Oral Ondansetron Offers Effective Antidiarrheal Activity for Carcinoid Syndrome Refractory to Somatostatin Analogs.


Journal

The oncologist
ISSN: 1549-490X
Titre abrégé: Oncologist
Pays: England
ID NLM: 9607837

Informations de publication

Date de publication:
02 2019
Historique:
received: 28 03 2018
accepted: 05 07 2018
pubmed: 2 9 2018
medline: 21 3 2020
entrez: 2 9 2018
Statut: ppublish

Résumé

Somatostatin analogs (SSAs) are standard for symptomatic patients with neuroendocrine tumors (NETs). However, most patients experience tachyphylaxis, and limited options exist for this so-called "refractory carcinoid syndrome." Recently, 5-HT We have analyzed patients given ondansetron as bridging therapy for refractory carcinoid syndrome. The dose was 2 × 8 mg for 5 days, followed by reduction to 1 × 8 mg in case of benefit. A total of 14 patients with small bowel NETs metastatic to the liver were identified. All patients had been treated with SSAs for a median time of 18 months before aggravation of diarrhea. One patient had to be excluded because of an underlying infectious cause of diarrhea. The median number of daily bowel movements was 7 (range, 5-13) before initiation of therapy. At this time, seven patients had stable disease, whereas six patients showed radiological progression with symptomatic breakthrough. All 13 patients were scheduled for salvage therapy. Remarkably, in 85% (11/13) ondansetron resulted in a clinically relevant decrease of bowel movements to a median of 3 (1-4). The median time of ondansetron intake was 29 days (7 days to 29 months). In four patients, diarrhea recurred after initial improvement at an interval of 22-43 days, whereas the remaining seven had an ongoing benefit, including two long-term responders who refused further therapy because of pronounced decrease of symptoms (ondansetron for 14+ and 29+ months). Ondansetron offers symptomatic relief in the majority of patients. Although there was no influence on 5-HIAA levels, evidence from two patients suggests prolonged benefit. Somatostatin analogs are standard treatment in patients with carcinoid syndrome and have an overall response rate of up to 50%. This symptomatic benefit, however, is lost in many patients because of the development of tachyphylaxis or tumor progression. Patients with this "refractory carcinoid syndrome" pose a therapeutic challenge and are sometimes faced with a detrimental effect on quality of life. In this article, the authors suggest the 5-HT

Identifiants

pubmed: 30171068
pii: theoncologist.2018-0191
doi: 10.1634/theoncologist.2018-0191
pmc: PMC6369958
doi:

Substances chimiques

Antidiarrheals 0
Serotonin Antagonists 0
Ondansetron 4AF302ESOS
Somatostatin 51110-01-1

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

255-258

Informations de copyright

© AlphaMed Press 2018.

Déclaration de conflit d'intérêts

Disclosures of potential conflicts of interest may be found at the end of this article.

Références

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Auteurs

Barbara Kiesewetter (B)

Division of Oncology, Department of Internal Medicine I, Medical University Vienna, Vienna, Austria.
Neuroendocrine Tumor Unit, Comprehensive Cancer Center Vienna, Medical University Vienna, Vienna, Austria.

Heying Duan (H)

Division of Nuclear Medicine, Department of Biomedical Imaging and Image-guided Therapy, Medical University Vienna, Vienna, Austria.

Wolfgang Lamm (W)

Division of Oncology, Department of Internal Medicine I, Medical University Vienna, Vienna, Austria.
Neuroendocrine Tumor Unit, Comprehensive Cancer Center Vienna, Medical University Vienna, Vienna, Austria.

Alexander Haug (A)

Division of Nuclear Medicine, Department of Biomedical Imaging and Image-guided Therapy, Medical University Vienna, Vienna, Austria.

Philipp Riss (P)

Section of Endocrine Surgery, Division of General Surgery, Department of Surgery, Medical University Vienna, Vienna, Austria.
Neuroendocrine Tumor Unit, Comprehensive Cancer Center Vienna, Medical University Vienna, Vienna, Austria.

Andreas Selberherr (A)

Section of Endocrine Surgery, Division of General Surgery, Department of Surgery, Medical University Vienna, Vienna, Austria.
Neuroendocrine Tumor Unit, Comprehensive Cancer Center Vienna, Medical University Vienna, Vienna, Austria.

Christian Scheuba (C)

Section of Endocrine Surgery, Division of General Surgery, Department of Surgery, Medical University Vienna, Vienna, Austria.
Neuroendocrine Tumor Unit, Comprehensive Cancer Center Vienna, Medical University Vienna, Vienna, Austria.

Markus Raderer (M)

Division of Oncology, Department of Internal Medicine I, Medical University Vienna, Vienna, Austria markus.raderer@meduniwien.ac.at.
Neuroendocrine Tumor Unit, Comprehensive Cancer Center Vienna, Medical University Vienna, Vienna, Austria.

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Classifications MeSH