Evidence map›Paper›PMID 31583575›Full record

ArticleEndocrine2020

Ophélie Bélissant Benesty, Valérie Nataf, Jessica Ohnona, Laure Michaud, Jules Zhang-Yin, Jérôme Bertherat, Philippe Chanson, Yves Reznik, Jean-Noël Talbot, Françoise Montravers

Abstract read
PubMed Publisher
In one paragraph

Article in Endocrine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

10 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Recognition and Management of Ectopic ACTH Secreting Tumors.Journal of the Endocrine Society · 2025
    Article
  3. Article
  4. Journal of clinical medicine · 2024
    Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
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

10 authors at 4 institutions in 1 country.

Ophélie Bélissant BenestyNuclear Medicine, Hôpital Tenon APHP and Sorbonne University, Paris, France. ophelie.benesty@gmail.com.ORCID http://orcid.org/0000-0002-7372-4152
Valérie NatafNuclear Medicine, Hôpital Tenon APHP and Sorbonne University, Paris, France.
Jessica OhnonaNuclear Medicine, Hôpital Tenon APHP and Sorbonne University, Paris, France.
Laure MichaudNuclear Medicine, Hôpital Tenon APHP and Sorbonne University, Paris, France.
Jules Zhang-YinNuclear Medicine, Hôpital Tenon APHP and Sorbonne University, Paris, France.
Jérôme BertheratEndocrinology, Hôpital Cochin APHP and Paris Descartes University, Paris, France.
Philippe ChansonEndocrinology, Hôpital Bicêtre APHP and Université Paris Sud, Le Kremlin-Bicêtre, France.
Yves ReznikEndocrinology, Centre Hospitalo-Universitaire de Caen and Université de Caen Normandie, Caen, France.
Jean-Noël TalbotNuclear Medicine, Hôpital Tenon APHP and Sorbonne University, Paris, France.
Françoise MontraversNuclear Medicine, Hôpital Tenon APHP and Sorbonne University, Paris, France.
Sorbonne Université · FRUniversité de Caen Normandie · FRUniversité Paris Cité · FRUniversité Paris-Sud · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeParaneoplastic Cushing's syndrome (PCS) is frequently caused by neuroendocrine tumours (NETs). Approximately 20% of tumours are still occult years later. Gallium-68 somatostatin receptor-PET/CT is promising for the detection of the causal primary NET, but its role in case of recurrent PCS is rarely reported. We report our experience with DOTATOC PET/CT in localising the causal NET in cases of initial but also recurrent PCS, and its clinical impact.

methodsA retrospective review of all DOTATOC PET/CTs performed in consecutive patients referred for PCS to our centre, between January 2011 and June 2017, was done. Nineteen patients underwent 26 PET/CTs, 13 for detection of a primary NET, seven for persistent or recurrent PCS after resection, and six for surveillance after resection of NETs previously detected on a DOTATOC PET/CT in our centre.

resultsAmong the 13 PET/CTs performed to search for primary NET, five were positive: four carcinoid lung tumours were confirmed after resection and one lung focus was not confirmed since surgery would have carried a high risk. Clinical impact was 23% (3/13). Among the seven PET/CTs performed for persistent or recurrent PCS, six were true-positive, with confirmation of metastatic lymph nodes after resection. Clinical impact was 57% (4/7). All PET/CTs performed for surveillance were true-negative.

conclusionsDOTATOC PET/CT seems to be a valuable tool for detection of the NET responsible for persistent or recurrent PCS after surgery. In this context, DOTATOC PET/CT was more effective than for the detection of the causal tumour in initial PCS.

Indexed as

Cushing SyndromeNeuroendocrine TumorsOrganometallic CompoundsGallium RadioisotopesHumansOctreotidePositron-Emission TomographyPositron Emission Tomography Computed TomographyRadiopharmaceuticalsRetrospective StudiesTomography, X-Ray ComputedEdotreotideGallium RadioisotopesOctreotideOrganometallic CompoundsRadiopharmaceuticalsCushingDOTATOCNeuroendocrine tumourPET/CTRecurrence

Identifiers

PMID31583575
OpenAlexW2977353535

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.