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Objective: Patients with growth hormone (GH)-secreting pituitary adenomas (PAs) experience various symptoms and comorbidities, which can ultimately lead to increased mortality. This study aimed to develop and validate a machine learning (ML) model for predicting long-term outcomes in patients with GH-secreting PAs following endonasal transsphenoidal surgery (ETS).
Methods: The authors conducted a retrospective three-institution cohort study that included patients with GH-secreting PAs treated with ETS between 2013 and 2023. Clinical, radiological, and biochemical data were collected. The main outcome of interest was the intervention-free rate (IFR) after primary ETS. Supervised ML algorithms, including decision trees and random forests, were developed to predict the IFR. Model performance was evaluated using area under the receiver operating characteristic curve (AUROC) and Shapley Additive Explanations (SHAP) values.
Results: The median follow-up for 100 patients with GH-secreting PAs (53% female) was 64 months (range 1-130 months). Additional intervention for persistent or recurrent acromegaly was required in 32% of patients. Following primary ETS alone, the 3-year IFR was 70% and the 5-year IFR was 67%. Multiple ML models were developed and evaluated using AUROCs. The decision tree analysis achieved an accuracy of 81% and emphasized the importance of both gross-total resection (GTR) and patient age in determining the long-term IFR. To better understand the factors that contributed to model performance, SHAP analysis was applied to the best-performing model. The SHAP dependence plots showed that key factors associated with a longer IFR included tumor size < 9 mm, GTR, patient age > 65 years, and Knosp grade 0.
Conclusions: This ML model offers a more nuanced and potentially more accurate approach to identify patients more likely to develop recurrent or persistent acromegaly following primary ETS and require additional treatment. Following external validation, this ML model could improve personalized treatment planning and follow-up strategies and enhance patient care and resource allocation in clinical practice.
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http://dx.doi.org/10.3171/2025.4.FOCUS2597 | DOI Listing |
CNS Neurosci Ther
August 2025
Department of Neurosurgery, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Background: Growth hormone-secreting pituitary neuroendocrine tumors (GH-secreting PitNETs) pose significant health risks due to hormone-related complications. Despite transsphenoidal surgical resection being the primary treatment, complete removal is often infeasible due to invasive growth patterns, leading to postoperative tumor residuals and uncertain hormone remission outcomes.
Methods: This retrospective study included 458 patients with GH-secreting PitNETs who underwent surgery at Beijing Tiantan Hospital.
Cureus
July 2025
Department of Neuroendocrinology, National Institute of Neurology and Neurosurgery "Manuel Velasco Suárez", Mexico City, MEX.
Background and objective Fractionated stereotactic radiotherapy (FSRT) and stereotactic radiosurgery (SRS) are commonly used in patients with growth hormone (GH)-secreting pituitary adenomas (PAs) who are not candidates for surgery, have residual disease postoperatively, or have failed or cannot access medical therapy. It is also considered a first-line option in elderly patients or those with comorbidities that contraindicate surgery. In this study, we aimed to evaluate the long-term outcomes of SRS and FSRT in patients with acromegaly who remained biochemically active despite prior surgical and/or medical treatment.
View Article and Find Full Text PDFPituitary
August 2025
Unit on Hypothalamic and Pituitary Disorders, Eunice Kennedy Shriver National Institute of Child Health, and Human Development (NICHD), National Institutes of Health, Bethesda, MD, USA.
Purpose: Pituitary adenomas (PAs) constitute a rare pediatric diagnosis and their pathogenetic mechanisms are not clearly understood. The aim of this study was to evaluate the prevalence of genetic defects in pediatric PAs through germline and tumor testing, and to describe genotype-phenotype correlations.
Methods: Fifty-four pediatric patients with PAs and available germline and/or tumor samples were studied.
Clin Neurol Neurosurg
October 2025
Department of Neurosurgery, Medical College of Wisconsin and Froedtert Hospital, 8701 Watertown Plank Rd, Wauwatosa, WI 53226, USA. Electronic address:
Introduction: Mixed gangliocytoma-pituitary adenomas (MGPAs) are rare sellar tumors, often presenting with signs and symptoms of acromegaly due to the somatotrophic component. The pathogenesis is not well understood, with few cases reported. We present our institutional experience in surgical management and compare surgical outcomes in growth hormone (GH)-secreting MGPAs and GH-secreting pituitary adenomas (GHPAs).
View Article and Find Full Text PDFDiscov Oncol
August 2025
Department of Neurosurgery, Chang Gung Memorial Hospital at Linkou, Chang Gung University, 5, Fuxing St., Guishan Dist., 333423, Taoyuan, Taiwan.
Introduction: Growth hormone (GH)-secreting pituitary tumors cause serious systemic comorbidities, necessitating the achievement of gross total resection (GTR) and biochemical remission. This study aims to identify predictors of resection status and biochemical remission.
Methods: We retrospectively reviewed the records of 54 GH adenoma patients receiving endoscopic endonasal transsphenoidal approach (EETSA).