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论治疗增益的系统与控制方法。

On systems and control approaches to therapeutic gain.

作者信息

Radivoyevitch Tomas, Loparo Kenneth A, Jackson Robert C, Sedwick W David

机构信息

Department of Epidemiology and Biostatistics Case Western Reserve University, Cleveland, Ohio 44106, USA.

出版信息

BMC Cancer. 2006 Apr 25;6:104. doi: 10.1186/1471-2407-6-104.

Abstract

BACKGROUND

Mathematical models of cancer relevant processes are being developed at an increasing rate. Conceptual frameworks are needed to support new treatment designs based on such models.

METHODS

A modern control perspective is used to formulate two therapeutic gain strategies.

RESULTS

Two conceptually distinct therapeutic gain strategies are provided. The first is direct in that its goal is to kill cancer cells more so than normal cells, the second is indirect in that its goal is to achieve implicit therapeutic gains by transferring states of cancer cells of non-curable cases to a target state defined by the cancer cells of curable cases. The direct strategy requires models that connect anti-cancer agents to an endpoint that is modulated by the cause of the cancer and that correlates with cell death. It is an abstraction of a strategy for treating mismatch repair (MMR) deficient cancers with iodinated uridine (IUdR); IU-DNA correlates with radiation induced cell killing and MMR modulates the relationship between IUdR and IU-DNA because loss of MMR decreases the removal of IU from the DNA. The second strategy is indirect. It assumes that non-curable patient outcomes will improve if the states of their malignant cells are first transferred toward a state that is similar to that of a curable patient. This strategy is difficult to employ because it requires a model that relates drugs to determinants of differences in patient survival times. It is an abstraction of a strategy for treating BCR-ABL pro-B cell childhood leukemia patients using curable cases as the guides.

CONCLUSION

Cancer therapeutic gain problem formulations define the purpose, and thus the scope, of cancer process modeling. Their abstractions facilitate considerations of alternative treatment strategies and support syntheses of learning experiences across different cancers.

摘要

背景

与癌症相关过程的数学模型正在以越来越快的速度被开发出来。需要概念框架来支持基于此类模型的新治疗设计。

方法

采用现代控制视角来制定两种治疗增益策略。

结果

提供了两种概念上不同的治疗增益策略。第一种是直接的,其目标是比正常细胞更有效地杀死癌细胞;第二种是间接的,其目标是通过将不可治愈病例的癌细胞状态转移到由可治愈病例的癌细胞定义的目标状态来实现隐含的治疗增益。直接策略需要将抗癌药物与由癌症病因调节且与细胞死亡相关的终点联系起来的模型。它是用碘化尿苷(IUdR)治疗错配修复(MMR)缺陷癌症策略的一种抽象;IU-DNA与辐射诱导的细胞杀伤相关,并且MMR调节IUdR与IU-DNA之间的关系,因为MMR的缺失会减少DNA中IU的去除。第二种策略是间接的。它假设如果将其恶性细胞的状态首先转移到与可治愈患者相似的状态,不可治愈患者的预后将会改善。这种策略难以应用,因为它需要一个将药物与患者生存时间差异的决定因素联系起来的模型。它是将可治愈病例作为指导来治疗BCR-ABL前B细胞儿童白血病患者策略的一种抽象。

结论

癌症治疗增益问题的表述定义了癌症过程建模的目的,进而定义了其范围。它们的抽象有助于考虑替代治疗策略,并支持对不同癌症学习经验的综合。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7cc5/1484487/7eb1bbbba4cc/1471-2407-6-104-1.jpg

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