Cancer
Conditions
Keywords
immune therapy, TILs, Adoptive cell therapy
Brief summary
This study will perform tumor-infiltrating lymphocyte (TIL)-based adoptive T-cell therapy in combination with checkpoint inhibition on cancer patients across all cancer diagnoses.
Detailed description
Adoptive cell therapy (ACT) is a personalized form of immunotherapy, where lymphocytes isolated from the patient's own tumor tissue are expanded 1000-fold ex-vivo and then infused back into the patient. The lymphocytes are then able to recognize and attack remaining cancer cells. This approach has shown remarkable clinical results in several trials conducted worldwide for patients with advanced melanoma - some with durable remissions. Promising clinical results were obtained in smaller trials where patients with disparate solid tumors were treated with tumor-infiltrating lymphocytes (TILs). At Center for Cancer Immune Therapy (CCIT) at Herlev Hospital, there are currently clinical trials undergoing in ovarian and renal cancer, and internationally ACT is being tested in an increasing number of cancer diagnoses, some trials are even recruiting patients across cancer types. Studies have shown that a high intratumoral infiltration with TILs in is correlated to the general clinical outcome of the disease in virtually all solid tumors, and thus clinical trials with TIL-based ACT to different cancer diagnoses have been undertaken. To support the TIL-mediated tumor elimination, in classical ACT protocols patients go through a highly specialized treatment regime before and after TIL infusion. This regime includes lymphodepletion with 7 days non-myeloablative chemotherapy, to provide an immunological window of opportunity for the infused TILs, and concomitant immune stimulation with interleukin-2 (IL-2). Checkpoint inhibition to support the anti-tumor activity of TILs is currently under extensive investigation in several other trials worldwide. Thus, lymphodepletion and IL-2 stimulation are well-established as supportive therapy and already an integrated part of current ACT protocols and while checkpoint inhibition is a new addition at CCIT; internationally other centers have ongoing comparable trials. Drug-based immunotherapy in the form of checkpoint inhibitors (anti-PD-1 and anti-CTLA-4) has yielded impressive clinical results across tumor histologies. Recent results indicate that the effect of immunotherapy relies not so much on the cancer diagnoses but rather on the genomic and immunologic features of the individual patient's cancer disease. Both ACT and checkpoint inhibition work by tipping the immunological balance in favor of activation and away from suppression or avoidance by the cancer cells. Scientific evidence now show that administering anti-CTLA-4 and PD-1 could provide a benefit in the ACT setting, and several ongoing clinical trials are testing combinations of ACT and checkpoint inhibition. To synergistically maximize the immunological potential, we wish to combine ACT with an anti-CTLA-4 antibody (Ipilimumab) prior to tumor resection and an anti-PD-1 antibody (Nivolumab) in combination with TIL infusion. Patients will be treated with one dose of Ipilimumab 14 days before undergoing surgery to harvest tumor material for TIL production. Patients is admitted on day -8 in order to undergo lymphodepleting chemotherapy with cyclophosphamide and fludara starting day -7. On day -2 patients will start treatment with Nivolumab every 2 weeks for a total of 4 doses to increase the activity of the infused TIL product. Available evidence indicates that ACT is a safe and feasible treatment option in an increasing number of solid tumors, and that it should be tested in all cancer patients regardless of their cancer diagnosis.
Interventions
Tumor-infiltrating lymphocytes grown ex-vivo from resected from cancer tissue and reapplied to the patient via an intravenous infusion.
DRUGIpilimumab
One treatment with ipilimumab (3 mg/kg) prior to tumor resection.
DRUGNivolumab
4 doses of nivolumab. Starting 2 days prior to TIL infusion and every 2 weeks hereafter.
