In this paper, we compare two types of stochastic models for the initial growth of cancerous tumors. In one type, the random element enters via the initial time of growth or via the initial size of the growth clone. In the other type, tumors differ from one another essentially via their growth rates. We present a simple test to distinguish between the two types when tumor size distributions are available from several time points. Size distributions are the key elements of such kinetic analysis given the limitation that an individual tumor can be measured only once, at the time of sacrifice of an experimental animal. We discuss these concepts in connection with data from particular experiments on carcinogenic growth in the livers of mice.
- scientific article; zbMATH DE number 3555176 (Why is no real title available?)
- scientific article; zbMATH DE number 3569467 (Why is no real title available?)
- scientific article; zbMATH DE number 3206712 (Why is no real title available?)
- scientific article; zbMATH DE number 3410334 (Why is no real title available?)
- scientific article; zbMATH DE number 3190745 (Why is no real title available?)
- Limit theorems for decomposable multi-dimensional Galton-Watson processes
- On estimating the growth function of tumors
- The particular role of cell loss in tumor growth
- Dynamics of tumor interaction with the host immune system
- From population dynamics to modelling the competition between tumors and immune system
- Tests for Differences in Tumor Incidence Based on Animal Carcinogenesis Experiments
- Modeling Tumor Growth with Random Onset
- Some stochastic models op cancer metastases
- Estimating tumor growth rates in vivo
This page was built for publication: The early growth of cancer
Report a bug (only for logged in users!)Click here to report a bug for this page (MaRDI item Q802483)