In cancer trials, the analysis of longitudinal toxicity data is a difficult task due to the presence of multiple adverse events with different extents of toxic burden. Models able to summarise and quantify the overall toxic risk and its evolution during cancer therapy, which deals with both the longitudinal and the categorical aspects of toxicity levels progression, are necessary, but still not well developed. In this work, a novel approach based on Latent Markov (LM) models for longitudinal toxicity data is proposed. The latent status of interest is the Latent Overall Toxicity (LOTox) condition of each patient, which affects the distribution of the observed toxic levels over treatment. By assuming the existence of a LM chain for LOTox dynamics, the new approach aims at identifying different latent states of overall toxicity burden (LOTox states). This approach investigates how patients move between latent states during chemotherapy treatment allowing for the reconstruction of personalized longitudinal LOTox profiles. This methodology has never been applied to osteosarcoma treatment and provides new insights for medical decisions in childhood cancer therapy.
翻译:在癌症试验中,对纵向毒性数据的分析是一项艰巨的任务,因为存在多种有毒负担程度不同的不良事件。能够总结和量化总体毒性风险及其在癌症治疗过程中的演变的模型是必要的,但这种模型涉及毒性水平递增的纵向和绝对方面。在这项工作中,根据Litent Markov(LM)模型提出了一个关于纵向毒性数据的新颖方法。潜在的关注状况是每个病人的低位总体毒性(LOTox)状况,它影响到所观察到的毒性水平在治疗中的分布。假设存在LOTox动态的LM链,新的方法旨在查明整个毒性负担的不同潜在状态(LOTox州)。这种方法调查了病人在化疗程治疗期间如何在潜伏状态之间移动,以便重建个性长距离LOTOox剖面。这种方法从未应用于骨质肿瘤治疗,并为儿童癌症治疗的医疗决定提供了新的见解。