Glioblastoma therapy with tumor-treating fields will be available in Germany

16

Apr 2020

Patients with a newly diagnosed glioblastoma will have an opportunity to benefit from the therapy with tumor-treating fields (TTF) at the expense of statutory health insurance. The Federal Joint Committee (G-BA) decided on March 20, 2020, the details concerning the indications and the quality assurance measures that will apply when prescribing this outpatient treatment method.

Glioblastoma is known as the most aggressive brain tumor. The cause of most cases of glioblastoma is not known. The typical duration of survival following diagnosis is 12 to 15 months, with fewer than 3 to 7% of people surviving longer than five years.

TTF treatment is a new method of inhibiting tumor growth based on electrostimulation. Electrical alternating current (AC) fields are locally transmitted to the tumor cells via the scalp; the electricity is generated in a small portable generator. The benefit assessment procedure found that those affected live an average of almost five months longer if TTF is also used in addition to standard therapy.

TTF treatment will be available for patients with a newly diagnosed glioblastoma if, after the complete possible surgery or after completion of chemoradiation, no early disease progression is detected. The TTF treatment is then used in the maintenance phase in addition to the further standard therapy, which includes adjuvant chemotherapy or after the first relapse occurs, relapse therapy. TTF treatment can be used until the second relapse.

The G-BA stipulated that the indication given by the prescribing specialist must be based on the recommendation of an interdisciplinary tumor consultation. As part of the regular follow-up, the use and tolerability of the TTF should be discussed as well.

Since the treatment with TTF takes place continuously at home, the patient and, if necessary, other auxiliary persons must be trained in the correct use of the device. In order to achieve the best possible therapy result, patients should use the TTF at least 18 hours a day.

The decision will be submitted to the Federal Ministry of Health for legal review and will enter into force after non-objection and publication in the Federal Gazette. Treatment with TTF can be provided as an outpatient service after the Evaluation Committee’s decision on the amount of reimbursement via the EBM (German Uniform Evaluation Standard).

The full details in German can be found here.

Subscribe to our newsletter delivered every second week not to miss important reimbursement information.

The latest related news

24

Mar 2022

The HTA body of the Tuscany Regional Healthcare issues two types of documents: HTA forms and motivational forms. With a regional decree 2472 of February 10, 2022, Tuscany Regional Healthcare has published assessments of five medical devices of various therapeutic areas, such as cardiovascular and peripheral vascular areas.

Read more

23

Mar 2022

In late January 2022, Swedish Medical Technologies Product (MTP) Council issued an updated version of recommendations regarding gene expression analysis for decision-making on the adjuvant breast cancer treatment, initially published in November 2021. The recommendation to the regions remains the same. The changes were only concerned with the clarification of some facts.

Read more

22

Mar 2022

On February 17, 2022, the Federal Joint Committee (G-BA) has decided to include the method of matrix-associated autologous chondrocyte implantation (M-ACI) on the knee joint in the case of symptomatic cartilage damage in the lists of reimbursed procedures in the hospital and ambulatory settings.

Read more

18

Mar 2022

On February 22, 2022, a repository of innovative acts outside the nomenclature of biology and anatomopathology (RIHN) and a Supplementary list of IVD tests were published. Minor changes were introduced in the 2022 RIHN list.

Read more

15

Mar 2022

The Belgian Health Care Knowledge Center (KCE) initiated a study aimed at defining a clear and transparent procedure for the evaluation of digital health technologies in Belgium.

Read more