News Release

Mayo Clinic: Genotyping errors plague CYP2D6 testing for tamoxifen therapy

Peer-Reviewed Publication

Mayo Clinic

ROCHESTER, Minn. -- Clinical recommendations discouraging the use of CYP2D6 gene testing to guide tamoxifen therapy in breast cancer patients are based on studies with flawed methodology and should be reconsidered, according to the results of a Mayo Clinic study published in the Journal of the National Cancer Institute.

For years, controversy has surrounded the CYP2D6 gene test for breast cancer. Women with certain inherited genetic deficiencies in the CYP2D6 gene metabolize tamoxifen less efficiently, and thus have lower levels of tamoxifen's active cancer-fighting metabolite endoxifen. Numerous studies have shown that these women gain less benefit from tamoxifen therapy and have higher rates of recurrence.

However, two large clinical trials found no link between the CYP2D6 genotype and tamoxifen effectiveness, prompting recommendations against testing. In the new Mayo Clinic study, researchers found that previous studies, which used tumor tissue instead of healthy tissue to determine the CYP2D6 genotype, were prone to error. The study found that up to 45 percent of breast tumors exhibit genetic alterations affecting the CYP2D6 gene. Thus, the use of tumor tissue to obtain DNA leads to a distortion of the patient's true or inherited CYP2D6 genotype.

"The potential benefit of CYP2D6 testing is obvious but has been difficult to establish. One major reason appears to be the lack of analytical validity," says Matthew Goetz, M.D., an oncologist at the Mayo Clinic Cancer Center and senior author of the study. "We found that if you use tumor tissue to determine the CYP2D6 genotype a patient was born with, you are going to get it wrong a substantial portion of the time."

CYP2D6, which stands for Cytochrome P450 2D6, is one of the most important enzymes involved in drug metabolism. It is responsible for the breakdown of nearly a quarter of all medicines prescribed. The CYP2D6 gene is highly variable. That variability is the main genetic factor affecting how the liver metabolizes tamoxifen, and the blood levels of the important metabolite endoxifen.

"It is sobering to consider that a decade of work by the oncology community has not produced a clear resolution of the value of CYP2D6 genotype for predicting tamoxifen efficacy," says James Ingle, M.D., an oncologist at Mayo Clinic Cancer Center and co-author of the study. "The potential impact of the delay in resolving this issue is quite large in that during this time over half a million women worldwide would have been expected to be poor metabolizers, and, if the relationship between CYP2D6 genotype and tamoxifen efficacy is correct, these women would have been given less than optimal adjuvant therapy had they received tamoxifen."

Most individuals carry two copies or alleles of the CYP2D6 gene, one inherited from each parent. However, Dr. Goetz and his colleagues identified that up to 45 percent of breast tumors lose one of these "parental" CYP2D6 alleles, a phenomenon known as loss of heterozygosity. Use of tumor DNA to derive CYP2D6 genotype resulted in a distortion of the inherited CYP2D6 genotype and the inability to predict the concentrations of endoxifen.

To explore whether use of tumor tissue to obtain DNA could result in CYP2D6 genotyping errors, the researchers first looked for loss of heterozygosity at the CYP2D6 locus in genomic tumor data from two large breast cancer datasets, the Cancer Genome Atlas and Foundation Medicine. They found loss of heterozygosity in over 40 percent of the breast tumors analyzed. These findings suggested that genotyping techniques using DNA extracted from tumor samples could misclassify a patient's CYP2D6 genotype.

Next, the researchers sought to directly compare CYP2D6 genotypes derived from patients who provided normal and tumor tissue. Using samples from patients enrolled in the NCCTG 89-30-52 tamoxifen trial, the researchers showed that there was perfect agreement between CYP2D6 genotypes derived from non-malignant tissue and those derived from cheek swabs. In contrast, 20 percent of the CYP2D6 genotypes were misclassified when tumor tissue was used.

The researchers say their results should prompt a careful reassessment of the data necessary to inform patients and clinicians properly about the value of CYP2D6 testing. "We believe that previously published studies should be re-examined in the context of potential genotyping errors, specifically in those studies that utilized tumor tissue as the primary DNA source," says Mark Ratain, M.D., professor of medicine at the University of Chicago and co-author of the study. "Given the difficulties of using tumor tissue for genotyping, we also recommend that blood for DNA be routinely obtained in large oncology clinical trials."


Co-authors from Mayo Clinic include Vera Suman, Ph.D., Stephanie Safgren, Mary Kuffel, Matthew Ames, Ph.D., and Krishna Kalari, Ph.D.

The study was funded by the National Institutes of Health, the Mayo Clinic Breast Cancer Specialized Program of Research Excellence (SPORE), and the Breast Cancer Research Foundation.

About Mayo Clinic Cancer Center

As a leading institution funded by the National Cancer Institute, Mayo Clinic Cancer Center conducts basic, clinical and population science research, translating discoveries into improved methods for prevention, diagnosis, prognosis and therapy. For information on cancer clinical trials, call 1-855-776-0015 (toll-free).

About Mayo Clinic

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