share_log

Broad Clinical Labs and Genomes2Veterans Partner on Veterans Affairs' Prostate Cancer, Genetic Risk, and Equitable Screening Study (ProGRESS)

Broad Clinical Labs and Genomes2Veterans Partner on Veterans Affairs' Prostate Cancer, Genetic Risk, and Equitable Screening Study (ProGRESS)

Broad Clinical Labs和Genomes2Veterans合作進行退伍軍人事務局的前列腺癌、遺傳風險和公平篩查研究(ProGRESS)
PR Newswire ·  00:00

BURLINGTON, Mass., Nov. 6, 2024 /PRNewswire/ -- Broad Clinical Labs (BCL) and the Genomes2Veterans (G2V) Research Program announced today that the Department of Veterans Affairs' (VA)-funded Prostate Cancer, Genetic Risk, and Equitable Screening Study (ProGRESS) clinical trial will use BCL's Blended Genome-Exome (BGE) assay and analytical and interpretative pipelines to return genomic risk for prostate cancer to Veteran(s) who enroll in the trial, which has now started recruitment.

馬薩諸塞州伯靈頓,2024年11月6日 /美通社/ -- 廣泛臨床實驗室(BCL)和基因組退伍軍人(G2V)研究計劃今天宣佈,退伍軍人事務部(VA)資助的前列腺癌、遺傳風險和公平篩查研究(ProGRESS)臨床試驗將使用BCL的混合基因組-外顯子(BGE)測定和分析解釋管道,向參與試驗的退伍軍人返回前列腺癌的基因風險,該試驗現已開始招募。

As healthcare shifts toward more personalized approaches, understanding individual risk is crucial for disease prevention. By leveraging biobank-linked healthcare systems like Veterans Affairs' Million Veteran Program (MVP), researchers developed a new genomic risk model for prostate cancer called Prostate CAncer integrated Risk Evaluation (P-CARE). The P-CARE model was developed using data from 585,418 male MVP participants, including 101,920 who identify as Black or African American. It combines genetic scores, family history, and genetic background to provide tailored risk assessments for prostate cancer. To ensure its accuracy, the model was validated in external datasets including those of the Prostate Cancer Association Group to Investigate Cancer Associated Alterations in the Genome (PRACTICAL) Consortium and from the NIH's All of Us Research Program. The model is now being used in the ProGRESS clinical trial of precision prostate cancer screening.

隨着醫療保健向更個性化方法轉變,了解個體風險對疾病預防至關重要。通過利用像退伍軍人事務部百萬退伍軍人計劃(MVP)這樣的生物庫鏈接的醫療保健系統,研究人員爲前列腺癌開發了一個名爲前列腺癌綜合風險評估(P-CARE)的新基因風險模型。P-CARE模型使用了來自585,418名男性MVP參與者的數據,其中包括101,920名自述爲黑人或非裔美國人。該模型結合了遺傳分數、家族史和遺傳背景,爲前列腺癌提供定製的風險評估。爲了確保其準確性,該模型在外部數據集中進行了驗證,包括前列腺癌協會調查癌症基因組變化(PRACTICAL)聯盟和NIH的All of Us研究計劃的數據。該模型現在正在用於精準前列腺癌篩查的ProGRESS臨床試驗中。

According to a study from the group, released this week as a preprint and presented at the American Society of Human Genetics national meeting, the P-CARE model describes a clinically important risk gradient for prostate cancer. For participants with high P-CARE scores (in the top 20%), the likelihood of developing prostate cancer was significantly increased. For example, in the MVP group, the risk of any prostate cancer was 2.75 times higher, while the risk for metastatic disease was 2.78 times greater, and the risk of fatal prostate cancer was 2.59 times higher compared to those with median scores. Among high-risk individuals, nearly 48% were expected to develop prostate cancer by age 90, compared to only 14% in the low-risk group. The ProGRESS trial is now testing whether this type of information allows healthcare providers to make better screening recommendations for men at lower and higher risk of disease.

根據該團體本週發佈的一項預印研究,並在美國人類遺傳學會全國會議上介紹,P-CARE模型描述了前列腺癌的臨床重要風險梯度。對於P-CARE評分高的參與者(前20%),患前列腺癌的可能性顯著增加。例如,在MVP團體中,任何前列腺癌的風險增加了2.75倍,轉移性疾病的風險增加了2.78倍,致命前列腺癌的風險增加了2.59倍,與評分中位數相比。在高風險個體中,有將近48%的人預計在90歲前患前列腺癌,而低風險群體只有14%。ProGRESS試驗現在正在測試這類信息是否能夠讓醫療保健提供者爲患有不同疾病風險的男性做出更好的篩查建議。

"Biobank-linked healthcare systems like Veterans Affairs give us a unique opportunity to learn from existing patient data, develop better models, and deliver new paradigms of preventive care to patients," said Jason Vassy, MD, MPH, MS clinician-investigator at Veterans Affairs Boston Healthcare System and lead author on the study. "Veteran(s) we are now enrolling into the ProGRESS trial will help us understand the potential impact of precision prostate cancer screening on health outcomes."

