NCCN Prostate Cancer Guidelines Reinforce Status of Myriad Genetics' Prolaris Test as an 'Advanced Tool' Recommended for Prognostic Assessment
NCCN Prostate Cancer Guidelines Reinforce Status of Myriad Genetics' Prolaris Test as an 'Advanced Tool' Recommended for Prognostic Assessment
Prolaris Remains a Long-Standing Fixture in the Guidelines for 10th Year Running
Prolaris在指南中保持了長達十年的固定地位
SALT LAKE CITY, Dec. 09, 2024 (GLOBE NEWSWIRE) -- Myriad Genetics, Inc. (NASDAQ: MYGN), a leader in genetic testing and precision medicine, today announced that its Prolaris prostate cancer prognostic test continues to be classified by the National Comprehensive Cancer Network (NCCN) as an 'Advanced Tool' in the fight against prostate cancer1. Like other gene expression-based tests, Prolaris for many years has been included in NCCN guidelines with category 2A level of evidence, meaning its inclusion has support from at least 85% of members on the NCCN prostate panel2.
鹽湖城,2024年12月09日(環球新聞通訊社) -- 萬基遺傳(NASDAQ: MYGN),基因檢測和精準醫療的領導者,今天宣佈其Prolaris前列腺癌預後測試繼續被國家綜合癌症網絡(NCCN)分類爲與前列腺癌鬥爭的'愛文思控股工具'。與其他基於基因表達的測試一樣,Prolaris多年來一直被納入NCCN指南,證據等級爲2A,意味着其被納入得到至少85% NCCN前列腺小組成員的支持。
"The updated NCCN Prostate Cancer Guidelines continue to solidify Prolaris' market position," said Paul J. Diaz, President and CEO, Myriad Genetics. "While there have been certain mischaracterizations regarding the updated guidelines leading to confusion, extensive published evidence shows that Prolaris is a clinically recognized and effective tool in managing patients with prostate cancer. We are confident that our highly engaged clinicians will continue to see the guidelines as an additional reason to incorporate Prolaris in treatment decisions."
"更新的NCCN前列腺癌指南繼續鞏固Prolaris的市場地位,"萬基遺傳總裁兼首席執行官保羅·J·迪亞茲(Paul J. Diaz)表示。"儘管關於更新指南的某些錯誤描述導致了混淆,但大量公開的證據顯示,Prolaris是一個在管理前列腺癌患者中被臨床公認和有效的工具。我們相信,我們高度參與的臨床醫生將繼續將這些指南視爲在治療決策中納入Prolaris的額外理由。"
"Prolaris is the Only test developed in untreated patients and the Only test with two clinically validated thresholds. With its active surveillance threshold, Prolaris identifies the most appropriate patients for active surveillance across all biomarkers," said George Daneker, Jr. MD, President and Chief Clinical Officer, Oncology, Myriad Genetics. "With its multimodal threshold, Prolaris can identify which patients may consider treatment intensification3."
"Prolaris是唯一在未治療患者中開發的測試,也是唯一有兩個臨床驗證閾值的測試。通過其主動監測閾值,Prolaris識別出所有生物標誌物中最適合主動監測的患者,"萬基遺傳總體臨床官員喬治·丹克爾(George Daneker, Jr.)博士表示。"通過其多模態閾值,Prolaris可以識別哪些患者可能考慮治療強化。"
Myriad has published more than 25 studies demonstrating the value of Prolaris in clinical decision-making for prostate cancer. This year alone, multiple studies have been published and presented as further evidence of the clinical utility of the Prolaris test. In an independent prospective study, investigators validated the Prolaris score's ability to predict both early metastasis within three years and a quicker time to definitive treatment for patients above the active surveillance threshold. Another study demonstrated that Prolaris can accurately predict the benefit of adding androgen deprivation therapy (ADT) to radiation therapy (RT) in men with localized prostate cancer.
