CI

At a glance

ClinicalIndex Comparison Record
Phase 2Recruiting· 332 target
Drug / intervention
Pembrolizumab (Keytruda) +4 moredrug
Likely dose
Pembrolizumab (Keytruda) 2mg/kgfrom record
Key inclusion· 9
  • Measurable metastatic cancer of specified types including colorectal, pancreatic, ovarian, breast, or endocrine/neuroendocrine tumors
  • At least one resectable lesion for TIL generation with minimal morbidity
  • Refractory to approved standard systemic therapy
  • Colorectal cancer patients must have received oxaliplatin or irinotecan
Key exclusion· 11
  • Pregnant or nursing
  • Concurrent systemic steroid therapy
  • Active systemic infections requiring anti-infective treatment, coagulation disorders, or active uncompensated major medical illnesses
  • Any form of primary immunodeficiency including SCID and AIDS

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

Search/NCT01174121
NCT01174121Phase 2RecruitingOn Track
Long Recruiting

A Phase II Study Using Short-Term Cultured, Autologous Tumor-Infiltrating Lymphocytes Following a Lymphodepleting Regimen in Metastatic Cancers Plus the Administration of Pembrolizumab

National Cancer Institute (NCI)·interventional·Posted Aug 3, 2010·Updated Jun 11, 2026

In Brief

A Phase 2 clinical trial evaluating Pembrolizumab (Keytruda), Fludarabine, and 3 other interventions for Metastatic Colorectal Cancer and 4 related conditions. Currently recruiting, targeting 332 participants across 1 site.

Detailed Summary

Background: The 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 200 patients with melanoma. Researchers want to know if TIL shrink s tumors in people with digestive tract, urothelial, breast, or ovarian/endometrial cancers. In this study, we are selecting a specific subset of white blood cells from the tumor that we think are the most effective in fighting tumors and will use only these cells in making the tumor fighting cells. Objective: The purpose of this study is to see if these specifically selected tumor fighting cells can cause digestive tract, urothelial, breast, or ovarian/endometrial tumors to shrink and to see if this treatment is safe. Eligibility: \- Adults age 18-72 with upper or lower gastrointestinal, hepatobiliary, genitourinary, breast, ovarian/endometrial cancer, or glioblastoma refractory to standard chemotherapy. Design: Work up stage: Patients will be seen as an outpatient at the NIH clinical Center and undergo a history and physical examination, scans, x-rays, lab tests, and other tests as needed. Surgery: If the patients meet all of the requirements for the study they will undergo surgery to remove a tumor that can be used to grow the TIL product. Leukapheresis: Patients may undergo leukapheresis to obtain additional white blood cells. (Leukapheresis is a common procedure, which removes only the white blood cells from the patient.) Treatment: Once their cells have grown, the patients will be admitted to the hospital for the conditioning chemotherapy, the TIL cells and aldesleukin. 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 will take up to 2 days.

Study Details

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

Timeline

Phase 2Recruiting
20112012201320142015201620172018201920202021202220232024202520262027202820292030
First PostedAug 3, 2010
Enrollment StartAug 26, 2010
Primary CompletionDec 27, 2028
Study CompletionDec 27, 2029
TodayJul 1, 2026
Enrollment to primary: 18.3 yearsPosted 15.9 years agoPrimary completion in 2.5 years

Arms & Interventions

1/CD8+ Enriched TIL (CLOSED)experimental

Non-myeloablative, lymphodepleting preparative regimen of cyclophosphamide and fludarabine + young CD8+ enriched TIL + high-dose aldesleukin (CLOSED)

Drug: FludarabineDrug: CyclophosphamideDrug: AldesleukinBiological: Young TIL
2/Unselected TIL (CLOSED)experimental

Non-myeloablative, lymphodepleting preparative regimen of cyclophosphamide and fludarabine + young unselected TIL + high-dose aldesleukin (CLOSED)

Drug: FludarabineDrug: CyclophosphamideDrug: AldesleukinBiological: Young TIL
3/Unselected TIL + Pembro Prior to Cellsexperimental

Non-myeloablative, lymphodepleting preparative regimen of cyclophosphamide and fludarabine + young unselected TIL + high-dose aldesleukin + pembrolizumab prior to cell administration and 3 additional doses every 3 weeks following cell infusion

Drug: Pembrolizumab (Keytruda)Drug: FludarabineDrug: CyclophosphamideDrug: AldesleukinBiological: Young TIL
4/Unselected TIL + Pembro at PODexperimental

Non-myeloablative, lymphodepleting preparative regimen of cyclophosphamide and fludarabine + young unselected TIL + high-dose aldesleukin + pembrolizumab within 4 weeks of progressive disease for up to 8 doses every 3 weeks

Drug: Pembrolizumab (Keytruda)Drug: FludarabineDrug: CyclophosphamideDrug: AldesleukinBiological: Young TIL
5/Unselected TIL + Pembro Prior to Cellsexperimental

Non-myeloablative, lymphodepleting preparative regimen of cyclophosphamide and fludarabine + young unselected TIL + high-dose aldesleukin + pembrolizumab prior to cell administration and 3 additional doses every 3 weeks following cell infusion

Drug: Pembrolizumab (Keytruda)Drug: FludarabineDrug: CyclophosphamideDrug: AldesleukinBiological: Young TIL

Interventions

Pembrolizumab (Keytruda)drug

Arm 3 or 5: Pembrolizumab 2mg/kg IV over approximately 30 minutes on Days -2, 21, 42, and 63 Arm 4: Pembrolizumab 2mg/kg IV over approximately 30 minutes (for patients who meet progressive disease per RECIST criteria and have resolved major toxicities after cell infusion or anytime during the post-treatment evaluation period; starting within 4 weeks of progression; may receive up to 8 doses every 3 weeks).

Fludarabinedrug

Days -7 to -3: Fludarabine 25 mg/m2/day IVPB daily over 30 minutes for 5 days.

Cyclophosphamidedrug

Days -7 and -6: Cyclophosphamide 60 mg/kg/day X 2 days IV in 250 ml D5W with Mesna 15 mg/kg/day X2 days over 1 hr.

Aldesleukindrug

Aldesleukin 720,000 IU/kg IV (based on total body weight) over 15 minutes every eight hours (+/- 1 hour) beginning within 24 hours of cell infusion and continuing for up to 4 days (maximum 12 doses.)

Young TILbiological

Day 0: Cells will be infused intravenously (IV) on the Patient Care Unit over 20-30 minutes (one to four days after the last dose of fludarabine).