Analysis showing patients treated with Optune® in combination with
temozolomide for newly diagnosed glioblastoma reported an unprecedented
five-year survival advantage to be shared during an oral presentation
ST. HELIER, Jersey--(BUSINESS WIRE)--
Novocure (NASDAQ: NVCR) announced today that ten data presentations
investigating the use of Tumor Treating Fields (TTFields) for the
treatment of glioblastoma will be presented at this year’s World
Federation of Neuro-oncology Societies (WFNOS) 5th
Quadrennial Meeting in Zurich from May 4-7.
The listing of TTFields presentations at WFNOS include:
-
(OS07.9) Standard of care temozolomide chemotherapy ± Tumor Treating
Fields (TTFields) in newly diagnosed glioblastoma. Final results of
the phase III EF-14 clinical trial. R. Stupp. Saturday, May 6, 11:50
a.m. – 12:00 p.m. CET. Location: Kongresssaal.
-
(P08.17) Mitotic checkpoint inhibition augments Tumor Treating Fields
(TTFields) effects on glioblastoma cells. C. Hagemann. Friday, May 5,
5:00 p.m. – 6:00 p.m. CET. Location: Poster section P08.
-
(P09.07) The use of programmable shunts in patients treated with Tumor
Treating Fields: multicentric case series. C.F. Freyschlag. Friday,
May 5, 5:00 p.m. – 6:00 p.m. CET. Location: Poster section P09a.
-
(P09.12) Durable remission with Tumor Treating Fields as adjuvant
treatment for glioblastoma relapse in a patient with grade IV
hematotoxicity during initial temozolomide radiochemotherapy. C. Hirt.
Friday, May 5, 5:00 p.m. – 6:00 p.m. CET. Location: Poster section
P09a.
-
(P09.21) Complete radiological response after subtotal resection in
two glioblastoma patients treated with Tumor Treating Fields. A.F.
Kessler. Friday, May 5, 5:00 p.m. – 6:00 p.m. CET. Location: Poster
section P09a.
-
(P09.23) Tumor Treating Fields delivery using second generation Optune
system for glioblastoma treatment: patient experience and compliance.
Friday, May 5, 5:00 p.m. – 6:00 p.m. CET. Location: Poster section
P09a.
-
(P09.47) Long-term survival after Tumor Treating Fields (TTFields)
therapy. A. Rulseh. Saturday, May 6, 6:00 p.m. – 7:00 p.m. CET.
Location: Poster section P09b.
-
(P09.32) High therapy compliance in patients treated with Optune
therapy does not depend on demographic data, stage of disease or
treatment duration. M. Misch. Saturday, May 6, 6:00 p.m. – 7:00 p.m.
CET. Location: Poster section P09b.
-
(P09.44) One year with Optune in Austria: first report on clinical
experiences. D. Pinggera. Saturday, May 6, 6:00 p.m. – 7:00 p.m. CET.
Location: Poster section P09b.
-
(P09.51) Simultaneous application of TTFields (Optune) and radiation
in a 60-year old male patient: a case report. S. Scharl. Saturday, May
6, 6:00 p.m. – 7:00 p.m. CET. Location: Poster section P09b.
In addition, Novocure will have an exhibit where WFNOS attendees can
meet with commercial and medical colleagues and learn more about Optune
and Tumor Treating Fields (TTFields). Novocure will also host a
scientific lunchtime symposium on Friday, May 5 from 12:35 to 2:00 p.m.
CET in the main auditorium.
About Novocure
Novocure is an oncology company developing a profoundly different cancer
treatment centered on a proprietary therapy called TTFields, the use of
electric fields tuned to specific frequencies to disrupt solid tumor
cancer cell division. Novocure’s commercialized product, Optune, is
approved for the treatment of adult patients with glioblastoma. Novocure
has ongoing or completed clinical trials investigating TTFields in brain
metastases, non-small cell lung cancer, pancreatic cancer, ovarian
cancer and mesothelioma.
