DigniCap Scalp Cooling System Now Available for Women With Breast Cancer at 10 U.S. Cancer Treatment Centers
Dignitana Inc. announced today that the DigniCap scalp cooling system, which was cleared by the U.S. Food and Drug Administration (FDA) in December 2015 to effectively reduce the likelihood of chemotherapy-induced hair loss in women with breast cancer, is now available at 10 cancer treatment centers across the United States. Scalp cooling is administered alongside chemotherapy in medical infusion centers.
The DigniCap system is the first and only scalp cooling device to complete FDA clinical trials in the U.S., where 7 out of 10 patients with early-stage breast cancer kept at least 50% of their hair.
The DigniCap scalp cooling system features a patented tight-fitting silicone cooling cap that is placed directly on the head, and an outer neoprene cap that insulates and secures the silicone cap. The cooling cap is connected to a cooling and control unit with touch screen prompts. A liquid coolant circulates throughout the silicone cap, delivering consistent and controlled cooling to all areas of the scalp. The cap is fitted to the head, and the temperature of the scalp is lowered, resulting in vasoconstriction with reduced delivery of chemotherapy to the scalp, as well as reduced cellular uptake of drugs due to decreased intra follicular metabolic rate. These factors together reduce the risk of chemotherapy-induced hair loss.
The following cancer treatment centers will be the first 10 sites in the U.S. to provide the DigniCapscalp cooling system in their breast cancer treatment regimens:
- Charleston Hematology Oncology Associates (Charleston, South Carolina)
- Chesapeake Oncology and Hematology Associates (Glen Burnie, Maryland)
- Florida Cancer Specialists & Research Institute (Sarasota, Florida)
- Mount Sinai Comprehensive Cancer Center (Miami Beach, Florida)
- Orange County Blood and Cancer Care (Fountain Valley, California)
- The Angeles Clinic and Research Institute, an affiliate of Cedars-Sinai (Los Angeles, California)
- Toledo Clinic Cancer Center (Toledo, Ohio)
- University of California, San Francisco (UCSF) Helen Diller Family Comprehensive Cancer Center (San Francisco, California)
- UT Health Science Center San Antonio’s Cancer Therapy & Research Center (San Antonio, Texas)
- Wake Forest Baptist Medical Center (Winston-Salem, North Carolina)
Hope Rugo, MD, of UCSF’s Helen Diller Family Comprehensive Cancer Center, Principal Investigator for the FDA multicenter clinical trial of the DigniCap, and Susan Melin, MD, of Wake Forest Baptist, Principal Investigator of the DigniCap trial at her institution, originated early clinical trials and shepherded studies throughout the FDA process.
“We are proud to have helped bring this new treatment option to women in the U.S.,” said Dr. Rugo. “A breast cancer diagnosis is traumatizing enough—there’s no need to add fear of hair loss to the experience.”
The content in this post has not been reviewed by the American Society of Clinical Oncology, Inc. (ASCO®) and does not necessarily reflect the ideas and opinions of ASCO®.
