OncoMatch/Clinical Trials/NCT01174121
Immunotherapy Using Tumor Infiltrating Lymphocytes for Patients With Metastatic Cancer
Is NCT01174121 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies multiple treatments for metastatic colorectal cancer.
Treatment: Pembrolizumab (Keytruda) · Fludarabine · Cyclophosphamide · Aldesleukin · Young TIL — 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.
Check if I qualifyExtracted eligibility criteria
Cancer type
Colorectal Cancer
Pancreatic Cancer
Ovarian Cancer
Breast Carcinoma
Neuroendocrine Tumor
Disease stage
Metastatic disease required
Performance status
ECOG 0–1(Restricted strenuous activity)
Prior therapy
Must have received: platinum-based chemotherapy (oxaliplatin)
Patients with metastatic colorectal cancer must have received oxaliplatin or irinotecan.
Must have received: topoisomerase inhibitor (irinotecan)
Patients with metastatic colorectal cancer must have received oxaliplatin or irinotecan.
Must have received: VEGFR inhibitor (sorafenib)
Patients with hepatocellular carcinoma must have received sorafenib (Nexavar(R)), since level 1 data support a survival benefit with this agent.
Must have received: cytotoxic chemotherapy — second-line
Patients with breast and ovarian cancer must be refractory to both first- and second-line treatments and must have received at least one second-line chemotherapy regimen.
Lab requirements
Blood counts
ANC > 1000/mm^3 without filgrastim; WBC ≥ 2500/mm^3; Platelet count ≥ 80,000/mm^3; Hemoglobin > 8.0 g/dL (transfusion allowed)
Kidney function
Serum creatinine ≤ 1.5 x ULN
Liver function
Serum ALT/AST ≤ 5.0 x ULN; total bilirubin ≤ 2.0 mg/dL (Gilbert's ≤ 3.0 mg/dL)
ANC > 1000/mm^3 without the support of filgrastim; WBC ≥ 2500/mm^3; Platelet count ≥ 80,000/mm^3; Hemoglobin > 8.0 g/dL. Serum ALT/AST ≤ 5.0 x ULN; Serum creatinine ≤ 1.5 x ULN; Total bilirubin ≤ 2.0 mg/dL, except in patients with Gilbert s Syndrome, who must have a total bilirubin < 3.0 mg/dL.
Structured fields extracted by AI. May contain errors — verify against the official protocol.
US trial sites
- National Institutes of Health Clinical Center · Bethesda, Maryland
Showing up to 5 US sites. See all sites on ClinicalTrials.gov →
Could you qualify for this trial?
Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.
Check if I qualify