Effects of therapy with [177Lu-DOTA 0,Tyr 3]octreotate on endocrine function

Eur J Nucl Med Mol Imaging. 2009 Nov;36(11):1758-66. doi: 10.1007/s00259-009-1151-8. Epub 2009 May 27.

Abstract

Purpose: Peptide receptor radionuclide therapy (PRRT) with radiolabelled somatostatin analogues is a novel therapy for patients with somatostatin receptor-positive tumours. We determined the effects of PRRT with [(177)Lu-DOTA(0),Tyr(3)]octreotate ((177)Lu-octreotate) on glucose homeostasis and the pituitary-gonadal, pituitary-thyroid and pituitary-adrenal axes.

Methods: Hormone levels were measured and adrenal function assessed at baseline and up to 24 months of follow-up.

Results: In 35 men, mean serum inhibin B levels were decreased at 3 months post-therapy (205 +/- 16 to 25 +/- 4 ng/l, p < 0.05) and follicle-stimulating hormone (FSH) levels increased (5.9 +/- 0.5 to 22.7 +/- 1.4 IU/l, p < 0.05). These levels returned to near baseline levels. Total testosterone and sex hormone binding globulin (SHBG) levels decreased (15.0 +/- 0.9 to 10.6 +/- 1.0 nmol/l, p < 0.05 and 61.8 +/- 8.7 to 33.2 +/- 3.7 nmol, p < 0.05), respectively, whereas non-SHBG-bound T did not change. An increase (5.2 +/- 0.6 to 7.7 +/- 0.7 IU/l, p < 0.05) of luteinizing hormone (LH) levels was found at 3 months of follow-up returning to baseline levels thereafter. In 21 postmenopausal women, a decrease in levels of FSH (74.4 +/- 5.6 to 62.4 +/- 7.7 IU/l, p < 0.05) and LH (26.8 +/- 2.1 to 21.1 +/- 3.0 IU/l, p < 0.05) was found. Of 66 patients, 2 developed persistent primary hypothyroidism. Free thyroxine (FT(4)) levels decreased (17.7 +/- 0.4 to 15.6 +/- 0.6 pmol/l, p < 0.05), whereas thyroid-stimulating hormone (TSH) and triiodothyronine (T(3)) levels did not change. Reverse triiodothyronine (rT(3)) levels decreased (0.38 +/- 0.03 to 0.30 +/- 0.01 nmol/l, p < 0.05). Before and after therapy adrenocorticotropic hormone (ACTH) stimulation tests showed an adequate response of serum cortisol (> 550 nmol/l, n = 18). Five patients developed elevated HbA(1c) levels (> 6.5%).

Conclusion: In men (177)Lu-octreotate therapy induced transient inhibitory effects on spermatogenesis, but non-SHBG-bound T levels remained unaffected. In the long term, gonadotropin levels decreased significantly in postmenopausal women. Only a few patients developed hypothyroidism or elevated levels of HbA(1c). Therefore, PRRT with (177)Lu-octreotate can be regarded as a safe treatment modality with respect to short- and long-term endocrine function.

MeSH terms

  • Adult
  • Aged
  • Endocrine Glands / metabolism
  • Endocrine Glands / physiology*
  • Endocrine Glands / radiation effects*
  • Female
  • Glucose / metabolism
  • Homeostasis / radiation effects
  • Hormones / blood
  • Humans
  • Longitudinal Studies
  • Male
  • Middle Aged
  • Neoplasms / blood
  • Neoplasms / metabolism
  • Neoplasms / physiopathology
  • Neoplasms / radiotherapy
  • Octreotide / adverse effects
  • Octreotide / analogs & derivatives*
  • Octreotide / therapeutic use
  • Organometallic Compounds / adverse effects*
  • Organometallic Compounds / therapeutic use
  • Receptors, Peptide / therapeutic use
  • Retrospective Studies
  • Somatostatin / chemistry
  • Somatostatin / therapeutic use
  • Time Factors
  • Young Adult

Substances

  • Hormones
  • Organometallic Compounds
  • Receptors, Peptide
  • Somatostatin
  • lutetium Lu 177 dotatate
  • Glucose
  • Octreotide