RO4929097and Bevacizumab in Treating Patients With Progressive or Recurrent Malignant Glioma

Adult Glioblastoma Clinical Trial

Official title:

Phase I/II Study of R04929097 With Bevacizumab in Patients With Recurrent Malignant Glioma

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT01189240
• Other study ID #: NCI-2011-02509
• Secondary ID: NCI-2011-02509CD
• Status: Terminated
• Phase: Phase 1/Phase 2
• First received: August 25, 2010
• Last updated: November 13, 2015
• Start date: December 2010
• Est. completion date: February 2015

Study information

• Verified date: October 2015
• Source: National Cancer Institute (NCI)
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

This phase I/II trial is studying the side effects and the best dose of RO4929097 to see how well it works when given together with bevacizumab compared to bevacizumab alone in treating patients with progressive or recurrent malignant glioma. RO4929097 may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Monoclonal antibodies, such as bevacizumab, can block tumor growth in different ways. Some block the ability of tumor cells to grow and spread. Others find tumor cells and help kill them or carry tumor-killing substances to them. Giving RO4929097 together with bevacizumab may kill more tumor cells.

Description:

Phase I

Primary Objective:

1. To assess the safety profile of R04929097 in combination with bevacizumab and to determine a recommended Phase II dose of R04929097 in combination with bevacizumab in patients with recurrent malignant glioma

Secondary Objectives:

2. To describe the toxicity associated with this combination regimen

3. To assess pharmacokinetics of R04929097 in combination with bevacizumab

Phase II I. Assess the safety profile and the recommended phase II dose of gamma-secretase inhibitor RO4929097 (RO4929097) in combination with bevacizumab in patients with recurrent malignant glioma.

II. Assess the progression-free survival at 6 months of patients treated with this regimen.

III. Compare the overall survival of patients with recurrent glioblastoma treated with RO4929097 and bevacizumab versus bevacizumab alone.

SECONDARY OBJECTIVES:

I. Describe the toxicity associated with this regimen in these patients. II. Assess the pharmacokinetics of this regimen in these patients. III. Estimate the proportion of patients alive and progression-free survival at 6 months in patients treated with RO4929097 and bevacizumab versus bevacizumab alone.

IV. Evaluate the safety and tolerability of these regimens in these patients. V. Explore potential prognostic biomarkers from glioma tissue at baseline and potential association with Notch pathway inhibition.

OUTLINE: This is a multicenter, phase I, dose-escalation study of gamma-secretase inhibitor RO4929097 (RO4929097) followed by a randomized phase II study.

PHASE I: Patients receive oral RO4929097 on days 1-3, 8-10, 15-17, and 22-24, and bevacizumab IV over 30-90 minutes on days 1 and 15 (days 2 or 3 and 15 of course 1 only). Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.

PHASE II: Patients are randomized* to 1 of 2 treatment arms.

ARM I: Patients receive oral RO4929097 on days 1-3, 8-10, 15-17, and 22-24, and bevacizumab IV over 30-90 minutes on days 1 and 15.

ARM II: Patients receive bevacizumab as in arm I.

In both arms, courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.

NOTE: *If phase II single-arm study demonstrates effectiveness, it will proceed to the phase II randomized study.

Some patients undergo blood sample collection for pharmacokinetic studies. Archived tumor tissue samples are analyzed for potential biomarkers and Notch pathway inhibition.

After completion of study therapy, patients are followed up every 2 months.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 13
• Est. completion date: February 2015
• Est. primary completion date: January 2013
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Histologically confirmed malignant glioma (phase I)

• Glioblastoma

• Anaplastic astrocytoma

• Anaplastic oligodendroglioma

• Mixed anaplastic oligoastrocytoma

• Histologically confirmed glioblastoma following radiotherapy and temozolomide (phase II)

• Progressive or recurrent disease after conformal external-beam radiation therapy and concurrent temozolomide, followed by = 1 adjuvant course of temozolomide

• Measurable disease by MRI within the past 2 weeks

• Tumor tissue form indicating availability of archived tissue from initial resection at diagnosis of malignant glioma completed and signed by a pathologist

• Karnofsky performance status 60-100%

• ANC = 1,500/mm³

• Platelet count = 100,000/mm³

• Hemoglobin = 9 g/dL

• Total bilirubin normal

• AST and ALT = 2.5 times upper limit of normal

• Creatinine normal OR creatinine clearance = 60 mL/min

• Urine protein: If proteinuria = +2 protein, a protein level should be < 1,000 mg by a 24-hour urine collection

• Electrolytes (calcium, chloride, magnesium, potassium, phosphorus, sodium) within institutional normal limits

• Fertile patients must use 2 forms of effective contraception before, during, and for = 12 months (6 months phase II, bevacizumab arm only) after treatment

• Negative pregnancy test

• Not pregnant or nursing

• At least 5 years since prior malignancy except nonmelanoma skin cancer, or carcinoma in situ of the cervix, breast, or bladder

• Mini Mental State Exam score of = 15

• Must be able to tolerate MRI

Exclusion Criteria:

• No serious concurrent infection or medical illness that would jeopardize the ability of the patient to receive the treatment outline in this protocol with reasonable safety

• No history of allergic reactions attributed to compounds of similar chemical or biological composition to gamma-secretase inhibitor RO4929097 or bevacizumab

• Must be able to swallow capsules

• No malabsorption syndrome or other condition that would interfere with intestinal absorption

• No baseline QTcF > 450 msec (male) or QTcF > 470 msec (female)

• Not history of being serologically positive for hepatitis A, B, or C

• No history of cirrhosis

• No uncontrolled hypocalcemia, hypomagnesemia, hyponatremia, or hypokalemia despite adequate electrolyte supplementation

