HOPKINS RESEARCHERS FIND GENETIC ALTERATIONS LINKED TO CANCER IN SOME BLOOD SAMPLES: MAY HELP IDENTIFY PATIENTS WITH ADVANCED CANCER

August 27, 1996
Media Contact: Karin Twilde or Kate Ruddon
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Using a recently developed molecular test, investigators at The Johns Hopkins University School of Medicine have detected genetic mutations specific to cancer in blood samples of six patients with head and neck cancer. Their findings are reported in the September issue of Nature Medicine.

"Although quite preliminary, these findings are interesting, because the presence of DNA alterations in the blood appears to be associated with large, advanced tumors and with cancer that has spread," says lead author David Sidransky, M.D., associate professor of otolaryngology/head and neck surgery, and oncology. Sidransky cautions that the test does not appear useful as a screening test for cancer. "But it might be helpful in patient management for identifying patients with a very poor prognosis who may benefit from aggressive therapy," he says.

The test works by identifying replication errors, or chromosomal deletions, in the DNA of cancer cells. In this study, the investigators examined DNA from patients' serum (a component of blood plasma) and compared this DNA pattern to normal DNA from circulating white blood cells. They found genetic alterations in the serum of 6 of 21 head and neck cancer patients that were identical to alterations from the tumor itself.

Examining disease outcomes, the researchers found that 4 out of the 6 patients with positive test results subsequently died of their cancer compared to only 3 of 15 with negative test results. Additionally, the three patients who developed distant metastases (disseminated cancer) were in the positive test group, further indicating that poor outcome may be associated with the presence of serum DNA alterations. These results must be confirmed in much larger clinical trials, Sidransky says.

The technique used in this study was developed by Sidransky's team and first used to detect cancer cells in urine. The test uses a series of DNA markers to seek out genetic mutations specific to each patient's cancer. "We decided to test serum samples based on evidence from scientists two decades ago which pointed to increased levels of serum DNA in cancer patients," Sidransky said. "More recent studies suggest that cancer cells circulating in the blood may die and release DNA, which is carried through the bloodstream by plasma."

In an accompanying study in Nature Medicine, a team from Switzerland (also co-authors of the Hopkins study) found genetic alterations in the blood plasma of over 70 percent of patients with small cell lung cancer. The authors speculate that the higher presence of alterations may be indicative of the high propensity of this cancer to spread.

In addition to Sidransky, other participants in the Hopkins study include Drs. Homaira Nawroz and Wayne Koch from the Department of Otolaryngology--Head and Neck Surgery, Division of Head and Neck Cancer Research at Johns Hopkins, and Drs. Philippe Anker and Maurice Stroun from the Laboratory of Plant Biochemistry and Physiology at the University of Geneva in Switzerland.

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Funding for this research was provided by a lung cancer SPORE (Specialized Program of Research Excellence) grant from the National Cancer Institute and by Oncor, Inc. of Gaithersburg, MD. Under an agreement between Oncor and The Johns Hopkins University, Dr. Sidransky is entitled to a share of sales royalty received by the University from Oncor. Under that agreement, the University and Dr. Sidransky also have received Oncor stock, which, under University policy, cannot be traded until two years after the first commercial sales of the products related to this research. Dr. Sidransky also serves as a member of the Scientific Advisory Board and has stock options in OncorMed, Inc., an Oncor subsidiary, which is commercializing some of Oncor's technology. The terms of this agreement have been reviewed and approved by the University in accordance with its conflict of interest policies.


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