萬基遺傳已發佈超過25項研究,證明Prolaris在前列腺癌臨床決策中的價值。今年,多個研究已被髮布並呈現出作爲Prolaris測試臨床效用的進一步證據。在一項獨立前瞻性研究中,研究人員驗證了Prolaris評分在預測三年內早期轉移和對超過主動監測閾值的患者迅速起始確切治療的能力。另有研究表明,Prolaris可以準確預測在侷限性前列腺癌男性中將雄激素剝奪治療(ADT)與放射治療(RT)結合的益處。
About the Prolaris Prostate Cancer Prognostic Test
Prolaris is a molecular diagnostic test that provides personalized information about the aggressiveness of a patient's prostate cancer, helping to identify whether it is safe to forgo treatment, whether to pursue treatment, and how much treatment is needed for the best possible outcome. Prolaris is the only biomarker test to quantify the benefits of adding androgen ADT to RT.
關於Prolaris前列腺癌預後測試
Prolaris是一種分子診斷測試,提供有關患者前列腺癌侵襲性的信息,幫助確定是否可以安全地放棄治療,是否應進行治療,以及爲獲得最佳結果需要多少治療。Prolaris是唯一一個量化將雄激素ADt添加到Rt的益處的生物標誌物測試。
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學公司,致力於推進所有人的健康和福祉。萬基遺傳開發並提供基因檢測,幫助評估發病風險或疾病進展,並指導治療決策,涉及醫療專業領域的基因洞察可以顯著改善患者護理,並降低醫療保健成本。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 statements relating to the company's Prolaris test and how with its active surveillance threshold, Prolaris identifies the most appropriate patients for active surveillance across all biomarkers, and that clinicians will continue to see the guidelines as an additional reason to incorporate Prolaris in treatment decisions. 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.
Safe Harbor聲明
本新聞稿包含1995年《私人證券訴訟改革法案》意義上的「前瞻性聲明」,包括與公司的Prolaris測試相關的聲明,以及如何通過其主動監測閾值,Prolaris識別所有生物標誌物中最適合主動監測的患者,並且臨床醫生將繼續將這些指南視爲將Prolaris納入治療決策的另一個理由。這些「前瞻性聲明」是管理層在此日期對未來事件的預期,受已知和未知的風險和不確定性的影響,這可能導致實際結果、情況和事件與預期顯著不同併產生不利影響。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,包括公司於2024年2月28日提交的10-K表格年度報告,以及隨時間推移公司在10-Q季度報告或8-K當前報告中提交的任何風險因素更新。萬基遺傳並不承擔任何義務,並明確拒絕更新或更改任何前瞻性聲明的義務,無論是由於新信息、未來事件還是其他原因,法律另有要求的除外。
1 "Advanced tools that have demonstrated superior prognostic performance beyond standard tools and/or serve as a predictive biomarker that identifies patients who will differentially benefit from a specific treatment." Version 1.2025, 12/04/24 2024 National Comprehensive Cancer Network (NCCN)
2
3 Tward JD, et al. Personalizing localized prostate cancer: Validation of a combined clinical cell-cycle risk (CCR) score threshold for prognosticating benefit from multimodality therapy. Clinical Genitourinary Cancer. 2021. Doi:10.1016/j.clgc.2021.01.003
1 「先進工具已證明其預後性能超越標準工具和/或作爲預測性生物標誌物,識別將從特定治療中獲得不同益處的患者。」 版本1.2025,12/04/24 2024年國家綜合癌症網絡(NCCN)
2
3 Tward JD等。個性化局部前列腺癌:驗證結合臨床電芯週期風險(CCR)評分閾值以預判多模式治療的益處。《臨床泌尿腫瘤學》。2021。Doi:10.1016/j.clgc.2021.01.003
National Comprehensive Cancer Network. NCCN makes no warranties of any kind whatsoever regarding their content, use or application and disclaims any responsibility for their application or use in any way.
國家綜合癌症網絡。NCCN對其內容、使用或應用不作任何形式的擔保,並對其以任何方式的應用或使用不承擔任何責任。
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譯文內容由第三人軟體翻譯。