UCLA Today News Logo
 

:: Home

:: News
:: Campus
:: People
:: Voices
:: Closeup
:: Briefs
:: Contact Us
Search Archive
:: UCLA HOME

 

 

 

 

©2004
The Regents of the University of California
 

 
VOL. 24. NO.11 MARCH 23, 2004
Photo by Reed Hutchinson UCLA Photographic Services
Researcher Dennis Slamon has been studying HER-2, a gene that drives breast-cancer growth, for nearly two decades. His work led to the development of Herceptin.

the hero of the herceptin story

He led pursuit of
breast-cancer villain

BY AJAY SINGH
UCLA Today Staff

Dennis Slamon, head of clinical/transitional research at UCLA’s Jonsson Cancer Center, has spent most of his career trying to beat HER. That’s short for human epidermal growth factor receptor, a gene that regulates cell growth and sometimes causes cancer. For nearly two decades, Slamon has been studying HER-2, one of the four siblings in the HER family, whose altered form is present in about 25% to 30% of women suffering from advanced breast cancer. Slamon’s work was honored Feb. 28 by the American Cancer Society, which awarded him the Medal of Honor, its most prestigious prize.

The award is in recognition of the research that led Slamon and his UCLA colleagues to develop Herceptin, a breast-cancer drug that was approved by the FDA in 1998. It is the first comprehensive breast-cancer therapy to arise from the cutting-edge world of molecular biology.

In a sense, the “Herceptin story,” as Slamon calls the drug’s development, began back in 1972 when he decided to devote his life to cancer research. It was a field at which, he recalled, a lot of people were looking at a time when “people were just learning about genes carrying oncogenic agents more potent than chemical agents or even radiation.”

In 1979, Slamon came to UCLA to complete a fellowship in medical oncology. By the time he began working with HER-2 in 1985, it was still not known that the gene is abnormally altered in about a quarter of breast-cancer cases. Slamon examined breast-cancer samples, hoping to isolate any gene even remotely responsible for regulating abnormal cell growth.

He discovered that HER-2 was indeed altered in one-third of the samples and that the women from whom the samples were taken had three things in common: They were free of cancer for relatively shorter periods, were less responsive to mainstream therapies and died more rapidly once they got sick.

But Slamon still needed to show that HER-2 was the cancer-causing villain he suspected, and that it could be therapeutically targeted. With the help of generous donors, he expanded his research and demonstrated that HER-2 does drive breast-cancer growth.

After testing antibodies aimed at checking the growth, Slamon and his team conducted eight clinical trials, which, together with 12 years of research, cost more than $100 million.

Slamon, who’s as famously tireless as he is affable, recently began an ambitious new trial to see if Herceptin is effective in 3,200 women worldwide who have recently been diagnosed with breast cancer. “That is where we think we’ll be able to impact the disease most and potentially cure patients,” he said. Indeed, if survivors from his Herceptin story are any indication, Slamon might already have achieved his goal — some patients from the last trial have been disease-free for up to 11 years.

“We’ve improved survival by 30%, and they may well be cured,” Slamon said. “But we’d like to do that for a much larger percentage of patients. So there is still a lot to be done.”

 

 

UCLA Today
CONNECTING STAFF AND FACULTY IN THE UCLA COMMUNITY

Home | News | Campus | People | Voices | Closeup | Briefs |
Contact Us
| Search Archive | UCLA Home