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Modelling uveal melanoma.

机译:葡萄膜黑色素瘤建模。

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BACKGROUND/AIM: There has been no consistent pattern reported on how mortality for uveal melanoma varies with age. This information can be useful to model the complexity of the disease. The authors have examined ocular cancer trends, as an indirect measure for uveal melanoma mortality, to see how rates vary with age and to compare the results with their other studies on predicting metastatic disease. METHODS: Age specific mortality was examined for England and Wales, the USA, and Canada. A log-log model was fitted to the data. The slopes of the log-log plots were used as measure of disease complexity and compared with the results of previous work on predicting metastatic disease. RESULTS: The log-log model provided a good fit for the US and Canadian data, but the observed rates deviated for England and Wales among people over the age of 65 years. The log-log model for mortality data suggests that the underlying process depends upon four rate limiting steps, while a similar model for the incidence data suggests between three and four rate limiting steps. Further analysis of previous data on predicting metastatic disease on the basis of tumour size and blood vessel density would indicate a single rate limiting step between developing the primary tumour and developing metastatic disease. CONCLUSIONS: There is significant underreporting or underdiagnosis of ocular melanoma for England and Wales in those over the age of 65 years. In those under the age of 65, a model is presented for ocular melanoma oncogenesis requiring three rate limiting steps to develop the primary tumour and a fourth rate limiting step to develop metastatic disease. The three steps in the generation of the primary tumour involve two key processes-namely, growth and angiogenesis within the primary tumour. The step from development of the primary to development of metastatic disease is likely to involve a single rate limiting process.
机译:背景/目的:关于葡萄膜黑色素瘤的死亡率如何随年龄变化没有一致的报道。该信息可用于对疾病的复杂性进行建模。作者检查了眼癌趋势,作为葡萄膜黑色素瘤死亡率的间接指标,以观察发病率如何随年龄变化,并将结果与​​他们的其他预测转移性疾病的研究进行比较。方法:检查了英格兰和威尔士,美国和加拿大的特定年龄死亡率。将对数-对数模型拟合到数据。对数-对数图的斜率用于衡量疾病的复杂性,并与先前预测转移性疾病的工作结果进行比较。结果:对数-对数模型非常适合美国和加拿大的数据,但在65岁以上的人群中,英格兰和威尔士的观测值存在偏差。死亡率数据的对数对数模型表明基本过程取决于四个限速步骤,而发病率数据的类似模型则建议在三个至四个限速步骤之间。对基于肿瘤大小和血管密度预测转移性疾病的先前数据的进一步分析将表明,在发展原发性肿瘤和发展性转移性疾病之间有一个限速步骤。结论:在65岁以上的英格兰和威尔士,眼黑色素瘤的报告或诊断明显不足。在65岁以下的人群中,提出了一种眼黑色素瘤致癌模型,该模型需要三个限速步骤来发展原发性肿瘤,而第四个限速步骤来发展转移性疾病。原发肿瘤产生的三个步骤涉及两个关键过程,即原发肿瘤内的生长和血管生成。从原发性疾病发展到转移性疾病的发展可能涉及单一的限速过程。

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