IKKb-matured, RNA-loaded Dendritic Cells for Metastasised Uveal Melanoma
Primary Purpose
Melanoma, Uveal Metastatic
Status
Active
Phase
Phase 1
Locations
Germany
Study Type
Interventional
Intervention
Vaccination with IKKb matured Dendritic Cells
Sponsored by
About this trial
This is an interventional treatment trial for Melanoma, Uveal Metastatic focused on measuring local treatment not sufficient, systemic treatment indicated
Eligibility Criteria
Inclusion Criteria:
- Histologically confirmed unresectable stage IV metastatic uveal melanoma as per AJCC staging system 2014, 7th edition (updated 2018) not curable with local therapy modalities
- WHO performance status of 0, 1 or 2
- age from 18 and ≤ 75 years
- negative pregnancy test
- signed informed consent
Exclusion Criteria:
- Major serious illness
- evidence for HIV-1, HIV-2, HTLV-1, HBV or HCV infection
- active autoimmune disease requiring immunosuppressive therapy
- splenectomy or radiation therapy of the spleen
- organ allografts
- pregnancy
- lactation
- psychiatric disorders
- severe organic brain syndrome
Sites / Locations
- University Hospital Erlangen Dept. of Dermatology
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
DC IKKb
Arm Description
Vaccination with IKKb matured RNA loaded Dendritic Cells
Outcomes
Primary Outcome Measures
Safety of DCIKKb
Assesment of side effects using the Common Toxicity Criteria (CTC v4.0)
Tolerability of DCIKKb
Assesment of Quality of life using Quality of life EORTC QLQ-C30, Version 2
Dose-limiting toxicities (DLTs) of DCIKKb
Assesment of side effects using the Common Toxicity Criteria (CTC v4.0)
Maximum tolerated dose (MTD) of DCIKKb
Assesment of side effects using the Common Toxicity Criteria (CTC v4.0)
Secondary Outcome Measures
Prolongation of median overall survival
Assesment of survival
Prolongation of overall survival (OS) after 1 and 2 years
Assesment of survival
Induction of antigen specific CD8+ T cells and / or CD4+ T cells against TAA and mutated drivers
Assesment of immune responses
Full Information
NCT ID
NCT04335890
First Posted
April 1, 2020
Last Updated
March 16, 2022
Sponsor
Hasumi International Research Foundation
1. Study Identification
Unique Protocol Identification Number
NCT04335890
Brief Title
IKKb-matured, RNA-loaded Dendritic Cells for Metastasised Uveal Melanoma
Official Title
Phase I Vaccination Trial in Metastatic Uveal Melanoma Using IKKb-matured Dendritic Cells Loaded With Autologous Tumor-RNA + RNA Coding for Defined Antigens and Driver Mutations
Study Type
Interventional
2. Study Status
Record Verification Date
March 2022
Overall Recruitment Status
Active, not recruiting
Study Start Date
June 24, 2020 (Actual)
Primary Completion Date
January 30, 2023 (Anticipated)
Study Completion Date
January 30, 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hasumi International Research Foundation
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
A Phase I vaccination trial in patients suffering from recently diagnosed metastatic uveal melanoma not cureable with local therapy and needing systemic therapy. IKKb-matured Dendritic Cells loaded with autologous tumor-RNA + RNA coding for defined antigens and driver mutations will be added to a standard therapy chosen by the tumor board (either checkpoint blockade or chemotherapy).
Detailed Description
Intravenous infusion of 7.5 to 30 mio DCIKKb at 9 vaccination time points (week 1, 3, 7, 13, 19, 25, 31, 37 and 42) and in intervals of 2, 4, and 6 intervals of 6 weeks) is scheduled; the first 4 patients will receive reduced doses for the first 4 vaccinations, namely 7.5 mio (1st and 2nd vaccination) and 15 mio (3rd and 4th vaccination) DC followed by the full dose of 30 mio for subsequent vaccinations. Patients number 5 to 8 will receive initially reduced doses of 15 mio (1st and 2nd vaccination) DC for the first 2 vaccinations, and the full dose of 30 mio for subsequent vaccinations. Patients number 8 to 12 will receive the full dose of 30 mio cells from vaccination 1 onwards provided that no major side effects occurred. Patients will be vaccinated in a staggered approach by selectively decelerating release of the vaccine.
