Clinical trial · Interventional
Phase II Trial of Carbon-ion Radiotherapy Combined With GM-CSF for the Treatment of Hepatocellular Carcinoma
A Prospective Phase II Single-institution Trial of Carbon-ion Radiotherapy Combined With Granulocyte-macrophage Colony-stimulating Factor for the Treatment of Hepatocellular Carcinoma
NCT02946138CI-TRIAL-00040457withdrawnPhase 2ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Why stopped (as posted): enrollment was too slow
Summary
Brief summary (as posted)
The aim of this research project is to assess the efficacy and toxicity of hypofractionated carbon-ion radiotherapy with concurrent granulocyte-macrophage colony-stimulating factor for the treatment of hepatocellular carcinoma
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Hepatocellular Carcinoma | Hepatocellular Carcinoma | ONTOLOGY_EXACT | 0.98 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| carbon-ion radiotherapy | Radiation | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- carbon-ion radiotherapy with GM-CSF
- description
- Hypofractionated carbon-ion radiotherapy was prescribed at a dose of 40Gray(Gy) \[relative biological effectiveness (RBE)\] in 5 fractions for intrahepatic cases away from gastro-intestinal (GI) tract (\>1cm) with concurrent GM-CSF 125ug/m2/d, subcutaneous injection d1-28;
- interventionNames
- Radiation: carbon-ion radiotherapy
Primary outcomes (1)
- measure
- Progression-free survival of all patients
- timeFrame
- 2 year
- description
- Time in months measured from treatment initiation until the date of progression or the date of last follow-up.
Secondary outcomes (3)
- measure
- Overall Survival
- timeFrame
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 80 Years
Show eligibility criteria text
Inclusion Criteria: 1. histologically confirmed hepatocellular carcinoma (HCC) or clinical diagnosis of HCC according to American association for the study of liver diseases (AASLD)-guidelines or clinical diagnosis criteria based on Alpha Fetoprotein (AFP), and radiological images proposed by Liver Cancer Society, Chinese Anti-Cancer Association; 2. no clinically distant metastasis; 3. the tumor is away from gastro-intestinal (GI) tract (\>1cm); 4. Child Push score A,technically unresectable, or medically inoperable; maximal tumor size is less than 10 cm; 5. age ≥ 18 and \<80 years of age; 6. Karnofsky Performance Score ≥ 70; 7. No previous invasive cancer (within 5 years before the HCC diagnosis)except for skin non-melanoma cancer or non muscle invasive bladder cancer; Ability to understand character and individual consequences of the clinical trial; 8. Willing to sign the written informed consent; Informed consent must be signed before the enrollment in the trial; Exclusion Criteria: 1. Distant metastasis (M1); 2. maximal tumor size is more than 10 cm; 3. tumor invading adjacent gastrointestine (T4); 4. Child push score B or C; 5. Previous hepatic radiotherapy; 6. Severe systemic disorders; 7. Previous malignancy (within 5 years) except for skin non-melanoma cancer or 3-year disease free interval from previous malignancy like in situ cervix cancer or non muscle invasive bladder cancer; 8. Non conformity of the radiotherapy dose distribution when compared to the dose constraints; 9. Psychiatric disorders or any other condition that can make unreliable the informed consent;
References
Publications (0)
Data not yet available
No reference posted for this study.