Safety and Tolerability Study of AlloVax(TM) in Patients With Metastatic or Recurrent Cancer of the Head and Neck

Squamous Cell Carcinoma of the Head and Neck Clinical Trial

— HNC  

Official title:

Phase II Study Designed To Evaluate Safety and Tumor Debulking Mechanism of an Individualized Cancer Vaccine (AllovaxTM) in Patients With Metastatic or Recurrent Cancer of the Head and Neck.

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01998542
• Other study ID #: ITL-010-HNC
• Status: Completed
• Phase: Phase 2
• Start date: January 2016
• Est. completion date: November 2017

Study information

• Verified date: August 2016
• Source: Immunovative Therapies, Ltd.
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to determine the safety and tumor debulking efficacy of personalized anti-cancer vaccine AlloVax(TM) in Subjects with confirmed recurrent or metastatic squamous cell carcinoma of the head and neck (SCCHN) who cannot be treated with surgery, chemotherapy or radiation. AlloVax(TM) is a personalized anti-cancer vaccine combining Chaperone Rich Cell Lysate (CRCL) as a source of tumor antigen prepared from patient's tumor and AlloStim(TM) as an adjuvant. The combination of CRCL and AlloStim(TM) is designed to provide cross-reactivity of alloantigen specific recognition with tumor-specific recognition. All the key components necessary to develop tumor-specific immunity by creating the inflammatory environment necessary to overcome the HNC immunosuppressive environment, breaking tumor immune tolerance, and provision of specific HNC antigens for generation of a specific adaptive anti-tumor response.

Description:

This is a Phase II study following up on a previous Phase I/II study in chemotherapy refractory metastatic disease with <90 day survival expectancy. In the Phase I/II study all patients progressed using RECIST criteria. However, 11/42 (26%) were alive at 1yr and 9/42 (21%) alive at 2 yr. Therefore, CT scans did not correlate with clinical presentation and "pseudo-progression" was suspected. This study was designed to select subjects with visible tumor burden on the head, neck or tongue that could be measured and photographed so as not to rely solely on CT scans to determine anti-tumor debulking efficacy. Subjects are initially primed with intradermal AlloStim(TM) injections creating systemic anti-allo-specific cellular immunity. Tumor biopsy samples taken prior to dosing were processed into personalized Chaperone Rich Cell Lysate (CRCL) vaccine containing enriched heat shock proteins which are believed to chaperone tumor-specific neoantigens . AlloStim(TM) was then injected with CRCL into primed subjects to create tumor-specific cellular immunity. Subsequently, subjects are infused with intravenous AlloStim(TM) to cause extravasation of memory cells to the tumor lesions. The protocol including intradermal AlloStim(TM) day 0, 3, 7, 10. Intradermal AlloStim(TM)+CRCL on days 14, 17, 21, 24. Intravenous AlloStim(TM) day 28. This experimental treatment schedule will continue for 3 cycles.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 12
• Est. completion date: November 2017
• Est. primary completion date: June 1, 2017
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 70 Years

Eligibility

Inclusion Criteria:

1. Adult males and female patients aged 18 to 70 years old, inclusive, at screening visit.

2. Patients with histopatholologically or cytologically confirmed diagnosis of recurrent or metastatic squamous cell carcinoma of the head and neck (SCCHN) that is incurable with surgery, chemotherapy or radiation. No nasopharyngeal primaries.

3. Patients must have a tumor safely accessable for biopsy resulting in a minimum of 0.1 g of tumor sample for CRCL processing.

4. Patients must have visible external tumors measurable with at least one lesion deemed to be safely accessible for serial biopsy.

5. ECOG =2.

6. The result of screening test were in the criteria:

6.1 Adequate organ function including:

A. Marrow:

• WBC >3000/mm3

• Platelets >100,000/mm3.

• Absolute neutrophil count = 1,500/mm³

• Hemoglobin = 10.0 g/dL (transfusion allowed)

B. Hepatic:

• Serum Total bilirubin < 2 x ULN mg/dL,

• ALT (SGPT) / AST (SGOT) =3 x upper limit of normal (ULN).

C. Renal:

• Serum creatinine (SCR) <2.0 x ULN, or

• Creatinine clearance (CCR) >30 mL/min.

6.2 All patients have a pre-study echocardiogram without significant abnormalities or Ejection fraction >50%.

6.3 All patients must be screened to be negative for HIV1, HIV2, HTLVI, HTLVII, HBV, HCV and RPR (syphilis).

6.4 Women of child-bearing potential must have a negative urine or serum pregnancy test result within 72 hours prior to the start of study drug administration.

7. All patients of child producing potential must agree to use contraception or avoidance of pregnancy measures while enrolled on study and receiving the experimental product.