• No uncontrolled intercurrent illness including, but not limited to, any of the following:

• Ongoing or active infection

• Symptomatic congestive heart failure

• Unstable angina pectoris

• A history of torsades de pointes or other significant cardiac arrhythmias other than chronic, stable atrial fibrillation

• Psychiatric illness and/or social situations that would limit compliance with study requirements

• No serious or non-healing wound, ulcer, or bone fracture

• No history of abdominal fistula, gastrointestinal perforation, or intra-abdominal abscess within the past 6 months

• No significant vascular disease (e.g., aortic aneurysm requiring surgical repair or recent peripheral arterial thrombosis) within the past 6 months

• No clinically significant cardiovascular disease, including any of the following:

• Inadequately controlled hypertension (systolic BP > 160 mm Hg and/or diastolic BP > 90 mm Hg) despite antihypertensive medication

• History of cerebrovascular accident or transient ischemic attack at any time

• Myocardial infarction or unstable angina within the past 12 months

• NYHA grade II-IV congestive heart failure

• Serious and inadequately controlled cardiac arrhythmia

• Significant vascular disease (e.g., aortic aneurysm or history of aortic dissection)

• Clinically significant peripheral vascular disease

• No evidence of bleeding diathesis or coagulopathy

• No known hypersensitivity to Chinese hamster ovary cell products or other recombinant human antibodies

• No requirement for antiarrhythmics or other medications known to prolong QTc

• One or 2 prior treatment regimens allowed

• Recovered from severe toxicity of prior therapy

• At least 3 months since prior radiotherapy

• At least 6 weeks since prior nitrosourea

• At least 3 weeks since prior chemotherapy

• At least 4 weeks since prior and no other concurrent investigational agents

• At least 2 weeks since prior non-cytotoxic, FDA-approved agent (e.g., Tarceva [erlotinib hydrochloride], hydroxychloroquine, bevacizumab, etc.)

• At least 28 days since any prior surgery

• No prior ?-secretase inhibitors and/or bevacizumab

• At least 10 days since prior and no concurrent enzyme-inducing anti-epileptic drug

• No concurrent combination antiretroviral therapy for HIV-positive patients

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Adult Anaplastic Astrocytoma
• Adult Anaplastic Oligodendroglioma
• Adult Giant Cell Glioblastoma
• Adult Glioblastoma
• Adult Gliosarcoma
• Astrocytoma
• Glioblastoma
• Gliosarcoma
• Oligodendroglioma
• Recurrent Adult Brain Tumor

Intervention

Drug:
• gamma-secretase/Notch signalling pathway inhibitor RO4929097
Given orally

Biological:
• bevacizumab
Given IV

Other:
• laboratory biomarker analysis
Correlative studies
• pharmacological study
Correlative studies

Locations

Country	Name	City	State
United States	University of California at Los Angeles (UCLA )	Los Angeles	California
United States	Memorial Sloan-Kettering Cancer Center	New York	New York
United States	University of California San Francisco Medical Center-Parnassus	San Francisco	California
United States	H. Lee Moffitt Cancer Center and Research Institute	Tampa	Florida

Sponsors (1)

Lead Sponsor	Collaborator
National Cancer Institute (NCI)

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Maximum-tolerated Dose and the Recommended Phase II Dose of Gamma-secretase Inhibitor RO4929097 in Combination With Bevacizumab Determined by Dose-limiting Toxicity Rate (Phase I)	Pts were treated at escalating dose levels of RO4929097 (Dose levels: 5, 10 or 20 mg) for an observed evaluation at the end of a 4week period. 3 pts treated at each cohort if less than or equal to 33% dose will be escalated. Pts must receive one dose of treatment to be evaluated for toxicity. A standard 3+3 dose escalation method will be used	28 days	Yes
Secondary	Toxicity Description (Dose Limiting Toxicity-DLT) of Gamma-secretase Inhibitor RO4929097 in Combination With Bevacizumab	Pts were treated at escalating dose levels of RO4929097 (Dose levels: 5, 10 or 20 mg) for an observed evaluation at the end of a 4week period. 3 pts treated at each cohort. Pts must receive one dose of treatment to be evaluated for toxicity. Toxcity description associated with combination of RO4929097 and Bevacizumab	28 days - 1 cycle	Yes
Secondary	Measurement of Cmax to Determine the Effect of Bevacizumab on the Plasma Pharmacokinetics of RO4929097 Day 1	all pts at all dose levels (5,10 and 20mg) will have pks collected. 10 samples will be collected at various time points over a 24 hour time point. Samples will be collected on the first day of treatment during cycle 1.; For initial cycle (Cycle 1) bevacizumab was not given until 2 or 3 days after all PKs samples of initial dose of RO49290977 was collected	24 hrs	No
Secondary	Measurement of Cmax to Determine the Effect of Bevacizumab on the Plasma Pharmacokinetics of RO4929097 Day 15	all pts at all dose levels (5,10 and 20mg) will have pks collected. 10 samples will be collected at various time points over a 24 hour time point. Samples will be collected on the 15th day of treatment during cycle 1.	24hr	No
Secondary	Measurement of AUC24 to Determine the Effect of Bevacizumab on the Plasma Pharmacokinetics of RO4929097 Day 1	all pts at all dose levels (5,10 and 20mg) will have pks collected. 10 samples will be collected at various time points over a 24 hour time point. Samples will be collected on the first day of treatment during cycle 1.	24hrs	No
Secondary	Measurement of AUC24 to Determine the Effect of Bevacizumab on the Plasma Pharmacokinetics of RO4929097 Day 15	all pts at all dose levels (5,10 and 20mg) will have pks collected. 10 samples will be collected at various time points over a 24 hour time point. Samples will be collected on the 15th day of treatment during cycle 1.	24hr	No