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Phase 2 N=40 Treatment

Vaccine Therapy in Treating Patients With Newly Diagnosed Glioblastoma Multiforme

Malignant Neoplasms of Brain

Enrolled (actual)
40
Serious AEs
10.0%
Results posted
Feb 2014
Primary outcome: Primary: Humoral and Cellular Immune Response — 3; 0; 7 participants

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
PEP-3 vaccine (Biological); sargramostim (Biological); Temozolomide (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
John Sampson
Primary completion
Jan 2012

Outcome Measures

OutcomeResultp-value
PRIMARY
Humoral and Cellular Immune Response
3; 0; 7
PRIMARY
Clinical Efficacy of Vaccination, in Terms of Progression-free Survival (PFS)
14.2; 12.1; 11.6
SECONDARY
Response to Vaccination
NA; NA; NA
SECONDARY
Toxicity to PEP-3 Vaccine Immunization
4; 1; 7

Summary

RATIONALE: Vaccines made from a peptide may help the body build an effective immune response to kill tumor cells. Colony-stimulating factors, such as GM-CSF, increase the number of white blood cells and platelets found in bone marrow or peripheral blood. Giving vaccine therapy after surgery may kill any tumor cells that remain after surgery. PURPOSE: This phase II trial is studying how well vaccine therapy works in treating patients with newly diagnosed glioblastoma multiforme.

Eligibility Criteria

Inclusion Criteria

  • Histologically confirmed newly diagnosed glioblastoma multiforme
  • Has undergone prior gross total resection (GTR) followed by conformal radiotherapy* with or without concurrent chemotherapy
  • GTR is defined as ≥ 95% volumetric resection of the contrast-enhancing component on the preoperative MRI
  • Residual radiographic contrast enhancement on post-resection CT scan or MRI must be ≤ 1 cm in maximal diameter in any two perpendicular axial planes
  • No evidence of disease progression after completion of radiotherapy* NOTE: *Patients may enroll in part 2 of the study within 2 weeks after surgery; these patients will receive radiotherapy with concurrent chemotherapy during the study
  • EGFRvIII-positive tumor by immunohistochemistry, polymerase chain reaction, or related molecular techniques
  • Karnofsky performance status 80-100%
  • Curran group status I-IV
  • Signed informed consent form

Exclusion Criteria

  • Absolute Neutrophil Count (ANC) 1.5 times normal
  • Positive hepatitis B (HB) surface antigen (HbsAg), antibody to hepatitis B surface antigen (anti-HBs), and antibody to hepatitis B core antigen (anti-HBc)
  • Pregnant or nursing
  • Positive pregnancy test
  • Active infection requiring treatment
  • Unexplained febrile illness (T max > 101.5 F)
  • Inflammatory bowel disease, lupus erythematosus, rheumatoid arthritis, or other autoimmune disease
  • Known immunosuppressive disease
  • Known HIV infection
  • Diffuse leptomeningeal disease
  • Unstable or severe concurrent medical condition, such as severe heart and lung disease or active hepatitis
  • Demonstrated allergy to temozolomide or inability to tolerate temozolomide for reasons other than lymphopenia
  • Concurrent corticosteroids (except for nasal or inhaled steroids) at a dose above physiologic levels (> 2 mg of dexamethasone/day).
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00643097). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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