Optune® Plus Bevacizumab in Bevacizumab-Refractory Recurrent Glioblastoma

NCT ID: NCT02743078

Last Updated: 2021-06-02

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: PHASE2
• Total Enrollment: 3 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2017-05-09
• Study Completion Date: 2019-10-15

Brief Summary

This phase II trial will investigate the efficacy and safety of the addition of Optune (Tumor Treating Fields [TTFields] Therapy) to bevacizumab for patients with bevacizumab-refractory recurrent glioblastoma.

Detailed Description

Patients that have recurrent glioblastoma that has progressed on bevacizumab continue to receive bevacizumab with the addition of Tumor Treating Fields Therapy. Treatment is given until disease progression or the development of adverse events that require complete discontinuation.

Conditions

Glioblastoma; Glioma; Gliosarcoma

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Bevacizumab and TTFields Therapy

Bevacizumab starts on the first day (+/- 1 day) of Tumor Treating Fields (TTFields) therapy. Treatment is given until disease progression or the development of adverse events that require complete discontinuation.

Group Type: EXPERIMENTAL

Bevacizumab

Intervention Type: DRUG

10 mg/kg every 2 weeks intravenously over 30 minutes.

TTFields Therapy

Intervention Type: DEVICE

Device is worn continuously at least 18 hours a day on average, with 1-3 days off every four weeks.

Interventions

Bevacizumab

10 mg/kg every 2 weeks intravenously over 30 minutes.

Intervention Type: DRUG

TTFields Therapy

Device is worn continuously at least 18 hours a day on average, with 1-3 days off every four weeks.

Intervention Type: DEVICE

Other Intervention Names

Avastin; Optune; Tumor Treating Fields Therapy; TTF Therapy

Eligibility Criteria

Inclusion Criteria

• Histologically proven diagnosis of glioblastoma or other grade IV malignant glioma (including variants of glioblastoma i.e., gliosarcoma, giant cell glioblastoma, etc.).
• Confirmation of tumor recurrence or progression on contrast magnetic resonance imaging (MRI) (with and without gadolinium contrast) as determined by Response assessment in neuro-oncology (RANO) criteria within 14 days prior to registration for patients who did not have recent resection of their glioblastoma or only had a stereotactic biopsy.
• Patients having undergone recent resection (within 5 weeks prior to registration) of their glioblastoma to treat current recurrence prior to study treatment must have recovered from the effects of surgery (including patient's skin having fully recovered from the surgical wound) Note: a 4-week window is required after surgery prior to starting treatment. For central nervous system (CNS) -related stereotactic biopsies, a minimum of 7 days must have elapsed prior to registration.
• Residual disease of recurrent glioblastoma is not mandated for eligibility into the study. To best assess the extent of residual disease post-operatively, a post-operative MRI scan must be performed prior to registration and is recommended to be within 96 hours post-surgery (although 24-48 hours would be optimum). Note: Patients who did have surgery with a post-operative contrast-enhanced scan falling outside the 5-week window prior to registration, must have a repeat MRI scan within 14 days prior to registration.
• Patients with up to two recurrences are allowed.
• Failure on bevacizumab (either as a monotherapy or a combination) as most recent regimen confirmed by tumor recurrence on MRI.

• The patient must have failed no more than one regimen of bevacizumab.
• The patient must not have received bevacizumab as an upfront treatment in newly diagnosed glioblastoma.
• There must be a minimum of 14 days (i.e., an interval equal to or greater than 14 days) since last treatment with bevacizumab and registration
• History/physical examination within 14 days prior to registration
• Karnofsky performance status ≥ 70 within 14 days prior to registration
• Age ≥ 22
• Absolute neutrophil count (ANC) ≥ 1,000 cells/mm3
• Platelets ≥ 75,000 cells/mm3
• Hemoglobin (Hgb) ≥ 9.0 g/dl (Note: The use of transfusion or other intervention to achieve Hgb ≥ 9.0 g/dl is acceptable.)
• Creatinine ≤ 1.5 mg/dl
• Urine protein: creatinine (UPC) ratio < 1.0 within 14 days prior to registration OR urine dipstick for proteinuria ≤ 2+ (patients discovered to have > 2+ proteinuria on dipstick urinalysis at baseline must have a UPC ratio done that is <1.0 to be eligible. If the UPC ratio is ≥ 1.0 then the patients should undergo a 24-hour urine collection and must demonstrate ≤ 1g of protein in 24 hours to be eligible).

