Clinical Application of Spectral Electromagnetic Interaction in Breast Cancer: Diagnostic Results of a Pilot Study

Author:

De Cicco Concetta1,Mariani Luigi2,Vedruccio Clarbruno3,Ricci Carla4,Balma Massimo5,Rotmensz Nicole1,Ferrari Mahila Esmeralda6,Alitino Elena5,Trifirò Giuseppe1,Sacchini Virgilio7,Viale Giuseppe8,Paganelli Giovanni1

Affiliation:

1. Division of Nuclear Medicine, European Institute of Oncology, Milan, Italy;

2. Epidemiology and Biostatistics, European Institute of Oncology and National Cancer Institute, Milan, Italy;

3. COMSUBIN Research Office, Italian Navy, La Spezia, Italy;

4. Consulting Engineer, Medicina, Bologna, Italy;

5. Galileo Avionica SpA, San Maurizio Canavese (Turin), Italy;

6. Physics Unit, European Institute of Oncology, Milan, Italy;

7. Department of Breast Surgery, Memorial Sloan-Kettering Cancer Center, New York, NY, USA;

8. Pathology Division, European Institute of Oncology and University of Milan, Milan, Italy

Abstract

Aims and background There is a need for a cost-effective method to safely reduce the number of diagnostic procedures women undergo for breast cancer. We tested a new procedure for breast cancer diagnosis based on breast tissue response to low level electromagnetic incident waves. Methods We tested 101 patients with suspicious palpable breast lesions detected by mammography or ultrasonography, who were scheduled to undergo an open biopsy. Using an electromagnetic field generator (tissue resonance interaction method probe [TRIMprobTM]), we passed the TRIMprobTM over the breast area and recorded the signal variation of one or more spectral lines (dB1, dB2, dB3). The results were compared with those of a control group as well as with pathology data obtained from excisional biopsy. Results No adverse effects of the test were observed. Pathology revealed 86 malignant breast cancers (72 invasive, 14 in situ) and 15 benign conditions. We achieved the best discrimination between normal breasts and lesions using dB1 (dB1 AUC-ROC = 0.8; dB2 AUC-ROC = 0.61; dB3 AUC-ROC = 0.76). With a specificity of 75% to 95%, the sensitivity ranged from 49% to 84%. Tumor or patient variables did not influence the results. Conclusions The TRIMprobTM test was able to provide some degree of discrimination between normal breast tissue and lesions but not between benign and malignant lesions. The lack of influence of patient age and tumor size on test results might be advantageous in terms of early diagnosis in young women. These preliminary results need to be verified and extended in a preclinical-stage disease setting before clinical applicability can be envisaged.

Publisher

SAGE Publications

Subject

Cancer Research,Oncology,General Medicine

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