8. Patients must have the ability to understand the study, its inherent risks, side effects and potential benefits and be able to give written informed consent to participate.

Exclusion Criteria:

1. Clinical evidence or radiological evidence of nasopharyngeal primaries.

2. Clinical evidence or radiological evidence of brain metastasis.

3. History of severe hypersensitivity to monoclonal antibody drugs or any contraindication to any of the study drugs.

4. Concomitant active autoimmune disease (e.g., rheumatoid arthritis, multiple sclerosis, autoimmune thyroid disease, uveitis).

5. Prior experimental therapy or cancer vaccine treatment (e.g., dendritic cell therapy, heat shock vaccine).

6. Clinical requirement for systemic steroids or current immunosuppressive therapy, including: cyclosporine, antithymocyte globulin, or tacrolimus within 1 month of study entry.

7. Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, requiring parenteral antibiotics, symptomatic congestive heart failure, severe myocardial insufficiency, cardiac arrhythmia

8. All infections must be resolved and the patient must remain a febrile for seven days prior to being placed in the study.

9. History of blood transfusion reactions.

10. Psychiatric or addictive disorders or other condition that, in the opinion of the investigator, would preclude study participation.

11. Pregnant or breast feeding.

The patient will discontinuation from the participation in the study:

1. Less than 12 doses of CRCL able to be produced

2. Tumor sample for CRCL processing contains less than 80% tumor.

Related Conditions & MeSH terms

• Cancer of Head and Neck
• Head and Neck Neoplasms
• Recurrence
• Squamous Cell Carcinoma of Head and Neck
• Squamous Cell Carcinoma of the Head and Neck

Intervention

Biological:
• AlloVax
Personalized anti-cancer vaccine with AlloStim(TM) and CRCL
• CRCL
autologous tumor-derived chaperone protein mixture
• AlloStim
AlloStim (ID) injection AlloStim (IV) infusion

Locations

Country	Name	City	State
Thailand	National Cancer Institute of Thailand	Bangkok

Sponsors (1)

Lead Sponsor	Collaborator
Immunovative Therapies, Ltd.

Country where clinical trial is conducted

Thailand, 

References & Publications (6)

Epple LM, Bemis LT, Cavanaugh RP, Skope A, Mayer-Sonnenfeld T, Frank C, Olver CS, Lencioni AM, Dusto NL, Tal A, Har-Noy M, Lillehei KO, Katsanis E, Graner MW. Prolonged remission of advanced bronchoalveolar adenocarcinoma in a dog treated with autologous, — View Citation

Har-Noy M, Slavin S. The anti-tumor effect of allogeneic bone marrow/stem cell transplant without graft vs. host disease toxicity and without a matched donor requirement? Med Hypotheses. 2008;70(6):1186-92. Epub 2007 Dec 3. — View Citation

Har-Noy M, Zeira M, Weiss L, Fingerut E, Or R, Slavin S. Allogeneic CD3/CD28 cross-linked Th1 memory cells provide potent adjuvant effects for active immunotherapy of leukemia/lymphoma. Leuk Res. 2009 Apr;33(4):525-38. doi: 10.1016/j.leukres.2008.08.017. — View Citation

Janikashvili N, LaCasse CJ, Larmonier C, Trad M, Herrell A, Bustamante S, Bonnotte B, Har-Noy M, Larmonier N, Katsanis E. Allogeneic effector/memory Th-1 cells impair FoxP3+ regulatory T lymphocytes and synergize with chaperone-rich cell lysate vaccine to — View Citation

LaCasse CJ, Janikashvili N, Larmonier CB, Alizadeh D, Hanke N, Kartchner J, Situ E, Centuori S, Har-Noy M, Bonnotte B, Katsanis E, Larmonier N. Th-1 lymphocytes induce dendritic cell tumor killing activity by an IFN-?-dependent mechanism. J Immunol. 2011 — View Citation

Mayer-Sonnenfeld T, Har-Noy M, Lillehei KO, Graner MW. Proteomic analyses of different human tumour-derived chaperone-rich cell lysate (CRCL) anti-cancer vaccines reveal antigen content and strong similarities amongst the vaccines along with a basis for C — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Tumor Response	Tumor response evaluation by clinical exam including photographs of visible tumor lesions on head, neck and/or tongue (endoscopic) and by CT scan assessment for change in target lesion tumor volume (TV). TV is defined as the volume occupied by macroscopic visible target lesion in two longest cross-sectional diameters.	baseline, every 28 days for 5 months (CT scan confirmation at baseline and day 90 and day 150)
Secondary	Anti-tumor immune response	change in tumor pathology and immune cell inflitration	baseline, 30 days after the last dose
Secondary	Anti-Tumor Response	expression of CTLA4.	baseline and 30 days after the last dose

External Links

•   Cancer
•   Head and Neck Cancer