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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

萬基遺傳的風險評分研究被評選爲《美國人類遺傳學雜誌》十大重要進展之一。
GlobeNewswire ·  12/20 05:15

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是乳腺癌風險的更準確預測指標,其準確性是Tyrer-Cuzick模型的兩倍

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(全球新聞社)—— 萬基遺傳(NASDAQ: MYGN),一家在遺傳和基因組檢測及精準醫療領域的領導者,宣佈其MyRisk遺傳癌症測試與RiskScore的研究被《美國人類遺傳學雜誌》評選爲基因組醫學的十大重要進展之一。該研究由國家人類基因組研究所的基因組醫學工作組選出。

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等人的研究,"結合多基因得分與傳統風險因素的臨牀乳腺癌風險評估工具的驗證,"展示了使用超過130,000名接受遺傳癌症基因檢測女性的數據,對MyRisk與RiskScore進行的縱向臨牀驗證。

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將適用於所有血統的多基因風險評分(PRS)與廣泛使用的Tyrer-Cuzick模型相結合。研究表明,萬基的PRS比單獨的Tyrer-Cuzick模型更準確地預測乳腺癌風險。實際上,RiskScore的乳腺癌風險預測能力是Tyrer-Cuzick模型的兩倍。此外,萬基是首批推出具有多血統乳腺癌PRS的商業實驗室之一,這一舉措旨在推進健康公平並提供更具包容性的基因洞察。

"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."

"我們很榮幸獲得這一認可,這強調了該研究的驗證研究的臨牀重要性和RiskScore的預測準確性,"萬基遺傳首席科學官Dale Muzzey博士說。"MyRisk與RiskScore可以幫助臨牀醫生和患者做出明智、主動的醫療管理決策,以幫助預防乳腺癌或早期發現。RiskScore在所有血統上的準確性強調了萬基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.

「我們希望我們的論文被選爲重大進展能夠繼續推動提供者和指南協會採用RiskScore。」穆澤說。

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MyRisk遺傳癌症測試與RiskScore
MyRisk遺傳癌症測試與RiskScore評估48個與遺傳癌症風險相關的基因,以識別與11種不同癌症相關的遺傳變化。當與家族史和其他臨牀因素(如乳腺密度)結合時,MyRisk與RiskScore爲符合條件的患者提供個性化的五年和剩餘生命週期乳腺癌風險評估。

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Myriad Genetics
萬基遺傳是一家領先的基因檢測和精準醫療公司,致力於提升所有人的健康和幸福。萬基開發並提供基因檢測,幫助評估患病風險或疾病進展,並在醫療專業領域指導治療決策,在這些領域,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,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「前瞻性聲明」,其中包括MyRisk與RiskScore作爲基因醫學的頂級創新被突出介紹,強化了廣泛臨牀實施MyRisk與RiskScore的必要性,因爲這些數據可能對醫療系統和實踐指南產生影響,而MyRisk與RiskScore可以幫助臨牀醫生和患者做出明智的、積極的醫療管理決策,以預防乳腺癌或早期發現乳腺癌。這些「前瞻性聲明」是管理層截至本日期對未來事件的預期,並且受到已知和未知的風險和不確定性的影響,這些因素可能導致實際結果、條件和事件顯著地及不利地與預期的不同。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那些風險,包括公司於2024年2月28日提交的10-K表格年度報告,以及不時在公司的10-Q表格季度報告或8-K表格當前報告中提交的這些風險因素的任何更新。萬基遺傳沒有任何義務,也明確否認任何義務去更新或更改任何前瞻性聲明,無論是由於新信息、未來事件還是其他情況,除非法律要求。

Investor Contact
Matt Scalo
(801) 584-3532
IR@myriad.com

投資者聯繫
馬特·斯卡洛
(801) 584-3532
IR@myriad.com

Media Contact
Glenn Farrell
(385) 318-3718
PR@myriad.com

媒體聯繫
格倫·法雷爾
(385) 318-3718
PR@myriad.com


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