A Humanitarian Device Exemption Treatment Protocol of TheraSphere For Treatment of Unresectable Hepatocellular Carcinoma
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Purpose
To provide Therasphere treatment for patients diagnosed with unresectable liver cancer.
| Condition | Intervention |
|---|---|
|
Liver Cancer |
Device: Theraspheres |
| Study Type: | Expanded Access What is Expanded Access? |
| Official Title: | A Humanitarian Device Exemption Treatment Protocol of TheraSphere For Treatment of Unresectable Hepatocellular Carcinoma |
| Study Start Date: | December 2008 |
| Estimated Study Completion Date: | December 2099 |
| Estimated Primary Completion Date: | December 2099 (Final data collection date for primary outcome measure) |
-
Device: Theraspheres
- HCC
- hepatocellular carcinoma treatment
Eligibility| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Patients over 18 years of age, of any race or sex, who have hepatocellular carcinoma of the liver, and who are able to give informed consent, will be eligible. Patients must have an ECOG Performance Status score of £ 2, with a life expectancy of >= 3 months, non-pregnant with an acceptable contraception in premenopausal women. Patients must be >4 weeks since prior radiation or prior surgery and at least 1 month post other chemotherapy.
Exclusion Criteria:
- Contraindications to angiography and selective visceral catheterization
- Evidence of potential delivery of greater than 16.5 mCi (30 Gy absorbed dose) of radiation to the lungs
- Evidence of any detectable Tc-99m MAA flow to the stomach or duodenum, after application of established angiographic techniques to stop or mitigate such flow (ex. placing catheter distal to gastric vessels)
- Significant extrahepatic disease representing an imminent life-threatening outcome
- Severe liver dysfunction or pulmonary insufficiency
- Active uncontrolled infection
- Significant underlying medical or psychiatric illness
- Pregnancy
Patients will be excluded: if they have pre-existing diarrhea/illness, or if they have a co-morbid disease or condition that would preclude safe delivery of TheraSphere treatment and place the patient at undue risk.
Contacts and Locations| Contact: Shyam Panchal | (650) 725-9810 | spanchal@stanford.edu |
| United States, California | |
| Stanford University School of Medicine | |
| Stanford, California, United States, 94305 | |
| Contact: Shyam Panchal 650-725-9810 spanchal@stanford.edu | |
| Contact: Cancer Clinical Trials Office (650) 498-7061 | |
| Principal Investigator: Daniel Yung-Ho Sze | |
| Sub-Investigator: Dr. Lawrence (Rusty) Hofmann MD | |
| Principal Investigator: | Daniel Yung-Ho Sze | Stanford University |
More Information
No publications provided
| Responsible Party: | Stanford University |
| ClinicalTrials.gov Identifier: | NCT01076517 History of Changes |
| Other Study ID Numbers: | XHEP0016-NOT-RESEARCH, HEP0016, 14324 |
| Study First Received: | February 24, 2010 |
| Last Updated: | January 18, 2013 |
| Health Authority: | United States: Institutional Review Board |
Additional relevant MeSH terms:
|
Carcinoma Liver Neoplasms Carcinoma, Hepatocellular Neoplasms, Glandular and Epithelial Neoplasms by Histologic Type Neoplasms |
Digestive System Neoplasms Neoplasms by Site Digestive System Diseases Liver Diseases Adenocarcinoma |
ClinicalTrials.gov processed this record on June 18, 2013