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Published on: January 17, 2018
Tumor Recurrence or Regrowth in Adults With Nonfunctioning Pituitary Adenomas Using GH Replacement Therapy
N C van Varsseveld1, C C van Bunderen1, A A M Franken1
1Department of Internal Medicine (N.C.v.V., C.C.v.B., M.L.D.), Endocrine Section, Neuroscience Campus Amsterdam, VU University Medical Center, 1007 MB Amsterdam, The Netherlands; Department of Internal Medicine (A.A.M.F.), Isala Clinics, 8000 GK Zwolle, The Netherlands; Emotional Brain and Alan Turing Institute for Multidisciplinary Health Research (H.P.F.K.), 1311 RL Almere, The Netherlands; and Division of Endocrinology and Metabolism (A.J.v.d.L.), Department of Internal Medicine, Erasmus Medical Center, 3000 CA Rotterdam, The Netherlands.
Context:
GH replacement therapy (GH-RT) is a widely accepted treatment in GH-deficient adults with nonfunctioning pituitary adenoma (NFPAs). However, some concerns have been raised about the safety of GH-RT because of its potentially stimulating effect on tumor growth.
Objective:
The aim of this study was to evaluate tumor progression in NFPA patients using GH-RT.
Design, Setting, And Patients:
From the Dutch National Registry of Growth Hormone Treatment in Adults, a nationwide surveillance study in severely GH-deficient adults (1998-2009), all NFPA patients with ≥ 30 days of GH-RT were selected (n = 783). Data were retrospectively collected from the start of GH-RT in adulthood (baseline).
Main Outcome Measure:
Tumor progression, including tumor recurrence after complete remission at baseline and regrowth of residual tumor.
Results:
Tumor progression developed in 12.1% of the patients after a median (range) time of 2.2 (0.1-14.9) years. Prior radiotherapy decreased tumor progression risk compared to no radiotherapy (hazard ratio = 0.16; 95% confidence interval, 0.09-0.26). Analysis in 577 patients with available baseline imaging data showed that residual tumor at baseline increased tumor progression risk compared to no residual tumor (hazard ratio = 4.5; 95% confidence interval, 2.4-8.2).
Conclusions:
The findings in this large study were in line with those reported in literature and provide further evidence that GH-RT does not appear to increase tumor progression risk in NFPA patients. Although only long-term randomized controlled trials will be able to draw firm conclusions, our data support the current view that GH-RT is safe in NFPA patients.
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