Effect of NovoTTF-100A in Recurrent Glioblastoma Multiforme (GBM)

Recurrent Glioblastoma Multiforme Clinical Trial

Official title:

A Prospective, Multi-center Trial of NovoTTF-100A Compared to Best Standard of Care in Patients With Progressive or Recurrent GBM

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00379470
• Other study ID #: EF-11
• Status: Completed
• Phase: Phase 3
• First received: September 20, 2006
• Last updated: April 29, 2012
• Start date: September 2006
• Est. completion date: January 2011

Study information

• Verified date: April 2012
• Source: NovoCure Ltd.
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

The study is a randomized, controlled trial, designed to test the efficacy and safety of a new medical device, the NovoTTF-100A. The device is an experimental, portable, battery operated device for chronic treatment of patients with recurrent or progressive glioblastoma multiforme (GBM) using alternating electric fields (termed TTFields).

Description:

PAST CLINICAL EXPERIENCE:

The effect of the electric fields generated by the NovoTTF-100A device (TTFields) has been tested in two pilot trials in humans. The data from these trials suggest NovoTTF-100A may improve time to disease progression and overall survival of recurrent GBM patients. Although the number of patients in the pilot trials is small, The FDA has determined that the data gathered so far warrant testing of NovoTTF-100A treatment as a possible therapy for patients with recurrent GBM.

DESCRIPTION OF THE TRIAL:

Patients with GBM whose disease has recurred or progressed despite standard treatment (Surgery, radiation therapy, Temozolomide treatment) and meet all of the requirements for participation in the study will be randomly assigned to one of two groups:

1. Treatment with the NovoTTF-100A device, or

2. Treatment with the best standard of care practiced at each of the participating centers.

If assigned to the best standard of care group, patients will receive a chemotherapeutic agent chosen based on their prior treatments and the standard of care practiced at each treating center.

If assigned to the NovoTTF-100A group, the patients will be treated continuously for as long as their disease is stable or regressing. NovoTTF-100A treatment will consist of wearing four electrically insulated electrodes on the head. Electrode placement will require shaving of the scalp before treatment. After an initial short hospitalization (24 hours) patients will be released to continue treatment at home where they can maintain their regular daily routine.

During the trial, regardless of whether assigned to the NovoTTF-100A treatment group or the best standard of care group, patients will need to return once every month the hospital outpatient clinics where they will be examined by a physician and undergo routine laboratory examinations. These routine visits will continue for as long as the patient's disease is not progressing. After progression, if such occurs, patients will need to return once per month for two more months to the outpatient clinic for similar follow up examinations.

During the visits to the clinic patients will be examined physically and neurologically. Additionally, routine blood tests and ECG will be performed. A routine MRI of the head will be performed at baseline and after 2, 4 and 6 months. After this follow up plan, patients will be contacted once per month by telephone to answer basic questions about their health status.

SCIENTIFIC BACKGROUND:

Electric fields exert forces on electric charges similar to the way a magnet exerts forces on metallic particles within a magnetic field. These forces cause movement and rotation of electrically charged biological building blocks, much like the alignment of metallic particles seen along the lines of force radiating outwards from a magnet.

Electric fields can also cause muscles to twitch and if strong enough may heat tissues. TTFields are alternating electric fields of low intensity. This means that they change their direction repetitively many times a second. Since they change direction very rapidly (200 thousand times a second), they do not cause muscles to twitch, nor do they have any effects on other electrically activated tissues in the body (brain, nerves and heart). Since the intensities of TTFields in the body are very low, they do not cause heating.

The breakthrough finding made by NovoCure was that finely tuned alternating fields of very low intensity, now termed TTFields (Tumor Treating Fields), cause a significant slowing in the growth of cancer cells. Due to the unique geometric shape of cancer cells when they are multiplying, TTFields cause the building blocks of these cells to move and pile up in such a way that the cells physically explode. In addition, cancer cells also contain miniature building blocks which act as tiny motors in moving essential parts of the cells from place to place. TTFields cause these tiny motors to fall apart since they have a special type of electric charge.

As a result of these two effects, cancer tumor growth is slowed and can even reverse after continuous exposure to TTFields.

Other cells in the body (normal healthy tissues) are affected much less than cancer cells since they multiply at a much slower rate if at all. In addition TTFields can be directed to a certain part of the body, leaving sensitive areas out of their reach.

In conclusion, TTField hold the promise of serving as a brand new cancer treatment with very few side effects and promising affectivity in slowing or reversing this disease.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 236
• Est. completion date: January 2011
• Est. primary completion date: November 2009
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Pathological evidence of GBM using WHO classification criteria.

• > 18 years of age.

• Not a candidate for further radiotherapy or additional resection of residual tumor.

• Patients with disease progression (by Macdonald criteria i.e., > 25% or new lesion) documented by CT or MRI within 4 weeks prior to enrollment

• Karnofsky scale = 70

• Life expectancy at least 3 months

• Participants of childbearing age must use effective contraception.

