Adoptive T Cell Therapy in Patients With Recurrent Ovarian Cancer

Ovarian Cancer Recurrent Clinical Trial

— OVACURE  

Official title:

Adoptive T Cell Therapy in Patients With Recurrent Ovarian Cancer

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04072263
• Other study ID #: OVACURE
• Status: Recruiting
• Phase: Phase 1/Phase 2
• Start date: August 1, 2018
• Est. completion date: December 1, 2021

Study information

• Verified date: March 2021
• Source: Leiden University Medical Center
• Contact: Judith Kroep, MD, PhD
• Phone: 0031715263464
• Email: j.r.kroep[@]lumc.nl
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The clinical benefit of standard treatment for patients with epithelial ovarian cancer (EOC) are poor. Ovarian cancer is a highly immunogenic tumor and good survival is tightly linked to the presence of tumor-infiltrating CD8+ T cells and the absence of immunosuppressive immune cells. This clear correlation between T cell infiltration and disease progression suggests that EOC may be sensitive to adoptive cell therapy by infusion of ex-vivo expanded autologous Tumor Infiltrating Lymphocytes (TIL) provided that immune suppression is reduced. Carboplatin+paclitaxel chemotherapy is directly killing tumor cells but was also shown to alleviate immunosuppression for 2 weeks coinciding with enhanced T-cell immunity, potentially creating a window of opportunity for T-cell based immunotherapy.

In addition, there is evidence that interferon alpha (IFNα) not only may work as a low toxic preconditioning regimens that creates the space required for the infused TIL but that it also supports the TIL by sustaining their persistence and indirectly their function, by upregulation of HLA class I on tumor cells and decreasing the numbers of regulatory T cells. Based on this we hypothesize that a synergistic clinical effect may be obtained when adoptive cell therapy with autologous TIL is administered during treatment with chemotherapy and IFNα. The feasibility and safety of TIL administration is studied in the window of opportunity created by carboplatin-paclitaxel chemotherapy with or without interferon alpha (IFNα). Furthermore, exploratory studies will be performed to analyze and confirm the proposed underlying mechanisms.

Tumor material for TIL production will be collected during first line debulking surgery in case of FIGO stage IIIC/IV disease (pre-OVACURE) or in case of recurrent platinum sensitive disease an extra biopsy can be planned (OVACURE).

Description:

Study the feasibility and safety of TIL administration in the window of opportunity created by carboplatin-paclitaxel chemotherapy with or without interferon alpha (IFNα). Furthermore, exploratory studies will be performed to analyze and confirm the proposed underlying mechanisms.

Intervention:

Cohort 1

• Carboplatin-paclitaxel day1, q3 weeks, 6x, plus

• TIL starting 14 days after the 2nd chemotherapy cycle, q3 weeks, 3x.

Cohort 2

• Carboplatin-paclitaxel day1, q3 weeks, 6x, plus

• TIL starting 14 days after the 2nd chemotherapy cycle, q3 weeks, 3x, plus

• IFNα (3x10e6 U daily) starting one week before the first TIL infusion for 12 weeks in total.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 12
• Est. completion date: December 1, 2021
• Est. primary completion date: August 1, 2021
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Age = 18 years.

• Histologically proven epithelial ovarian cancer (EOC).

• Recurrent ovarian cancer amenable to carboplatin and paclitaxel chemotherapy. Patient with primary stage III or IV EOC can participate in the pre-OVACURE to collect rest tumor during debulking surgery for TILs preservation, so TILs will be available in case of recurrent disease will develop in the future.

• Presence of measurable progressive disease according to RECIST version 1.1 or elevated CA125 = 2 times the upper normal limit (UNL) within 3 months and confirmed.

• Expected survival of at least 3 months.

• WHO performance status 0-2.

• Within the last 2 weeks prior to study day 0, vital laboratory parameters should be within normal range, except for the following laboratory parameters, which should be within the ranges specified:

Lab Parameter Range Hemoglobin = 6,0 mmol/l Granulocytes = 1,500/µl Lymphocytes = 700/µl Platelets = 100,000/µl Creatinine clearance = 50 min/ml Serum bilirubin = 40 mol/l ASAT and ALAT = 5 times the normal upper limit LDH = 2 times the normal upper limit

• Viral tests:

• Negative for HIV type 1/2, HTLV and TPHA

• No HBV (hepatitis B virus) antigen or antibodies against HBc in the serum

• No antibodies against HCV (hepatitis C virus) in the serum

• Able and willing to give valid written informed consent.

• Prior treatment, including immunotherapy e.g. with anti-PD(L)1, is allowed but systemic therapy and radiotherapy must have been discontinued for at least two weeks before study entry.

• Patients should have disease progression.

Exclusion Criteria:

• Patients with brain metastases.

• Clinically significant heart disease (NYHA Class III or IV).

• Other serious acute or chronic illnesses, e.g. active infections requiring antibiotics, bleeding disorders, or other conditions requiring concurrent medications not allowed during this study.

• Active immunodeficiency disease or autoimmune disease requiring immune suppressive drugs. Vitiligo is not an exclusion criterion.

• Other malignancy within 2 years prior to entry into the study, except for treated non-melanoma skin cancer and in situ cervical or vulva carcinoma.

• Mental impairment that may compromise the ability to give informed consent and comply with the requirements of the study.

• Lack of availability for follow-up assessments.

• Pregnancy or breastfeeding.

Related Conditions & MeSH terms

• Carcinoma, Ovarian Epithelial
• Ovarian Cancer Recurrent
• Ovarian Neoplasms

Intervention

Biological:
• Tumor Infiltrating Lymphocytes (TIL)
Adoptive cell therapy using Tumor-Infiltrating Lymphocytes (TIL) i.v.

Drug:
• Interferon Alfa 2A
Interferon alpha (IFNa) s.c., may work as a low toxic preconditioning regimens that creates the space required for the infused TIL but that it also supports the TIL by sustaining their persistence and indirectly their function, by upregulation of HLA class I on tumor cells and decreasing the numbers of regulatory T cells.
• Carboplatin
chemotherapy i.v.
• Paclitaxel
Chemotherapy i.v.

Locations

Country	Name	City	State
Netherlands	Leiden University Medical Center	Leiden	ZH

Sponsors (1)

Lead Sponsor	Collaborator
Leiden University Medical Center

Country where clinical trial is conducted

Netherlands, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	NCI CTC criteria	If a DLT occurs in more than one out of the three patients, the study will be stopped. If < 1 out of 3 patients have a DLT, then three additional patients will be treated. Therefore, a minimum of 3 and a maximum of 6 patients will be treated in both cohorts.	3 years
Secondary	Clinical Response	Clinical response according to RECIST 1.1 criteria and immune response criteria (irRC)	3 years
Secondary	Disease Control rate	Disease control rate (DCR: CR+PR+SD) at 6 months	3 years
Secondary	Progression free survival (PFS)	Progression free survival (PFS) is defined as: the duration from the time of start chemotherapy until first observation of radiologically confirmed progressive disease or death due to any cause, whichever occurred first.	3 years
Secondary	Overall Survival (OS)	Overall Survival (OS) is defined as: the duration from the time of start of chemotherapy until death from any cause.	3 years