Skip to main content
Erschienen in: Medical Oncology 3/2009

01.09.2009 | Original Paper

The effect of Saccharomyces boulardii on reducing irinotecan-induced intestinal mucositis and diarrhea

verfasst von: Atakan Sezer, Ufuk Usta, Irfan Cicin

Erschienen in: Medical Oncology | Ausgabe 3/2009

Einloggen, um Zugang zu erhalten

Abstract

To investigate the efficiency of Saccharomyces boulardii on irinotecan-induced mucosal damage and diarrhea in rats, fifty rats were randomized into three groups with 20 rats in two study groups and 10 rats in the control group. Control group did not receive any treatment. Irinotecan (60 mg/kg) alone was administered intravenously once a day for four consecutive days to the rats of Group A. Throughout the experiment, Group B rats were additionally given Saccharomyces boulardii (800 mg/kg) for 3 days before administration of irinotecan and 7 days throughout the experiment. Delayed diarrhea was more severe in Group A than Group B (P = 0.009). The weight loss was 34.7 ± 3.8 mg for Group A, while it was 17.4 ± 1.7 mg for Group B (P < 0.001). Findings of mucositis most clearly appeared in the jejunum. Regarding edema (P = 0.003), leukocyte migration (P = 0.038), and inflammation (P = 0.006) significant recovery was detected in the mucosa of rats receiving Saccharomyces boulardii. Villous thickness was significantly greater in Group A than Group B (P < 0.001). The results indicate that Saccharomyces boulardii provided significant improvement in irinotecan-induced diarrhea and mucositis.
Literatur
1.
Zurück zum Zitat Tanizawa A, Fujimori A, Fujimori Y, Pommier Y. Comparison of topoisomerase I inhibition, DNA damage, and cytotoxicity of camptothecin derivatives presently in clinical trials. J Natl Cancer Inst (Bethesda). 1994;86:836–42. doi:10.1093/jnci/86.11.836.CrossRef Tanizawa A, Fujimori A, Fujimori Y, Pommier Y. Comparison of topoisomerase I inhibition, DNA damage, and cytotoxicity of camptothecin derivatives presently in clinical trials. J Natl Cancer Inst (Bethesda). 1994;86:836–42. doi:10.​1093/​jnci/​86.​11.​836.CrossRef
3.
Zurück zum Zitat Park SH, et al. Randomized phase II study of irinotecan, leucovorin and 5-fluorouracil (ILF) versus cisplatin plus ILF (PILF) combination chemotherapy for advanced gastric cancer. Ann Oncol. 2008;19:729–33. doi:10.1093/annonc/mdm502.PubMedCrossRef Park SH, et al. Randomized phase II study of irinotecan, leucovorin and 5-fluorouracil (ILF) versus cisplatin plus ILF (PILF) combination chemotherapy for advanced gastric cancer. Ann Oncol. 2008;19:729–33. doi:10.​1093/​annonc/​mdm502.PubMedCrossRef
4.
Zurück zum Zitat Hanna N, et al. Randomized phase III trial comparing irinotecan/cisplatin with etoposide/cisplatin in patients with previously untreated extensive-stage disease small-cell lung cancer. J Clin Oncol. 2006;24:2038–43. doi:10.1200/JCO.2005.04.8595.PubMedCrossRef Hanna N, et al. Randomized phase III trial comparing irinotecan/cisplatin with etoposide/cisplatin in patients with previously untreated extensive-stage disease small-cell lung cancer. J Clin Oncol. 2006;24:2038–43. doi:10.​1200/​JCO.​2005.​04.​8595.PubMedCrossRef
7.
Zurück zum Zitat Stringer AM, et al. Chemotherapy-induced mucositis: the role of gastrointestinal microflora and mucins in the luminal environment. J Support Oncol. 2007;5:259–67.PubMed Stringer AM, et al. Chemotherapy-induced mucositis: the role of gastrointestinal microflora and mucins in the luminal environment. J Support Oncol. 2007;5:259–67.PubMed
9.
Zurück zum Zitat Buts JP. Twenty-five years of research on Saccharomyces boulardii trophic effects: updates and perspectives. Dig Dis Sci. 2008 (in press). Buts JP. Twenty-five years of research on Saccharomyces boulardii trophic effects: updates and perspectives. Dig Dis Sci. 2008 (in press).
10.
Zurück zum Zitat Surawicz CM, et al. Prevention of antibiotic associated diarrhoea by Saccharomyces boulardii: a prospective study. Gastroenterology. 1989;96:981–8.PubMed Surawicz CM, et al. Prevention of antibiotic associated diarrhoea by Saccharomyces boulardii: a prospective study. Gastroenterology. 1989;96:981–8.PubMed
