Temsirolimus as Second-line Therapy in HCC
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Purpose
The purpose of this study is to evaluate the activity of temsirolimus in patients who have advanced hepatocellular carcinoma (HCC) and have been treated with one previous chemotherapy or biologic therapy like sorafenib, but have experienced disease progression or intolerance to that therapy.
| Condition | Intervention | Phase |
|---|---|---|
|
Unresectable or Metastatic Hepatocellular Carcinoma |
Drug: Temsirolimus |
Phase 2 |
| Study Type: | Interventional |
| Study Design: | Endpoint Classification: Efficacy Study Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | A Phase II Study of Temsirolimus as Second-line Therapy in Patients With Advanced, Unresectable Hepatocellular Carcinoma |
- Disease Progression [ Designated as safety issue: No ]The primary outcome measure is to determine the proportion of patients who are progression free at 3 months.
- Response rate [ Designated as safety issue: No ]Response rate, clinical benefit rate (complete + partial response + stable disease > 12 weeks) and overall survival with temsirolimus
- Safety and tolerability [ Designated as safety issue: Yes ]Number and frequency of adverse events and serious adverse events will be monitored.
- Biochemical response [ Designated as safety issue: No ]Biochemical response (>50% decline in AFP levels from baseline) with temsirolimus
- Pharmacokinetics [ Designated as safety issue: No ]Pharmacokinetics will be assessed: AUC pre-dose, 1, 3, 24,48, 72 and 162 hours post dose.
- Circulating tumor cells levels [ Designated as safety issue: No ]Feasibility and utility of circulating tumor cells in this patient population
| Estimated Enrollment: | 25 |
| Study Start Date: | February 2010 |
| Estimated Study Completion Date: | March 2013 |
| Estimated Primary Completion Date: | December 2012 (Final data collection date for primary outcome measure) |
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Drug: Temsirolimus
Currently, no standard therapy exists for patients who progress on sorafenib. mTOR signaling is often up-regulated in HCC promoting cell growth and survival. This process is inhibited by rapamycin, a specific inhibitor of mTOR. Temsirolimus, a rapamycin analog, may delay tumor progression by inhibiting mTOR in HCC.Intervention: Temsirolimus IV
Eligible patients will receive temsirolimus IV on days 1,8,15 every 21 days. Treatment will continue till disease progression or untolerable side effects
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Patients must have advanced unresectable or metastatic hepatocellular carcinoma (HCC). Prior diagnosis of HCC could have been established histologically or based on one of the following criteria:
- Liver mass > 2cm: Characteristic enhancement on at least one imaging technique(triphasic CT scan, MRI, or contrast enhanced ultrasound) or AFP > 200 ng/ml.
- Liver mass between 1 and 2 cm: Characteristic enhancement on two imaging techniques.Diagnosis of HCC must have been confirmed by biopsy if non-characteristic enhancement on imaging.
- All patients must have received exactly one prior systemic therapy (cytotoxic chemotherapy or targeted therapies) and must not be eligible for further locoregional treatment modalities.
- All patients must have measurable disease per RECIST criteria.
- Patients with previous locoregional therapies, including but not limited to radio-frequency ablation, cryoablation, percutaneous ethanol injection, chemo-embolization, hepatic artery embolization, and hepatic artery infused FUDR, stereotactic radiotherapy are eligible provided they have documented progression of their disease or have measurable extrahepatic disease.
- Patients must have an ECOG performance status of 0 - 2 (see Appendix B).
- Patients must be greater than or equal to 18 years of age.
- Patients with Child-Pugh class A (score of 5-6) or class B (score of 7-9) are eligible.
Patients must have adequate organ function as defined by:
- AST, ALT and Alkaline phosphatase ≤ 5x upper limit of normal (ULN)
- Total Bilirubin < 2 mg/dl.
- Creatinine clearance ≥ 15ml/min & patients must not be dialysis dependent.
Patients must have adequate bone marrow function as defined by:
- Leukocytes ≥ 2000 / mm3 or absolute neutrophil count (ANC) ≥ 1000 / mm3
- Platelet count ≥ 75000 / mm3
- Pregnant and nursing women will be excluded from this study. All patients of reproductive potential must agree to use adequate birth control measures to be eligible for study enrollment.
- Prior palliative radiotherapy is permissible provided it has been completed at least 2 weeks prior to study entry and the patient has recovered from any radiation-related side effects.
- Patients must not be receiving any other investigational agents or other anti-cancer therapies. At least 28 days must have elapsed since completion of previous systemic therapy prior to study entry and the patient should have recovered from all toxicities related to prior therapy.
- Patients must not have a history of other malignancies that are active and require therapy (other than non-melanoma skin cancers).
Exclusion Criteria:
- Patients with prior treatment with any mTOR inhibitor are not eligible.
- Patients with a history of an uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris,cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements are not eligible.
- Patients taking cytochrome P450 enzyme-inducers or inhibitors are not eligible.
- Patients with a known history of HIV infection are not eligible.
- Patients with uncontrolled hyperlipidemia or hypercholesterolemia are not eligible (fasting serum cholesterol > 350 mg/dL or fasting serum triglycerides > 400 mg/dL).
- Patients with a known history or clinical evidence of CNS metastases are not eligible.
- Patients who, in the best judgment of the investigator, will not be able to comply with the requirements of the protocol are not eligible.
Patients with Child-Pugh class C liver disease are not eligible.
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Contacts and Locations| Contact: Steve West, BS, CCRP | 901.226.1493 | steve.west@bmhcc.org |
| United States, Tennessee | |
| Boston Baskin Cancer Foundation | Recruiting |
| Memphis, Tennessee, United States, 38120 | |
| Principal Investigator: | Jasgit Sachdev, MD | University of Tennessee Cancer Institute |
More Information
No publications provided
| Responsible Party: | University of Tennessee Cancer Institute |
| ClinicalTrials.gov Identifier: | NCT01567930 History of Changes |
| Other Study ID Numbers: | 3066K1‐2247 |
| Study First Received: | February 1, 2012 |
| Last Updated: | December 13, 2012 |
| Health Authority: | United States: Food and Drug Administration |
Keywords provided by University of Tennessee Cancer Institute:
|
Temsirolimus HCC Advanced hepatocellular carcinoma |
Additional relevant MeSH terms:
|
Carcinoma Carcinoma, Hepatocellular Neoplasms, Glandular and Epithelial Neoplasms by Histologic Type Neoplasms Adenocarcinoma Liver Neoplasms Digestive System Neoplasms Neoplasms by Site Digestive System Diseases Liver Diseases Sirolimus |
Everolimus Antibiotics, Antineoplastic Antineoplastic Agents Therapeutic Uses Pharmacologic Actions Antifungal Agents Anti-Infective Agents Immunosuppressive Agents Immunologic Factors Physiological Effects of Drugs Anti-Bacterial Agents |
ClinicalTrials.gov processed this record on May 19, 2013