Evidence map›Paper›PMID 40384778›Full record

ArticleEndocrine oncology (Bristol, England)2025

Octreotide infusion pump in patients with functional neuroendocrine tumors and refractory hormonal syndrome.

Kalyan Mansukhbhai Shekhda, Eleni Armeni, Dalvinder Mandair, Aspasia Manta, George Parker, Akanksha Sarma, Aimee Hayes, Martyn Caplin, Christos Toumpanakis

Abstract read
In one paragraph

Article in Endocrine oncology (Bristol, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Kalyan Mansukhbhai ShekhdaNeuroendocrine Tumour Unit, ENETS Centre of Excellence, Royal Free Hospital NHS Foundation Trust, London, UK.ORCID https://orcid.org/0000-0001-7884-0403
Eleni ArmeniNeuroendocrine Tumour Unit, ENETS Centre of Excellence, Royal Free Hospital NHS Foundation Trust, London, UK.ORCID https://orcid.org/0000-0003-3310-1521
Dalvinder MandairNeuroendocrine Tumour Unit, ENETS Centre of Excellence, Royal Free Hospital NHS Foundation Trust, London, UK.ORCID https://orcid.org/0000-0002-5237-8641
Aspasia MantaEndocrine Unit, 2nd Propaedeutic Department of Internal Medicine, Attikon University Hospital, Medical School, National & Kapodistrian University of Athens, Athens, Greece.ORCID https://orcid.org/0000-0002-3420-1420
George ParkerNeuroendocrine Tumour Unit, ENETS Centre of Excellence, Royal Free Hospital NHS Foundation Trust, London, UK.
Akanksha SarmaNeuroendocrine Tumour Unit, ENETS Centre of Excellence, Royal Free Hospital NHS Foundation Trust, London, UK.
Aimee HayesNeuroendocrine Tumour Unit, ENETS Centre of Excellence, Royal Free Hospital NHS Foundation Trust, London, UK.ORCID https://orcid.org/0000-0003-4417-7716
Martyn CaplinNeuroendocrine Tumour Unit, ENETS Centre of Excellence, Royal Free Hospital NHS Foundation Trust, London, UK.ORCID https://orcid.org/0000-0003-0177-1352
Christos ToumpanakisNeuroendocrine Tumour Unit, ENETS Centre of Excellence, Royal Free Hospital NHS Foundation Trust, London, UK.ORCID https://orcid.org/0000-0002-1152-7727

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: To evaluate clinical outcomes, safety and survival measures of octreotide infusion pump (OIP) therapy in patients with metastatic neuroendocrine tumors (NETs) and refractory hormonal syndrome. Design: A retrospective analysis was conducted using data from patients treated with OIP therapy at a single center. Methods: Data on demographics, disease characteristics, biochemical profiles and treatment outcomes were extracted from electronic patient records. Results: Eighteen patients with NETs and debilitating symptoms refractory to maximum approved doses of somatostatin analogs (SSTAs) were included. The cohort comprised 18 patients (12 males (67%) and six females (33%)) with a median age of 64.5 years (IQR: 49.5-71). The most common tumor site was midgut (72.2%), followed by pancreas (22.2%). Refractory carcinoid syndrome was the primary indication for initiation of OIP therapy in 15 patients and VIPoma in three. Most tumors were WHO grade 1 or 2 (89%), and liver metastases were prevalent (94% of patients). At presentation, the median 24-h urinary 5-hydroxyindoleacetic acid (5-HIAA) level was 421.5 μmoL/24 h ( Conclusion: OIP therapy is an effective treatment option for symptom control in patients with refractory NET-related hormonal syndrome. Randomized controlled trials are warranted to confirm these findings and assess long-term outcomes.

Indexed as

carcinoid syndromeneuroendocrine tumorsoctreotide infusion pumprefractory hormonal syndrome

Identifiers

PMID40384778
PMCPMC12084797

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.