Multiple indications of disease progression found in a cancer patient by loco-regional relapse, distant metastasis and death. Early identification of these indications is necessary to change the treatment strategy. Biomarkers play an essential role in this aspect. The biomarkers can influence how particular cancer behaves and how it may respond to a specific treatment. The survival chance of a patient is dependent on the biomarker, and the treatment strategy also differs accordingly, e.g., the survival prediction of breast cancer patients diagnosed with HER2 positive status is different from the same with HER2 negative status. This results in a different treatment strategy. So, the heterogeneity of the biomarker statuses or levels should be taken into consideration while modelling the survival outcome. This heterogeneity factor which is often unobserved, is called frailty. When multiple indications are present simultaneously, the scenario becomes more complex as only one of them can occur, which will censor the occurrence of other events. The events indicating cancer progression are likely to be inter-related. So, the correlation should be incorporated through the frailties of different events. In our study, we considered a multiple events or risks model with a heterogeneity component. Based on the estimated variance of the frailty, the threshold levels of a biomarker are utilised as early detection tool of the disease progression or death. Additive-gamma frailty model is considered to account the correlation between different frailty components and estimation of parameters are performed using Expectation-Maximization Algorithm. With the extensive algorithm in R, we have obtained the threshold levels of activity of a biomarker in a multiple events scenario.
翻译:癌症患者的存活机会取决于生物标志, 治疗战略也因此不同, 例如, 被诊断为HER2阳性状态的乳腺癌患者的存活率预测与HER2的负参数不同。 这导致不同的治疗战略。 因此, 在模拟生存结果时,应该考虑到生物标记状态或水平的异质性。 生物标志可以影响特定癌症的行为方式, 以及它如何对特定治疗作出反应。 生物标志可以影响特定癌症的行为方式。 生物标志可以影响特定癌症的行为方式, 以及它如何对特定治疗方式作出反应。 当多重迹象同时出现时, 情况会变得更为复杂, 因为只有其中一种症状, 这会限制其他事件的发生。 表明癌症进展的事件可能与 HER2 的负值不同。 因此, 在不同的治疗战略中, 在模拟生存结果时,应该考虑到生物标记状态或水平的异质性 。 我们的研究认为, 使用生物标记的多异质性成分的检测 或基础的 模型 水平是 一种多质性 的模型 。