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[癌症多步骤治疗的原则与1977年概念。新时机选择的生理基础。选择性局部热疗(作者译)]

[Principles and 1977 concept of cancer multistep therapy. Physiological fundamentals of the new timing. Selectotherm local hyperthermy (author's transl)].

作者信息

von Ardenne M

出版信息

Arch Geschwulstforsch. 1978;48(6):504-20.

PMID:31849
Abstract

A report is given on the further development of the Cancer Multistep Therapy (CMT) Concept. With a clinically applied blood glucose concentration of 5 . 10(-3) g ml-1 the pH value in tumour tissue reduces to about 6.0 which, in turn, causes an increase in thermal sensitivity of cancer cells by approximately 2 degrees C. At the same time, their proliferation ceases almost completely. In addition, the pH value at the venous end of capillaries in tumour tissue increases to about 6.5 so that the flexibility of the erythrocytes gets lost in a selective mode. From this it follows that, under CMT conditions, there will be a total decrease of microcirculation in tumour tissues. All the aforementioned facts have been considered by a new timing: applying cancerostatic drugs and/or ionizing radiation prior to the said drop of microcirculations and of cancer cell proliferation rate. The begin of the hyperthermy step is then planned to take place immediately after the decrease of microcirculation in tumour tissue since the action of the discussed local hyperthermy then becomes very strong (pronounced selective reduction of convection cooling by the blood stream; further enhanced thermal sensitivity of cancer cells). Local hyperthermy then is performed by superposing the Selectotherm Process on 40 degrees C whole-body hyperthermy which allows high power densities also with deep-seated tumour tissues. Finally calculated temperature profiles in tumour tissue of various diameters are discussed together with the practice-considered parameters used in the respective equations.

摘要

本文报告了癌症多步治疗(CMT)概念的进一步发展。当临床应用的血糖浓度为5×10⁻³g/ml时,肿瘤组织中的pH值降至约6.0,这反过来又使癌细胞的热敏感性提高约2℃。同时,癌细胞的增殖几乎完全停止。此外,肿瘤组织中毛细血管静脉端的pH值升至约6.5,从而使红细胞的柔韧性以选择性方式丧失。由此可知,在CMT条件下,肿瘤组织中的微循环将总体减少。通过一种新的时间安排考虑了上述所有事实:在微循环和癌细胞增殖率下降之前应用抗癌药物和/或电离辐射。然后计划在肿瘤组织微循环减少后立即开始热疗步骤,因为此时所讨论的局部热疗的作用会变得非常强(显著的血流对流冷却选择性降低;癌细胞热敏感性进一步增强)。然后通过将Selectotherm过程叠加在40℃的全身热疗上来进行局部热疗,这对于深部肿瘤组织也能实现高功率密度。最后讨论了不同直径肿瘤组织中计算得出的温度分布以及各方程中考虑实际情况的参数。

相似文献

1
[Principles and 1977 concept of cancer multistep therapy. Physiological fundamentals of the new timing. Selectotherm local hyperthermy (author's transl)].[癌症多步骤治疗的原则与1977年概念。新时机选择的生理基础。选择性局部热疗(作者译)]
Arch Geschwulstforsch. 1978;48(6):504-20.
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[Calculation of the dynamic heating process in multilayer model tissues during local hyperthermy using the CMT Selectotherm technique (author's transl)].
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[Selective local hyperthermy of tumor tissue. Homogenized energy supply also to deep-seated tissues by high-performance decametric wave coil section plus dual system raster motion (author's transl)].
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On the optimization of local hyperthermy in tumors based on a new radiofrequency procedure. Local hyperthermy of large body areas using the CMT selectotherm method.
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Principles and concept 1993 of the Systemic Cancer Multistep Therapy (sCMT). Extreme whole-body hyperthermia using the infrared-A technique IRATHERM 2000--selective thermosensitisation by hyperglycemia--circulatory back-up by adapted hyperoxemia.全身癌症多步骤治疗(sCMT)的1993年原则与概念。采用红外A技术(IRATHERM 2000)进行极端全身热疗——通过高血糖实现选择性热敏化——通过适应性高氧血症进行循环支持。
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[Clinical examination of the conception '86 of "Canoer Multistep-Therapie" (CMT) by M. v. Ardene. First communication: the standard, the control-parameters, and the course of therapy (author's transl)].[对M. v. Ardene的“独木舟多步疗法”(CMT)'86概念的临床检查。首次报告:标准、对照参数及治疗过程(作者译)]
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[Pharmacokinetic aspects of tumor tissue impairment by cancerostatics. Ways for the intensification of the induced attack in the multiple step cancer therapy. CMT-Selectine].[癌症化疗药物对肿瘤组织损伤的药代动力学方面。多步骤癌症治疗中强化诱导攻击的方法。CMT-选择性]
Arzneimittelforschung. 1975 Jun;25(6):863-70.
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[Mesenchyme theory on the increase in resistance experienced during repetition of cancer therapy processes (author's transl)].[癌症治疗过程重复中所经历的阻力增加的间充质理论(作者译)]
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Arrhenius relationships from the molecule and cell to the clinic.从分子、细胞到临床的阿伦尼乌斯关系。
Int J Hyperthermia. 2009 Feb;25(1):3-20. doi: 10.1080/02656730902747919.

引用本文的文献

1
Hyperthermia and cancer therapy.
Cancer Chemother Pharmacol. 1980;4(3):137-8. doi: 10.1007/BF00254010.
2
On the optimization of local hyperthermy in tumors based on a new radiofrequency procedure. Local hyperthermy of large body areas using the CMT selectotherm method.
J Cancer Res Clin Oncol. 1979 Jun 8;94(2):163-84. doi: 10.1007/BF00422496.
3
Histological proof for selective stop of microcirculation in tumor tissue at pH 6.1 and 41 degrees C.
Naturwissenschaften. 1979 Jan;66(1):59-60. doi: 10.1007/BF00369370.