Aldesleukin With or Without Ziv-Aflibercept in Treating Patients With Stage III-IV Melanoma That Cannot Be Removed By Surgery
This randomized phase II clinical trial studies how well aldesleukin with or without ziv-aflibercept works in treating patients with stage III-IV melanoma that cannot be removed by surgery. Aldesleukin may stimulate the white blood cells to kill cancer. Ziv-aflibercept may stop the growth of melanoma by blocking blood flow to the tumor. It is not yet known whether aldesleukin is more effective with or without ziv-aflibercept in treating melanoma.
Stage IIIA Melanoma
Stage IIIB Melanoma
Stage IIIC Melanoma
Stage IV Melanoma
Other: laboratory biomarker analysis
|Study Design:||Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
|Official Title:||A Randomized Phase II Study of Sequential Biotherapy With Aflibercept and High Dose IL-2 Versus High Dose IL-2 Alone in Patients With Inoperable Stage III or Stage IV Melanoma: Efficacy and Biomarker Study|
- Progression-free survival [ Time Frame: The time from the date of randomization until date of progression, death, or recurrence, assessed up to 5 years ] [ Designated as safety issue: No ]The primary comparison will be based on the log-rank test for comparison of progression-free survival, which will be estimated by the Kaplan-Meier method. Cox regression will also be conducted for progression-free survival.
- Overall survival [ Time Frame: Up to 5 years ] [ Designated as safety issue: No ]Cox regression will be conducted for survival. Survival endpoints will be evaluated from data of randomization and will be also reported on the as-treated populations for comparison.
- 1-year survival [ Time Frame: 1 year ] [ Designated as safety issue: No ]Cox regression will be conducted for survival.
- Response rate, evaluated using the RECIST v1.1 [ Time Frame: Up to 5 years ] [ Designated as safety issue: No ]Response rate will be estimated and a 95% confidence interval (CI) provided for each arm.
- Incidence of adverse events, graded according to National Cancer Institute Common Terminology Criteria for Adverse Events version 4.0 [ Time Frame: Up to 5 years ] [ Designated as safety issue: Yes ]Toxicity will be primarily be evaluated by examining the number of doses of aldesleukin administered during the first course of combination therapy; the percentage of patients who receive all 56 doses will also be summarized. The toxicity after the scheduled 10th dose of aldesleukin, the frequency of grade III and IV toxicities, and unusual toxicities will also be summarized.
- Changes in VEGF levels [ Time Frame: Baseline up to 5 years ] [ Designated as safety issue: No ]Explored using multivariate Cox regression.
|Study Start Date:||January 2011|
|Estimated Primary Completion Date:||December 2014 (Final data collection date for primary outcome measure)|
Experimental: Arm I (ziv-aflibercept and aldesleukin)
Patients receive ziv-aflibercept IV over at least 1 hour in weeks 1, 3, 5, and 7 (and in week 9 of course 1 only) and high-dose aldesleukin IV over 15 minutes every 8 hours for 5 days in weeks 1 and 3 (and in weeks 3 and 5 of course 1 only). Treatment repeats every 8 weeks for 3 courses in the absence of disease progression or unacceptable toxicity. Patients then receive maintenance therapy comprising ziv-aflibercept IV on day 1. Courses repeat every 14 days in the absence of disease progression or unacceptable toxicity.
Other Names:Biological: aldesleukin
Other Names:Other: laboratory biomarker analysis
Experimental: Arm II (aldesleukin)
Patients receive high-dose aldesleukin IV over 15 minutes every 8 hours for 5 days in weeks 1 and 3. Treatment repeats every 4 weeks for up to 3 courses in the absence of disease progression or unacceptable toxicity.
Other Names:Other: laboratory biomarker analysis
I. Test the hypothesis that combination biotherapy with aflibercept (ziv-aflibercept) and high-dose (HD) interleukin (IL)-2 (aldesleukin) will improve the progression-free survival compared to HD IL-2 alone.
I. Evaluate the response rate (complete response [CR] + partial response [PR]) of aflibercept and HD IL-2 as assessed by Response Evaluation Criteria In Solid Tumors (RECIST) criteria version 1.1 and compare to results of HD IL-2 alone.
II. Evaluate the toxicities and tolerance of combination biotherapy with aflibercept and HD IL-2 and maintenance aflibercept alone in this patient population and compare to HD-IL2 alone.
III. Test the hypotheses related to the laboratory correlative studies. IV. Evaluate the overall survival of patients treated with aflibercept and HD IL-2 and HD IL-2 alone.
OUTLINE: Patients are randomized to 1 of 2 treatment arms.
ARM I: Patients receive ziv-aflibercept intravenously (IV) over at least 1 hour on day 1 of weeks 1, 3, 5, and 7 (and in week 9 of course 1 only) and high-dose aldesleukin IV over 15 minutes every 8 hours for 5 days in weeks 1 and 3 (and in weeks 3 and 5 of course 1 only). Treatment repeats every 8 weeks for 3 courses in the absence of disease progression or unacceptable toxicity. Patients then receive maintenance therapy comprising ziv-aflibercept IV on day 1. Courses repeat every 14 days in the absence of disease progression or unacceptable toxicity.
