Sioux Community Cancer Consortium/Sioux Valley Clinic Oncology Participated in Clinical Trial
Initial results of the Study of Tamoxifen and Raloxifene, or STAR, show that the drug Raloxifene, currently used to prevent and treat osteoporosis in postmenopausal women, works as well as Tamoxifen in reducing breast cancer risk for postmenopausal women at increased risk of the disease. Sioux Community Cancer Consortium/Sioux Valley Clinic Oncology participated in this clinical trial, one of the largest breast cancer prevention trials ever conducted.
In STAR, both drugs reduced the risk of developing invasive breast cancer by about 50 percent. In addition, within the study, women who were prospectively and randomly assigned to take Raloxifene daily, and who were followed for an average of about four years, had 36 percent fewer uterine cancers and 29 percent fewer blood clots than the women who were assigned to take Tamoxifen. Uterine cancers, especially endometrial cancers, are a rare but serious side effect of Tamoxifen. Both Tamoxifen and Raloxifene are known to increase a womans risk of blood clots.
STAR enrolled 19,747 postmenopausal women who were at increased risk of the disease. At Sioux Community Cancer Consortium/Sioux Valley Clinic Oncology, 79 women were enrolled, and in
Dr. Loren Tschetter, Principal Investigator of the Sioux Community Cancer Consortium, Sioux Valley Clinic Oncology, states, "The results with Raloxifene showing less toxicity than Tamoxifen are important for patients in this region." Dr. Tschetter wishes to thank all the women who participated in this trial so that this new information could be available for the women of our region.
"In 1998, the landmark Breast Cancer Prevention Trial showed that Tamoxifen could reduce the risk of invasive breast cancer in premenopausal and postmenopausal women by nearly 50 percent," said Norman Wolmark, M.D., NSABP chairman. "Today, we can tell you that for postmenopausal women at increased risk of breast cancer, raloxifene is just as effective, without some of the serious side effects known to occur with Tamoxifen."
Women taking either drug had equivalent numbers of strokes, heart attacks, and bone fractures. Both Raloxifene and Tamoxifen are known to protect bone health; it is estimated that half a million postmenopausal women are currently taking Raloxifene by prescription to prevent or treat osteoporosis. Additionally, the initial results from STAR suggest that Raloxifene does not increase the risk of developing a cataract, as Tamoxifen does.
"Although no drugs are without side effects, Tamoxifen and Raloxifene are vital options for women who are at increased risk of breast cancer and want to take action," said Leslie Ford, M.D., associate director for clinical research in NCIs Division of Cancer Prevention. "For many women, Raloxifenes benefits will outweigh its risks in a way that Tamoxifens benefits do not."
The STAR researchers also tracked known menopausal side effects that occur with both drugs and monitored the participants quality of life. The data show that side effects of both drugs were mild to moderate in severity, and quality of life was the same for both drugs.
Participants in STAR are now receiving information about which drug they were taking. Women assigned to Raloxifene will continue to be provided with the drug until they have completed five years of treatment. Those women assigned to Tamoxifen can choose to continue taking Tamoxifen or to receive Raloxifene to complete their five years of treatment.
Study details include:
- STAR enrolled 19,747 women. This data analysis is based on the 19,471 women for whom complete study information was available.
- The numbers of invasive breast cancers in both groups of women were statistically equivalent. Among the 9,745 women in the Raloxifene group, 167 developed invasive breast cancer, compared to 163 of 9,726 women in the Tamoxifen group.
- More than half of the women who joined STAR had had a hysterectomy and, therefore, were not at risk of uterine cancer. For those women with a uterus, 36 of 4,732 who were assigned to take Tamoxifen developed uterine cancers (mainly endometrial cancer) compared to 23 of 4,712 women who were assigned to take Raloxifene.
- In STAR, women in the Raloxifene group had 29 percent fewer deep vein thromboses (blood clots in a major vein) and pulmonary embolisms (blood clots in the lung) than women in the Tamoxifen group. Specifically, 87 of 9,726 women in the Tamoxifen group had a deep vein thrombosis compared to 65 of 9,745 women taking Raloxifene. In addition, 54 of 9,726 women taking Tamoxifen developed pulmonary embolisms compared to 35 of 9,745 women taking Raloxifene.
- The number of strokes occurring in both groups of women was statistically equivalent: 53 of 9,726 women in the tamoxifen group and 51 of 9,745 women in the Raloxifene group had a stroke during the trial. There was no difference in deaths from strokes: 6 of 9,726 women in the Tamoxifen group and 4 of 9,745 women in the Raloxifene group died from this event. Women at increased risk of stroke (those with uncontrolled hypertension or uncontrolled diabetes, or a history of stroke, transient ischemic attack, or atrial fibrillation) were not eligible to participate in STAR.
- While Tamoxifen has been shown to reduce, by half, the incidence of lobular carcinoma in situ (LCIS) and ductal carcinoma in situ (DCIS), Raloxifene did not have an effect on these diagnoses. (LCIS and DCIS are sometimes called noninvasive breast cancers.) Of the 9,726 women taking Tamoxifen, 57 developed LCIS or DCIS, compared to 81 of 9,745 taking Raloxifene. This result confirms data reported in a large study of Raloxifene in the treatment of osteoporosis (the Continued Outcomes Relevant to Evista or CORE Trial) in 2004.
Women who participated in STAR were postmenopausal, at least 35 years old, and had an increased risk of breast cancer as determined by their age, family history of breast cancer, personal medical history, age at first menstrual period, and age at first live birth. Before participating in the study, the women were instructed about the potential risks and benefits of Tamoxifen and Raloxifene and then were asked to sign an informed consent document.
The maker of Tamoxifen, AstraZeneca Pharmaceuticals,
For more information about STAR, including links to media materials and a fact sheet, visit NCI's STAR home page at http://www.cancer.gov/star or one of NSABPs Web sites at http://www.nsabp.pitt.edu and http://foundation.nsabp.org.
For a Q&A related to the STAR results, go to: http://www.cancer.gov/newscenter/pressreleases/STARresultsQandA.
For B-roll related to the STAR results, go to www.thenewsmarket.com for digitized, downloadable B-roll, or call the
For tools used to calculate a womans risk of breast cancer, visit http://cancer.gov/bcrisktool or http://breastcancerprevention.com.