Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Observational Study
. 2019 Jan-Dec:18:1534735419878505.
doi: 10.1177/1534735419878505.

Modulated Electro-Hyperthermia as Palliative Treatment for Pancreatic Cancer: A Retrospective Observational Study on 106 Patients

Affiliations
Observational Study

Modulated Electro-Hyperthermia as Palliative Treatment for Pancreatic Cancer: A Retrospective Observational Study on 106 Patients

Giammaria Fiorentini et al. Integr Cancer Ther. 2019 Jan-Dec.

Abstract

Background: Pancreatic adenocarcinoma has a poor prognosis, resulting in a <10% survival rate at 5 years. Modulated electro-hyperthermia (mEHT) has been increasingly used for pancreatic cancer palliative care and therapy. Objective: To monitor the efficacy and safety of mEHT for the treatment of advanced pancreatic cancer. Methods: We collected data retrospectively on 106 patients affected by stage III-IV pancreatic adenocarcinoma. They were divided into 2 groups: patients who did not receive mEHT (no-mEHT) and patients who were treated with mEHT. We performed mEHT applying a power of 60 to 150 W for 40 to 90 minutes. The mEHT treatment was associated with chemotherapy and/or radiotherapy for 33 (84.6%) patients, whereas 6 (15.4%) patients received mEHT alone. The patients of the no-mEHT group received chemotherapy and/or radiotherapy in 55.2% of cases. Results: Median age of the sample was 65.3 years (range = 31-80 years). After 3 months of therapy, the mEHT group had partial response in 22/34 patients (64.7%), stable disease in 10/34 patients (29.4%), and progressive disease in 2/34 patients (8.3%). The no-mEHT group had partial response in 3/36 patients (8.3%), stable disease in 10/36 patients (27.8%), and progressive disease in 23/36 patients (34.3%). The median overall survival of the mEHT group was 18.0 months (range = 1.5-68.0 months) and 10.9 months (range = 0.4-55.4 months) for the non-mEHT group. Conclusions: mEHT may improve tumor response and survival of pancreatic cancer patients.

Keywords: FOLFIRINOX; gemcitabine; modulated electro-hyperthermia; pancreatic cancer; survival; tumor response.

PubMed Disclaimer

Conflict of interest statement

Declaration of Conflicting Interests: The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

Figures

Figure 1.
Figure 1.
Tumor response at 3 months.PR, partial response; SD, stable disease; PD, progressive disease; mEHT, modulated electro-hyperthermia.
Figure 2.
Figure 2.
OS (overall survival) of the 2 groups of the study. The solid line is the survival of modulated electro-hyperthermia (mEHT) group and the dashed line the non-mEHT. The “x” indicates the censored patients.
Figure 3.
Figure 3.
OS (overall survival) grouped by metastatic patients of the 2 groups of the study. The solid line is the survival of modulated electro-hyperthermia (mEHT) group and the dashed line the non-mEHT. The “x” indicates the censored patients.
Figure 4.
Figure 4.
OS (overall survival) grouped by the first-line treatments of the 2 groups of the study. The solid line is the survival of modulated electro-hyperthermia (mEHT) group and the dashed line the non-mEHT. The “x” indicates the censored patients.
Figure 5.
Figure 5.
OS (overall survival) grouped for non-resected patients of the 2 groups of the study. The solid line is the survival of modulated electro-hyperthermia (mEHT) treated, the dashed line the non-mEHT treated survival curve, and the “x” indicates the censored patients.

References

    1. Siegel RL, Miller KD, Jemal A. Cancer statistics, 2015. CA Cancer J Clin. 2015;65:5-29. - PubMed
    1. Von Hoff DD, Ervin T, Arena FP, et al. Increased survival in pancreatic cancer with nab-paclitaxel plus gemcitabine. N Engl J Med. 2013;369:1691-1703. - PMC - PubMed
    1. Long J, Luo GP, Xiao ZW, et al. Cancer statistics: current diagnosis and treatment of pancreatic cancer in Shanghai, China. Cancer Lett. 2014;346:273-277. - PubMed
    1. Schrag D. Optimizing treatment for locally advanced pancreas cancer: progress but no precision. JAMA. 2016;315:1837-1838. - PubMed
    1. Pancreatic Cancer Europe. Pancreatic Cancer Europe’s General Assembly Meeting—Barcelona, July 4, 2019. https://www.pancreaticcancereurope.eu/. Accessed September 16, 2019.

Publication types