The association between acromegaly and cancer had been assessed mainly in population studies with inconsistent results. The objective of this study was to investigate the risk of cancer in a large cohort of patients with acromegaly compared with matched controls. The comprehensive computerized database of the largest healthcare provider organization in Israel was searched for patients diagnosed with acromegaly in 2000-2021. All diagnoses were qualitatively validated. Patients were individually matched 1:5 with a control group for age, sex, and socioeconomic status. Clinical and outcome data were collected from the medical files. The final cohort consisted of 470 patients (54% male) with acromegaly and 2330 control subjects. Mean age at diagnosis was 53 years, and mean duration of follow-up after diagnosis was 10.4 years. The prevalence of solid malignancies was 21.3% in the acromegaly group and 14.8% in the control group (OR 1.6, 95% CI 1.2-2.0). Patients with acromegaly had a higher rate of thyroid cancer (2.8% vs 0.6%; OR 5.1, CI 2.3-11.0) and a tendency for a higher risk of colorectal cancer (3.6% vs 2.8%; OR 1.3, CI 0.7-2.2), prostate cancer (2.8% vs 1.7%; OR 1.6, CI 0.8-3.1), and renal cancer (1.5% vs 0.8%; OR 1.8, CI 0.8-4.4), but not hematological malignancies. They also had a higher mortality rate (21.3% vs 15.7%; OR 1.5, CI 1.1-1.9). In conclusion, the higher prevalence of malignant solid tumors in patients with acromegaly compared with control subjects suggests that periodic screening for early detection of solid cancers may be considered in this patient population.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1530/ERC-24-0087 | DOI Listing |
Front Endocrinol (Lausanne)
March 2025
Hospices Civils de Lyon, Hôpital Femme Mère Enfant, Service d'Endocrinologie Pédiatrique et Pédiatrie Générale, Bron, France.
Introduction: McCune-Albright syndrome (MAS) is a rare disease caused by somatic gain-of-function variants in the gene that lead to constitutive activation of the G protein alpha subunit (Gsα). Pathologic consequences can involve several tissues. Fibrous dysplasia (FD), café-au-lait skin macules and hyperfunctioning endocrinopathies are classic manifestations.
View Article and Find Full Text PDFEndokrynol Pol
March 2025
Department of Endocrinology and Internal Medicine, Medical University Wrocław, Wroclaw, Poland.
Introduction: The analysis of the costs associated with treating acromegaly and its complications is important in planning diagnostics and treatment for a single patient, as well as in establishing the standard of care for the entire population of acromegaly patients. Data on the actual costs of treating patients with acromegaly in Poland are limited.
Aims Of The Study: To determine the direct cost (hospital stays, diagnostic imaging, surgical treatment, pharmacotherapy, tumour irradiation) of treating patients with acromegaly and its complications, assessing the relationship between acromegaly treatment costs and the radical nature of the treatment.
Eur J Endocrinol
March 2025
Centre for Endocrinology, Barts and The London School of Medicine, Queen Mary University of London, London, UK.
Objective: Heterozygous germline loss-of-function variants in AIP are associated with young-onset growth hormone and/or prolactin-secreting pituitary tumours. However, the pathogenic role of the c.911G>A; p.
View Article and Find Full Text PDFEur J Endocrinol
March 2025
Alexion, AstraZeneca Rare Disease, Boston, MA, USA.
Objective: Acromegaly is an endocrine disorder caused by the hypersecretion of growth hormone (GH) by a benign tumor of the pituitary that leads to insulin-like growth factor-1 (IGF1) overproduction. In most patients, somatostatin analogs (SSAs), the current first line medical therapy for acromegaly, do not normalize IGF1 levels. This study aims to investigate the pre-clinical efficacy of ALXN2420, a novel, small peptide antagonist of the growth hormone receptor (GHR), being developed as a combination therapy to SSAs to further suppress and normalize IGF1 levels.
View Article and Find Full Text PDFFront Endocrinol (Lausanne)
March 2025
Key Laboratory of Endocrinology of National Health Commission, Department of Endocrinology, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Science and Peking Union Medical College, Beijing, China.
Introduction: Long-term biochemical nonremission and long-delayed diagnosis can increase the incidence of comorbidities of acromegaly and seriously affect patients' quality of life. To identify predictors of biochemical remission and quantify the relationship between delayed diagnosis and comorbidities, we performed a retrospective study of a large, single-centre cohort.
Methods: This retrospective cohort included 1692 hospitalised patients with acromegaly seen in a single referral centre between 2012 and 2020.
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!