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Probiotic Bacteria Cannot Mitigate the Adverse Effects of Radioactive Iodine-131 Treatment Publisher



Mortazavi SMJ1 ; Nowroozi S2 ; Haghani M3 ; Zarrinimonfared Z4 ; Gheisari F5 ; Sihver L6, 7
Authors
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Authors Affiliations
  1. 1. Medical Physics and Engineering Department, School of Medicine, Shiraz University of Medical Sciences, Shiraz, 71348-14336, Iran
  2. 2. School of Medicine, Shiraz University of Medical Sciences, Shiraz, 71348-14336, Iran
  3. 3. Radiology and Radiobiology Department, School of Paramedical Sciences, Shiraz University of Medical Sciences, Shiraz, 71348-14336, Iran
  4. 4. Department of Medical Physics & Biomedical Engineering, School of Medicine, Tehran University of Medical Sciences, Tehran, 19835-178, Iran
  5. 5. Nuclear Medicine Department, School of Medicine, Shiraz University of Medical Sciences, Shiraz, 71348-14336, Iran
  6. 6. Department of Radiation Dosimetry, Nuclear Physics Institute of the CAS, Prague, 180 00, Czech Republic
  7. 7. Technische Universitat Wien, Atominstitut, Vienna, 1020, Austria

Source: Cancers Published:2023


Abstract

Thyroid carcinoma is the most common cancer of the endocrine system, accounting for 12% of all cancer cases in adolescents in the United States. Radioiodine therapy plays a key role in differentiated thyroid cancer (DTC) treatment. This double-blind, randomized, placebo-controlled clinical trial was aimed at evaluating the effect of probiotics supplementation in reducing the acute side-effects of radioiodine therapy in PTC patients. Fifty-six patients were randomly divided into four groups: one placebo and three intervention groups. The probiotics product used in this study was LactoCare (ZistTakhmir Co., Tehran, Iran), a multi-strain commercially available symbiotic containing 12 strains of probiotic species including Lactobacillus strains, Bifidobacteria strains, and Streptococcus thermophilus, plus Fructo-oligosaccharides as the prebiotic. Group 0 was our placebo group (no probiotics), while the other three groups received probiotics capsules for 2/4 days, starting only 2 days prior to radioiodine therapy, only 4 days after radioiodine therapy or 2 days prior and 4 days after radioiodine therapy. Six patients were withdrawn during the study because of poor compliance or at their own request. The symptoms reported by patients including data about the incidence and duration of each complication were recorded. The probiotics’ effectiveness was confirmed for dry mouth and taste loss or change when it was administered prior to the radioiodine treatment. The benefit was not confirmed for other radiation-induced complications such as pain and swelling in the neck, nausea and vomiting, salivary gland swelling, and diarrhea. Further large-scale clinical trials are warranted to improve our knowledge in this quickly evolving field. © 2023 by the authors.