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Myriad Genetics to Present New Data at San Antonio Breast Cancer Symposium

Myriad Genetics to Present New Data at San Antonio Breast Cancer Symposium

万基遗传将在圣安东尼奥乳腺癌 symposium 上发布新数据
GlobeNewswire ·  2024/12/10 05:05

Presentations include analytical validation of Myriad's high-definition tumor informed MRD assay for breast cancer and its Breast Cancer Risk Assessment Tool MyRisk with RiskScore

演示包括对万基遗传高分辨率肿瘤知情MRD检测的分析验证,该检测用于乳腺癌,以及其乳腺癌风险评估工具MyRisk与风险评分。

SALT LAKE CITY, Dec. 09, 2024 (GLOBE NEWSWIRE) -- Myriad Genetics, Inc. (NASDAQ: MYGN), a leader in genetic testing and precision medicine, announced it will present new data at the 2024 San Antonio Breast Cancer Symposium (SABCS), including a spotlight presentation on a breast cancer risk assessment tool that combines a polygenic score for all ancestries.

盐湖城,2024年12月09日 (全球新闻网) -- 万基遗传公司(纳斯达克:MYGN),一家在基因检测和精准医疗领域领先的公司,宣布将于2024年圣安东尼奥乳腺癌研讨会(SABCS)上展示新数据,包括关于一种结合了所有祖先的多基因评分的乳腺癌风险评估工具的精彩演讲。

Additional new data will show how Myriad's second-generation tumor-informed molecular residual disease (MRD) assay demonstrated high sensitivity, specificity and measurement accuracy, which, together, will facilitate improved resolution in residual-disease detection and extend lead times in recurrence detection.

额外的新数据将展示万基遗传的第二代肿瘤知情分子残留病(MRD)检测如何显示出高灵敏度、特异性和测量准确性,这将共同促进残留病检测的改进以及复发检测的提前时间。

"We are very excited to share validation data of our MRD assay. SABCS gives us the opportunity to showcase our clinical expertise in the prevention and treatment of early and advanced breast cancer," said George Daneker, MD, President and Chief Clinical Officer, Oncology, Myriad Genetics. "Myriad is one of the only labs that can offer germline and tumor genomic testing, combined with customizable workflow solutions and point-of-care patient education sessions. Our test results are supported by treatment-focused reporting, concordance checks between germline and tumor genomic results, and a summary sheet designed to help oncologists and breast surgeons interpret actionable insights more effectively."

"我们非常高兴能够分享我们的MRD检测的验证数据。SABCS为我们提供了展示我们在早期和晚期乳腺癌预防与治疗方面临床专业知识的机会,"万基遗传的肿瘤学首席医生兼总裁乔治·丹克尔博士表示。"万基是少数能提供生殖系和肿瘤基因检测的实验室之一,结合定制的工作流程解决方案和临床护理现场患者教育会议。我们的检测结果通过以治疗为中心的报告、生殖系与肿瘤基因结果之间的一致性检查,以及旨在帮助肿瘤科医生和乳腺外科医生更有效地解读可操作见解的总结表进行支持。"

Myriad Genetics Data Presentations

万基遗传数据展示

Spotlight Presentation: Session 16, PS16-01: Polygenic Risk
Date: Thursday, Dec. 12, 2024, 5:30-7:00 pm (CST), Hemisfair Ballroom 3
Presenter: Timothy Simmons, PhD, Biostatistician III, Myriad Genetics
The presentation will share longitudinal validation in the UK Biobank of a breast cancer risk assessment tool that combines a polygenic score for all ancestries with traditional risk factors.

聚光灯演示:会议16,PS16-01:多基因风险
日期:2024年12月12日,星期四,下午5:30-7:00(中央标准时间),Hemisfair舞厅3
演讲者:Timothy Simmons,博士,生物统计学家III,万基遗传
此次演示将分享在英国生物银行中对结合所有祖先的多基因评分与传统风险因素的乳腺癌风险评估工具的长期验证。

Rapid-Fire Presentation: RF1-06
Date: Wednesday, Dec. 11, 2024, 12:00-12:50 pm (CST), Hall 1
Presenter: Katie Johansen Taber, PhD, Vice President, Clinical Product Research & Partnerships, Myriad Genetics
Dr. Johansen Taber will share data detailing the association of polygenic-based breast cancer risk prediction with patient management.

快速演示:RF1-06
日期:2024年12月11日,下午12:00-12:50(中央标准时间),1号厅
演讲者:凯蒂·约汉森·塔贝,博士,副总裁,临床产品研究与合作,万基遗传
约翰森·塔伯博士将分享数据,详细说明基于多基因的乳腺癌风险预测与患者管理的关联。

Poster Presentation: P2-04-23
Date: Wednesday, Dec. 11, 2024, 5:30-7:00 pm (CST), Halls 2-3
Presenter: Ashley Acevedo, PhD, Staff Computational Scientist, Myriad Genetics
This poster shares the analytical validation of a high-definition tumor-informed Molecular Residual Disease (MRD) assay to demonstrate robust detection at low-tumor fractions, which are common in breast cancer.

海报展示:P2-04-23
日期:2024年12月11日,下午5:30-7:00(中央标准时间),2-3号厅
演讲者:阿什莉·阿塞维多,博士,万基遗传的计算科学家
该海报分享了一种高分辨率肿瘤知情的分子残留病(MRD)检测的分析验证,旨在展示在乳腺癌中常见的低肿瘤比例下的强大检测能力。

Poster Presentation: P3-02-10
Date: Thursday, Dec. 12, 2024, 12:30-2:00 pm (CST), Halls 2-3
Presenter: Holly Pederson, MD, Cleveland Clinic
Dr. Pederson will share her evaluation of a polygenic risk score as a predictor of breast cancer, triple-negative breast cancer, and early-onset disease in Hispanic women.

