HeberFERON®, therapeutic alternative for non-melanoma skin cancer in primary care
Abstract
Introduction: Non-melanoma skin cancer is, in a sustained manner, the first cause of morbidity due to malignant tumors in Cuba. HeberFERON® is applied as a therapeutic modality with favorable experiences in this disease.
Objective: To evaluate the clinical effectiveness of HeberFERON® in non-melanoma skin cancer.
Methods: An observational, descriptive and prospective study was conducted between January 1st, 2017 and December 2023, at the Teaching Polyclinic Dr. Carlos J. Finlay, in the municipality of Colón, province of Matanzas. It included 176 patients and 201 lesions. The dose was 10.5 million international units, three times a week, for three weeks, perilesional and intradermal. The variables were age, sex, phototype, number of tumors, tumor profile, location, tumor type, evolution time, diameter, cancer variants, subtypes and histological differentiation. Four response categories were considered: complete, partial, stable and progressive disease. The objective response (complete plus partial) was included. A clinical record was prepared. The SPSS package was used for statistical processing and ethical principles were met.
Results: Male sex, phototype II, and patients with single lesions predominated. Primary tumors and head-face-neck location predominated. In the tumor with the highest incidence, lesions of 20 mm or less predominated. In the other neoplastic variant, the lesions frequently exceed 20 mm. The objective response in both tumors exceeded the effectiveness indicator, although basal cell carcinoma experienced better responses.
Conclusions: The mixture of interferons was effective in both variants of non-melanoma skin cancer.
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