ICTR in the News: Blood Test That Detects Changes in Tumor DNA Predicts Survival of Women with Advanced Breast Cancers
Posted by: Crystal Williams on: February 1, 2017 | Print This Page
The following article profiles work performed by ICTR researchers Antonio Wolff, M.D., professor of oncology at the Johns Hopkins University School of Medicine and member of the Kimmel Cancer Center, Sara Sukumar, Ph.D., professor of oncology at the Johns Hopkins University School of Medicine and member of the Kimmel Cancer Center, and Kala Visvanathan, M.D., M.H.S., professor of epidemiology at the Johns Hopkins Bloomberg School of Public Health, professor of oncology at the Johns Hopkins University School of Medicine and director of the Clinical Cancer Genetics Program at the Johns Hopkins Kimmel Cancer Center.
Results of a multicenter study of 129 women with advanced breast cancer show that a blood test that spots cancer-linked DNA correctly predicted that most of those patients with higher levels of the tumor markers died significantly earlier than those with lower levels.
The Johns Hopkins Kimmel Cancer Center scientists, who developed the test and led the study, say the results, if confirmed in more studies, suggest that the DNA detector, called cMethDNA, could be widely used to identify breast cancers at higher risk for recurrence and track the success or failure of treatment. Results of the study were published online Nov. 21 in the Journal of Clinical Oncology.
“There’s a great need in cancer patients to be able to quickly and easily assess if a particular treatment is working in order to switch to another if it’s not, thus avoiding wasted time, potential side effects and cost,” says Kala Visvanathan, M.D., M.H.S., professor of epidemiology at the Johns Hopkins Bloomberg School of Public Health, professor of oncology at the Johns Hopkins University School of Medicine and director of the Clinical Cancer Genetics Program at the Johns Hopkins Kimmel Cancer Center. “Our study results, although preliminary, suggest that cMethDNA has the potential to be an effective way to do this for breast cancer patients.”
For the biomarker study, the Johns Hopkins scientists prospectively analyzed blood samples collected from 141 women with advanced breast cancer (cancer that had spread to other organs) who were beginning a new treatment at seven cancer centers in the U.S., including The Johns Hopkins Hospital. The scientists collected the samples at the start of therapy, four weeks later and when the women’s cancers were “restaged,” usually after 12 weeks.
The cMethDNA test analyzes a filtered portion of the blood called serum, which contains proteins and genetic material, such as DNA, released by cells. The test searches for evidence of so-called hypermethylation, a type of chemical tag affixed to DNA in one or more of six breast cancer-specific genes. Biologically, hypermethylation often silences genes that keep runaway cell growth in check, and its appearance in the DNA code of breast cancer-related genes shed into the blood may indicate that a patient’s cancer growth is increasing and the disease has worsened.
To figure out how well the test reflected disease trends, results of the blood tests were analyzed to look at two measures of survival: progression-free and overall survival over the study period.
The scientists then used statistical models to evaluate the distribution of cancer-linked DNA in the patients’ blood samples over the seven-year study to find the largest degree of differences between patients with low and high levels of evidence of hypermethylation in their DNA.
The cut off value for women with high versus low levels of cancer DNA in their blood was determined for progression-free and overall survival separately. Therefore the absolute number of women with high and low levels of cancer DNA in their blood in the analysis of progression-free survival was different from that of the overall survival analysis.
Among 128 of the 141 patients, the scientists found that the median progression-free survival of 71 patients identified with high levels of cancer DNA in their blood was 2.1 months, compared with 5.8 months for 57 patients with low levels.
In 129 patients, median overall survival for 62 patients identified with high levels of cancer DNA in their blood was 12.3 months, compared with 21.7 for 67 patients with low levels.
Median follow-up of the women in the study was 19.5 months (range 0.8-86.3 months). By the end of the seven-year study period, nearly all the women enrolled in the study had died of their metastatic cancer.
“What we see is an association between shorter periods of progression-free survival and overall survival in patients whose blood has higher levels of hypermethylated DNA, and we can see this very early on, after just four weeks of treatment,” says Sara Sukumar, Ph.D., professor of oncology at the Johns Hopkins University School of Medicine and member of the Kimmel Cancer Center, who developed the test with Johns Hopkins scientist Mary Jo Fackler, Ph.D., and others.
Visvanathan says the current study did not look at the blood test’s benefits with regard to specific anti-cancer therapies. More research to determine the blood test’s predictive ability among women with earlier-stage disease is also underway, led by Antonio Wolff, M.D., professor of oncology at the Johns Hopkins University School of Medicine and member of the Kimmel Cancer Center, who also co-led the current study with Visvanathan and Sukumar.
The research team estimates that verification and use of the new hypermethylation test is years away, and the cMethDNA assay is not yet available for general use.
The National Cancer Institute estimates that there have been more than 246,000 new cases of breast cancer diagnosed this year. Approximately 6 percent of those women are diagnosed at an advanced stage, and some 26.3 percent of them survive beyond five years.
Funding for this study, conducted in the Translational Breast Cancer Research Consortium, was provided by the Avon Foundation for Women, the Rubenstein Family Fund, the Breast Cancer Research Foundation, Janssen Diagnostics, the Susan G. Komen Foundation and the National Institutes of Health’s National Cancer Institute (P30CA006973 and P30CA58223).
Additional scientists who contributed to the work include Zhe Zhang, Zoila A. Lopez-Bujanda, Wei Wen Teo, Stacie C. Jeter, Lori J. Sokoll, Leslie M. Cope, Christopher B. Umbricht and David M. Euhus from Johns Hopkins; Elizabeth Garrett-Mayer from the Medical University of South Carolina; Andres Forero from the University of Alabama at Birmingham; Anna M. Storniolo from Indiana University; Rita Nanda from the University of Chicago; Nancy U. Lin from the Dana-Farber Cancer Institute; Lisa A. Carey from the University of North Carolina; and James N. Ingle from Mayo Clinic.
Under a license agreement between Cepheid and the Johns Hopkins University, Sukumar and Wolff are entitled to future royalty distributions associated with an invention described in this publication. Additionally, Sukumar and Fackler are paid consultants to Cepheid. These arrangements have been reviewed and approved by the Johns Hopkins University in accordance with its conflict of interest policies.
FOR THE MEDIA