Evidence map›Paper›PMID 25743263›Full record

Trial reportEndocrine2015

The treatment with pasireotide in Cushing's disease: effects of long-term treatment on tumor mass in the experience of a single center.

Chiara Simeoli, Renata Simona Auriemma, Fabio Tortora, Monica De Leo, Davide Iacuaniello, Alessia Cozzolino, Maria Cristina De Martino, Claudia Pivonello, Ciro Gabriele Mainolfi, Riccardo Rossi and 3 more

Erratum issuedAbstract readCase ReportsRandomized Controlled Trial
PubMed Publisher
In one paragraph

Trial report in Endocrine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
5.6field-weighted citation impact, top 3% 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

23 citing papers in PubMed, 1 synthesis or guideline pooled it, 49 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Trial
  5. Trial
  6. Trial
  7. Review
  8. Review
  9. Pasireotide-a novel somatostatin receptor ligand after 20 years of use.Reviews in endocrine & metabolic disorders · 2022
    Review
  10. Review
  11. Review
  12. Article
  13. Review
  14. Pituitary-Directed Therapies for Cushing's Disease.Frontiers in endocrinology · 2018
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 3 institutions in 1 country.

Chiara SimeoliDipartimento di Medicina Clinica e Chirurgia, Sezione di Endocrinologia, Università "Federico II", Via Sergio Pansini 5, 80131, Naples, Italy.
Renata Simona AuriemmaIos & Coleman Medicina Futura Medical Center, Naples, Italy.
Fabio TortoraDepartment of Internal and Experimental Medicine, Division of Neurological Sciences, Second University of Naples, Naples, Italy.
Monica De LeoDipartimento di Medicina Clinica e Chirurgia, Sezione di Endocrinologia, Università "Federico II", Via Sergio Pansini 5, 80131, Naples, Italy.
Davide IacuanielloDipartimento di Medicina Clinica e Chirurgia, Sezione di Endocrinologia, Università "Federico II", Via Sergio Pansini 5, 80131, Naples, Italy.
Alessia CozzolinoDipartimento di Medicina Clinica e Chirurgia, Sezione di Endocrinologia, Università "Federico II", Via Sergio Pansini 5, 80131, Naples, Italy.
Maria Cristina De MartinoDipartimento di Medicina Clinica e Chirurgia, Sezione di Endocrinologia, Università "Federico II", Via Sergio Pansini 5, 80131, Naples, Italy.
Claudia PivonelloDipartimento di Medicina Clinica e Chirurgia, Sezione di Endocrinologia, Università "Federico II", Via Sergio Pansini 5, 80131, Naples, Italy.
Ciro Gabriele MainolfiDipartimento di Scienze Biomediche Avanzate, Università "Federico II", Naples, Italy.
Riccardo RossiDipartimento di Medicina Clinica e Chirurgia, Sezione di Endocrinologia, Università "Federico II", Via Sergio Pansini 5, 80131, Naples, Italy.
Sossio CirilloDepartment of Internal and Experimental Medicine, Division of Neurological Sciences, Second University of Naples, Naples, Italy.
Annamaria ColaoDipartimento di Medicina Clinica e Chirurgia, Sezione di Endocrinologia, Università "Federico II", Via Sergio Pansini 5, 80131, Naples, Italy.
Rosario PivonelloDipartimento di Medicina Clinica e Chirurgia, Sezione di Endocrinologia, Università "Federico II", Via Sergio Pansini 5, 80131, Naples, Italy. rosario.pivonello@unina.it.
University of Naples Federico II · ITTecnologie Avanzate (Italy) · ITUniversity of Campania "Luigi Vanvitelli" · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pasireotide is the first medical therapy officially approved for the treatment of adult patients with Cushing's disease (CD) who experienced a failure of pituitary surgery or are not candidates for surgery and require medical therapeutic intervention. The current study aimed at investigating the effects of long-term treatment with pasireotide (up to 24 months) on tumor mass in a group of patients with CD, participating to a phase III study. Fourteen CD patients entered the phase III clinical trial CSOM230B2305 at Naples Center, and eight (seven women, one man, aged 38.9 ± 17.6 years), including seven with a microadenoma and one with a macroadenoma, received treatment with pasireotide at the dose of 600-1200 µg bid for at least 6 months, and were considered for the analysis of the study. These eight patients were subjected to the evaluation of pituitary tumor volume by pituitary MRI, together with the evaluation of urinary cortisol levels, at baseline and every 6 months for the entire period of treatment. Pasireotide treatment induced full disease control in 37.5 % and partial disease control in 37.5 % after 6 months, whereas full and partial disease control after 12 months was obtained in 28.6 % and in 57.1 % of patients, respectively. A significant (>25 %) reduction in tumor volume was found in 62.5 % and in 100 % of patients, after 6 and 12 months, respectively. In particular, after 6 months, a slight tumor shrinkage (between 25.1 and 50 %) was observed in 25 %, moderate (50.1-75 %) in 25 %, and marked (>75 %) in 12.5 % of patients, whereas after 12 months, a slight tumor shrinkage was observed in 43 %, moderate in 14 %, and marked in 43 % of patients. In 25 % of patients (two patients), a marked tumor shrinkage was recorded, with tumor mass disappearance in one case; this tumor shrinkage was associated to rapid and sustained biochemical remission up to 24 months of continuous pasireotide treatment. These two cases represent the first cases with a documentation of such a notable effect of pasireotide on tumor mass. Pasireotide induces significant tumor shrinkage in 62.5 % of patients after 6 months and in 100 % of patients after 12 months, and occasionally induces a radiological disappearance of the tumor. This evidence supports and strengthens the role of pasireotide as medical treatment specifically addressed to patients with CD, particularly in those who had unsuccessful pituitary surgery, or are not candidates for surgery.

Indexed as

AdolescentAdultFemaleHumansMaleMiddle AgedPituitary ACTH HypersecretionProspective StudiesSomatostatinTreatment OutcomeYoung AdultpasireotideSomatostatinACTH-secreting pituitary tumorCushing’s diseaseCushing’s syndromePasireotideSomatostatin analogsTumor mass

Identifiers

PMID25743263
OpenAlexW2037435440

What Socratic 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 Socratic graph.