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Clinical Trial on the Combination of Avelumab and Axitinib for the Treatment of Patients With Recurrent Glioblastoma (GliAvAx)

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ClinicalTrials.gov Identifier: NCT03291314
Recruitment Status : Recruiting
First Posted : September 25, 2017
Last Update Posted : September 25, 2017
Sponsor:
Information provided by (Responsible Party):
Bart Neyns, Universitair Ziekenhuis Brussel

Brief Summary:
Phase II clinical trial on the combination of avelumab and axitinib for the treatment of patients with recurrent glioblastoma (histologically confirmed WHO grade IV glioma), at documented recurrence/progression following prior treatment with surgery, radiation therapy and temozolomide.

Condition or disease Intervention/treatment Phase
Recurrent Glioblastoma (WHO-Grade IV Glioma) Drug: Axitinib Drug: Avelumab Phase 2

  Show Detailed Description

Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 52 participants
Allocation: Non-Randomized
Intervention Model: Parallel Assignment
Intervention Model Description:

Open label, single-center, stratified phase II clinical trial.

Patients will be stratified according to their baseline use of corticosteroids: <Stratum A> = no need for corticosteroids and <Stratum B> = baseline need for steroid treatment

Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Phase II Clinical Trial on the Combination of Avelumab and Axitinib for the Treatment of Patients With Recurrent Glioblastoma
Actual Study Start Date : May 3, 2017
Estimated Primary Completion Date : September 30, 2018
Estimated Study Completion Date : September 30, 2018

Resource links provided by the National Library of Medicine

U.S. FDA Resources

Arm Intervention/treatment
Experimental: Axitinib + Avelumab
On day 1 of the treatment phase, patients recruited to this arm will initiate concomitant continuous daily treatment with axitinib (InlytaTM, 5 mg comp BID) in combination with avelumab (10 mg/kg IV Q2 weeks)
Drug: Axitinib
1. Axitinib, a VEGFR-specific small molecule tyrosine kinase inhibitor (Tki) has demonstrated anti-tumor activity when evaluated as a mono-therapy and in combination with lomustine for the treatment of patients with recGB (EudraCT 2011-000900-16) [7].
Other Name: InlytaTM
Drug: Avelumab
2. Avelumab (MSB00107; anti-PD-L1) is a fully human anti-PD-L1 IgG1 monoclonal antibody (mAb) that has demonstrated anti-tumor activity in several tumor types.
Other Name: MSB00107
Experimental: Axitinib (+Avelumab)

On day 1 of the treatment phase, patients recruited to this arm will initiate treatment with continuous daily axitinib (InlytaTM, 5 mg comp BID).

Patients who tolerate treatment with axitinib and are able to taper the dose of corticosteroids to a maximal daily dose of 8 mg methylprednisolone (or an equivalent dose of another oral corticosteroid) will initiate combination therapy with avelumab (10 mg/kg IV Q2 weeks) on day 43, following the the first MRI-based tumor response evaluation in week 6.

Patients who do not tolerate monotherapy with axitinib, or cannot decrease their daily dose of corticosteroids to a maximal daily dose of 8 mg methylprednisolone will not be allowed to initiate avelumab treatment.

Drug: Axitinib
1. Axitinib, a VEGFR-specific small molecule tyrosine kinase inhibitor (Tki) has demonstrated anti-tumor activity when evaluated as a mono-therapy and in combination with lomustine for the treatment of patients with recGB (EudraCT 2011-000900-16) [7].
Other Name: InlytaTM
Drug: Avelumab
2. Avelumab (MSB00107; anti-PD-L1) is a fully human anti-PD-L1 IgG1 monoclonal antibody (mAb) that has demonstrated anti-tumor activity in several tumor types.
Other Name: MSB00107



Primary Outcome Measures :
  1. 6-month PFS% [ Time Frame: 24 weeks ]
    The percentage of patients who are alive and free-from confirmed tumor progression at 6-month (24 weeks).


Secondary Outcome Measures :
  1. Median OS (Overall survival) [ Time Frame: an average of 1 year ]
    Estimate OS according to stratum and for the total study population by Kaplan-Meier estimates.

  2. Objective Tumor Response (OR) [ Time Frame: up to 24 weeks ]
    To assess anti-tumor activity by evaluating the OR as assessed by iRANO criteria.

  3. Overall Safety profile [ Time Frame: Overall safety will be continuously monitored throughout the duration of the treatment, until one month after last patient visit. ]
    To evaluate the overall safety profile of avelumab in combination with axitinib by evaluating the adverse events (AEs) and laboratory abnormalities as graded by National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) v4.03.

  4. Evolution of neuro-cognitive function [ Time Frame: Up to 24 weeks; on week 1, week 9 of the treatment phase and week 20 of the follow-up phase ]
    Document neuro-cognitive function by Cogstate computer based neurocognitive assessment during study treatment.