11.
Zurück zum Zitat McFarland LV, et al. Prevention of ß–lactam associated diarrhoea by Saccharomyces boulardii compared with placebo. Am J Gastroenterol. 1995;90:439–48.PubMed McFarland LV, et al. Prevention of ß–lactam associated diarrhoea by Saccharomyces boulardii compared with placebo. Am J Gastroenterol. 1995;90:439–48.PubMed
13.
Zurück zum Zitat Surawicz CM, et al. The search for a better treatment for Clostridium difficile disease: use of high-dose vancomycin combined with Saccharomyces boulardii. Clin Infect Dis. 2000;31:1012–7. doi:10.1086/318130.PubMedCrossRef Surawicz CM, et al. The search for a better treatment for Clostridium difficile disease: use of high-dose vancomycin combined with Saccharomyces boulardii. Clin Infect Dis. 2000;31:1012–7. doi:10.​1086/​318130.PubMedCrossRef
14.
Zurück zum Zitat Buts JP, Corthier G, Delm’ee M. Saccharomyces boulardii for Clostridium difficile-associated enterocolopathies in infants. J Pediatr Gastroenterol Nutr. 1993;16:1497–504. doi:10.1097/00005176-199305000-00013. Buts JP, Corthier G, Delm’ee M. Saccharomyces boulardii for Clostridium difficile-associated enterocolopathies in infants. J Pediatr Gastroenterol Nutr. 1993;16:1497–504. doi:10.​1097/​00005176-199305000-00013.
15.
Zurück zum Zitat Höchter W, Chase D, Hegenhoff G. Saccharomyces boulardii in treatment of acute adult diarrhoea efficacy and tolerance of treatment. Münch Med Wochenschr. 1990;132:188–92. Höchter W, Chase D, Hegenhoff G. Saccharomyces boulardii in treatment of acute adult diarrhoea efficacy and tolerance of treatment. Münch Med Wochenschr. 1990;132:188–92.
16.
Zurück zum Zitat Kollaritsch H, Holst H, Grobara P, Wiedermann G. Prevention of traveler’s diarrhea with Saccharomyces boulardii. Results of a placebo controlled double-blind study. Forstchr Med. 1993;111:152–6. Kollaritsch H, Holst H, Grobara P, Wiedermann G. Prevention of traveler’s diarrhea with Saccharomyces boulardii. Results of a placebo controlled double-blind study. Forstchr Med. 1993;111:152–6.
17.
Zurück zum Zitat Bleichner G, Bléhaut H, Mentec H, Moyse D. Sacchromyces boulardii prevents diarrhoea in critically ill tube-fed patients. A multicenter, randomized, double-blind-placebo-controlled trial. Intensive Care Med. 1997;23:517–23. doi:10.1007/s001340050367.PubMedCrossRef Bleichner G, Bléhaut H, Mentec H, Moyse D. Sacchromyces boulardii prevents diarrhoea in critically ill tube-fed patients. A multicenter, randomized, double-blind-placebo-controlled trial. Intensive Care Med. 1997;23:517–23. doi:10.​1007/​s001340050367.PubMedCrossRef
18.
Zurück zum Zitat Saint-Marc T, Bl’ehaut H, Musial C, Touraine JL. Efficacit’e de Saccharomyces boulardii dans le traitement des diarrh’ees du SIDA. Am Med Int. 1991;142:64–5. Saint-Marc T, Bl’ehaut H, Musial C, Touraine JL. Efficacit’e de Saccharomyces boulardii dans le traitement des diarrh’ees du SIDA. Am Med Int. 1991;142:64–5.
21.
Zurück zum Zitat Pothoulakis C, et al. Saccharomyces boulardii inhibits Clostridium difficile toxin. A binding and enterotoxicity in rat ileum. Gastroenterology. 1993;104:1108–15.PubMed Pothoulakis C, et al. Saccharomyces boulardii inhibits Clostridium difficile toxin. A binding and enterotoxicity in rat ileum. Gastroenterology. 1993;104:1108–15.PubMed
22.
Zurück zum Zitat Czerucka D, Roux I, Rampal P. Saccharomyces boulardii inhibits secretagogue-mediated adenosine 3′,5′-cyclic monophosphate induction in intestinal cells. Gastroenterology. 1994;106:65–72.PubMed Czerucka D, Roux I, Rampal P. Saccharomyces boulardii inhibits secretagogue-mediated adenosine 3′,5′-cyclic monophosphate induction in intestinal cells. Gastroenterology. 1994;106:65–72.PubMed
24.
28.
29.
Zurück zum Zitat Lee SK, Kim YW, Chi SG, Joo YS, Kim HJ. The effect of Saccharomyces boulardii on human colon cells and inflammation in rats with trinitrobenzene sulfonic acid-induced colitis. Dig Dis Sci. 2008 (in press). Lee SK, Kim YW, Chi SG, Joo YS, Kim HJ. The effect of Saccharomyces boulardii on human colon cells and inflammation in rats with trinitrobenzene sulfonic acid-induced colitis. Dig Dis Sci. 2008 (in press).