• All patients must sign written informed consent.

Exclusion Criteria:

• Actively participating in another clinical treatment trial

• Within 4 weeks from surgery for recurrence

• Within 4 weeks from any prior chemotherapy.

• Within 4 weeks from radiation therapy

• Pregnant

• Significant co-morbidities (within 4 weeks prior to enrollment):

1. Significant liver function impairment - AST or ALT > 3 times the upper limit of normal

2. Total bilirubin > upper limit of normal

3. Significant renal impairment (serum creatinine > 1.7 mg/dL)

4. Coagulopathy (as evidenced by PT or APTT >1.5 times control in patients not undergoing anticoagulation)

5. Thrombocytopenia (platelet count < 100 x 103/µL)

6. Neutropenia (absolute neutrophil count < 1 x 103/µL)

7. Anemia (Hb < 10 g/L)

8. Severe acute infection

• Implanted pacemaker, defibrillator or deep brain stimulator, or documented clinically significant arrhythmias.

• Infra-tentorial tumor

• Evidence of increased intracranial pressure (midline shift > 5mm, clinically significant papilledema, vomiting and nausea or reduced level of consciousness)

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Glioblastoma
• Recurrent Glioblastoma Multiforme

Intervention

Device:
• NovoTTF-100A
multiple four-week courses of continuous NovoTTF-100A treatment

Locations

Country	Name	City	State
Austria	University Hospital Graz	Graz
Czech Republic	FN Brno - Masaryk University	Brno
Czech Republic	Na Homolce Hospital	Prague
France	Hospital of Neurology Lyon - University Claude Bernard Lyon 1	Lyon
France	Group Hospitals Pitie-Salpetriere	Paris
Germany	University Hospital Augsburg	Augsburg
Germany	University Medical Center Hamburg-Eppendorf	Hamburg
Germany	University Hospital of Schleswig-Holstein	Kiel
Israel	Tel Aviv Sourasky Medical Center	Tel Aviv
Switzerland	Centre Hospitalier Universitaire Vaudois	Lausanne
United States	Beth Israel Deaconess Medical Center	Boston	Massachusetts
United States	Boston University Medical Center	Boston	Massachusetts
United States	Lahey Clinic Medical Center	Burlington	Massachusetts
United States	University of Virginia	Charlottesville	Virginia
United States	Northwestern University	Chicago	Illinois
United States	University of Illinois in Chicago	Chicago	Illinois
United States	Cleveland Clinic	Cleveland	Ohio
United States	University Hospitals of Cleveland	Cleveland	Ohio
United States	NJ Neuroscience Institute - JFK Medical Center	Edison	New Jersey
United States	Evanston Northwestern Healthcare	Evanston	Illinois
United States	Medical College of Wisconsin	Milwaukee	Wisconsin
United States	Columbia University Medical Center	New York	New York
United States	Memorial Sloan Kettering Cancer Center	New York	New York
United States	Weill Cornell Medical College	New York	New York
United States	University of Pittsburgh Medical Center (UPMC)	Pittsburgh	Pennsylvania

Sponsors (1)

Lead Sponsor	Collaborator
NovoCure Ltd.

Countries where clinical trial is conducted

United States,  Austria,  Czech Republic,  France,  Germany,  Israel,  Switzerland, 

References & Publications (3)

Kirson ED, Dbalý V, Tovarys F, Vymazal J, Soustiel JF, Itzhaki A, Mordechovich D, Steinberg-Shapira S, Gurvich Z, Schneiderman R, Wasserman Y, Salzberg M, Ryffel B, Goldsher D, Dekel E, Palti Y. Alternating electric fields arrest cell proliferation in animal tumor models and human brain tumors. Proc Natl Acad Sci U S A. 2007 Jun 12;104(24):10152-7. Epub 2007 Jun 5. — View Citation

Kirson ED, Gurvich Z, Schneiderman R, Dekel E, Itzhaki A, Wasserman Y, Schatzberger R, Palti Y. Disruption of cancer cell replication by alternating electric fields. Cancer Res. 2004 May 1;64(9):3288-95. — View Citation

Salzberg M, Kirson E, Palti Y, Rochlitz C. A pilot study with very low-intensity, intermediate-frequency electric fields in patients with locally advanced and/or metastatic solid tumors. Onkologie. 2008 Jul;31(7):362-5. doi: 10.1159/000137713. Epub 2008 Jun 24. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Overall Survival		2 years from initiation of accrual	No
Secondary	Progression free survival at 6 months (PFS6)		2 years from initiation of accrual	No
Secondary	Median Time to Disease Progression (TTP)		2 years from initiation of accrual	No
Secondary	% 1-year survival		2 years from initiation of accrual	No
Secondary	Radiological response (Macdonald criteria)		2 years from initiation of accrual	No
Secondary	Quality of life assessment (EORTC QLQ-C30)		2 years from initiation of accrual	No
Secondary	Adverse events severity and frequency		2 years from initiation of accrual	Yes