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Boston Scientific Announces FDA Clearance And CE Mark For WallFlex(R) Fully Covered Esophageal Stent

Main Category: Cancer / Oncology
Also Included In: GastroIntestinal / Gastroenterology | Regulatory Affairs / Drug Approvals
Article Date: 24 Nov 2009

Boston Scientific Corporation (NYSE: BSX) announced that it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) and CE Mark approval to market its WallFlex® Fully Covered Esophageal Stent for the treatment of malignant esophageal strictures (obstructions) caused by tumors in patients with resectable or non-resectable esophageal cancer.

The WallFlex® Partially Covered Esophageal Stent was cleared by the FDA and received CE Mark in 2008. Both stents -- along with the complete WallFlex Stent family of self-expanding metal stents (SEMS) -- will be available for hands-on demonstration at the GASTRO 2009 conference, which is being held November 21-25 in London.

"The low profile delivery system (18.5 Fr) of the WallFlex Esophageal Stents has allowed me to traverse tight strictures, facilitating stent placement within malignancies that, in the past, needed to be pre-dilated," said Drew Schembre, M.D., Chief of Gastroenterology at Virginia Mason Medical Center in Seattle, Washington. "Moreover, the fully covered option may be a viable choice for patients with operable esophageal cancer who are undergoing chemotherapy and radiation treatment in preparation for surgery."

Patients with obstructions due to esophageal cancer may have difficulty swallowing, resulting in severely limited quality of life. Complete blockages of the esophagus can prevent liquid consumption. The WallFlex Esophageal Stent allows physicians to re-establish patency (openness) of the esophagus, enabling resumption of oral intake.

The WallFlex Fully and Partially Covered Stents employ a proprietary Permalume® silicone covering designed to prevent tumor ingrowth, seal concurrent esophageal fistulas and help reduce food impaction. The stents' progressive-step, flared ends are designed to reduce the risk of migration and may assist in anchoring the fully covered stent within the esophageal lumen. The multiple wire-braided construction is engineered to allow the stent to adjust to forces within the esophagus such as peristalsis (involuntary contractions) and strictures. In addition, the WallFlex Fully Covered Stent may be reconstrained up to 75 percent deployment.

"The availability of the complete line of WallFlex Fully and Partially Covered Esophageal Stents represents a tremendous milestone for Boston Scientific," said Michael Phalen, President, Boston Scientific Endoscopy. "This advanced line of esophageal stents is designed to improve the quality of life for the thousands of patients suffering from esophageal cancer. We are pleased that our entire WallFlex Stent family -- biliary, enteral and now esophageal -- is available in the U.S., Europe and other strategic international markets. This underscores our mission to meet the high expectations of our customers and deliver a complete range of innovative treatment options to diagnose, palliate and treat patients with diseases of the gastrointestinal tract."

Symposium at GASTRO 2009

Boston Scientific will host a symposium titled "Esophageal Stenting: Changing Algorithms, Changing Outcomes" on Tuesday, November 24 at 7:00 a.m. at GASTRO 2009 in London. The event will be moderated by Professor Horst Neuhaus of Evangelisches Krankenhaus in Dusseldorf, Germany. Panelists and topics include Dr. Marc Giovannini, Institut Paoli-Calmettes in Marseille, France, who will discuss advancing treatment options; Professor Jacques Deviere, Erasme Hospital in Brussels, Belgium, who will address benign conditions and expanding the role of stents; and Professor Peter Siersema, University Medical Center Utrecht in The Netherlands who will discuss minimizing reintervention rates in stenting.

Source
Boston Scientific

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Boston Scientific Announces FDA Clearance And CE Mark For WallFlex(R) Fully Covered Esophageal Stent

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