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Updated: Aug 17, 2026

Endoscopic Endonasal Trans-sphenoidal Approach: Minimally Invasive Surgery for Pituitary Adenomas
Published on: January 17, 2018
Postoperative treatment of clinically nonfunctioning pituitary adenomas with dopamine agonists decreases tumour
Y Greenman1, K Tordjman, E Osher
1Institute of Endocrinology, Metabolism and Hypertension, Tel Aviv-Sourasky Medical Center and Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel. greenman@tasmc.health.gov.il
Objective:
There is no consensus as to the optimal postoperative treatment of patients with clinically nonfunctioning pituitary adenomas (NFPA) in whom total tumour removal has not been achieved. In this study we assessed whether dopamine agonist (DA) treatment can prevent postoperative remnant enlargement in NFPA.
Design And Methods:
Thirty-three patients (25 men/8 women; mean age, 61.7 +/- 11.2 years; mean follow-up, 40.6 +/- 4.8 months) were treated with DA, and their outcome was compared to that of 47 untreated patients (33 men/14 women; mean age, 59 +/- 2 years; mean follow-up, 42.9 +/- 4.2 months).
Results:
Tumour mass decreased or remained stable in 18/20 patients in whom DA treatment was initiated upon detection of residual tumour on postoperative MRI (group I). In 13 subjects (group II), DA therapy was started when tumour remnant growth became evident during the course of routine follow-up. Tumour growth stabilized or decreased in 8/13 (61.5%) of these patients. In contrast, tumour size remained stable in only 38.3% (18/47) of the untreated subjects (P < 0.0001 for comparisons among the three groups) and increased in the remaining 29 patients. Tumour enlargement free mean survival time was 103.7 +/- 8.8 months (CI 86.3-121) for group I, 43.9 +/- 9.6 months (CI 25.2-62.8) for group II and 36.7 +/- 3.8 (CI 29.2-44.2) for the control group (P = 0.0017). Treatment vs. control hazard ratio for tumour enlargement was 0.135 for group I (P = 0.007, 95% CI 0.032-0.577) and 0.892 for group II (P = 0.817; 95% CI 0.34-2.34).
Conclusions:
Dopamine agonist therapy is associated with a decreased prevalence of residual tumour enlargement in patients with nonfunctioning pituitary adenomas, particularly when treatment is instituted before tumour remnant growth is detected.
Insights
Dopamine agonist (DA) treatment can prevent nonfunctioning pituitary adenoma (NFPA) remnant enlargement after surgery. Early DA intervention in NFPA patients significantly reduces tumor growth compared to delayed treatment or no treatment.
Area of Science:
- Endocrinology
- Neurosurgery
- Oncology
Background:
- Optimal postoperative management for nonfunctioning pituitary adenomas (NFPA) with residual tumor is debated.
- Assessing dopamine agonist (DA) efficacy in preventing remnant enlargement is crucial.
Purpose of the Study:
- To evaluate the effectiveness of dopamine agonist (DA) treatment in preventing the enlargement of residual nonfunctioning pituitary adenomas (NFPA) after surgical resection.
Main Methods:
- A retrospective study comparing 33 patients treated with DA to 47 untreated patients.
- Outcomes were analyzed based on the timing of DA initiation (upon detection vs. evident growth).
Main Results:
- DA treatment significantly reduced tumor remnant enlargement compared to controls (P < 0.0001).
- Early DA initiation (Group I) showed a hazard ratio of 0.135 for enlargement (P = 0.007).
- Tumor enlargement-free survival was significantly longer in the early DA treatment group.
Conclusions:
- Dopamine agonist therapy is associated with a reduced prevalence of residual tumor enlargement in NFPA patients.
- Proactive DA treatment, initiated before evident remnant growth, offers the most significant benefit.
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