「像退伍軍人事務部等與生物庫相關的醫療系統爲我們提供了從現有患者數據中學習、開發更好模型並向患者提供新的預防護理範式的獨特機會,」退伍軍人事務部波士頓醫療保健系統的臨床研究員兼研究報告的主要作者Jason Vassy醫學博士、公共衛生碩士、數學碩士說:「我們正將參與 ProGRESS 試驗的以往退伍軍人幫助我們了解精準前列腺癌篩查對健康結果的潛在影響。」

"We are so proud to support this important study with G2V and Veterans Affairs," said Niall Lennon, PhD, CSO, and Chair of Broad Clinical Labs. "This trial leverages the power of our Blended Genome-Exome platform, where the imputed genome region can be used to compute polygenic scores and the exome region to look for monogenic risk factors. Our team is delighted to have worked with the team at Veterans Affairs to validate and launch this new pipeline and we look forward to delivering results to participants very soon."

「我們很自豪能支持G2V和退伍軍人事務這一重要研究,」Broad臨床實驗室的CSO兼主席Niall Lennon博士說:「這項試驗利用我們融合基因組-外顯子平台的強大功能,其中推定的基因組區域可用於計算多基因分數,而外顯子區域可用於尋找單基因風險因素。我們團隊很高興與退伍軍人事務團隊合作驗證和啓動這一新流程,我們期待儘快向參與者交付結果。」

The rollout of the ProGRESS trial highlights how biobank-linked healthcare systems can quickly turn research into real-world evidence-generating activities. Veteran(s) between the ages of 55-69, who are in receipt of regular Veterans Affairs care, and who are without a personal history of prostate cancer are eligible to enroll in the study (more information can be found at ClinicalTrials.gov by searching for Trial ID NCT05926102).

ProGRESS 試驗的推出凸顯出與生物庫相關醫療系統如何能迅速將研究轉化爲產生真實世界證據的活動。55歲至69歲之間、定期接受退伍軍人事務護理、且個人無前列腺癌病史的退伍軍人有資格參與本研究(更多信息可在 ClinicalTrials.gov 上搜索 Trial ID NCT05926102 方可了解)。

About Broad Clinical Labs:
Broad Clinical Laboratories was founded in 2013 as a subsidiary of Broad Institute of MIT and Harvard to accelerate the world toward a better understanding, diagnosis, and treatment of disease by pursuing projects, developing products, and driving adoption of cutting-edge 'omics technologies and novel molecular assays. Broad Clinical Labs is a leader in human whole genome sequencing, having sequenced over 680,000 genomes in service of its mission to accelerate the understanding and diagnosis of human disease.

關於 Broad 臨床實驗室:
Broad 臨床實驗室成立於2013年,作爲斯坦福大學和哈佛大學 Broad 研究所的子公司,通過開展項目、開發產品並推動尖端的組學技術和新型分子檢測方法的採用,加速使世界朝着更好地理解、診斷和治療疾病的方向發展。Broad 臨床實驗室是人類全基因組測序的領導者,已在其使命中測序了超過 68 萬個基因組,加速了對人類疾病的理解和診斷。

About Genomes2Veterans:
Based at the VA Boston Healthcare System and spanning the larger ecosystem of Harvard Medical School, Mass General Brigham, Ariadne Labs, and the U.S. Department of Veterans Affairs, the Genomes2Veterans (G2V) Research Program conducts genomic and precision medicine implementation research to bring these new technologies to the healthcare of US Veterans.

關於 Genomes2Veterans:
總部設在VA波士頓醫療中心,涵蓋哈佛醫學院、馬薩諸塞州總醫院、Ariadne Labs和美國退伍軍人事務部較大生態系統,Genomes2Veterans(G2V)研究計劃進行基因組和精準醫學實施研究,將這些新技術引入美國退伍軍人的醫療保健中。

For more information, please contact:
[email protected]

更多信息,請聯繫:
[email protected]

SOURCE Broad Clinical Labs

資訊 Broad 臨床實驗室

WANT YOUR COMPANY'S NEWS FEATURED ON PRNEWSWIRE.COM?

想要您公司的新聞在PRNEWSWIRE.COM上特色呈現嗎?

440k+
440k+

Newsrooms &
新聞發佈室&

Influencers
影響力人士
9k+
9k+

Digital Media
數字媒體

Outlets
Outlets
270k+
270k+

Journalists
記者

Opted In
Opted In
GET STARTED
開始使用

譯文內容由第三人軟體翻譯。


以上內容僅用作資訊或教育之目的,不構成與富途相關的任何投資建議。富途竭力但無法保證上述全部內容的真實性、準確性和原創性。
    搶先評論