IDO Peptid Vaccination for Stage III-IV Non Small-cell Lung Cancer Patients.

Phase 1

Completed

• Conditions: NSCLC; Lung Cancer

• Registration Number: NCT01219348
• Lead Sponsor: Inge Marie Svane

Brief Summary

Title: IDO peptid vaccination in combination with immune stimulating agent Aldara and the adjuvant Montanide, for treatment of patients with locally advanced or metastatic non small-cell lung cancer. A first-in-man phase I trial.

Hypothesis: In this trial the investigators assess a new immunotherapeutic strategy targeting the immune inhibiting enzyme, IDO to investigate the potential of vaccination against IDO as a possible anticancer target.

Detailed Description

Background: Non small-cell lung cancer (NSCLC) is a common disease with a poor prognosis when locally advanced or metastasized, despite advances in surgery, chemo- and radiation therapy.

In this trial the investigators assess a new immunotherapeutic strategy targeting the immune inhibiting enzyme, IDO to investigate the potential of vaccination against IDO as a possible anticancer target.

IDO has recently been recognized as an important factor in immune regulation and development of immune tolerance in the microenvironment of cancer cells. Cells that represent IDO at their surface are known to inhibit the immune system. IDO expression is seen both in cancer cells and antigen presenting cells. The vaccination against IDO expressing cells is therefore two-sided. The vaccination therapy is thought to block the development of immune tolerance induced by IDO expressing cells. At the same time the investigators aim to stimulate the production of IDO specific T-cells, hence facilitating the elimination of IDO positive tumour cells. The primary end points are safety and toxicity evaluation. Secondary end points are immunological and clinical response.

Study Timeline

• Study First Submitted: 2010-05-10
• Study Start: 2010-06
• Study First Submitted QC: 2010-10-12
• Study First Posted: 2010-10-13
• Primary Completion: 2012-08
• Study Completion: 2012-08
• Status Verified: 2015-08
• Last Update Submitted: 2015-08-17
• Last Update Posted: 2015-08-18

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 14

Inclusion Criteria

1. Histological or cytological verified non small cell lung cancer 2. Metastatic or locally advanced incurable stage III-IV NSCLC 3. Patients need to be off chemotherapy treatment 4. Evaluable disease according to RECIST V. 1,1 criteria 5. Patients must be HLA-A2 positive 6. Patients > 18 years old 7. Performance status 0-1 8. Life expectancy of > 3 months 9. Acceptable bone marrow function, defined as

a. White blood cell count > 2,5 * 109 /l b. Neutrophil count> 1,5 * 109 /l c. Platelet count > 75 * 109/l 10. Creatinin measured < 2,5 * upper limit value 11. Acceptable liver function, defined as

1. ASAT < 100 U/L

2. Bilirubin < 30 U/L 12. Women with child-bearing potential must have controlled s-hcg before inclusion 13. Patients must provide written informed concent before inclusion 13. Termination of chemotherapy treatment > 28 days before inclusion

   14. Termination of radiotherapy treatment > 28 days before inclusion

   15. Inclusion at least > 4 weeks after complicated gastric surgery

Exclusion Criteria

1. Other malignancies except from non-melanoma skin cancer in the previous 5 years until study inclusion 2. Brain metastasis are allowed after radical excision, and if the patient at least 1 month afterwards is not in clinical or radiographic progression 3. Patients with active gastric ulcer disease; patients taking antacid treatment can be included. 4. Severe medical condition, severe asthma, severe COLD, severe arteriosclerosis or diabetic disease 5. Acute or chronic infection (ie. HIV, hepatitis, tuberculosis) 6. Severe allergic reaction or previous anaphylactic shock 7. Autoimmune diseases (ie. autoimmune neutropenia/thrombopenia, hæmolytic anaemia, systemic lupus erythematosis, Sjøgrens disease, sclerodermia, Goodpastures syndrome, Addisons disease, active Graves disease) 8. Pregnant or lactating women 9. Psychiatric disease, which can influence compliance 10. Known hypersensitivity towards the adjuvance Montanide, the Aldara creme, or adhesive tape. 11. Treatment with immunosuppressive therapy (ie. dexamethasone, methotrexate) 12. Treatment with other experimental therapy 13. Treatment with other anti-cancer therapy, except from treatment of osteoporosis 14. No systemic chemotherapy, immunotherapy or radiation therapy (except locally) are allowed until 28 days before inclusion.

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Primary Outcome Measures

Name	Time	Method
evidence of toxicity	12 months	CTCAE = Common Terminology Criteria for Adverse Events v. 3.0 will be used for registration of toxicity

Secondary Outcome Measures

Name	Time	Method
evaluation of immunological and clinical responses	18 months	immunological assays will be used to identify immunological responses. CT scans will be used for evaluation of clinical responses.

Trial Locations

Locations (2)

Center for Cancer ImmuneTherapy; 🇩🇰 Herlev, Copenhagen, Denmark

Center for Cancer Immune Therapy, Dept. og Haematology/Oncology; 🇩🇰 Copenhagen, Herlev, Copenhagen, Denmark