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Status unknownNCT02854228PITUICARE-LyonUpdated Aug 3, 2016

PITUItary Carcinoma or Aggressive Tumors REgistry -Lyon

An observational study in Pituitary Tumor, sponsored by Hospices Civils de Lyon. Status unknown at 1 site in France. Per ClinicalTrials.gov, last updated 2016-08-03.

Sponsored by Hospices Civils de Lyon · Observational

The sponsor has not verified this record recently (last verified Jul 2016), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
1,300
Sex
All
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Study summary

The purpose of this study is to observe predictors of pituitary tumor recurrence and markers of persistent disease activity through computerized collection of comprehensive demographic, therapeutic, pathologic and outcome information on patients harboring pituitary mass lesions of all types.

02

Conditions studied

  • Pituitary Tumor

Keywords

  • Pituitary tumor
  • pituitary carcinoma
  • acromegaly
  • cushing
  • prolactinoma
03

In context

Pituitary Neoplasms

180 studies on the registry are indexed under Pituitary Neoplasms; 48 are open to participants now.

This study's planned enrollment of 1,300 is above the median of 150 across 75 observational studies indexed under Pituitary Neoplasms.

Browse Pituitary Neoplasms studies →

Lead sponsor

Hospices Civils de Lyon is the lead sponsor of 1,854 studies on the registry; 441 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

tertiary referral center

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • patients with confirmed pituitary disease

Exclusion criteria

Exclusion Criteria:

  • patients who do not have confirmed pituitary disease
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
1,300 participants (estimated)
Patient registry
No
Biospecimen retention
Samples with dna
06

What researchers measure

Primary outcomes

  1. Progression free survival after pituitary surgery according to the clinicopathological classification (HYPOPRONOS)

    Clinical, biochemical et imaging evaluation of a cohort of patient operated in the referral center for pituitary tumor. Identification of recurrence or progression an analysis of the clinicopathological classification. Evaluation of the different therapeutic strategies (med, surgery, chemotherapies, radiation therapy) to prevent recurrence or tumor progression.

    Time frame: up to 10 years (postoperatively)

Secondary outcomes

  1. Correlation between percentage of SSTR expression of the pituitary tumor and somatostatine analogs efficacy.

    Analysis of the expression of SST receptors in GH, PRL and ACTH secreting pituitary tumors: SSTR expression accessed by immunohistochemistry of the pituitary tumor. Evaluation of the response to somatostatine analogs: somatostatine analogs efficacy evaluated by normalization of hormone hypersecretion in ACTH, GH and PRL secreting pituitary tumor.

    Time frame: 2007-2020

  2. Correlation between percentage of MGMT expression of the pituitary tumor and tumor response to temozolomide.

    Evaluation of MGMT expression (accessed by immunohistochemistry of the pituitary tumor) and response to temozolomide treatment (evaluated according to RECIST criteria) for patient presenting multirecurrent tumors resistant to conventional treatment.

    Time frame: 2007-2020

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Study locations

1 of 1 sites recruiting
08

References and documents

Publications

  • Raverot G, Dantony E, Beauvy J, Vasiljevic A, Mikolasek S, Borson-Chazot F, Jouanneau E, Roy P, Trouillas J. Risk of Recurrence in Pituitary Neuroendocrine Tumors: A Prospective Study Using a Five-Tiered Classification. J Clin Endocrinol Metab. 2017 Sep 1;102(9):3368-3374. doi: 10.1210/jc.2017-00773. PubMed 28651368 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 3, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT02854228
Responsible party
Sponsor
First posted
Aug 3, 2016
Start date
Feb 2007
Primary completion
Dec 2015
Completion
Dec 2020 (estimated)
Last update
Aug 3, 2016

Study contacts

Gerald Raverot, MD PhD
Contact
gerald.raverot@chu-lyon.fr
(0)472119325 ext. +33
Emmanuel Jouanneau, MD PhD
Contact
emmanuel.jouanneau@chu-lyon.fr
(0)472357411 ext. +33
Gerald Raverot, MD PhD
principal investigator · Hospices Civils de Lyon

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Jul 2016. You cannot join it, but the record below documents what was studied.

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