Tolerability and Efficacy of UV1 Vaccine in Patients With Recurrent or Metastatic Head and Neck Squamous Cell Carcinoma Planned for First-line Treatment With Pembrolizumab

Head and Neck Squamous Cell Carcinoma Clinical Trial

— FOCUS  

Official title:

Phase 2 Multicenter Study Investigating the Tolerability and Efficacy of UV1 Vaccine in Patients With Recurrent or Metastatic PD-L1 Positive (CPS≥1) Head and Neck Squamous Cell Carcinoma Planned for First-line Treatment With Pembrolizumab

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05075122
• Other study ID #: KKSH176
• Secondary ID: 2020-005910-17
• Status: Recruiting
• Phase: Phase 2
• Start date: August 2, 2021
• Est. completion date: February 2025

Study information

• Verified date: March 2022
• Source: Martin-Luther-Universität Halle-Wittenberg
• Contact: Mascha Binder, MD
• Phone: 0049 345 557
• Email: mascha.binder[@]uk-halle.de
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The primary objective of this study is to determine the clinical performance of UV1 vaccination as add on to standard pembrolizumab treatment in patients with recurrent or metastatic PD-L1 positive (CPS >=1) head and neck squamous cell carcinoma. Secondary objectives are to determine the efficacy in terms of overall survival ,objective response rate and duration of response. Moreover, this study will explore patient subgroups most likely deriving benefit from a targeted immunotherapy approach combining a checkpoint inhibitor with a cancer vaccine and help to establish liquid biopsy tumor monitoring in HNSCC.

Description:

Overall survival of patients with metastatic or recurrent HNSCC has improved over the past decade but remains poor overall. Median overall survival is limited to less than 15 months, with the current standard of care (immune checkpoint blockade with or without chemotherapy). Many patients with HNSCC are frail and therefore cannot tolerate chemotherapy, reducing their treatment options to checkpoint inhibitor. Therefore, the development of effective and tolerable combination regimens is urgently needed, especially in first-line therapy. The FOCUS study will evaluate such a combination regimen in patients with metastatic or recurrent HNSCC. The experimental regimen evaluated in this study will test the first-line standard drug pembrolizumab in combination with the novel UV1 cancer vaccine. In the comparator arm, patients receive pembrolizumab as the standard of care. The aim is to assess whether the addition of UVI can increase the efficacy of the checkpoint inhibitor. Based on currently available data, a decrease in efficacy due to the combination of standard first-line therapy with pembrolizumab is unlikely. The FOCUS study could therefore establish a new 1st-line regimen with increased efficacy and acceptable tolerability, which would need to be compared with the standard of care in a larger phase III trial. Based on the biomarker data from the FOCUS study, a subsequent Phase 3 study would potentially test the regimen only in subpopulations with increased response probability. From the perspective of the individual patient, participants may benefit from the experimental combination through improved efficacy. On the other hand, this is a novel combination study for HNSCC, and there is a risk that efficacy may not improve.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 75
• Est. completion date: February 2025
• Est. primary completion date: August 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Histologically confirmed diagnosis of a non-resectable recurrent or metastatic head and neck squamous cell carcinoma (not necessarily reconfirmed at time of enrolment)

• At least one measurable tumor lesion as per RECIST v1.1, (Scan not older than 4 weeks before randomization)

• Eligible for pembrolizumab monotherapy (PD-L1 CPS >/= 1% and adequate laboratory parameters for pembrolizumab monotherapy as assessed by the investigator)

• ECOG-performance score 0-2

• Written informed consent obtained according to international guidelines and local laws

• Ability to understand and give informed consent.

• Safe contraception measures for males and females. Procedures with a pearl index of less than 1% apply as safe pregnancy prevention measures.

Exclusion Criteria:

• Patients for whom a combination therapy of a checkpoint inhibitor and a chemotherapy is deemed necessary in the opinion of the investigator

• Participation in another interventional study simultaneously and within the last 30 days prior to inclusion (registries or observational studies allowed)

• Concurrent malignancies other than disease under study within 5 years prior to inclusion, with the exception of those with a negligible risk of metastasis or death (e.g., expected 5-year OS > 90%) treated with expected curative outcome

• Active, known, or suspected autoimmune disease requiring systemic treatment.

• A concomitant therapy with systemic immune suppression: use of chronic systemic steroid medication (up to 5 mg/day prednisolone equivalent is allowed; patients using physiological replacement doses of prednisone for adrenal or pituitary insufficiency are eligible)

• History of severe autoimmune disorder or history of organ transplant

• Any serious or uncontrolled medical disorder or active infection that, in the opinion of the investigator, may increase the risk associated with study participation, study drug administration, or would impair the ability of the subject to receive study drug.