DRUGproleukin
2 MIE s.c. injection, after TIL infusion and continuing for 2 weeks
DRUGCyclophosphamide
2 doses (60 mg/kg) prior to TIL infusion
DRUGFludara
5 doses (25 mg/m2) prior to TIL infusion
Sponsors
Inge Marie Svane
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No
Inclusion criteria
Only patients within the Danish Healthcare system are eligible for enrollment. Inclusion Criteria: * Histologically verified metastatic or locally advanced cancer diagnosis * At least one lesion (\>1 cm3) available for surgical resection * Not candidate for standard treatment options * Age of 18-70 years * Performance status of 1 or 0. * Life expectancy \> 6 months * One or more measurable parameter according to RECIST 1.1. * No significant toxicity from previous cancer treatments (CTC≤1). Except alopecia (CTC≤2) or neuropathy (CTC≤2) * Sufficient organ function, including: * Absolute neutrophil count (ANC) ≥ 1.500 /µl * Leucocyte count ≥ normal limit * Platelets ≥ 100.000 /µl and \<700.000 /µl * Hemoglobin ≥ 6,0 mmol/l (regardless of prior transfusion) * S-creatinine \< 140 * S-bilirubin ≤ 1,5 times upper normal limit * ASAT/ALAT ≤ 2,5 times upper normal limit * Alkaline phosphatase ≤ 5 times upper normal limit * Lactate dehydrogenase (LDH) ≤ 5 times upper normal limit * Sufficient coagulation: PP-time\>40 and INR\<1,5 * Women in the fertile age must use effective contraception. This applies from inclusion and until 6 months after treatment. Birth control pills, spiral, depot injection with gestagen, subdermal implantation, hormonal vaginal ring and transdermal depot patch are all considered safe contraceptives. * Signed statement of consent after receiving oral and written study information * Willingness to participate in the planned treatment and follow-up and capable of handling toxicities.
Exclusion criteria
* A history of prior malignancies. Patients treated for another malignancy can only participate if they are without signs of disease for a minimum of 3 years after last treatment. * Primary brain tumor or verified brain metastases * Known hypersensitivity to one of the active drugs or excipients. * Significant medical conditions, including but not limited to severe asthma/COLD, significant cardiac disease, poorly regulated insulin dependent diabetes mellitus. * Creatinine clearance below 70 ml/min . * Acute or chronic infections with HIV, hepatitis, syphilis etc. * Severe allergies or previous anaphylactic reactions. * Active autoimmune disease, such as autoimmune neutropenia/thrombocytopenia or hemolytic anemia, systemic lupus erythematosus, Sjögren's syndrome, sclerodermia, myasthenia gravis, goodpastures disease, addison's disease, hashimoto's thyroiditis, graves' disease etc. * Pregnant women and women who are breastfeeding. * Simultaneous treatment with systemic immunosuppressive drugs (including prednisolone methotrexate etc.) * Simultaneous treatment with other experimental drugs. * Simultaneous treatment with other systemic anti-cancer treatments. * Patients with active or uncontrollable hypercalcemia.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Number of Participants and Type of Reported Adverse Events | Up to 2,5 years from begin of study | Determine the safety of the administration of TIL therapy including checkpoint inhibitors, lymphodepleting chemotherapy and Interleukin-2 for patients with cancer by reporting grade \>2 adverse events according to CTCAE v. 4.0 |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Time to Disease Progression | Until study completion | Days of follow-up from TIL infusion until progressive cancer disease, end of follow-up or death. Progression is defined using Response Evaluation Criteria In Solid Tumors Criteria (RECIST v1.0), as a 20% increase in the sum of the longest diameter of target lesions, or a measurable increase in a non-target lesion, or the appearance of new lesions |
| Overall Survival | Until study completion | Duration of survival measured in days after adoptive cell therapy until death or end of follow-up/censoring. |
| Overall Response Rate | The patients were evaluated every 6-12 weeks (median 90 days) and after therapy and until study completion (max 220 days). | Per Response Evaluation Criteria In Solid Tumors Criteria (RECIST v1.0) for target lesions and assessed by CAT scan: Complete Response (CR), Disappearance of all target lesions; Partial Response (PR), \>=30% decrease in the sum of the longest diameter of target lesions; Overall Response (OR) = CR + PR. |
Countries
Denmark
Participant flow
Participants by arm
| Arm | Count |
|---|---|
| All Participants Autologous tumor-infiltrating lymphocytes: Tumor-infiltrating lymphocytes grown ex-vivo from resected from cancer tissue and reapplied to the patient via an intravenous infusion.
Ipilimumab: One treatment with ipilimumab (3 mg/kg) prior to tumor resection.
