Clinical Trial Details
Braintumor Website

[Information provided by: ClinicalTrials.gov, which provides patients, family members, and members of the public easy and free access to information on clinical studies for a wide range of diseases and conditions.]

NCT02510950 : Neoepitope-based Personalized Vaccine Approach in Patients With Newly Diagnosed Glioblastoma
PhasePhase 1
AgesMin: 18 Years Max: N/A
Eligibility
Inclusion Criteria:

- Newly diagnosed histologically confirmed glioblastoma multiforme (WHO grade IV).
Patients with secondary glioblastoma, in particular those who are IDH1 or IDH2 mutant,
will not be excluded.

- Patients who had craniotomy with biopsy, subtotal resection, total gross resection, or
re-resection will be permitted.

- Consented to genome sequencing and dbGaP-based data sharing and has provided or will
provide germline (PBMC) and tumor DNA/RNA samples of adequate quality for sequencing.
(Acquisition of specimens for sequencing and the sequencing itself may be done under
this study or as part of routine care or another research project.)

- At least 18 years of age.

- Karnofsky performance status ? 60%

- Normal bone marrow and organ function as defined below:

- Absolute neutrophil count ? 1,500/mcL

- Platelets ? 100,000/mcL

- Total bilirubin ? 1.5 x IULN

- AST(SGOT)/ALT(SGPT) ? 3.0 x IULN

- Creatinine ? IULN OR creatinine clearance ? 60 mL/min/1.73 m2 for patients with
creatinine levels above institutional normal

- Systemic corticosteroid therapy is permitted provided dosing is no greater than 4 mg
per day (dexamethasone or equivalent) on the day of vaccine administration

- Bevacizumab will be allowed if given for symptomatic control of vasogenic edema and to
avoid high dose of corticosteroids

- Women of childbearing potential and men must agree to use adequate contraception
(hormonal or barrier method of birth control, abstinence) prior to study entry and for
the duration of study participation. Should a woman become pregnant or suspect she is
pregnant while participating in this study, she must inform her treating physician
immediately.

- Ability to understand and willingness to sign an IRB approved written informed consent
document (or that of legally authorized representative, if applicable).

Exclusion Criteria:

- As this is a safety and feasibility study, prior immunotherapy will be permitted.
However, any prior immunotherapy must be discontinued at least 2 weeks before peptide
vaccine administration. Non-immunologic therapy may be continued.

- Inadequate tissue acquisition to allow for neoantigen screening

- No candidate neoantigen identified during screening

- A history of other malignancy ? 3 years previous with the exception of non-melanoma
skin cancer, any in situ cancer that has been successfully resected and cured, treated
superficial bladder cancer, or any early-stage solid tumor that was successfully
resected without need for adjuvant radiation or chemotherapy.

- Currently receiving any other investigational agents.

- Known allergy, or history of serious adverse reaction to, vaccines such as
anaphylaxis, hives, or respiratory difficulty.

- A history of allergic reactions attributed to compounds of similar chemical or
biologic composition to poly-ICLC or other agents used in the study.

- Uncontrolled intercurrent illness including, but not limited to, ongoing or active
infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac
arrhythmia, or psychiatric illness/social situations that would limit compliance with
study requirements.

- History of pre-existing immunodeficiency disorder including chronic infection (i.e.
hepatitis B, hepatitis C, HIV), or autoimmune condition requiring immunosuppressive
therapy. This includes inflammatory bowel disease, ulcerative colitis, Crohn's
disease, systemic vasculitis, scleroderma, psoriasis, multiple sclerosis, hemolytic
anemia, immune-mediated thrombocytopenia, rheumatoid arthritis, systemic lupus
erythematosus, Sjogren's syndrome, sarcoidosis, or other rheumatologic disease or any
other medical condition or use of medication which might make it difficult for the
patient to complete the full course of treatments or to generate an immune response to
vaccines.

- Presence of clinically significant increased intracranial pressure (e.g. impending
herniation) or hemorrhage, uncontrolled seizures, or requirement for immediate
palliative treatment.

- Pregnant and/or breastfeeding. Women of childbearing potential must have a negative
pregnancy test within 7 days of first dose of vaccine.
LinksPermanent Link to THIS page: http://virtualtrials.com/nct/display1trial.cfm?nct=NCT02510950      |      Link to official Clinicaltrials.gov listing
Locations
Saint Louis, Missouri
Facility: Washington University School of Medicine
Investigator: William E Gillanders, M.D.
Contact: Gavin Dunn, M.D., Ph.D. Phone: 314-362-3570
Click HERE to send email to this center




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