Myriad Genetics' RiskScore Study Named One of the Top 10 Significant Advances in Genomic Medicine in American Journal of Human Genetics
Myriad Genetics' RiskScore Study Named One of the Top 10 Significant Advances in Genomic Medicine in American Journal of Human Genetics
Study Demonstrates RiskScore as a More Accurate Predictor of Breast Cancer Risk, Doubling Accuracy Compared to the Tyrer-Cuzick Model
研究表明,RiskScore是更準確的乳腺癌風險預測指標,與Tyrer-Cuzick模型相比,準確率提高了一倍
SALT LAKE CITY, Dec. 19, 2024 (GLOBE NEWSWIRE) -- Myriad Genetics, Inc. (NASDAQ: MYGN), a leader in genetic and genomic testing and precision medicine, announced that a MyRisk Hereditary Cancer Test with RiskScore study has been named in the American Journal of Human Genetics as one of its top 10 significant advances in genomic medicine. The study was selected by the Genomic Medicine Working Group at the National Human Genome Research Institute.
鹽湖城,2024年12月19日(GLOBE NEWSWIRE)——遺傳和基因組測試及精準醫療領域的領導者Myriad Genetics, Inc.(納斯達克股票代碼:MYGN)宣佈,一項基於RiskScore的MyRisk遺傳性癌症測試研究已被《美國人類遺傳學雜誌》列爲其基因組醫學十大重大進展之一。該研究由國家人類基因組研究所的基因組醫學工作組選定。
The study by Mabey et al., "Validation of a clinical breast cancer risk assessment tool combining a polygenic score for all ancestries with traditional risk factors," presented a longitudinal clinical validation of MyRisk with RiskScore using data from more than 130,000 women referred for hereditary cancer genetic testing.
Mabey等人的這項研究 「驗證了將所有祖先的多基因評分與傳統風險因素相結合的臨牀乳腺癌風險評估工具」,使用來自13萬多名轉診接受遺傳性癌症基因檢測的女性的數據,使用RiskScore對MyRisk進行了縱向臨牀驗證。
RiskScore integrates a polygenic risk score (PRS) for all ancestries with the widely used Tyrer-Cuzick model. The study demonstrated that Myriad's PRS is a more accurate predictor of breast cancer risk than Tyrer-Cuzick alone. In fact, RiskScore delivered two times the ability to predict breast cancer risk than the Tyrer-Cuzick model. Additionally, Myriad was one of the first commercial laboratories to market with a multi-ancestry breast-cancer PRS, driven by its mission to advance health equity and deliver more inclusive genetic insights.
RiskScore將所有祖先的多基因風險評分(PRS)與廣泛使用的泰勒-庫齊克模型整合在一起。該研究表明,與單獨的泰勒-庫齊克相比,Myriad的PRS可以更準確地預測乳腺癌的風險。實際上,RiskScore提供的乳腺癌風險預測能力是泰勒-庫齊克模型的兩倍。此外,Myriad是首批推出多祖系乳腺癌PRS的商業實驗室之一,其使命是促進健康公平和提供更具包容性的遺傳見解。
"We are honored by this recognition, which underscores the clinical significance of the validation research from the study and predictive accuracy of RiskScore," said Dale Muzzey, PhD, Chief Scientific Officer at Myriad Genetics. "MyRisk with RiskScore can assist both clinicians and patients in making informed, proactive medical management decisions to help prevent breast cancer or detect it early. The accuracy of RiskScore across all ancestries emphasizes Myriad's commitment and contribution to health equity."
Myriad Genetics首席科學官戴爾·穆齊博士說:「這一認可令我們感到榮幸,這凸顯了RiskScore研究和預測準確性中驗證研究的臨牀意義。」「帶有RiskScore的MyRisk可以幫助臨牀醫生和患者做出明智、積極的醫療管理決策,以幫助預防或及早發現乳腺癌。RiskScore在所有祖先中的準確性凸顯了Myriad對健康公平的承諾和貢獻。」
"We hope that the selection of our paper as a major advance will continue to drive the adoption of RiskScore by providers and guideline societies," continued Muzzey.