*Note: UPC ratio of spot urine is an estimation of the 24-hour urine protein excretion; a UPC ratio of 1 is roughly equivalent to a 24-hour urine protein of 1 gm. UPC ratio is calculated using one of the following formulas:

• [urine protein]/[urine creatinine]: if both protein and creatinine are reported in mg/dL
• [(urine protein) x0.088]/[urine creatinine]: if urine creatinine is reported in mmol/L
• Serum total bilirubin ≤ 1.5 x upper limit of normal (ULN) within 14 days prior to registration
• Alanine transaminase (ALT) and aspartate transaminase (AST) ≤ 3.0 x ULN within 14 days prior to registration
• Patients on full dose anticoagulants (e.g., warfarin or low molecular weight (LMW) heparin) must meet both of the following criteria:

1. No active bleeding or pathological condition that carries a high risk of bleeding (e.g., tumor involving major vessels or known varices) within 14 days prior to registration

2. One of the below criteria must be met based on patient's therapy:

1. Warfarin: In-range international normalized ratio (INR) (usually between 2 and 3) within 14 days prior to registration

2. LMW heparin or novel oral anti-coagulant: stable dose within 14 days prior to registration

• Patients must have recovered from the toxic effects of prior therapy at the time of registration as follows:

• 28 days from the administration of any investigational agent
• 28 days from administration of prior cytotoxic therapy with the following exceptions:

• 14 days from administration of vincristine or irinotecan
• 42 days from administration of nitrosoureas
• 21 days from administration of procarbazine
• 7 days from administration of non-cytotoxic agents [e.g., interferon, tamoxifen, thalidomide, cis-retinoic acid, etc. (radiosensitizer does not count)]

• Female patients of child-bearing potential must have a negative serum pregnancy test within 14 days prior to registration.
• Patient must be maintained on a stable or decreasing dose of corticosteroid for at least 5 days before the baseline scan.
• Minimum interval since completion of radiation treatment at the time of registration is 90 days.
• Patient must provide study specific informed consent prior to study entry.

Exclusion Criteria

• Prior invasive malignancy (except non-melanomatous skin cancer) unless disease free for a minimum of 3 years. (For example, carcinoma in situ of the breast, oral cavity, or cervix are all permissible).
• Infra-tentorial tumor.
• > 1 cm diameter of blood seen on contrast MRI (with and without gadolinium contrast)
• Major surgery such as intra-thoracic, intra-abdominal or intra-pelvic (with the exception of craniotomy), open biopsy or significant traumatic injury ≤ 4 weeks prior to registration, or patients who have had minor procedures, percutaneous biopsies or placement of vascular access device ≤ 1 week prior to registration, or who have not recovered from side effects of such procedure or injury.
• Implanted pacemaker, defibrillator or deep brain stimulator, other implanted electronic devices in the brain.
• Unstable angina and/or congestive heart failure requiring hospitalization within the last 6 months prior to registration.
• Transmural myocardial infarction within the last 6 months prior to registration
• Cerebrovascular accident (CVA), transient ischemic attack (TIA) within the last 6 months prior to registration
• Pulmonary embolism (PE) within the last 6 months prior to registration
• Uncontrolled hypertension (defined by a systolic blood pressure (SBP) ≥ 160 mm Hg or diastolic blood pressure (DBP) ≥ 100 mm Hg while on anti-hypertensive medications) within 14 days prior to registration.
• Acute bacterial or fungal infection requiring intravenous antibiotics at the time of registration.
• Chronic lung disease or Chronic Obstructive Pulmonary Disease exacerbation or other respiratory illness requiring hospitalization or precluding study therapy at the time of registration.
• Severe hepatic disease, defined as a diagnosis of Child-Pugh Class B or C hepatic disease.
• Known HIV positive patients.
• Other concurrent severe and/or uncontrolled concomitant medical conditions (e.g. active or uncontrolled infection, uncontrolled diabetes) that could cause unacceptable safety risks or compromise compliance with the protocol.
• Skull defects such as missing bone flap, a shunt, or bullet fragments.
• Significant intracranial pressure as per treating physician that may require surgical intervention.
• Pregnancy or women of childbearing potential and men who are sexually active and not willing/able to use medically acceptable forms of contraception.
• Breast feeding women.
• Prior allergic reaction to bevacizumab or severe adverse event with bevacizumab.
• Known sensitivity to conductive hydrogels.
• Prior treatment with the Optune® system.
• Active treatment on another clinical trial.

• Minimum Eligible Age: 22 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

NovoCure Ltd.

INDUSTRY

Sponsor Role: collaborator

RTOG Foundation, Inc.

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Manmeet Ahluwalia, MD, FACP

Role: PRINCIPAL_INVESTIGATOR

RTOG Foundation

Locations

University of California, San Diego

La Jolla, California, United States

University of California Irvine, Chao Family Comprehensive Cancer Center

Orange, California, United States

Miami Cancer Institute at Baptist Health

Miami, Florida, United States

UF Health Cancer Center at Orlando Health

Orlando, Florida, United States

Emory University

Atlanta, Georgia, United States

Washington University School of Medicine

St Louis, Missouri, United States

University of Rochester

Rochester, New York, United States

Cleveland Clinic Foundation

Cleveland, Ohio, United States

Thomas Jefferson University

Philadelphia, Pennsylvania, United States

Medical University of South Carolina

Charleston, South Carolina, United States

Medical College of Wisconsin

Milwaukee, Wisconsin, United States

Countries

United States

Provided Documents

Document Type: Study Protocol and Statistical Analysis Plan

View Document

Document Type: Informed Consent Form

View Document

Other Identifiers

RF 3503

Identifier Type: OTHER

Identifier Source: secondary_id

RTOG 3503

Identifier Type: -

Identifier Source: org_study_id