Abstract | BACKGROUND: Gastric carcinoid tumours type 1 (GCA1) originate from hyperplastic enterochromaffin-like (ECL) cells secondary to hypergastrinaemia. Treatment with somatostatin analogues (SSA) might impede ECL-cell hyperplasia by suppressing gastrin secretion and/or by a direct anti-proliferative effect on ECL cells. We conducted a multicentre prospective study to assess the effects of long-acting SSA on hypergastrinaemia and ECL-cell proliferation in patients with GCA1. METHODS: We studied 15 patients with GCA1 treated with monthly long-acting release octreotide (LAR) (20-30 mg; n=14) or Lanreotide 90 mg (n=1) for at least 6 months. Patients had serum gastrin and chromogranin A measurements performed and biopsies taken from both tumours and surrounding mucosa before, and every 6-12 months following treatment. Sections were immunostained for neuroendocrine markers. The cell proliferation index Ki-67, intensity of staining before and after treatment and the degree of gastric wall invasion were also assessed. RESULTS: All patients tolerated treatment well (mean follow-up of 18 months). In 11 patients (73%), a complete disappearance of the tumours at 1 year of treatment was observed on endoscopy, while in three patients (20%), the tumours decreased significantly in number and size. Gastrin levels normalized in 25% of patients, and were reduced by more than 80% in the remaining 75%. CONCLUSIONS: Treatment with SSAs in GCA1 leads to a substantial tumour load reduction, with a concomitant decrease of serum gastrin levels. Our data indicate an important anti-proliferative effect of SSA on ECL cells, providing clinical benefit and obviating, at least temporarily, the need for invasive therapies for GCA1.
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Authors | Simona Grozinsky-Glasberg, Gregory Kaltsas, Chamutal Gur, Eyal Gal, Dimitrios Thomas, Susana Fichman, Krystallenia Alexandraki, Dganit Barak, Benjamin Glaser, Ilan Shimon, David J Gross |
Journal | European journal of endocrinology
(Eur J Endocrinol)
Vol. 159
Issue 4
Pg. 475-82
(Oct 2008)
ISSN: 1479-683X [Electronic] England |
PMID | 18662970
(Publication Type: Clinical Trial, Journal Article, Multicenter Study)
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Chemical References |
- Antineoplastic Agents, Hormonal
- Octreotide
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Topics |
- Antineoplastic Agents, Hormonal
(administration & dosage)
- Carcinoid Tumor
(drug therapy, pathology)
- Enterochromaffin Cells
(pathology)
- Female
- Follow-Up Studies
- Humans
- Male
- Middle Aged
- Octreotide
(administration & dosage)
- Prospective Studies
- Stomach Neoplasms
(drug therapy, pathology)
- Treatment Outcome
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