海报展示: P3-02-10
日期: 2024年12月12日,星期四,下午12:30-2:00(中部时间),展厅2-3
报告人: Holly Pederson,医学博士,克利夫兰诊所
Pederson博士将分享她对聚合风险评分作为乳腺癌、三阴性乳腺癌和西班牙裔女性早发病的预测因子的评估。

In addition to data presentations, Myriad will welcome attendees to its booth (#1327) during exhibition hours. Among the Myriad products highlighted in the company's SABCS exhibit are:

除了数据展示,万基遗传将在展览期间欢迎与会者到其展位(#1327)参观。在公司的SABCS展览中突出的万基产品包括:

  • MyRisk Hereditary Cancer Test evaluates 48 genes to help healthcare providers identify their patients' risk of developing 11 different types of hereditary cancer. MyRisk's clear, actionable results are the foundation for personalized care plans to help patients make confident, informed decisions about medical management. MyRisk with RiskScore provides unaffected patients with a comprehensive, personalized assessment of the five-year risk and remaining lifetime risk of developing breast cancer.
  • Precise Tumor Molecular Profile Test is a pan-cancer solid tumor comprehensive genomic profiling test that helps clinicians with straightforward interpretations, prioritization of therapies, and the next steps specific to each patient's genomic result.
  • MyChoice CDx is one of the most comprehensive homologous recombination deficiency (HRD) tests available, enabling physicians to identify patients with tumors that have lost the ability to repair double-stranded DNA breaks, resulting in increased susceptibility to DNA-damaging drugs such as platinum drugs or PARP inhibitors. The MyChoice test comprises tumor sequencing of the BRCA1 and BRCA2 genes and a composite of three proprietary technologies (loss of heterozygosity, telomeric allelic imbalance and large-scale state transitions).
  • EndoPredict Breast Cancer Prognostic Test is for patients with ER+, HER2-, node negative or node positive breast cancer. The test provides three individualized results used to help determine the most appropriate breast cancer treatment.
  • 我的风险 遗传性癌症检测 评估48个基因,帮助医疗服务提供者识别患者发展11种不同类型遗传性癌症的风险。我的风险的清晰、可操作的结果是个性化护理计划的基础,帮助患者做出自信、明智的医疗管理决策。 我的风险与风险评分 为未受影响的患者提供全面的个性化评估,评估五年风险和终身风险以研究乳腺癌的发生。
  • 精确肿瘤 分子特征检测 是一种全癌症实体肿瘤综合基因组分析测试,帮助临床医生进行简单的财报解读、治疗优先级排序和针对每位患者基因组结果的下一步措施。
  • MyChoice CDx 是目前最全面的同源重组缺陷(HRD)测试之一,使医生能够识别那些失去修复双链DNA断裂能力的肿瘤患者,从而增加对铂金药物或PARP抑制剂等DNA损伤药物的易感性。MyChoice测试包含BRCA1和BRCA2基因的肿瘤测序,以及三项专有技术的组合(杂合性缺失、端粒等位基因失衡和大规模状态转变)。
  • EndoPredict 乳腺癌预后测试适用于ER+、HER2-、淋巴结阴性或淋巴结阳性的乳腺癌患者。该测试提供三个个性化结果,用于帮助判断最合适的乳腺癌治疗方案。

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 .

万基遗传(Myriad Genetics)是一家领先的遗传测试和精准医疗公司,致力于推进全民健康和福祉。万基遗传开发并提供能够帮助评估疾病或疾病进展风险并指导治疗决策的遗传测试,适用于遗传知识可以显著改善患者护理和降低医疗保健成本的医学专业领域。了解更多信息,请访问 。
万基遗传是一家领先的基因检测和精准医疗公司,致力于促进所有人的健康和福祉。万基开发和提供基因检测,帮助评估疾病发生或进展的风险,并指导在基因见解可以显著改善患者护理和降低医疗成本的医疗专科中的治疗决策。有关更多信息,请访问 .

Safe Harbor Statement
This press release contains "forward-looking statements" within the meaning of the Private Securities Litigation Reform Act of 1995, including that the company will present new data at SABCS and that the company's new data that will be shared at SABCS will show how the company's second-generation tumor-informed MRD assay demonstrated high sensitivity, specificity and measurement accuracy, which, together, will facilitate improved resolution in residual-disease detection and extend lead times in recurrence detection. 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.

安全港声明
本新闻稿包含根据1995年私人证券诉讼改革法案的定义的“前瞻性陈述”,其中包括公司将在SABCS上发布新数据,以及将在SABCS上分享的公司新数据将表明公司的第二代肿瘤信息MRD检测显示出高灵敏度、高特异性和测量准确性,这些因素将有助于改善残余疾病检测的分辨率,并延长复发检测的提前时间。这些“前瞻性陈述”是管理层截至本日期对未来事件的期望,并受到已知和未知的风险和不确定性的影响,这些风险可能导致实际结果、状况和事件与预期有所不同。这些因素包括公司向美国证券交易委员会提交的文件中描述的那些风险,包括在2024年2月28日提交的10-K表格的公司年度报告,以及不时在公司10-Q季度报告或8-K当前报告中提交的这些风险因素的任何更新。万基遗传没有义务,也明确声明没有义务更新或修改任何前瞻性陈述,无论是由于新信息、未来事件还是其他原因,法律要求的除外。

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

投资者联系
马特·斯卡洛
(801) 584-3532
IR@myriad.com

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

媒体联系
格伦·法雷尔
(385) 318-3718
PR@myriad.com


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