ARM II: Patients receive high-dose aldesleukin IV over 15 minutes every 8 hours for 5 days in weeks 1 and 3. Treatment repeats every 4 weeks for up to 3 courses in the absence of disease progression or unacceptable toxicity.
After completion of study treatment, patients are followed up every 3-4 months for 5 years.
Please refer to this study by its ClinicalTrials.gov identifier: NCT01258855
|United States, California|
|City of Hope Medical Center||Recruiting|
|Duarte, California, United States, 91010|
|Contact: Sanjay Awasthi 626-359-8111ext69200 email@example.com|
|Principal Investigator: Sanjay Awasthi|
|University of Southern California/Norris Cancer Center||Recruiting|
|Los Angeles, California, United States, 90033|
|Contact: Heinz-Josef Lenz 323-865-3955 firstname.lastname@example.org|
|Principal Investigator: Heinz-Josef Lenz|
|City of Hope Medical Group Inc||Recruiting|
|Pasadena, California, United States, 91105|
|Contact: Stephen C. Koehler 626-396-2900 Skhehler@cohmg.com|
|Principal Investigator: Stephen C. Koehler|
|University of California at Davis Cancer Center||Recruiting|
|Sacramento, California, United States, 95817|
|Contact: Scott D. Christensen 916-734-3772 email@example.com|
|Principal Investigator: Scott D. Christensen|
|United States, Colorado|
|University of Colorado Cancer Center - Anschutz Cancer Pavilion||Recruiting|
|Aurora, Colorado, United States, 80045|
|Contact: Karl D. Lewis 720-848-0584 firstname.lastname@example.org|
|Principal Investigator: Karl D. Lewis|
|United States, Georgia|
|Emory University/Winship Cancer Institute||Recruiting|
|Atlanta, Georgia, United States, 30322|
|Contact: David H. Lawson 404-778-1900 email@example.com|
|Principal Investigator: David H. Lawson|
|United States, Illinois|
|Robert H. Lurie Comprehensive Cancer Center||Recruiting|
|Chicago, Illinois, United States, 60611|
|Contact: Timothy M. Kuzel 312-695-4518 firstname.lastname@example.org|
|Principal Investigator: Timothy M. Kuzel|
|United States, Indiana|
|Indiana University Health||Recruiting|
|Indianapolis, Indiana, United States, 46206|
|Contact: Theodore F. Logan 317-948-7576 email@example.com|
|Principal Investigator: Theodore F. Logan|
|United States, Michigan|
|Barbara Ann Karmanos Cancer Institute||Recruiting|
|Detroit, Michigan, United States, 48201|
|Contact: Lawrence E. Flaherty 313-576-8725 firstname.lastname@example.org|
|Principal Investigator: Lawrence E. Flaherty|
|United States, Minnesota|
|Saint Louis Park, Minnesota, United States, 55416|
|Contact: Patrick J. Flynn 612-863-8585 email@example.com|
|Principal Investigator: Patrick J. Flynn|
|United States, New Hampshire|
|Dartmouth Hitchcock Medical Center||Recruiting|
|Lebanon, New Hampshire, United States, 03756|
|Contact: Marc S. Ernstoff 603-650-5534 firstname.lastname@example.org|
|Principal Investigator: Marc S. Ernstoff|
|United States, New York|
|Roswell Park Cancer Institute||Recruiting|
|Buffalo, New York, United States, 14263|
|Contact: Nikhil I. Khushalani 716-845-3099 Nikhil.Khushalani@RoswellPark.org|
|Principal Investigator: Nikhil I. Khushalani|
|United States, Ohio|
|University Hospitals Case Medical Center||Recruiting|
|Cleveland, Ohio, United States, 44106|
|Contact: Henry B. Koon 216-368-1175 Henry.Koon@UHhospitals.org|
|Principal Investigator: Henry B. Koon|
|Ohio State University||Recruiting|
|Columbus, Ohio, United States, 43210|
|Contact: Thomas E. Olencki 614-293-4680 Thomas.Olencki@osumc.edu|
|Principal Investigator: Thomas E. Olencki|
|United States, Pennsylvania|
|Penn State Milton S Hershey Medical Center||Recruiting|
|Hershey, Pennsylvania, United States, 17033-0850|
|Contact: Chandra P. Belani 717-531-1078 email@example.com|
|Principal Investigator: Chandra P. Belani|
|University of Pittsburgh||Recruiting|
|Pittsburgh, Pennsylvania, United States, 15232|
|Contact: Ahmad A. Tarhini 412-648-6507 firstname.lastname@example.org|
|Principal Investigator: Ahmad A. Tarhini|
|United States, Tennessee|
|Vanderbilt University Medical Center||Recruiting|
|Nashville, Tennessee, United States, 37240|
|Contact: Igor Puzanov 615-936-6938 email@example.com|
|Principal Investigator: Igor Puzanov|
|United States, Virginia|
|University of Virginia||Recruiting|
|Charlottesville, Virginia, United States, 22908|
|Contact: Geoffrey R. Weiss 434-243-0066 firstname.lastname@example.org|
|Principal Investigator: Geoffrey R. Weiss|
|Principal Investigator:||Ahmad Tarhini||Beckman Research Institute|