DCIKKb = autologous, monocyte-derived DC that are matured with the standard cocktail (TNF-alpha, IL-1 beta, IL-6 and PGE2) and IKKb-RNA loaded by electroporation with 1) autologous PCR-amplified total tumor mRNA, 2) RNA coding for defined tumor associated antigens (TAA) namely gp100, tyrosinase, PRAME, MAGE-A3, IDO) and 3) RNA coding for driver mutations (GNAQ/GNA11Q209 or R183, or the less frequently occurring SF3B1R625, CYSLTR2L129Q or PLCB4D630) by electroporation; RNAs for selected TAAs are in stock and will be transfected into the DCs only if expressed in the individual tumor of a patient (shown by RNA sequencing of the tumor); RNAs for selected driver mutations are in stock and will be loaded into the DCs only if the respective mutation is found (proven by exome and RNA sequencing) in the individual tumor.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Melanoma, Uveal Metastatic
Keywords
local treatment not sufficient, systemic treatment indicated
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
12 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
DC IKKb
Arm Type
Experimental
Arm Description
Vaccination with IKKb matured RNA loaded Dendritic Cells
Intervention Type
Biological
Intervention Name(s)
Vaccination with IKKb matured Dendritic Cells
Other Intervention Name(s)
Dendritic Cell vaccine
Intervention Description
IKKb matured autologous monocyte derived dendritic cells loaded with RNAs; intravenous Infusion with a dose escalation starting with 7.5 mio Dendritic Cells for the first vaccination up to 30 mio cells per vaccination
Primary Outcome Measure Information:
Title
Safety of DCIKKb
Description
Assesment of side effects using the Common Toxicity Criteria (CTC v4.0)
Time Frame
1 year
Title
Tolerability of DCIKKb
Description
Assesment of Quality of life using Quality of life EORTC QLQ-C30, Version 2
Time Frame
1 year
Title
Dose-limiting toxicities (DLTs) of DCIKKb
Description
Assesment of side effects using the Common Toxicity Criteria (CTC v4.0)
Time Frame
1 year
Title
Maximum tolerated dose (MTD) of DCIKKb
Description
Assesment of side effects using the Common Toxicity Criteria (CTC v4.0)
Time Frame
1 year
Secondary Outcome Measure Information:
Title
Prolongation of median overall survival
Description
Assesment of survival
Time Frame
2 years
Title
Prolongation of overall survival (OS) after 1 and 2 years
Description
Assesment of survival
Time Frame
2 years
Title
Induction of antigen specific CD8+ T cells and / or CD4+ T cells against TAA and mutated drivers
Description
Assesment of immune responses
Time Frame
2 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Histologically confirmed unresectable stage IV metastatic uveal melanoma as per AJCC staging system 2014, 7th edition (updated 2018) not curable with local therapy modalities
WHO performance status of 0, 1 or 2
age from 18 and ≤ 75 years
negative pregnancy test
signed informed consent
Exclusion Criteria:
Major serious illness
evidence for HIV-1, HIV-2, HTLV-1, HBV or HCV infection
active autoimmune disease requiring immunosuppressive therapy
splenectomy or radiation therapy of the spleen
organ allografts
pregnancy
lactation
psychiatric disorders
severe organic brain syndrome
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Beatrice Schuler-Thurner, MD
Organizational Affiliation
University Hospital Erlangen, Germany
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Hospital Erlangen Dept. of Dermatology
City
Erlangen
State/Province
Bavaria
ZIP/Postal Code
91054
Country
Germany
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
25100611
Citation
Pfeiffer IA, Hoyer S, Gerer KF, Voll RE, Knippertz I, Guckel E, Schuler G, Schaft N, Dorrie J. Triggering of NF-kappaB in cytokine-matured human DCs generates superior DCs for T-cell priming in cancer immunotherapy. Eur J Immunol. 2014 Nov;44(11):3413-28. doi: 10.1002/eji.201344417. Epub 2014 Sep 16.
Results Reference
result
PubMed Identifier
28717398
Citation
Gerer KF, Erdmann M, Hadrup SR, Lyngaa R, Martin LM, Voll RE, Schuler-Thurner B, Schuler G, Schaft N, Hoyer S, Dorrie J. Preclinical evaluation of NF-kappaB-triggered dendritic cells expressing the viral oncogenic driver of Merkel cell carcinoma for therapeutic vaccination. Ther Adv Med Oncol. 2017 Jul;9(7):451-464. doi: 10.1177/1758834017712630. Epub 2017 Jun 13.
Results Reference
result
PubMed Identifier
26602097
Citation
Schuler-Thurner B, Bartz-Schmidt KU, Bornfeld N, Cursiefen C, Fuisting B, Grisanti S, Heindl LM, Holbach L, Keseru M, Knorr H, Koch K, Kruse F, Meiller R, Metz C, Meyer-ter-Vehn T, Much M, Reinsberg M, Schliep S, Seitz B, Schuler G, Susskind D, Viestenz A, Wagenfeld L, Zeschnigk M. [Immunotherapy of uveal melanoma: vaccination against cancer. Multicenter adjuvant phase 3 vaccination study using dendritic cells laden with tumor RNA for large newly diagnosed uveal melanoma]. Ophthalmologe. 2015 Dec;112(12):1017-21. doi: 10.1007/s00347-015-0162-z. German.
Results Reference
result
PubMed Identifier
35185883
Citation
Koch EAT, Schaft N, Kummer M, Berking C, Schuler G, Hasumi K, Dorrie J, Schuler-Thurner B. A One-Armed Phase I Dose Escalation Trial Design: Personalized Vaccination with IKKbeta-Matured, RNA-Loaded Dendritic Cells for Metastatic Uveal Melanoma. Front Immunol. 2022 Feb 4;13:785231. doi: 10.3389/fimmu.2022.785231. eCollection 2022.
Results Reference
derived
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IKKb-matured, RNA-loaded Dendritic Cells for Metastasised Uveal Melanoma
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