33.
Zurück zum Zitat Logan RM, et al. Characterisation of mucosal changes in the alimentary tract following administration of irinotecan: implications for the pathobiology of mucositis. Cancer Chemother Pharmacol. 2008;62:33–41. doi:10.1007/s00280-007-0570-0.PubMedCrossRef Logan RM, et al. Characterisation of mucosal changes in the alimentary tract following administration of irinotecan: implications for the pathobiology of mucositis. Cancer Chemother Pharmacol. 2008;62:33–41. doi:10.​1007/​s00280-007-0570-0.PubMedCrossRef
35.
Zurück zum Zitat Takasuna K, et al. Involvement of β-glucuronidase in intestinal microflora in the intestinal toxicity of the antitumor camptothecin derivative irinotecan hydrochloride (CPT-11) in rats. Cancer Res. 1996;56:3752–7.PubMed Takasuna K, et al. Involvement of β-glucuronidase in intestinal microflora in the intestinal toxicity of the antitumor camptothecin derivative irinotecan hydrochloride (CPT-11) in rats. Cancer Res. 1996;56:3752–7.PubMed
36.
Zurück zum Zitat Kehrer DF, et al. Modulation of irinotecan-induced diarrhea by cotreatment with neomycin in cancer patients. Clin Cancer Res. 2001;7:1136–41.PubMed Kehrer DF, et al. Modulation of irinotecan-induced diarrhea by cotreatment with neomycin in cancer patients. Clin Cancer Res. 2001;7:1136–41.PubMed
39.
Zurück zum Zitat Jahn HU, et al. Immunological and trophical effects of Saccharomyces boulardii on the small intestine in healthy human volunteers. Digestion. 1996;57:95–104.PubMedCrossRef Jahn HU, et al. Immunological and trophical effects of Saccharomyces boulardii on the small intestine in healthy human volunteers. Digestion. 1996;57:95–104.PubMedCrossRef
40.
Zurück zum Zitat Harms HK, Bertele-Harms RM, Bruer-Kleis D. Enzyme substitution therapy with the yeast Saccharomyces cerevisiae in congenital sucrase isomaltase deficiency. N Engl J Med. 1987;316:1306–9.PubMed Harms HK, Bertele-Harms RM, Bruer-Kleis D. Enzyme substitution therapy with the yeast Saccharomyces cerevisiae in congenital sucrase isomaltase deficiency. N Engl J Med. 1987;316:1306–9.PubMed
41.
Zurück zum Zitat Buts JP, De Keyser N, Stilmant C, Sokal E, Marandi S. Saccharomyces boulardii enhances N-terminal peptide hydrolysis in suckling rat small intestine by endoluminal release of a zinc binding metalloprotease. Pediatr Res. 2002;51:528–34. doi:10.1203/00006450-200204000-00021.PubMedCrossRef Buts JP, De Keyser N, Stilmant C, Sokal E, Marandi S. Saccharomyces boulardii enhances N-terminal peptide hydrolysis in suckling rat small intestine by endoluminal release of a zinc binding metalloprotease. Pediatr Res. 2002;51:528–34. doi:10.​1203/​00006450-200204000-00021.PubMedCrossRef
42.
Zurück zum Zitat Buts JP, et al. Saccharomyces boulardii upgrades cellular adaptation after proximal enterectomy in rats. Gut. 1999;45:89–96.PubMedCrossRef Buts JP, et al. Saccharomyces boulardii upgrades cellular adaptation after proximal enterectomy in rats. Gut. 1999;45:89–96.PubMedCrossRef
43.
Zurück zum Zitat Baum B, Liebler-Tenorio EM, Enss ML, Pohlenz JF, Breves G. Saccharomyces boulardii and Bacillus cereus var. Toyoi influence the morphology and the mucins of the intestine of pigs. Z Gastroenterol. 2002;40:277–84. doi:10.1055/s-2002-30116.PubMedCrossRef Baum B, Liebler-Tenorio EM, Enss ML, Pohlenz JF, Breves G. Saccharomyces boulardii and Bacillus cereus var. Toyoi influence the morphology and the mucins of the intestine of pigs. Z Gastroenterol. 2002;40:277–84. doi:10.​1055/​s-2002-30116.PubMedCrossRef
Metadaten
Titel
The effect of Saccharomyces boulardii on reducing irinotecan-induced intestinal mucositis and diarrhea
verfasst von
Atakan Sezer
Ufuk Usta
Irfan Cicin
Publikationsdatum
01.09.2009
Verlag
Humana Press Inc
Erschienen in
Medical Oncology / Ausgabe 3/2009
Print ISSN: 1357-0560
Elektronische ISSN: 1559-131X
DOI
https://doi.org/10.1007/s12032-008-9128-1