Nivolumab: 4 doses of nivolumab. Starting 2 days prior to TIL infusion and every 2 weeks hereafter.
proleukin: 2 MIE s.c. injection, after TIL infusion and continuing for 2 weeks
Cyclophosphamide: 2 doses (60 mg/kg) prior to TIL infusion
Fludara: 5 doses (25 mg/m2) prior to TIL infusion | 25 |
| Total | 25 |
Baseline characteristics
| Characteristic | All Participants | — |
|---|---|---|
| Age, Categorical <=18 years | 0 Participants | — |
| Age, Categorical >=65 years | 3 Participants | — |
| Age, Categorical Between 18 and 65 years | 22 Participants | — |
| Race and Ethnicity Not Collected | — | — Participants |
| Sex: Female, Male Female | 14 Participants | — |
| Sex: Female, Male Male | 11 Participants | — |
Adverse events
| Event type | EG000 affected / at risk |
|---|---|
| deaths Total, all-cause mortality | 23 / 25 |
| other Total, other adverse events | 25 / 25 |
| serious Total, serious adverse events | 9 / 25 |
Outcome results
Primary
Number of Participants and Type of Reported Adverse Events
Determine the safety of the administration of TIL therapy including checkpoint inhibitors, lymphodepleting chemotherapy and Interleukin-2 for patients with cancer by reporting grade \>2 adverse events according to CTCAE v. 4.0
Time frame: Up to 2,5 years from begin of study
Population: Patients who received TIL therapy
| Arm | Measure | Group | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|---|
| All Participants | Number of Participants and Type of Reported Adverse Events | Neutropenia | 25 Participants |
| All Participants | Number of Participants and Type of Reported Adverse Events | Trombocytopenia | 22 Participants |
| All Participants | Number of Participants and Type of Reported Adverse Events | Anemia | 22 Participants |
| All Participants | Number of Participants and Type of Reported Adverse Events | Infection | 6 Participants |
| All Participants | Number of Participants and Type of Reported Adverse Events | Hyponatremia | 2 Participants |
| All Participants | Number of Participants and Type of Reported Adverse Events | Hemorrhagic cystitis | 1 Participants |
| All Participants | Number of Participants and Type of Reported Adverse Events | Fatique | 6 Participants |
| All Participants | Number of Participants and Type of Reported Adverse Events | Vertigo | 1 Participants |
| All Participants | Number of Participants and Type of Reported Adverse Events | Performance status drop | 4 Participants |
| All Participants | Number of Participants and Type of Reported Adverse Events | Thrombosis | 1 Participants |
| All Participants | Number of Participants and Type of Reported Adverse Events | Fever | 16 Participants |
| All Participants | Number of Participants and Type of Reported Adverse Events | Dyspnea | 6 Participants |
| All Participants | Number of Participants and Type of Reported Adverse Events | Hepatitis | 2 Participants |
| All Participants | Number of Participants and Type of Reported Adverse Events | Colitis | 2 Participants |
| All Participants | Number of Participants and Type of Reported Adverse Events | Transaminase elevation | 2 Participants |
| All Participants | Number of Participants and Type of Reported Adverse Events | Vomiting | 2 Participants |
| All Participants | Number of Participants and Type of Reported Adverse Events | Hallucination | 1 Participants |
| All Participants | Number of Participants and Type of Reported Adverse Events | Elevated creatinine | 1 Participants |
Secondary
Overall Response Rate
Per Response Evaluation Criteria In Solid Tumors Criteria (RECIST v1.0) for target lesions and assessed by CAT scan: Complete Response (CR), Disappearance of all target lesions; Partial Response (PR), \>=30% decrease in the sum of the longest diameter of target lesions; Overall Response (OR) = CR + PR.
Time frame: The patients were evaluated every 6-12 weeks (median 90 days) and after therapy and until study completion (max 220 days).
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| All Participants | Overall Response Rate | 2 Participants |
Secondary
Overall Survival
Duration of survival measured in days after adoptive cell therapy until death or end of follow-up/censoring.
Time frame: Until study completion
| Arm | Measure | Value (MEDIAN) |
|---|---|---|
| All Participants | Overall Survival | 227 Days |
Secondary
Time to Disease Progression
Days of follow-up from TIL infusion until progressive cancer disease, end of follow-up or death. Progression is defined using Response Evaluation Criteria In Solid Tumors Criteria (RECIST v1.0), as a 20% increase in the sum of the longest diameter of target lesions, or a measurable increase in a non-target lesion, or the appearance of new lesions
Time frame: Until study completion
| Arm | Measure | Value (MEDIAN) |
|---|---|---|
| All Participants | Time to Disease Progression | 89 Days |