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Breakthrough method predicts risk of invasive breast cancer

Date:
April 29, 2010
Source:
University of California - San Francisco
Summary:
For the first time, scientists have discovered a way to predict whether women with ductal carcinoma in situ -- the most common form of non-invasive breast cancer -- are at risk of developing more invasive tumors in later years.

For the first time, scientists have discovered a way to predict whether women with ductal carcinoma in situ (DCIS) -- the most common form of non-invasive breast cancer -- are at risk of developing more invasive tumors in later years.

As a result of the finding, women with DCIS will have the opportunity to be more selective about their treatment, according to the scientists.

"Women will have much more information, so they can better know their risk of developing invasive cancer,'' said lead author Karla Kerlikowske, MD. "It will lead to a more personalized approach to treatment. As many as 44 percent of patients with DCIS may not require any further treatment, and can rely instead on surveillance.''

The study was led by researchers at the University of California, San Francisco and the San Francisco Veterans Affairs Medical Center, and is reported online by the Journal of the National Cancer Institute.

The authors followed the medical histories of 1,162 women aged 40 years and older who were diagnosed with DCIS and treated with lumpectomy. They found that two factors were predictors of risk of developing invasive cancer within eight years after a diagnosis of DCIS: the method by which it was detected and expression of several biomarkers. Findings showed that a breast lump that is diagnosed as DCIS was more predictive of a high risk of subsequent invasive cancer than DCIS diagnosis by mammography.

The study also found that different combinations of biomarkers measured on the initial DCIS tissue were associated with varying levels of risk of invasive cancer or DCIS. These biomarkers include estrogen receptor, progesterone receptor, Ki67 antigen, p53, p16, epidermal growth factor receptor-2, and cyclooxygenase-2. Women who express high levels of p16, cyclooxygenase-2 and Ki67 were more likely to develop invasive cancer after their initial DCIS diagnosis.

Because of the research, physicians will now be able to predict whether a DCIS patient treated by lumpectomy only will subsequently develop invasive cancer, DCIS, or be at very low risk of developing further tumors, according to Kerlikowske, professor of medicine, and epidemiology and biostatistics at the UCSF Helen Diller Family Comprehensive Cancer Center, and co-director of the Women Veteran's Comprehensive Health Center at SFVAMC.

Scientists have been trying to solve the DCIS problem for more than 20 years, said Kerlikowske, but until now have been unable to stratify women into risk groups.

"It is novel to be able to separate women into those three groups,'' she said. "In the past, women were told they had a certain risk of developing further tumors, but could not be told whether they were at risk of an invasive cancer or DCIS -- risk of further tumors was lumped together into one risk group.''

The data shows definite markers that will predict as far as eight years into the future, said Thea D. Tlsty, PhD, one of the principal investigators of the study. She is a professor of pathology and UCSF leader of the Cell Cycling and Signaling Program at the UCSF Helen Diller Family Comprehensive Cancer Center.

"This is an exciting and powerful beginning, to be able to predict which pre-cancers will lie dormant and which will lead to invasive cancers,'' said Tlsty. "For the first time, we've identified that group of patients who have the lowest risk and the group at highest risk of developing invasive cancer. It's a big step forward.''

DCIS rarely leads to death from breast cancer -- approximately 11 out of 100 women treated by lumpectomy only go on to develop invasive cancer within eight years of the initial diagnosis of DCIS, and only 1 to 2 percent of women die of breast cancer within 10 years of diagnosis. Yet, women diagnosed with DCIS have historically had an inaccurate perception of their risk of later developing invasive cancer, and as a result have chosen fairly aggressive courses of treatment, said Tlsty.

Currently, approximately 35 percent opt for a lumpectomy, about 25 percent for a complete mastectomy, 3 to 5 percent for active surveillance only, and the remainder for lumpectomy plus radiation or hormone treatment or both.

"Women choose their treatment based on their level of concern of developing invasive cancer,'' said Kerlikowske. "DCIS is non-invasive so women do not die of it. Their real concern arises if they develop invasive cancer and the cancer spreads.''

According to the study, the group of patients with the lowest risk has only a 2 percent chance of developing invasive cancer at 5 years and a 4 percent chance at 8 years.

"Now we are able to identify the group at highest risk of developing an invasive cancer,'' said Tlsty. "Factors such as palpable DCIS and expression of protein levels of p16, cyclooxygenase-2 and Ki67 are found in approximately 50 percent of patients with DCIS who later develop invasive cancer. In collaboration with co-authors Hal Berman, MD, and Mona Gauthier, PhD, both faculty members of the Campbell Family Breast Cancer Research Institute in Toronto, Canada, we are identifying molecular markers that will stratify risk for the remaining patients.''

Other study co-authors include Fred Waldman, MD, PhD; Henry Sanchez, MD; Karen Chew, BA, CT, and Britt-Marie Ljung, MD, all of the UCSF Helen Diller Family Comprehensive Cancer Center; Cynthia Jimenez, medical student at UCSF, and Annette Molinaro, PhD, Yale University.

Funding for the research was provided by the NCI-funded UCSF Breast Cancer SPORE Project (Specialized Program of Research Interest) and by the California Breast Cancer Research Program.


Story Source:

The above story is based on materials provided by University of California - San Francisco. Note: Materials may be edited for content and length.


Journal Reference:

  1. Karla Kerlikowske, Annette M. Molinaro, Mona L. Gauthier, Hal K. Berman, Fred Waldman, James Bennington, Henry Sanchez, Cynthia Jimenez, Kim Stewart, Karen Chew, Britt-Marie Ljung, and Thea D. Tlsty. Biomarker Expression and Risk of Subsequent Tumors After Initial Ductal Carcinoma In Situ Diagnosis. Journal of the National Cancer Institute, April 28, 2010 DOI: 10.1093/jnci/djq101

Cite This Page:

University of California - San Francisco. "Breakthrough method predicts risk of invasive breast cancer." ScienceDaily. ScienceDaily, 29 April 2010. <www.sciencedaily.com/releases/2010/04/100428173335.htm>.
University of California - San Francisco. (2010, April 29). Breakthrough method predicts risk of invasive breast cancer. ScienceDaily. Retrieved July 31, 2014 from www.sciencedaily.com/releases/2010/04/100428173335.htm
University of California - San Francisco. "Breakthrough method predicts risk of invasive breast cancer." ScienceDaily. www.sciencedaily.com/releases/2010/04/100428173335.htm (accessed July 31, 2014).

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