• Significant acute or chronic infections including, among others (test not older than 4 weeks prior to randomization): Any positive test for human immunodeficiency virus (HIV) or known acquired immunodeficiency syndrome (AIDS), Any positive test result for hepatitis B virus or hepatitis C virus indicating acute or chronic infection.

• Pregnancy or lactation

• (Bacterial) infections requiring systemic antibiotic treatment within 2 weeks prior to first dose of study treatment (depending on group assignment: either prior to first UV1 or prior to first pembrolizumab administration).

• History of allergy or hypersensitivity to study drug or human granulocyte-macrophage colony stimulating factor, yeast-derived products or any constituent of the products

• Receipt of a live vaccine within 30 days prior to start of therapy

• Patient who has been incarcerated or involuntarily institutionalized by court order or by the authorities.

• Patients who are unable to consent because they do not understand the nature, significance and implications of the clinical study and therefore cannot form a rational intention in the light of the facts.

Related Conditions & MeSH terms

• Carcinoma
• Carcinoma, Squamous Cell
• Head and Neck Squamous Cell Carcinoma
• Squamous Cell Carcinoma of Head and Neck

Intervention

Biological:
• UV1
UV1 vaccination (300 µg) UV1 vaccination will be applied in a dense schedule with three vaccinations during one week before initiation of pembrolizumab, followed by 5 additional vaccinations every 3 weeks on d1 of each cycle (5 cycles in total, duration of treatment will be 13 weeks in total, regular EOT at week 14)

Drug:
• Sargramostim for Injection
75 µg GM-CSF as adjuvant per vaccination. Applied in a dense schedule with three injections during one week before initiation of pembrolizumab, followed by 5 additional injections every 3 weeks on d1 of each cycle (5 cycles in total, duration of treatment will be 13 weeks in total, regular EOT at week 14).
• Pembrolizumab injection
200mg flat dose iv every 3 weeks. Pembrolizumab will be administered beyond the EOT visit at physician discretion until disease progression and up to a maximum of two years (standard of care)

Locations

Country	Name	City	State
Germany	Universitätsklinikum Aachen, Klinik für Hämatologie, Onkologie, Hämostaseologie	Aachen
Germany	Charité Universitätsmedizin, Comprehensive Cancer Center, Medizinische Klinik m.S. Hämatologie, Onkologie und Tumorimmunologie	Berlin
Germany	Universitätsklinikum Greifswald, Klinik für Hals-, Nasen-, Ohrenkrankheiten, Kopf- und Halschirurgie	Greifswald
Germany	Universitätsklinikum Halle (Saale), Klinik und Poliklinik für Innere Medizin IV	Halle (Saale)
Germany	Universitätsklinikum Hamburg, Universitäres Cancer Center Hamburg UCCH, Hubertus Wald Tumorzentrum	Hamburg
Germany	Klinikum St. Georg gGmbH	Leipzig
Germany	Universitätsklinikum Leipzig, Klinik und Poliklinik für HNO Heilkunde	Leipzig
Germany	Universitätsklinikum Mainz, III. Medizinische Klinik und Poliklinik	Mainz
Germany	Klinikum Stuttgart, Klinik für Hämatologie, Onkologie und Palliativmedizin	Stuttgart
Germany	Universitätsklinikum Würzburg, Comprehensive Cancer Center Mainfranken	Würzburg

Sponsors (4)

Lead Sponsor	Collaborator
Martin-Luther-Universität Halle-Wittenberg	Apotheke der Universitätsmedizin der Johannes Gutenberg-Universität Mainz (Germany), Axel Hinke. CCRC Cancer Clinical Research Consulting (Düsseldorf, Germany, Ultimovacs ASA

Country where clinical trial is conducted

Germany, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Progression free survival rate	according to iRECIST	6 months after first administration of study medication
Secondary	Progression free survival	according to iRECIST	every three months, until progression of disease, maximum 12 months from the date of LPI (last patient in)
Secondary	Overall survival		every three months, until death, maximum 12 months from the date of LPI (last patient in)
Secondary	Objective Response Rate	Complete Remission (CR) + Partial Remission (PR) according to iRECIST	every three months, until death, maximum 12 months from the date of LPI (last patient in)
Secondary	Duration of Response	according to iRECIST	every three months, until death, maximum 12 months from the date of LPI (last patient in)
Secondary	Rate of immune responses against hTERT peptides	measured by 3H-Thymidine proliferation and IFNgamma ELISPOT assays	Baseline, up to 8 weeks, time of progression (max. 12 months after LPI)
Secondary	Rate of clearance of ctDNA from blood on treatment		Baseline, week 5, week 8 and 1, 3, 6 months after EOT (max. 14 weeks), time of progression (max. 12 months after LPI)
Secondary	Adverse Events	according to NCI CTC AE v5.0	3 months after EOT (maximum 25 weeks after start of treatment)