# Natural history of non-functioning pituitary neuroendocrine tumours: impact of baseline characteristics and gender-specific clinical presentations

**Authors:** Alessandro Bavaresco, Giulia Bovo, Alessandro Mondin, Carla Scaroni, Giacomo Voltan, Pierluigi Mazzeo, Irene Tizianel, Filippo Ceccato, Mattia Barbot

PMC · DOI: 10.1007/s11102-026-01669-7 · 2026-03-27

## TL;DR

This study explores how gender affects the presentation and progression of non-functioning pituitary tumors, finding that men tend to have larger, more symptomatic tumors while women are often diagnosed earlier.

## Contribution

The study identifies gender-specific clinical patterns in NF-PitNETs and emphasizes the need for individualized treatment approaches based on tumor characteristics.

## Key findings

- Males had larger tumors and more symptoms compared to females, who were often diagnosed earlier due to reproductive-age monitoring.
- Long-term tumor progression was similar between genders, with tumor size and visual impairment predicting progression in surveillance cases.
- Surgical outcomes showed that residual tumor increased progression risk, while significant volume reduction improved visual outcomes.

## Abstract

Non-functioning pituitary neuroendocrine tumours (NF-PitNETs) are the most common pituitary macroadenomas, with highly variable clinical behaviour. Although tumor growth and functional impairment are key considerations, the impact of patient sex on presentation and outcomes remains incompletely characterized.

To investigate clinical, radiological and histopathological predictors of long-term outcomes in NF-PitNETs managed conservatively or surgically and to evaluate gender impact on initial presentation and tumour natural history.

We retrospectively analyzed 170 patients with NF-PitNETs, including those under active surveillance and those treated surgically, with or without adjuvant therapies. Long-term clinical, endocrine and radiological follow-up was performed.

Compared with female patients, males exhibited larger tumour dimensions and a higher prevalence of both visual field defects and endocrine dysfunction. Women, particularly in the surveillance cohort, had smaller tumours, often detected earlier, likely due to reproductive-age clinical monitoring. Despite these baseline differences, progression rates were similar between genders. In patients under surveillance, five-year tumour growth risk was higher for macroadenomas than microadenomas (45.7% vs. 22.5%, p = 0.030), and baseline tumour volume and visual impairment predicted progression. In the surgical cohort, residual tumour increased progression risk, while a > 40% volume reduction was associated with visual improvement. The Trouillas clinicopathological classification was not predictive of outcomes. Adjuvant therapies, including stereotactic radiosurgery and temozolomide, stabilized disease in most treated cases.

Gender significantly influences NF-PitNETs presentation, with males harbouring larger, more symptomatic tumours whereas females tended to have an earlier detection. However, long-term progression seems to be independent of gender. These findings pinpoint the importance of individualized approach combining anatomical, volumetric, and functional assessments to optimize outcomes.

## Linked entities

- **Chemicals:** temozolomide (PubChem CID 5394)

## Full-text entities

- **Genes:** NFASC (neurofascin) [NCBI Gene 23114] {aka NEDCPMD, NF, NRCAML}, GHRH (growth hormone releasing hormone) [NCBI Gene 2691] {aka GHRF, GRF, INN}, TP53 (tumor protein p53) [NCBI Gene 7157] {aka BCC7, BMFS5, LFS1, P53, TRP53}, SF1 (splicing factor 1) [NCBI Gene 7536] {aka BBP, D11S636, MBBP, ZCCHC25, ZFM1, ZNF162}, GGH (gamma-glutamyl hydrolase) [NCBI Gene 8836] {aka GATD10, GH}
- **Diseases:** Adenomas (MESH:D000236), pituitary hormone deficiencies (MESH:C580003), pituitary disfunction (MESH:D057215), TSS (MESH:D000267), Tumour (MESH:D009369), volume reduction (MESH:D015431), visual field defects (MESH:D005128), Visual disturbances (MESH:D014786), GH deficiency (MESH:D006432), central hypothyroidism (MESH:D007037), anterior hypopituitarism (MESH:D007018), NF-PitNETs (MESH:D010911), nausea (MESH:D009325), endocrinopathies (MESH:C567425), panhypopituitarism (MESH:C563172), syncope (MESH:D013575), oligo/amenorrhoea (MESH:C537962), endocrine dysfunction (MESH:D004700), cranial nerve deficits (MESH:D003389), headache (MESH:D006261), Hypogonadotropic hypogonadism (MESH:D007006), pituitary dysfunction (MESH:D010900), Growth hormone deficiency (MESH:D004393), vertigo (MESH:D014717), vomiting (MESH:D014839), hyperprolactinemia (MESH:D006966), AVP deficiency (MESH:D020790), hormonal deficits (MESH:D009461), pituitary apoplexy (MESH:D010899), Central adrenal insufficiency (MESH:D000309), NF (MESH:D016518)
- **Chemicals:** TMZ (MESH:D000077204), formalin (MESH:D005557), thyroxine (MESH:D013974), oestradiol (MESH:D004958), testosterone (MESH:D013739), SRS (MESH:D013324), arginine (MESH:D001120)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13031247/full.md

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Source: https://tomesphere.com/paper/PMC13031247