  5. Continuous activity [ Time Frame: Activity will be continuously monitored for 2 weeks, two times with an interval of 6 weeks during the treatment phase. ]
    Assess the activity level in treated recGB patients by continuous activity tracking during study treatment by means of an activity tracking device.



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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  1. Diagnosis:

    • Histologically confirmed diagnosis of World Health Organization Grade IV malignant glioma (glioblastoma or gliosarcoma);
    • Documentation of recurrent (or progressive according to RNAO criteria) glioblastoma following prior treatment with surgery (resection or biopsy), radiation therapy and temozolomide chemotherapy;
    • A formalin-fixed, paraffin-embedded (FFPE) tumor tissue block or 15 unstained slides (10 minimum) obtained from an archival FFPE tumor tissue block will be required.
    • Presence of a measurable tumor lesion that is characterized by gadolinium enhancement on T1-MRI of the brain (with a shortest diameter of >5 mm) and enhanced lesion to normal brain uptake on FET-PET imaging of the brain;
    • If first recurrence of GBM is documented by MRI, an interval of at least 12 weeks after the end of prior radiation therapy is required unless there is either: i) histopathologic confirmation of recurrent tumor, or ii) new enhancement on MRI outside of the radiotherapy treatment field.
    • An interval of >28 days and full recovery (ie, no ongoing safety issues) from surgical resection and an interval of >4 weeks after the last administration of any other treatment for glioblastoma.
  2. Evidence of a personally signed and dated informed consent document indicating that the patient (or a legally acceptable representative, as allowed by local guidance/practice) has been informed of all pertinent aspects of the study.
  3. Patients who are willing and able to comply with scheduled visits, treatment plans, laboratory tests, and other study procedures.
  4. Age ≥ 18 years.
  5. Estimated life expectancy of at least 3 months.
  6. Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0 or 1.
  7. No evidence of pre-existing uncontrolled hypertension as documented by 2 baseline blood pressure (BP) readings taken at least 1 hour apart. The baseline systolic BP readings must be ≤ 140 mm Hg, and the baseline diastolic BP readings must be ≤ 90 mm Hg. Use of antihypertensive medications to control BP is allowed.
  8. Adequate bone marrow function, including:

    1. Absolute neutrophil count (ANC) ≥ 1,500/mm3 or ≥ 1.5 x 109/L;
    2. Platelets ≥ 100,000/mm3 or ≥ 100 x 109/L;
    3. Hemoglobin ≥ 9 g/dL (may have been transfused).
  9. Adequate renal function, including:

    1. Estimated creatinine clearance ≥ 30 mL/min as calculated using the Cockcroft-Gault (CG) equation;
    2. Urinary protein <2+ by urine dipstick. If dipstick is ≥ 2+, then 24-hour urinary protein <2 g per 24 hours.
  10. Adequate liver function, including:

    1. Total serum bilirubin ≤ 1.5 x upper limit of normal (ULN);
    2. AST and ALT ≤ 2.5 x ULN.
  11. Serum pregnancy test (for females of childbearing potential) negative at screening.
  12. Male patients able to father children and female patients of childbearing potential and at risk for pregnancy must agree to use 2 highly effective methods of contraception throughout the study and for at least 90 days after the last dose of assigned treatment.

Exclusion criteria:

  1. Any of the following prior cancer therapies:

    • Prior immunotherapy with an anti-PD-1, anti-PD-L1, anti-PD-L2, anti-CD137, or anti-cytotoxic T-lymphocyte-associated antigen-4 (CTLA-4) antibody (including ipilimumab), or any other antibody or drug specifically targeting T-cell co-stimulation or immune checkpoint pathways;
    • Prior therapy with axitinib as well as any prior therapies with other VEGF pathway inhibitors (including bevacizumab).
  2. Participation in other therapeutic studies within 4 weeks prior to enrollment in the current study.
  3. Persisting toxicity related to prior therapy NCI CTCAE v4.03 Grade > 1; however, sensory neuropathy Grade ≤ 2 is acceptable.
  4. Current or prior use of immunosuppressive medication within 7 days prior to enrollment, except for steroid treatment needed to palliate glioblastoma associated neurological symptoms and intranasal, inhaled, topical steroids, or local steroid injections (e.g., intra-articular injection);
  5. No treatment with enzyme inducing anti-epileptic drugs (EIAED) during and at least 14 days before the administration of axitinib;
  6. Known severe hypersensitivity reactions to monoclonal antibodies (Grade > 3), any history of anaphylaxis.
  7. Known prior or suspected hypersensitivity to study drugs or any component in their formulations.
  8. Diagnosis of any other malignancy within 5 years prior to enrollment, except for adequately treated basal cell or squamous cell skin cancer, or carcinoma in situ of the breast or of the cervix, or low-grade (Gleason 6 or below) prostate cancer on surveillance with no plans for treatment intervention (eg, surgery, radiation or castration).
  9. Active autoimmune disease that might deteriorate when receiving an immunostimulatory agents. Patients with diabetes type I, vitiligo, psoriasis, hypo- or hyperthyroid disease not requiring immunosuppressive treatment are eligible.
  10. Gastrointestinal abnormalities including:

