Evidence map›Paper›PMID 29949120›Full record

ReviewJournal of endocrinological investigation2019

Peptide receptor radionuclide therapy with

D Magalhães, I L Sampaio, G Ferreira, P Bogalho, D Martins-Branco, R Santos, H Duarte

Open access · bronzeAbstract readCase ReportsReview
PubMed Publisher
In one paragraph

Review in Journal of endocrinological investigation, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
3.1field-weighted citation impact, top 8% of its field
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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 37 citations in OpenAlex.

  1. Ectopic insulinoma: a systematic review.Reviews in endocrine & metabolic disorders · 2023
    Pooled it
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  12. The functioning side of the pancreas: a review on insulinomas.Journal of endocrinological investigation · 2020
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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

7 authors at 3 institutions in 1 country.

D MagalhãesEndocrinology, Diabetes and Metabolism Department, Centro Hospitalar de São João, Alameda Prof. Hernâni Monteiro, 4200-319, Porto, Portugal. danielascmagalhaes@gmail.com.ORCID http://orcid.org/0000-0002-8822-1179
I L SampaioNuclear Medicine Department, Instituto Português de Oncologia do Porto, Rua Dr. António Bernardino de Almeida, 4200-072, Porto, Portugal.
G FerreiraNuclear Medicine Department, Instituto Português de Oncologia do Porto, Rua Dr. António Bernardino de Almeida, 4200-072, Porto, Portugal.
P BogalhoEndocrinology Department, Hospital Curry Cabral, Rua da Beneficência, n.º 8, 1069-166, Lisboa, Portugal.
D Martins-BrancoOncology Department, Instituto Português de Oncologia de Lisboa, R. Prof. Lima Basto, 1099-023, Lisboa, Portugal.
R SantosEndocrinology Department, Instituto Português de Oncologia de Lisboa, R. Prof. Lima Basto, 1099-023, Lisboa, Portugal.
H DuarteNuclear Medicine Department, Instituto Português de Oncologia do Porto, Rua Dr. António Bernardino de Almeida, 4200-072, Porto, Portugal.
IPO Porto · PTHospital Curry Cabral · PTUniversidade do Porto · PT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionInsulinomas are a rare type of pancreatic neuroendocrine tumours characterized by insulin hypersecretion. They are considered malignant when metastases are present. Traditional therapies often promote only temporarily symptomatic relief and may be associated with severe adverse effects. There is scarce experience in treating malignant insulinomas with peptide receptors radionuclide therapy (PRRNT). PATIENTS AND

methodsWe describe PRRNT results in four patients with inoperable malignant insulinomas with poorly controllable hypoglycaemia. All patients received therapy with

resultsPatient 1 presented significant clinical benefit for 13 months after PRRNT, with imaging improvement. Patient 2 obtained reduction of the number and severity of hypoglycaemic episodes during 15 months after therapy. Patient 3 is asymptomatic since PRRNT first cycle performed 23 months ago and revealed significant imaging improvement. Patient 4 had resolution of hypoglycaemia only 3 days after PRRNT first cycle and today, 16 months after therapy, the disease seems to be in remission and the patient maintains euglycaemic state. PRRNT was well tolerated, with only hematologic grade 2 toxicity in patient 1 and mild kidney toxicity in patient 3.

conclusionsAfter the start of

Indexed as

AgedFemaleHumansInsulinomaMiddle AgedNeuroendocrine TumorsOctreotideOrganometallic CompoundsReceptors, PeptideRetrospective StudiesTreatment Outcomelutetium Lu 177 dotatateOctreotideOrganometallic CompoundsReceptors, PeptideInsulinomaLutetiumNeuroendocrine tumourPRRNTRadiolabeled somatostatin analoguesSomatostatin receptors

Identifiers

PMID29949120
OpenAlexW2806735378

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.