The Role of Somatostatin Analogues in the Control of Diarrhea and Flushing as Markers of Carcinoid Syndrome: A Systematic Review and Meta-Analysis

Author:

Alexandraki Krystallenia I.1ORCID,Angelousi Anna2ORCID,Chatzellis Eleftherios3ORCID,Chrisoulidou Alexandra4,Kalogeris Nikolaos5,Kanakis Georgios6,Savvidis Christos7,Vassiliadi Dimitra8,Spyroglou Ariadni1ORCID,Kostopoulos Georgios9ORCID,Markussis Vyron10ORCID,Toulis Konstantinos9,Tsagarakis Stylianos8,Kaltsas Gregory A.11

Affiliation:

1. Endocrine Unit, 2nd Department of Surgery, Aretaieio Hospital, National and Kapodistrian University of Athens, 11528 Athens, Greece

2. Unit of Endocrinology, 1st Department of Internal Medicine, Laiko University Hospital, Medical School, National and Kapodistrian University of Athens, 11527 Athens, Greece

3. 251 HAF and VA Hospital, 11525 Athens, Greece

4. Unit of Endocrinology, Theagenio Hospital, 54639 Thessaloniki, Greece

5. Department of Endocrinology and Diabetes, Hellenic Red Cross Hospital, 11526 Athens, Greece

6. Department of Endocrinology, Diabetes and Metabolism, Athens Naval & VA Hospital, 11521 Athens, Greece

7. Department of Endocrinology and Metabolism, Hippocratio General Hospital of Athens, 11527 Athens, Greece

8. Department of Endocrinology, Diabetes and Metabolism, Evangelismos Hospital, 10676 Athens, Greece

9. Department of Endocrinology, 424 General Military Hospital, 56429 Thessaloniki, Greece

10. Independent Researcher, 18535 Athens, Greece

11. Endocrine Unit, 1st Department of Propaedeutic Medicine, Laiko University Hospital, Medical School, National and Kapodistrian University of Athens, 11527 Athens, Greece

Abstract

Background: Somatostatin analogues (SSAs) are the cornerstone of treatment for carcinoid syndrome (CS)-related symptoms. The aim of this systematic review and meta-analysis is to evaluate the percentage of patients achieving partial (PR) or complete response (CR) with the use of long-acting SSAs in patients with CS. Methods: A systematic electronic literature search was conducted in PubMed, Cochrane, and Scopus to identify eligible studies. Any clinical trials reporting data on the efficacy of SSAs to alleviate symptoms in adult patients were considered as potentially eligible. Results: A total of 17 studies reported extractable outcomes (PR/CR) for quantitative synthesis. The pooled percentage of patients with PR/CR for diarrhea was estimated to be 0.67 (95% confidence interval (CI): 0.52–0.79, I2 = 83%). Subgroup analyses of specific drugs provided no evidence of a differential response. With regards to flushing, the pooled percentage of patients with PR/CR was estimated to be 0.68 (95% CI: 0.52–0.81, I2 = 86%). Similarly, no evidence of a significant differential response in flushing control was documented. Conclusions: We estimate there is a 67–68% overall reduction in symptoms of CS associated with SSA treatment. However, significant heterogeneity was detected, possibly revealing differences in the disease course, in management and in outcome definition.

Publisher

MDPI AG

Subject

Medicine (miscellaneous)

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