    • Inability to take oral medication;
    • Requirement for intravenous alimentation;
    • Prior surgical procedures affecting absorption including total gastric resection;
    • Treatment for active peptic ulcer disease in the past 6 months;
    • Active gastrointestinal bleeding, unrelated to cancer, as evidenced by clinically significant hematemesis, hematochezia or melena in the past 3 months without evidence of resolution documented by endoscopy or colonoscopy;
    • Malabsorption syndromes.
  11. Active infection requiring systemic therapy.
  12. Diagnosis of prior immunodeficiency or organ transplant requiring immunosuppressive therapy, or known human immunodeficiency virus (HIV) or acquired immunodeficiency syndrome (AIDS)-related illness.
  13. Any test for hepatitis B virus (HBV) or hepatitis C virus (HCV) indicating acute or chronic infection.
  14. Vaccination within 4 weeks of the first dose of avelumab and while on trial is prohibited except for administration of inactivated vaccines (for example, inactivated influenza vaccines).
  15. Requirement of anticoagulant therapy with oral vitamin K antagonists. Low-dose anticoagulants for maintenance of patency of central venous access device or prevention of deep venous thrombosis is allowed. Therapeutic use of low molecular weight heparin is allowed.
  16. Evidence of inadequate wound healing (including dehiscence of the craniotomy scar).
  17. Grade ≥ 3 hemorrhage within 4 weeks of patient enrollment.
  18. Any of the following in the previous 12 months: myocardial infarction, severe/unstable angina, coronary/peripheral artery bypass graft, symptomatic congestive heart failure, LVEF less than LLN, clinically significant pericardial effusion, cerebrovascular accident, transient ischemic attack.
  19. Any of the following in the previous 6 months: deep vein thrombosis or symptomatic pulmonary embolism.
  20. Evidence of tumor involvement of the myocardium or pericardium or tumor thrombus extending to the heart.
  21. Current use or anticipated need for treatment with drugs or foods that are known strong CYP3A4/5 inhibitors, including their administration within 10 days prior to patient enrollment (eg, grapefruit juice or grapefruit/grapefruit-related citrus fruits [eg, Seville oranges, pomelos], ketoconazole, miconazole, itraconazole, voriconazole, posaconazole, clarithromycin, telithromycin, indinavir, saquinavir, ritonavir, nelfinavir, amprenavir, fosamprenavir nefazodone, lopinavir, troleandomycin, mibefradil, and conivaptan). The topical use of these medications (if applicable), such as 2% ketoconazole cream, is allowed.
  22. Current use or anticipated need for drugs that are known strong CYP3A4/5 inducers, including their administration with 10 days prior to patient enrollment(eg, phenobarbital, rifampin, phenytoin, carbamazepine, rifabutin, rifapentin, clevidipine, St John's wort).
  23. Pregnant female patients, breastfeeding female patients.
  24. Other severe acute or chronic medical conditions including colitis, inflammatory bowel disease, uncontrolled asthma, and pneumonitis or psychiatric condition, including recent (within the past year) or active suicidal ideation or behavior, or laboratory abnormality that may increase the risk associated with study participation or investigational product administration or may interfere with the interpretation of study results and, in the judgment of the investigator, would make the patient inappropriate for entry into this study.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03291314


Contacts
Contact: Bart Neyns, MD, PhD +3224775447 Bart.Neyns@uzbrussel.be
Contact: Laila Ben Salama, Ir +3224749922 Laila.BenSalama@uzbrussel.be

Locations
Belgium
UZ Brussel Recruiting
Brussel, Belgium, 1090
Contact: Bart Neyns, Phd,Md    +32 2 477 ext 54 47    bart.neyns@uzbrussel.be   
Principal Investigator: Bart Neyns, Phd,Md         
Sponsors and Collaborators
Universitair Ziekenhuis Brussel

Publications:

Responsible Party: Bart Neyns, Prof. Dr., Universitair Ziekenhuis Brussel
ClinicalTrials.gov Identifier: NCT03291314     History of Changes
Other Study ID Numbers: 2017-BN-001
First Posted: September 25, 2017    Key Record Dates
Last Update Posted: September 25, 2017
Last Verified: July 2017
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Product Manufactured in and Exported from the U.S.: No

Additional relevant MeSH terms:
Glioblastoma
Astrocytoma
Glioma
Neoplasms, Neuroepithelial
Neuroectodermal Tumors
Neoplasms, Germ Cell and Embryonal
Neoplasms by Histologic Type
Neoplasms
Neoplasms, Glandular and Epithelial
Neoplasms, Nerve Tissue
Antibodies, Monoclonal
Axitinib
Immunologic Factors
Physiological Effects of Drugs
Protein Kinase Inhibitors
Enzyme Inhibitors
Molecular Mechanisms of Pharmacological Action