Adoptive Tumor-infiltrating Lymphocyte Transfer With Nivolumab for Melanoma

Advanced Melanoma Clinical Trial

— BaseTIL  

Official title:

A Phase I Study of Adoptive Tumor-infiltrating Lymphocyte Transfer in Combination With Nivolumab in Patients With Advanced Melanoma

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04165967
• Other study ID #: 2019-01908; me18Laeubli
• Status: Completed
• Phase: Phase 1
• Start date: September 17, 2020
• Est. completion date: March 30, 2023

Study information

• Verified date: August 2023
• Source: University Hospital, Basel, Switzerland
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study is to investigate safety and feasibility of a combination therapy of a tumor infiltrating lymphocytes (TIL) transfer with anti-programmed cell death protein (PD)-1 therapy in patients with metastatic melanoma that failed immunotherapy.Tumor-infiltrating lymphocytes will be expanded from resected melanoma samples from the patient and expanded TILs will be transferred to the patient after non-myeloablative chemotherapy with cyclophosphamide and fludarabine. TIL transfer will be combined with low dose Interleukin (IL)-2 and nivolumab anti-PD-1 treatment.

The study uses a personalized Investigational Medicinal Product (IMP), i.e. TIL product and in combination with IL-2 treatment and nivolumab.

Description:

Adoptive cell therapy has been previously shown to be an effective treatment option for patients with melanoma. Due to an immunosuppressive microenvironment, not all patients respond to this therapy. In this trial, the immune suppressive microenvironment will be targeted by adding a PD-1 blocking antibody in combination with a TIL Transfer. Tumor-infiltrating lymphocytes will be expanded from resected melanoma samples from the patient and expanded TILs will be transferred to the patient after non-myeloablative chemotherapy with cyclophosphamide and fludarabine. TIL transfer will be combined with low dose IL-2 and nivolumab anti-PD-1 treatment. The study uses a personalized IMP, i.e. TIL product and in combination with IL-2 treatment and nivolumab.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 9
• Est. completion date: March 30, 2023
• Est. primary completion date: March 30, 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

• Histologically confirmed unresectable or metastatic melanoma

• At least 1 PD-1 targeted immunotherapy and BRAF inhibition in case of BRAF mutated melanoma

• Resectable tumor mass and measurable disease by CT or MRI per RECIST 1.1 criteria (in addition to the resected lesion)

• World Health Organization (WHO) clinical performance Status (ECOG) 0-1

• Adequate organ function

• Patients of both genders must be willing to practice a highly effective method of birth control during treatment and for five months after receiving the last dose of nivolumab for women and seven months for men

• Patients must be able to understand and sign the Informed consent document

• Hematology: Absolute neutrophil count greater than 1.5 x 109/L without support of filgrastim. Platelet count greater than 100 x 109/L. Hemoglobin greater than 5 mmol/L, or 80 g/L.

• Chemistry: Serum alanine aminotransferase (ALAT)/ aspartate transaminase (ASAT) less than 3 times the upper limit of normal, unless patients have liver metastases (< 5 times ULN). Serum creatinine clearance 50 ml/min or higher. Total Bilirubin less than or equal to 20 micromol/L, except in patients with Gilbert's Syndrome who must have a total bilirubin less than 50 micromol/L. Lactate dehydrogenase (LDH) = 2x ULN

• Serology: Seronegative for HIV antibody. Seronegative for hepatitis B antigen, and hepatitis C antibody. Seronegative for syphilis.

Exclusion Criteria:

• Life expectancy of less than three months

• Patients with metastatic ocular/ mucosal or other non-cutaneous melanoma.

• Requirement for immunosuppressive doses of systemic corticosteroids (>10 mg/day prednisone or equivalent) or other immunosuppressive drugs within the last 3 weeks prior to randomization

• Uncontrolled central nervous system (CNS) metastases. Controlled CNS metastases must be for at least 4 weeks stable.

• Documented Forced expiratory volume at one second (FEV1) less than or equal to 50% predicted for patients with:

• A prolonged history of cigarette smoking (greater than 20 pack/year within the past 2 years)

• Symptoms of respiratory distress

• All patients' toxicities due to prior non-systemic treatment must have recovered to a grade 1 or less. Patients may have undergone minor surgical procedures or focal palliative radiotherapy (to non-target lesions) within the past 4 weeks, as long as all toxicities have recovered to grade 1 or less.

• Women who are pregnant or breastfeeding, because of the potentially dangerous effects of the preparative chemotherapy on the fetus or infant.

• Any active systemic infections, coagulation disorders or other active major medical illnesses.

• Contraindication for IL-2 or nivolumab (allergies etc.).

