Study of Everolimus With Paclitaxel and Carboplatin in Patients With Metastatic Melanoma
This study is ongoing, but not recruiting participants.
Sponsor:
Sarah Cannon Research Institute
Collaborator:
Novartis
Information provided by (Responsible Party):
Sarah Cannon Research Institute
ClinicalTrials.gov Identifier:
NCT01014351
First received: November 16, 2009
Last updated: March 20, 2013
Last verified: December 2012
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Purpose
Based on data demonstrating synergy between paclitaxel and mammalian target of rapamycin (mTOR) inhibition, the investigators propose that the addition of everolimus to paclitaxel with carboplatin should lead to improvements in efficacy as measured by progression-free survival and response rate.
| Condition | Intervention | Phase |
|---|---|---|
|
Metastatic Melanoma |
Drug: Paclitaxel Drug: Carboplatin Drug: Everolimus |
Phase 2 |
| Study Type: | Interventional |
| Study Design: | Endpoint Classification: Safety/Efficacy Study Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | A Phase II Study of Everolimus in Combination With Paclitaxel and Carboplatin in Patients With Metastatic Melanoma |
Resource links provided by NLM:
Further study details as provided by Sarah Cannon Research Institute:
Primary Outcome Measures:
- To evaluate the progression-free survival (PFS) of patients with metastatic melanoma treated with the combination of everolimus, paclitaxel, and carboplatin [ Time Frame: 18 months ] [ Designated as safety issue: No ]
Secondary Outcome Measures:
- To determine the response rate, disease control rate, and overall survival of patients with metastatic melanoma treated with everolimus, paclitaxel, and carboplatin [ Time Frame: 18 months ] [ Designated as safety issue: No ]
- To determine the toxicity profile of the combination of everolimus, paclitaxel, and carboplatin in this patient population [ Time Frame: 18 months ] [ Designated as safety issue: Yes ]
- To correlate immunohistochemical tissue microarray with response rates, PFS, and overall survival [ Time Frame: 18 months ] [ Designated as safety issue: No ]
| Estimated Enrollment: | 70 |
| Study Start Date: | February 2010 |
| Estimated Study Completion Date: | June 2013 |
| Estimated Primary Completion Date: | May 2013 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: Paclitaxel/Carboplatin/Everolimus
Systemic Therapy using everolimus, paclitaxel and carboplatin given during a 21-day treatment cycle
|
Drug: Paclitaxel
Paclitaxel, 175mg/m2 by IV infusion over 1-3 hours on day 1 of every 21 day cycle
Other Names:
Drug: Carboplatin
Carboplatin, AUC 6 given by IV infusion over 20-30 minutes on day 1 of every 21 day cycle
Other Names:
Drug: Everolimus
Everolimus, 5 mg by mouth (PO) once a day, continuous dosing every 21-day cycle
Other Names:
|
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- Histologically confirmed metastatic melanoma.
- Stage III or IV disease that is not amenable to resection.
- Measurable disease by Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1. If the patient has had previous radiation to the target lesion(s), there must be evidence of progression since the radiation.
- ECOG Performance Status of 0 or 1.
- Life expectancy ≥12 weeks.
- No prior cytotoxic chemotherapy or targeted therapy. Immunotherapy is allowed (i.e., interleukin-2 or interferon).
Adequate hematological function:
- absolute neutrophil count (ANC) ≥1500/µL and
- platelets ≥100,000/µL and
- hemoglobin >9 g/dL
- Adequate renal function: serum creatinine ≤2.0 mg/dL or calculated (measured) GFR ≥50 mL/min.
Adequate hepatic function:
- serum bilirubin ≤1.5 x institutional upper limit of normal (ULN);
- aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤2.5 × ULN, or ≤5 × ULN in patients with documented liver metastases.
- Normal PT, INR. Patients on coumadin anticoagulation are eligible if they are on a stable dose, with an INR in the therapeutic range.
- Fasting serum cholesterol ≤300 mg/dL OR ≤7.75 mmol/L AND fasting triglycerides ≤ 2.5 x ULN. NOTE: In case one or both of these thresholds are exceeded, the patient can be included after initiation of appropriate lipid lowering medication.
- Age ≥18 years.
- Ability to swallow whole pills.
- Patient must be accessible for treatment and follow-up.
- Patients must be able to understand the investigational nature of this study and give written informed consent prior to study entry.
Exclusion Criteria:
- Previous treatment with an mTOR inhibitor (sirolimus, temsirolimus, everolimus), paclitaxel, or carboplatin.
- Treatment with any investigational agent ≤4 weeks of protocol treatment.
- Patients currently receiving anticancer therapies or who have received anticancer therapies ≤3 weeks of the start of the study drug (including radiation therapy, immunotherapy).
- Patients, who have had a major surgery or significant traumatic injury ≤4 weeks of start of study drug or patients who have not recovered from the side effects of any major surgery (defined as requiring general anesthesia).
- Patients receiving chronic, systemic treatment with corticosteroids (dose >10 mg daily of methylprednisolone or equivalent) or other immunosuppressive agents. Topical or inhaled steroids are allowed.
- Immunization with attenuated live vaccine ≤1 week of study or anytime during study treatment period.
- Patients with active brain metastases are ineligible. Patients with treated brain metastases are eligible if (1) radiation therapy was completed ≥4 weeks prior to study entry; (2) surgery was completed ≥4 weeks prior to study entry; (3) follow-up scan shows no disease progression; and (4) patient does not require steroids.
