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The Clinical Validation of Modulated Electro-Hyperthermia (mEHT)
SIMPLE SUMMARY: Modulated electro-hyperthermia (mEHT) is a heating therapy that uses synergized thermal and nonthermal effects to heat and destroy malignant cells selectively without damaging healthy cells. This article presents the clinical validation of mEHT. The therapy is dominantly applied for...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10526385/ https://www.ncbi.nlm.nih.gov/pubmed/37760538 http://dx.doi.org/10.3390/cancers15184569 |
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author | Lee, Sun-Young Lorant, Gergo Grand, Laszlo Szasz, Attila Marcell |
author_facet | Lee, Sun-Young Lorant, Gergo Grand, Laszlo Szasz, Attila Marcell |
author_sort | Lee, Sun-Young |
collection | PubMed |
description | SIMPLE SUMMARY: Modulated electro-hyperthermia (mEHT) is a heating therapy that uses synergized thermal and nonthermal effects to heat and destroy malignant cells selectively without damaging healthy cells. This article presents the clinical validation of mEHT. The therapy is dominantly applied for such advanced malignancies when the conventional oncotherapies fail to apply. Survival results of mEHT were collected and compared with other methods. The results demonstrate the superiority of the mEHT method. ABSTRACT: The mEHT method uses tissues’ thermal and bioelectromagnetic heterogeneity for the selective mechanisms. The success of the therapy for advanced, relapsed, and metastatic aggressive tumors can only be demonstrated by measuring survival time and quality of life (QoL). The complication is that mEHT-treated patients cannot be curatively treated any longer with “gold standards”, where the permanent progression of the disease, the refractory, relapsing situation, the organ failure, the worsening of blood counts, etc., block them. Collecting a cohort of these patients is frequently impossible. Only an intent-to-treat (ITT) patient group was available. Due to the above limitations, many studies have single-arm data collection. The Phase III trial of advanced cervix tumors subgrouping of HIV-negative and -positive patients showed the stable efficacy of mEHT in all patients’ subgroups. The single-arm represents lower-level evidence, which can be improved by comparing the survival data of various studies from different institutes. The Kaplan–Meier probability comparison had no significant differences, so pooled data were compared to other methods. Following this approach, we demonstrate the feasibility and superiority of mEHT in the cases of glioblastoma multiform, pancreas carcinomas, lung tumors, and colorectal tumors. |
format | Online Article Text |
id | pubmed-10526385 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-105263852023-09-28 The Clinical Validation of Modulated Electro-Hyperthermia (mEHT) Lee, Sun-Young Lorant, Gergo Grand, Laszlo Szasz, Attila Marcell Cancers (Basel) Review SIMPLE SUMMARY: Modulated electro-hyperthermia (mEHT) is a heating therapy that uses synergized thermal and nonthermal effects to heat and destroy malignant cells selectively without damaging healthy cells. This article presents the clinical validation of mEHT. The therapy is dominantly applied for such advanced malignancies when the conventional oncotherapies fail to apply. Survival results of mEHT were collected and compared with other methods. The results demonstrate the superiority of the mEHT method. ABSTRACT: The mEHT method uses tissues’ thermal and bioelectromagnetic heterogeneity for the selective mechanisms. The success of the therapy for advanced, relapsed, and metastatic aggressive tumors can only be demonstrated by measuring survival time and quality of life (QoL). The complication is that mEHT-treated patients cannot be curatively treated any longer with “gold standards”, where the permanent progression of the disease, the refractory, relapsing situation, the organ failure, the worsening of blood counts, etc., block them. Collecting a cohort of these patients is frequently impossible. Only an intent-to-treat (ITT) patient group was available. Due to the above limitations, many studies have single-arm data collection. The Phase III trial of advanced cervix tumors subgrouping of HIV-negative and -positive patients showed the stable efficacy of mEHT in all patients’ subgroups. The single-arm represents lower-level evidence, which can be improved by comparing the survival data of various studies from different institutes. The Kaplan–Meier probability comparison had no significant differences, so pooled data were compared to other methods. Following this approach, we demonstrate the feasibility and superiority of mEHT in the cases of glioblastoma multiform, pancreas carcinomas, lung tumors, and colorectal tumors. MDPI 2023-09-15 /pmc/articles/PMC10526385/ /pubmed/37760538 http://dx.doi.org/10.3390/cancers15184569 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Lee, Sun-Young Lorant, Gergo Grand, Laszlo Szasz, Attila Marcell The Clinical Validation of Modulated Electro-Hyperthermia (mEHT) |
title | The Clinical Validation of Modulated Electro-Hyperthermia (mEHT) |
title_full | The Clinical Validation of Modulated Electro-Hyperthermia (mEHT) |
title_fullStr | The Clinical Validation of Modulated Electro-Hyperthermia (mEHT) |
title_full_unstemmed | The Clinical Validation of Modulated Electro-Hyperthermia (mEHT) |
title_short | The Clinical Validation of Modulated Electro-Hyperthermia (mEHT) |
title_sort | clinical validation of modulated electro-hyperthermia (meht) |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10526385/ https://www.ncbi.nlm.nih.gov/pubmed/37760538 http://dx.doi.org/10.3390/cancers15184569 |
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