Weitere Artikel der Ausgabe 3/2009

Medical Oncology 3/2009 Zur Ausgabe

Adjuvante Immuntherapie verlängert Leben bei RCC

25.04.2024 Nierenkarzinom Nachrichten

Nun gibt es auch Resultate zum Gesamtüberleben: Eine adjuvante Pembrolizumab-Therapie konnte in einer Phase-3-Studie das Leben von Menschen mit Nierenzellkarzinom deutlich verlängern. Die Sterberate war im Vergleich zu Placebo um 38% geringer.

Alectinib verbessert krankheitsfreies Überleben bei ALK-positivem NSCLC

25.04.2024 NSCLC Nachrichten

Das Risiko für Rezidiv oder Tod von Patienten und Patientinnen mit reseziertem ALK-positivem NSCLC ist unter einer adjuvanten Therapie mit dem Tyrosinkinase-Inhibitor Alectinib signifikant geringer als unter platinbasierter Chemotherapie.

Bei Senioren mit Prostatakarzinom auf Anämie achten!

24.04.2024 DGIM 2024 Nachrichten

Patienten, die zur Behandlung ihres Prostatakarzinoms eine Androgendeprivationstherapie erhalten, entwickeln nicht selten eine Anämie. Wer ältere Patienten internistisch mitbetreut, sollte auf diese Nebenwirkung achten.

ICI-Therapie in der Schwangerschaft wird gut toleriert

Müssen sich Schwangere einer Krebstherapie unterziehen, rufen Immuncheckpointinhibitoren offenbar nicht mehr unerwünschte Wirkungen hervor als andere Mittel gegen Krebs.

Update Onkologie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.