Any severe and/or uncontrolled medical conditions or other conditions that could affect participation in the study such as:
- severely impaired lung function defined as a DLCO ≤50% of the normal predicted value and/or O2 saturation ≤88% at rest on room air.
- symptomatic congestive heart failure of New York Heart Association Class III or IV.
- unstable angina pectoris, symptomatic congestive heart failure, myocardial infarction ≤6 months of start of study drug, serious uncontrolled cardiac arrhythmia or any other clinically significant disease.
- uncontrolled diabetes as defined by fasting serum glucose >1.5 x ULN.
- active (acute or chronic) uncontrolled severe infections.
- liver disease such as cirrhosis, chronic active hepatitis or chronic persistent hepatitis.
- Active, bleeding diathesis.
- Impairment of gastrointestinal (GI) function or GI disease that may significantly alter the absorption of everolimus (e.g., ulcerative disease, uncontrolled nausea, vomiting, diarrhea, malabsorption syndrome, or small bowel resection).
- A known history of human immunodeficiency virus (HIV) seropositivity.
- Known hypersensitivity to everolimus or other rapamycins (sirolimus, temsirolimus) or to its excipients.
- Use of St. John's Wort is prohibited. Drugs or substances (e.g., grapefruits, star fruits, seville oranges, and their juices and products), known to be inhibitors or inducers of the isoenzyme CYP3A4 should be avoided. Co-administration with substrates, inducers, or inhibitors of P glycoprotein should also be avoided.
- Female patients who are pregnant or breastfeeding or adults of reproductive potential who are not using effective birth control methods. If barrier contraceptives are being used, these must be continued throughout the trial by both sexes. Hormonal contraceptives are not acceptable as a sole method of contraception. (Women of childbearing potential [WOCBP] must have a negative urine or serum pregnancy test within 7 days prior to administration of everolimus.) WOCBP should continue to use effective contraception for 8 weeks after ending everolimus treatment.
- Other malignancies within the past 3 years except for adequately treated carcinoma of the cervix or basal or squamous cell carcinomas of the skin.
- History of noncompliance to medical regimens. Patients unwilling to, or unable to, comply with the protocol.
- History of any other disease, physical examination finding, or clinical laboratory finding that gives reasonable suspicion of a disease or a condition that may render the patient at high risk for treatment complications using these agents.
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01014351
Locations
| United States, Florida | |
| Florida Cancer Specialists | |
| Fort Myers, Florida, United States, 33901 | |
| United States, Georgia | |
| Northeast Georgia Medical Center | |
| Gainesville, Georgia, United States, 30501 | |
| United States, Indiana | |
| Oncology Hematology of SW Indiana | |
| Evansville, Indiana, United States, 47630 | |
| United States, Louisiana | |
| Hematology Oncology Clinic, LLP | |
| Baton Rouge, Louisiana, United States, 70809 | |
| United States, Maryland | |
| Center for Cancer and Blood Disorders | |
| Bethesda, Maryland, United States, 20817 | |
| United States, Michigan | |
| Grand Rapids Oncology Program | |
| Grand Rapids, Michigan, United States, 49503 | |
| United States, Missouri | |
| Research Medical Center | |
| Kansas City, Missouri, United States, 64132 | |
| United States, Nebraska | |
| Nebraska Methodist Cancer Center | |
| Omaha, Nebraska, United States, 68114 | |
| United States, Ohio | |
| Oncology Hematology Care | |
| Cincinnati, Ohio, United States, 45242 | |
| United States, Tennessee | |
| Chattanooga Oncology Hematology Associates | |
| Chattanooga, Tennessee, United States, 37404 | |
| Tennessee Oncology, PLLC | |
| Nashville, Tennessee, United States, 37023 | |
| United States, Virginia | |
| Peninsula Cancer Institute | |
| Newport News, Virginia, United States, 23601 | |
Sponsors and Collaborators
Sarah Cannon Research Institute
Novartis
Investigators
| Study Chair: | John D. Hainsworth, M.D. | Sarah Cannon Research Institute |
More Information
No publications provided
| Responsible Party: | Sarah Cannon Research Institute |
| ClinicalTrials.gov Identifier: | NCT01014351 History of Changes |
| Other Study ID Numbers: | SCRI MEL 19 |
| Study First Received: | November 16, 2009 |
| Last Updated: | March 20, 2013 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by Sarah Cannon Research Institute:
|
Metastatic Melanoma Everolimus Paclitaxel Carboplatin |
Additional relevant MeSH terms:
|
Melanoma Neuroendocrine Tumors Neuroectodermal Tumors Neoplasms, Germ Cell and Embryonal Neoplasms by Histologic Type Neoplasms Neoplasms, Nerve Tissue Nevi and Melanomas Everolimus Sirolimus Carboplatin Paclitaxel Immunosuppressive Agents Immunologic Factors |
Physiological Effects of Drugs Pharmacologic Actions Antibiotics, Antineoplastic Antineoplastic Agents Therapeutic Uses Antifungal Agents Anti-Infective Agents Anti-Bacterial Agents Tubulin Modulators Antimitotic Agents Mitosis Modulators Molecular Mechanisms of Pharmacological Action Antineoplastic Agents, Phytogenic |
ClinicalTrials.gov processed this record on May 23, 2013