# Aggressive and malignant pituitary tumours: does the sex matter?

**Authors:** Anna Lucia Carretti, Chrysi Kaparounaki, Gérald Raverot

PMC · DOI: 10.1007/s11102-026-01656-y · Pituitary · 2026-03-07

## TL;DR

This review finds that sex influences the behavior and treatment response of aggressive pituitary tumors, with men showing more aggressive disease and women responding better to certain therapies.

## Contribution

The study identifies sex-specific differences in clinical features and treatment outcomes of aggressive pituitary tumors.

## Key findings

- Men with corticotroph tumors had more non-functioning lesions and invasive disease compared to women.
- Women with lactotroph tumors showed better responses to temozolomide than men.
- Sex-specific patterns suggest the need for personalized treatment strategies in aggressive pituitary tumors.

## Abstract

Aggressive pituitary tumours (APT) and pituitary carcinomas (PC) are rare pituitary neoplasms and occur more frequently in men. Corticotroph and lactotroph tumours represent the most frequent secreting subtypes, showing different sex-related distribution, clinical features, and behaviour compared with benign disease. This review evaluates whether these sex-related differences persist in APT/PC and their clinical and therapeutic implications.

A literature review of case reports, series, and clinical studies, published between 2000 and October 2025, reporting sex-related data on corticotroph and lactotroph APT/PC, was conducted. Clinical presentation, pathological features, and outcomes were extracted and analysed by sex.

93 corticotroph APT/PC (38 W, 55 M) and 80 lactotroph APT/PC (29 W, 51 M) were included. Among corticotroph APT/PC, men more commonly had non-functioning lesions (36.5%, vs. 17.6%), showed loss of hormonal secretion (7.7%, n = 4/52), and had invasive disease (100%, vs. 73.3%, p: 0.03). Women more frequently harboured Crooke’s cell tumours (26.3% vs. 5.5%, p: 0.006) and showed complete radiological responses (22.2%, vs. 9.1%). In lactotroph APT/PC, men had giant tumours (27.3%, vs. 5.0%), invasive disease (83.3%, vs. 63.6%), higher prolactin levels, and dopamine agonist resistance. Complete tumour responses to temozolomide occurred exclusively in women (22.7%, n = 5/22, p: 0.02), whereas partial durable responses predominated in men (46.2%, n = 18/39).

Male sex is associated with higher prevalence and more aggressive disease, whereas women achieve more profound tumour and hormonal responses. Sex-specific stratification may support personalized management of these rare pituitary tumours.

The online version contains supplementary material available at 10.1007/s11102-026-01656-y.

## Linked entities

- **Chemicals:** temozolomide (PubChem CID 5394), dopamine (PubChem CID 681)

## Full-text entities

- **Genes:** PGR (progesterone receptor) [NCBI Gene 5241] {aka NR3C3, PR}, USP8 (ubiquitin specific peptidase 8) [NCBI Gene 9101] {aka HumORF8, PITA4, SPG59, UBPY}, VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422] {aka L-VEGF, MVCD1, VEGF, VPF}, MIB1 (MIB E3 ubiquitin protein ligase 1) [NCBI Gene 57534] {aka DIP-1, DIP1, LVNC7, MIB, ZZANK2, ZZZ6}, GGH (gamma-glutamyl hydrolase) [NCBI Gene 8836] {aka GATD10, GH}, TP53 (tumor protein p53) [NCBI Gene 7157] {aka BCC7, BMFS5, LFS1, P53, TRP53}, MTOR (mechanistic target of rapamycin kinase) [NCBI Gene 2475] {aka FRAP, FRAP1, FRAP2, RAFT1, RAPT1, SKS}, SF3B1 (splicing factor 3b subunit 1) [NCBI Gene 23451] {aka Hsh155, MDS, PRP10, PRPF10, SAP155, SF3b155}, ESR1 (estrogen receptor 1) [NCBI Gene 2099] {aka ER, ESR, ESRA, ESTRR, Era, NR3A1}, PRL (prolactin) [NCBI Gene 5617] {aka GHA1, pPRL}
- **Diseases:** Metastatic disease (MESH:D000092182), SD (MESH:D060050), Tumour (MESH:D009369), Aggressive pituitary tumours (MESH:D010911), PD (MESH:D010300), impaired vision and visual field (MESH:D014786), benign disease (MESH:D004194), NF (MESH:C536126), CR (MESH:D001766), hypercortisolism (MESH:D003480), adenomas (MESH:D000236), Nelson's syndrome (MESH:D009347), PR (MESH:D004828), Crooke cell tumours (MESH:D018295), lactotroph (MESH:D015175), osteoporosis (MESH:D010024), vertebral fractures (MESH:C535781), pituitary apoplexy (MESH:D010899), death (MESH:D003643), pituitary diseases (MESH:D010900), Metastases (MESH:D009362), invasive (MESH:D009361), aggressive (MESH:D010554), CD (MESH:D047748), Corticotroph (MESH:D049913)
- **Chemicals:** cortisol (MESH:D006854), tamoxifen (MESH:D013629), octreotide (MESH:D015282), lapatinib (MESH:D000077341), BVZ (MESH:D000068258), ipilimumab (MESH:D000074324), pembrolizumab (MESH:C582435), TMZ (MESH:D000077204), mitotane (MESH:D008939), NA (MESH:D012964), everolimus (MESH:D000068338), carboplatin (MESH:D016190), CHT (-), nivolumab (MESH:D000077594), dopamine (MESH:D004298), steroid (MESH:D013256)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** F298L, F in 3

## Full text

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## Figures

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Source: https://tomesphere.com/paper/PMC12967545