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Biology subjects

Lopez Alfonso, J. C.

Publications and source records attributed to Lopez Alfonso, J. C..

4 recordsLinked to original sources

Bayesian combination of mechanistic modeling and machine learning (BaM3): improving clinical tumor growth predictions

In clinical practice, a plethora of medical examinations are conducted to assess the state of a patients pathology producing a variety of clinical data. However, exploiting these data faces the following challenges: (C1) we lack the knowledge of the mechanisms involved in regulating these data variables, and (C2) data collection is sparse in time since it relies on patients clinical presentation. (C1) implies that only a small subset of the relevant variables can be modeled by virtue of mathematical modeling. This limitation allows models to be effective in analyzing the qualitative dynamics of the system, but limits their predictive accuracy. On the other hand, statistical learning methods are well-suited for quantitative reproduction of data, but they do not provide mechanistic understanding of the investigated problem. Moreover, due to (C2) any algorithm is challenged in learning the corresponding disease dynamics. Herein, we propose a novel method, based on the Bayesian coupling of mathematical modeling and machine learning (BaM3), aiming at improving individualized predictions by addressing the aforementioned challenges. As a proof of concept, we evaluate the proposed method on a synthetic dataset for brain tumor growth and analyze its performance in predicting two major clinical outputs, namely tumor burden and infiltration. The BaM3 method results in improved predictions in almost all simulated patients, especially for those with a late clinical presentation. In addition, we test the proposed methodology in two settings dealing with real patient cohorts. In both cases, namely cancer growth in chronic lymphocytic leukemia and ovarian cancer, BaM3 predictions show excellent agreement with reported clinical data.

bioinformatics↗

Harnessing tumor immune ecosystem dynamics to personalize radiotherapy

Radiotherapy is a pillar of cancer care and augments the response to immunotherapies. However, little is known regarding the relationships between the tumor immune ecosystem (TIES) and intrinsic radiosensitivity, and a pressing question in oncology is how to optimize radiotherapy to improve patient responses to immune therapies. To address this challenge, we profiled over 10,000 primary tumors for their metrics of radiosensitivity and immune cell infiltrate (ICI), and applied a new integrated in silico model that mimics the dynamic relationships between tumor growth, ICI flux and the response to radiation. We then validated this model with a separate cohort of 59 lung cancer patients treated with radiotherapy. These analyses explain radiation response based on its effect on the TIES and quantifies the likelihood that radiation can promote a shift to anti-tumor immunity. Dynamic modeling of the relationship between tumor radiosensitivity and the TIES may provide opportunity to personalize combined radiation and immunotherapy approaches.

cancer biology↗

A novel averaging principle provides insights in the impact of intratumoral heterogeneity on tumor progression

Typically stochastic differential equations (SDEs) involve an additive or multiplicative noise term. Here, we are interested in stochastic differential equations for which the white noise is non-linearly integrated in the corresponding evolution term, typically termed as random ordinary differential equations (RODEs). The classical averaging methods fail to treat such RODEs. Therefore, we introduce a novel averaging method appropriate to be applied on RODEs. To exemplify the importance of our method, we apply it in an important biomedical problem, i.e. the assessment of intratumoral heterogeneity impact on tumor dynamics. In particular, we model gliomas according to a well-known Go or Grow (GoG) model and tumor heterogeneity is modelled as a stochastic process. It has been shown that this GoG model exhibits an emerging Allee effect (bistability). We analytically and computationally show that the introduction of white noise, as a model of intratumoral heterogeneity, leads to a monostable tumor growth. This monostability behaviour is also derived even when spatial cell diffusion is taking into account.

systems biology↗

On the impact of chemo-mechanically induced phenotypic transitions in gliomas

Tumor microenvironment is a critical player in glioma progression and novel therapies for its targeting have been recently proposed. In particular, stress-alleviation strategies act on the tumor by reducing its stiffness, decreasing solid stresses and improving blood perfusion. However, these microenvironmental changes trigger chemo-mechanically induced cellular phenotypic transitions whose impact on therapy outcomes is not completely understood. In this work, we perform experiments to analyze the effects of mechanical compression on migration and proliferation of two glioma cell lines. From these experiments, we derive a mathematical model of glioma progression focusing on cellular phenotypic plasticity. The model reveals a trade-off between tumor infiltration and cellular content as a consequence of stress-alleviation approaches. We discuss how these findings can improve the current understanding of glioma/microenvironment interactions, and suggest strategies to improve therapeutic outcomes.

biophysics↗