• Any autoimmune disease: patients with a documented history of inflammatory bowel disease, including ulcerative colitis and Crohn's disease are excluded from this study as are patients with a history of symptomatic disease (e.g., rheumatoid arthritis, autoimmune thyroiditis (e.g. Hashimoto's disease), autoimmune hepatitis, systemic progressive sclerosis (scleroderma), Systemic Lupus Erythematosus, autoimmune vasculitis (e.g., Wegener's Granulomatosis). Subjects with motor neuropathy considered of autoimmune origin (e.g., Guillain-Barré Syndrome) are excluded from this study. Patients with vitiligo are eligible to enter the study

Related Conditions & MeSH terms

• Advanced Melanoma
• Melanoma

Intervention

Drug:
• Combination of TIL Transfer with anti-PD-1 Therapy and low dose IL-2
The study uses a personalized IMP, i.e. TIL product and in combination with IL-2 treatment and nivolumab. Day 0: Autologous TIL: (minimum 5 x 109 and up to a maximum of 2 x 1011 lymphocytes) administered intravenously over 20 to 30 minutes. Day 0: Interleukin-2 (Proleukin): 125.000 IU/kg/day s.c. for maximum 12 days as inpatients with a 2 days break after the first 4-5 doses (maximum 10 days dosing). Actual body weight will be used in calculating the dose of interleukin-2. Starting Day 14: Nivolumab application 240 mg i.v. over 30 minutes ever 2 weeks with a maximum to 2 years, or until disease progression or inacceptable toxicity.

Locations

Country	Name	City	State
Switzerland	Division of Medical Oncology and Cancer Immunology, University Hospital Basel	Basel

Sponsors (2)

Lead Sponsor	Collaborator
University Hospital, Basel, Switzerland	GMP network of Basel

Country where clinical trial is conducted

Switzerland, 

References & Publications (33)

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* Note: There are 33 references in all — Click here to view all references

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number of Adverse Events	Number of Adverse Events to analyze safety of the combination of TIL transfer with IL-2 therapy	First 3 months during treatment
Primary	Change in body temperature (Degree Celsius)	Change in Vital signs ( body temperature) to analyze the safety of the combination of TIL transfer with IL-2 therapy	at each treatment visit (Day 0, and for maximum 12 days as inpatients with a 2 days break after the first 4-5 doses (maximum 10 days dosing)
Primary	Change in blood pressure (mmHg)	Change in Vital signs ( blood pressure) to analyze the safety of the combination of TIL transfer with IL-2 therapy	at each treatment visit (Day 0, and for maximum 12 days as inpatients with a 2 days break after the first 4-5 doses (maximum 10 days dosing)
Primary	Change in heart beat (beats/minute)	Change in Vital signs (heart beat) to analyze the safety of the combination of TIL transfer with IL-2 therapy	at each treatment visit (Day 0, and for maximum 12 days as inpatients with a 2 days break after the first 4-5 doses (maximum 10 days dosing)
Primary	Change in respiratory frequency (inspiration/minute)	Change in Vital signs (respiratory frequency) to analyze the safety of the combination of TIL transfer with IL-2 therapy	at each treatment visit (Day 0, and for maximum 12 days as inpatients with a 2 days break after the first 4-5 doses (maximum 10 days dosing)
Primary	Change in full blood Counts (number of cells)	Change in Laboratory Parameter (full blood counts) to analyze haematological toxicity	at each treatment visit (every 2 weeks) from Day 0= Baseline to week 42
Secondary	Overall Response Rate (ORR) fluorodeoxyglucose (FDG)-positron emission tomography (PET)/CT scan	Changes of Tumor volume according to RECIST 1.1	First 3 months after TIL administration
Secondary	Progression Free Survival (PFS)	Progression free survival, defined as the time between registration to progression or death whichever occurs first.	between pre-treatment and 3-months post-treatment
Secondary	Overall Survival (OS) defined as the time between registration to death due to any cause	Overall survival will be measured from the beginning of the treatment to the death of the patient or to survival status analysis acquired during the last follow up.	2 years after TIL transfer
Secondary	Tumor response according to revised Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 criteria	Tumor response according to revised Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 criteria	between pre-treatment and 3-months post-treatment
Secondary	Objective response rate (ORR)	In order to assess the objective response rate CT scans and FDG-PET/CT scans will be performed. Response will be measured by best reduction of tumor volume according to RECIST 1.1	2 years after TIL transfer
Secondary	Number of Adverse Events according to CTCAE 4.0	Overall Safety during whole treatment period analyzed by collection of Adverse Events according to CTCAE 4.0	2 years after TIL transfer
Secondary	Metabolic Response	Response measured by 18FDG-uptake	during the first 3 months after TIL transfer
Secondary	Number of Serious Adverse Events according to CTCAE 4.0	Overall Safety during whole treatment period analyzed by collection of Serious Adverse Events according to CTCAE 4.0	2 years after TIL transfer