Headquartered in Jersey, Novocure has U.S. operations in Portsmouth, New
Hampshire, Malvern, Pennsylvania, and New York City. Additionally, the
company has offices in Germany, Switzerland and Japan, and a research
center in Israel. For additional information about the company, please
visit www.novocure.com
or follow us at www.twitter.com/novocure.
Approved Indications
In the United States, Optune is intended as a treatment for adult
patients (22 years of age or older) with histologically-confirmed
glioblastoma multiforme (GBM).
In the United States, Optune with temozolomide is indicated for the
treatment of adult patients with newly diagnosed, supratentorial
glioblastoma following maximal debulking surgery and completion of
radiation therapy together with concomitant standard of care
chemotherapy.
In the United States, for the treatment of recurrent GBM, Optune is
indicated following histologically-or radiologically-confirmed
recurrence in the supratentorial region of the brain after receiving
chemotherapy. The device is intended to be used as a monotherapy, and is
intended as an alternative to standard medical therapy for GBM after
surgical and radiation options have been exhausted.
In the European Union, Optune is intended for the treatment of patients
with newly diagnosed GBM, after surgery and radiotherapy with adjuvant
temozolomide, concomitant to maintenance temozolomide. The treatment is
intended for adult patients, 18 years of age or older, and should be
started more than 4 weeks after surgery and radiation therapy with
adjuvant temozolomide. Treatment may be given together with maintenance
temozolomide and after maintenance temozolomide is stopped.
In the European Union, Optune is also intended for the treatment of
patients with recurrent GBM who have progressed after surgery,
radiotherapy and temozolomide treatment for their primary disease. The
treatment is intended for adult patients, 18 years of age or older, and
should be started more than 4 weeks after the latest surgery, radiation
therapy or chemotherapy.
Patients should only use Optune under the supervision of a physician
properly trained in use of the device. Full prescribing information is
available at www.optune.com/safety
or by calling toll free 1-855-281-9301 in the US or by email at supportEMEA@novocure.com
in the European Union.
Important Safety Information
Contraindications: Do not use Optune if you have an active
implanted medical device, a skull defect (such as, missing bone with no
replacement), or bullet fragments. Use of Optune together with implanted
electronic devices has not been tested and may theoretically lead to
malfunctioning of the implanted device. Use of Optune together with
skull defects or bullet fragments has not been tested and may possibly
lead to tissue damage or render Optune ineffective.
Do not use Optune if you are known to be sensitive to conductive
hydrogels. In this case, skin contact with the gel used with Optune may
commonly cause increased redness and itching, and rarely may even lead
to severe allergic reactions such as shock and respiratory failure.
Warnings and Precautions: Use Optune only after receiving
training from qualified personnel, such as your doctor, a nurse, or
other medical personnel who have completed a training course given by
Novocure (the device manufacturer).
Do not use Optune if you are pregnant, you think you might be pregnant
or are trying to get pregnant. It is not known if Optune is safe or
effective in these populations.
The most common (≥10%) adverse events involving Optune in combination
with temozolomide were low blood platelet count, nausea, constipation,
vomiting, fatigue, scalp irritation from device use, headache,
convulsions, and depression.
The most common (≥10%) adverse events seen when using Optune alone were
scalp irritation from device use and headache.
The following adverse reactions were considered related to Optune when
using the device alone: scalp irritation from device use, headache,
malaise, muscle twitching, fall and skin ulcer.
All servicing procedures must be performed by qualified and trained
personnel.
Do not use any parts that do not come with the Optune Treatment Kit, or
that were not sent to you by the device manufacturer or given to you by
your doctor.
Do not wet the device or transducer arrays.
If you have an underlying serious skin condition on the scalp, discuss
with your doctor whether this may prevent or temporarily interfere with
Optune treatment.
Please see http://www.optune.com/safety
to see the Optune Instructions For Use (IFU) for complete information
regarding the device’s indications, contraindications, warnings, and
precautions.

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Source: Novocure