibility Criteria
Criteria
Inclusion Criteria:
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histologically confirmed HCC or diagnosis of HCC according to AASLD-guidelines
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macroscopic tumor
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liver-confined disease without extrahepatic disease as diagnosed by CT, MRT, ultrasound and bone scan
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minimal distance of tumor edge to the intestines of 1cm
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age ≥ 18 years of age
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Karnofsky Performance Score ³60
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For women with childbearing potential, (and men) adequate contraception.
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Ability of subject to understand character and individual consequences of the clinical trial
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Written informed consent (must be available before enrolment in the trial)
Exclusion Criteria:
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refusal of the patients to take part in the study
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previous radiotherapy of the hepatobiliary system
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margin of < 1cm between tumor edge and intestines
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Patients who have not yet recovered from acute toxicities of prior therapies
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Known carcinoma < 2 years ago (excluding Carcinoma in situ of the cervix, basal cell carcinoma, squamous cell carcinoma of the skin) requiring immediate treatment interfering with study therapy
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Pregnant or lactating women
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Participation in another clinical study or observation period of competing trials, respectively
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | University Hospital of Heidelberg, Radiation Oncology | Heidelberg | Germany | 69120 |
Sponsors and Collaborators
- University Hospital Heidelberg
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- PROMETHEUS-01