This is great news. Hopefully the FDA will quickly approve the Optune system for newly diagnosed GBM patients. Right now it is only approved for recurrent GBM patients but with results like this ( a 48% increase in 2 year survival rate), of course newly diagnosed patients should be using it.
Newly diagnosed patients can use it now off label. I just had a patient request my help in fighting his insurance company - they rejected the claim for Optune for his newly diagnosed GBM saying it is experimental for newly diagnosed. I sent a nice letter along with the research and they reversed the decision, saying they will now pay for it. Getting the FDA - then the NCCN - to support it's use for newly diagnosed will speed things up and avoid that problem.
11 May 2015 FDA Grants Priority Review Status for Novocure’s PMA Supplement Application of Optune in Newly Diagnosed Glioblastoma
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PMA Supplement application for Tumor Treating Fields in combination with temozolomide chemotherapy for newly diagnosed glioblastoma accepted for filing and review St. Helier, Jersey – May 11, 2015 – Novocure, a commercial stage oncology company, announced today that its Premarket Approval (PMA) application for Optune has been accepted for filing and review and granted priority review status by the United States Food and Drug Administration (FDA). The PMA application seeks approval for Tumor Treating Fields (TTFields), in combination with temozolomide chemotherapy, as a first-line treatment for glioblastoma (GBM). The submission is based on the successful interim analysis of EF-14, a randomized, Phase III trial comparing TTFields plus temozolomide to temozolomide alone in newly diagnosed glioblastoma. The FDA’s granting of priority review status means that the PMA application is placed at the beginning of the appropriate review queue and receives additional review resources, as needed. This status is granted to devices that are intended to treat a life-threatening disease and which offer significant, clinically meaningful advantages over existing approved alternatives. The FDA also confirmed that a filing review was conducted and the PMA application was found to contain all of the information needed to proceed with substantive review. "The FDA has been extremely responsive in working with Novocure on the Optune PMA supplement and we appreciate their partnership. We are very pleased to have received priority review and are fully committed to working closely with the FDA to ensure that Optune is approved as quickly as possible for newly diagnosed GBM,“ said Asaf Danziger, Chief Executive Officer of Novocure. “The FDA’s acceptance of the PMA supplement application for Optune is a very important milestone for Novocure and an even more important milestone for patients suffering from GBM who are in need of new and effective treatments.” The pre-specified, interim analysis of EF-14 showed that:
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