Cold Cap to Prevent Hair Loss During Chemo Cleared in US

Zosia Chustecka

Disclosures

December 08, 2015

UPDATED WITH INTERVIEW December 18, 2015 // Many cancer patients facing chemotherapy are aghast at the prospect of losing their hair, and for some years now in Europe and elsewhere there have been various scalp-cooling devices that promise to reduce this side effect.

Now the Food and Drug Administration (FDA) has cleared the first such device for marketing in the United States. The DigniCap Cooling System (manufactured by Dignitana Inc, in Lund, Sweden) has undergone a pivotal trial conducted at several centers in the US, and has been cleared for use to reduce hair loss in female breast cancer patients undergoing chemotherapy.

"We are pleased to see a product for breast cancer patients that can minimize chemotherapy-induced hair loss and contribute to the quality of life of these individuals," said William Maisel, MD, MPH, acting director of the Office of Device Evaluation in the FDA's Center for Devices and Radiological Health. "Managing the side effects of chemotherapy is a critical component to overall health and recovery."

Hair loss is a big deal for many patients. "For many women, this is the most emotionally distressing and disturbing impact from their diagnosis," said Hope S. Rugo, MD, professor of medicine at University of California San Francisco School of Medicine and lead investigator on the DigniCap study. "A short course of chemotherapy results in total hair loss, taking many months to grow back," she told journalists earlier this year. Some women even think about skipping the chemotherapy "because it will adversely affect them at work when they lose their hair," she said.

DigniCap is a computer-controlled system that circulates cooled liquid to a cap worn on the head during chemotherapy treatment. The cooling cap is covered by a second cap made from neoprene, which fastens under the chin and holds the cooling cap in place. It also acts as an insulation cover to prevent loss of cooling, the agency explains.

The device is on show in the exhibition hall at the San Antonio Breast Cancer Symposium, which began today.

The cooling action is intended to constrict blood vessels in the scalp, which, in theory, reduces the amount of chemotherapy that reaches cells in the hair follicles. The cold also decreases the activity of the hair follicles, which slows down cell division and makes them less affected by chemotherapy. The combined actions are thought to reduce the effect chemotherapy has on the cells, which may reduce hair loss, the agency explains.

The efficacy of the device was studied in 122 women with stage 1 and stage 2 breast cancer who were undergoing chemotherapy, using recognized chemotherapy regimens that have been associated with hair loss, the FDA notes. The data from this study may also be applied to some stage 3 and stage 4 breast cancer patients because they may have a benefit-risk profile comparable to that of the patients enrolled in this study.

The primary endpoint was a self-assessment of hair loss by the women using standardized photographs at 1 month (3 to 6 weeks) after the last chemotherapy cycle. More than two thirds (66%) of patients treated who wore the device reported losing less than half their hair.

Results from this study were reported earlier this year at the American Society of Clinical Oncology annual meeting.

One of the investigators was Tessa Cigler MD, MPH, from the Weill Cornell Breast Center in New York City, where 30 breast cancer patients were treated with the DigniCap. "Hair loss with chemotherapy is the most dreaded side effect," Dr Cigler said in an interview with Medscape Medical News. Some women refuse to have it, while others comprise the type of chemotherapy they will receive in order to avoid the hair loss, she said. Generally the most active chemotherapy for early stage breast cancer, which includes anthracyclines and taxanes, are associated with hair loss, she added, and these women are compromising the effectiveness of their prevention treatment.

"Hair loss is so much greater than vanity," Dr Cigler commented. "It is linked to a woman's sense of well-being, self-esteem, sense of control, and privacy," she added. Some are women who want to keep working through their treatment, others are mothers who do not want their children to know they are undergoing treatment.

In the clinical trial, the chemotherapy regimens for early breast cancer that were used are known to cause 100% of hair loss in 100% of women. In the portion of the study that Dr Cigler headed, which involved 30 women, the DigniCap cooling system allowed 70% of women to keep "a significant amount of their hair," she said. "The vast majority of the women at our center said they didn't feel the need to wear a wig or a head covering, and to me that's the best outcome," she added.

The device is well tolerated, she said. None of the 30 participants at her center withdrew from the study because of discomfort, and overall only three of 122 women did so.

It would likely work in patients with other solid tumors that are being treated with the same chemotherapy regimens, but the use of the DigniCap is not recommended for use in patients with hematological malignancies. The cooling of the scalp reduces the amount of chemotherapy reaching the scalps, and while this poses a minimum risk for patients with solid tumors, for blood cancers this risk is greater, she explained.

The FDA said in the approval notice for DigniCap that prevention of hair loss in these patients may be a significant benefit to their quality of life, and the risk of the chemotherapy drug missing an isolated grouping of the breast cancer cells in the scalp because of the cold cap is extremely rare, the FDA notes.

The most common side effects of the cooling system include cold-induced headaches and neck and shoulder discomfort, chills, and pain associated with wearing the cooling cap for an extended period of time.

The FDA reviewed data for DigniCap cooling system through the de novo classification process, a regulatory pathway for some low- to moderate-risk devices that are novel and not substantially equivalent to any legally marketed device.

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