Muzzey繼續說:「我們希望,選擇我們的論文作爲一項重大進展將繼續推動提供商和指導協會採用RiskScore。」
About MyRisk Hereditary Cancer Test with RiskScore
MyRisk Hereditary Cancer Test with RiskScore evaluates 48 genes associated with hereditary cancer risk to identify genetic changes associated with an increased cancer risk for 11 different cancers. When combined with family history and other clinical factors such as breast density, MyRisk with RiskScore provides eligible patients with a five-year and remaining lifetime breast cancer risk assessment individualized to them.
關於使用 riskScore 進行的 MyRisk 遺傳性癌症檢測
使用 RiskScore 進行的 MyRisk 遺傳性癌症測試可評估 48 個與遺傳性癌症風險相關的基因,以確定與 11 種不同癌症的癌症風險增加相關的基因變化。結合家族史和其他臨牀因素(例如乳房密度)時,帶有RiskScore的MyRisk爲符合條件的患者提供爲他們量身定製的五年及剩餘壽命乳腺癌風險評估。
About Myriad Genetics
Myriad Genetics is a leading genetic testing and precision medicine company dedicated to advancing health and well-being for all. Myriad develops and offers genetic tests that help assess the risk of developing disease or disease progression and guide treatment decisions across medical specialties where genetic insights can significantly improve patient care and lower healthcare costs. For more information, visit .
關於《無數遺傳學》
Myriad Genetics是一家領先的基因檢測和精準醫療公司,致力於促進所有人的健康和福祉。Myriad 開發並提供基因檢測,幫助評估發生疾病或疾病進展的風險,指導各醫學專業的治療決策,在這些專業領域,基因洞察可以顯著改善患者護理並降低醫療成本。欲了解更多信息,請訪問。
Safe Harbor Statement
This press release contains "forward-looking statements" within the meaning of the Private Securities Litigation Reform Act of 1995, including that MyRisk with RiskScore being featured as a top innovation in genomic medicine reinforces the need for more wide-scale clinical implementation of MyRisk with RiskScore, as this data is likely to have implications for healthcare systems and practice guidelines, and MyRisk with RiskScore can assist both clinicians and patients in making informed, proactive medical management decisions to help prevent breast cancer or detect it early. These "forward-looking statements" are management's expectations of future events as of the date hereof and are subject to known and unknown risks and uncertainties that could cause actual results, conditions, and events to differ materially and adversely from those anticipated. Such factors include those risks described in the company's filings with the U.S. Securities and Exchange Commission, including the company's Annual Report on Form 10-K filed on February 28, 2024, as well as any updates to those risk factors filed from time to time in the company's Quarterly Reports on Form 10-Q or Current Reports on Form 8-K. Myriad is not under any obligation, and it expressly disclaims any obligation, to update or alter any forward-looking statements, whether as a result of new information, future events or otherwise except as required by law.
安全港聲明
本新聞稿包含1995年《私人證券訴訟改革法》所指的 「前瞻性陳述」,包括將RiskScore列爲基因組醫學的頂級創新的MyRisk突顯了在臨牀上更廣泛地實施帶有RiskScore的MyRisk的必要性,因爲這些數據可能會對醫療系統和實踐指南產生影響,而帶有RiskScore的MyRisk可以幫助臨牀醫生和患者做出明智、積極的醫療管理決策幫助預防乳腺癌或儘早發現它。這些 「前瞻性陳述」 是管理層截至本文發佈之日對未來事件的預期,受已知和未知的風險和不確定性的影響,這些風險和不確定性可能導致實際業績、狀況和事件與預期存在重大不利差異。這些因素包括公司向美國證券交易委員會提交的文件中描述的風險,包括該公司於2024年2月28日提交的10-k表年度報告,以及不時在公司10-Q表季度報告或8-k表最新報告中對這些風險因素的任何更新。除非法律要求,否則Myriad沒有任何義務更新或修改任何前瞻性陳述,無論是由於新信息、未來事件還是其他原因。
Investor Contact
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PR@myriad.com
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