Evaluation of Dopamin Agonists Effect on Tumour Progression in Patients with Non-Functioning Pituitary Adenomas

2021 ◽  
Vol 45 (7) ◽  
pp. S19
Author(s):  
Ariane Labarre ◽  
Joanne Nguyen ◽  
Matthieu St-Jean ◽  
Fabienne Langlois ◽  
Ghislaine Houde
2009 ◽  
Vol 161 (5) ◽  
pp. 663-669 ◽  
Author(s):  
D S Olsson ◽  
M Buchfelder ◽  
S Schlaffer ◽  
B-Å Bengtsson ◽  
K-E Jakobsson ◽  
...  

ObjectiveAn important safety issue with GH replacement therapy (GHRT) in hypopituitary patients with a history of a pituitary adenoma is the risk for tumour recurrence or enlargement.DesignCase–control study.Subjects and methodsWe studied tumour progression rate in 121 patients with hypopituitarism on the basis of non-functioning pituitary adenomas (NFPA) receiving long-term GHRT. A group of 114 NFPA patients not receiving GHRT who were matched in terms of duration of follow-up, gender, age, age at diagnosis and radiotherapy status were used as a control population. The average duration of GHRT was 10±4 years (range 2–17).ResultsIn patients with a known residual adenoma, 63% had no detectable enlargement of tumour during the study. In patients who had no visible residual tumour prior to GHRT, 90% did not suffer from recurrence. In total, the 10-year tumour progression-free survival rate in patients with NFPA receiving GHRT was 74%. In the control population not receiving GHRT, the 10-year progression-free survival rate was 70%. Radiotherapy as part of the initial tumour treatment reduced the rate of tumour progression in both GHRT and non-GHRT patients to a similar extent.ConclusionsThe rate of tumour progression was similar in this large group of GHRT patients and the control population not receiving GHRT. Our results provide further support that long-term use of GH replacement in hypopituitarism may be considered safe in patients with residual pituitary adenomas.


2021 ◽  
Author(s):  
Tobias Hallén ◽  
Daniel S Olsson ◽  
Casper Hammarstrand ◽  
Charlotte Örndal ◽  
Angelica Engvall ◽  
...  

Objective: Current markers predicting tumour progression of pituitary adenomas after surgery are insufficient. Our objective was to investigate if minichromosome maintenance protein 7 (MCM7) expression predicts tumour progression in non-functioning pituitary adenomas (NFPAs). Methods: In a cohort study of surgically treated NFPAs, two groups with distinctly different behaviour of a residual tumour were selected: one group requiring reintervention due to tumour progression (reintervention group, n=57) and one with residual tumours without progression (radiologically stable group, n=40). MCM7, Ki-67, estrogen receptor-⍺ expression, mitotic index and tumour subtype was assessed by immunohistochemistry and their association with tumour progression requiring reintervention was analysed. Results: Median (IQR) MCM7 expression was 7.4% (2.4–15.2) in the reintervention group compared with 2.0% (0.6–5.3) in the radiologically stable group (P<0.0001). Cox regression analysis showed an association between high (>13%) MCM7 expression and reintervention (HR 3.1; 95%CI:1.7-5.4; P=0.00012). The probability for reintervention within 6 years for patients with high MCM7 was 93%. Ki-67 expression >3% (P=0.00062), age ≤55 years (P=0.00034) and mitotic index ≥1 (P=0.024) were also associated with reintervention. Using a receiver operating characteristics curve, a predictive model for reintervention with all the above predictors yielded an area under the curve of 82%. All eight patients with both high MCM7 and high Ki-67 needed reintervention. Conclusion: This cohort study shows that expression of MCM7 is a predictor for clinically significant postoperative tumour progression. Together with age, Ki-67 and mitotic index, MCM7 might be of added value as a predictive marker when managing patients with NFPA after surgery.


2014 ◽  
Author(s):  
Sandra Rotondi ◽  
Maria Antonietta Oliva ◽  
Vincenzo Esposito ◽  
Luca Ventura ◽  
Felice Giangaspero ◽  
...  

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