CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 33 enrolled
Drug / intervention
Aldesleukin +7 moredrug
Likely dose
Aldesleukin 720,000 IUfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01993719
NCT01993719Phase 2Completed

A Phase II Study for Metastatic Melanoma Using High-Dose Chemotherapy Preparative Regimen Followed by Cell Transfer Therapy Using Tumor-Infiltrating Lymphocytes Plus IL-2 With the Administration of Pembrolizumab in the Retreatment Arm

National Cancer Institute (NCI)·interventional·Posted Nov 25, 2013·Updated Jan 18, 2023

In Brief

A Phase 2 clinical trial evaluating Aldesleukin, Fludarabine, and 3 other interventions for Metastatic Melanoma. Completed, enrolled 33 participants across 1 site.

Detailed Summary

Background: * The National Cancer Institute (NCI) Surgery Branch has developed an experimental therapy that involves taking white blood cells from patients' tumors, growing them in the laboratory in large numbers, and then giving the cells back to the patient. These cells are called Tumor Infiltrating Lymphocytes, or TIL and we have given this type of treatment to over 400 patients with melanoma. * In this trial, we are determining if there is a difference in the response between patients who have received prior anti-programmed cell death-1 (PD-1) treatment to those who have not received this prior ant-PD1 treatment. Objectives: \- To determine if there is a difference in the rate of response between patients who have received prior anti-PD1 and those who have not. Eligibility: \- Individuals at least 18 years and less than or equal to 70 years of age who have metastatic melanoma. Design: * Work up stage: Participants will be screened with a physical exam and medical history. Blood and urine samples will be collected. * Surgery: Surgery or biopsy will be performed to obtain tumor from which to grow white blood cells. White blood cells will be grown from the tumor in the laboratory. * Leukapheresis: Participants will have leukapheresis to collect additional white blood cells. (Leukapheresis is a common procedure which removes only the white blood cells from the patient.) * Treatment: Participants will receive standard dose chemotherapy to prepare their immune system to accept the white blood cells. Participants will receive an infusion of their own white blood cells grown from tumor. They will also receive aldesleukin for up to five days to boost the immune system s response to the white blood cells. They will stay in the hospital for about 4 weeks for the treatment. * Follow up: Patients will return to the clinic for a physical exam, review of side effects, lab tests, and scans about every 1-3 months for the first year, and then every 6 months to 1 year as long as their tumors are shrinking. Follow up visits take up to 2 days.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 2CompletedFinished
2014201520162017201820192020202120222023202420252026
First PostedNov 25, 2013
Enrollment StartDec 12, 2013
Primary CompletionOct 14, 2021
Study CompletionJul 6, 2022
TodayJul 2, 2026
Enrollment to primary: 7.8 yearsPosted 12.6 years ago

Interventions

Aldesleukindrug

720,000 IU/kg intravenous (IV) every eight hours (+/- 1 hour) beginning within 24 hours of cell infusion and continuing for up to 4 days (maximum 12 doses).

Fludarabinedrug

25 mg/m\^2/day intravenous piggy-back (IVPB) daily for 5 days

Fludarabinedrug

30 mg/kg/day intravenous piggy-back (IVPB) daily for 3 days.

Cyclophosphamidedrug

60 mg/kg/day X 2 days intravenous (IV)

Cyclophosphamidedrug

Days -5 to -3 (low-dose arm):30 mg/kg IV over 60 minutes for 2 days

Cyclophosphamidedrug

Days -5 to -3 (low-dose arm): 300 mg/m\^2 IV over 60 minutes.

Young TILbiological

Day 0: Cells will be infused intravenously (IV)

Pembrolizumabdrug

2 mg/kg intravenous (IV) on Days -2, 21 (+/- 2 days), 42 (+/- 2 days), and 63 (+/- 2 days).