HCG Manavta Cancer Centre, Nashik, Maharashtra, India.
HealthCare Global Enterprises Limited, City Cancer Centre, Vijayawada, India.
Cancer Rep (Hoboken). 2024 Nov;7(11):e70042. doi: 10.1002/cnr2.70042.
Detection of cancer at the early stage currently offers the only viable strategy for reducing disease-related morbidity and mortality. Various approaches for multi-cancer early detection are being explored, which largely rely on capturing signals from circulating analytes shed by tumors into the blood. The fact that biomarker concentrations are limiting in the early stages of cancer, however, compromises the accuracy of these tests. We, therefore, adopted an alternate approach that involved interrogation of the serum metabolome with machine learning-based data analytics. Here, we monitored for modulations in metabolite patterns that correlated with the presence or absence of cancer. Results obtained confirmed the efficacy of this approach by demonstrating that it could detect a total of 15 cancers in women with an average accuracy of about 99%.
To further increase the scope of our test, we conducted an investigator-initiated clinical trial involving a total of 6445 study participants, which included both cancer patients and non-cancer volunteers. Our goal here was to maximize the number of cancers that could be detected, while also covering cancers in both females and males.
Metabolites extracted from individual serum samples were profiled by ultra-performance liquid chromatography coupled to a high-resolution mass spectrometer using an untargeted protocol. After processing, the data were analyzed by our cancer detection machine-learning algorithm to differentiate cancer from non-cancer samples. Results revealed that our test platform could indeed detect a total of 30 cancers, covering both females and males, with an average accuracy of ~98%. Importantly, the high detection accuracy remained invariant across all four stages of the cancers.
Thus, our approach of integrating untargeted metabolomics with machine learning-powered data analytics offers a powerful strategy for early-stage multi-cancer detection with high accuracy.
Registration No: CTRI/2023/03/050316.
目前,早期癌症检测是降低疾病相关发病率和死亡率的唯一可行策略。目前正在探索多种多癌早期检测方法,这些方法主要依赖于捕获肿瘤进入血液的循环分析物发出的信号。然而,由于在癌症的早期阶段生物标志物浓度有限,这些检测的准确性受到影响。因此,我们采用了一种替代方法,涉及使用基于机器学习的数据分析来检测血清代谢组。在这里,我们监测了与癌症存在或不存在相关的代谢物模式的调制。获得的结果证实了这种方法的有效性,表明它可以检测到女性中总共 15 种癌症,平均准确率约为 99%。
为了进一步扩大我们的测试范围,我们进行了一项由研究人员发起的临床试验,共涉及 6445 名研究参与者,包括癌症患者和非癌症志愿者。我们的目标是最大限度地增加可以检测到的癌症数量,同时覆盖女性和男性的癌症。
通过超高效液相色谱-高分辨率质谱联用仪,采用非靶向方法对来自个体血清样本的代谢物进行了分析。在处理后,通过我们的癌症检测机器学习算法对数据进行分析,以区分癌症和非癌症样本。结果表明,我们的测试平台确实可以检测到总共 30 种癌症,涵盖女性和男性,平均准确率约为 98%。重要的是,高检测准确性在癌症的所有四个阶段都保持不变。
因此,我们将非靶向代谢组学与基于机器学习的数据分析相结合的方法为早期多癌检测提供了一种具有高精度的强大策略。
注册号:CTRI/2023/03/050316。