# Temozolomide in aggressive and metastatic pituitary tumors: a Brazilian multicenter real-world cohort study

**Authors:** Isabelle Pinheiro Amaro de Magalhães, Camila Regina Pereira Batista de Macedo, Luciana Ansaneli Naves, Mauro Antonio Czepielewski, Isabella Naves Rosa, Lidiana Bandeira de Santana, Tobias Skrebsky de Almeida, Mario Padula, Paula Condé Lamparelli Elias, Margaret de Castro, Leandro Kasuki, Monica Roberto Gadelha, Carolina Garcia Soares Leães Rech, Heraldo Mendes Garmes, Cesar Luiz Boguszewski, Raquel Soares Jallad, Marilena Nakaguma, Maria Candida Barisson Villares Fragoso, Marcio Carlos Machado, Andrea Glezer, Malebranche Berardo Carneiro da Cunha Neto, Olavo Feher, Rafael Loch Batista

PMC · DOI: 10.1007/s11102-026-01663-z · Pituitary · 2026-03-27

## TL;DR

This study evaluates how well temozolomide works and is tolerated in treating aggressive pituitary tumors in Brazil, finding it effective and safe.

## Contribution

Provides real-world evidence on temozolomide's efficacy and safety in aggressive/metastatic pituitary tumors in a Latin American cohort.

## Key findings

- Temozolomide achieved 93.3% radiological disease control in aggressive/metastatic pituitary tumors.
- Biochemical disease control was observed in 81.2% of functioning tumors.
- Temozolomide was associated with an acceptable safety profile, with common adverse events being nausea and myelotoxicity.

## Abstract

To evaluate the real-world efficacy and safety of temozolomide (TMZ) in aggressive and metastatic pituitary neuroendocrine tumors in a Latin American setting, and to address whether TMZ achieves meaningful radiological and biochemical disease control with acceptable toxicity.

We conducted a retrospective multicenter study across Brazilian reference centers including patients with aggressive/metastatic pituitary adenomas treated with TMZ and followed for ≥ 6 months. The radiological response was assessed via RECIST 1.1. For functioning pituitary adenomas, biochemical response was assessed using prespecified hormonal criteria. Adverse events were collected from medical records.

Thirty patients were included (mean age 29.5 years; 53% female). All the tumors were macroadenomas, and 56% were giant (> 4 cm). Twenty-one pituitary adenomas were functioning and four were metastatic. Ki-67 was > 3% in 73% of the patients. The mean time from diagnosis to TMZ initiation was 102 months. The radiological disease control rate (partial response or stable disease) was 93.3%. Among functioning tumors, the biochemical disease control rate was 81.2%, with an objective biochemical response rate (complete + partial response) of 68.8%. Adverse events, most commonly nausea and myelotoxicity, occurred in 66% of patients.

In this multicenter Brazilian real-world cohort, TMZ provided high radiological and biochemical disease control with an acceptable safety profile, suggesting that TMZ is the preferred first-line systemic chemotherapy for aggressive/metastatic pituitary adenomas after the failure of standard therapies.

## Linked entities

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

## Full-text entities

- **Genes:** IGF1 (insulin like growth factor 1) [NCBI Gene 3479] {aka IGF, IGF-I, IGFI, MGF}, MGMT (O-6-methylguanine-DNA methyltransferase) [NCBI Gene 4255], TBX19 (T-box transcription factor 19) [NCBI Gene 9095] {aka TBS19, TPIT, dJ747L4.1}, 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}, SST (somatostatin) [NCBI Gene 6750] {aka SMST, SST1}, PGR (progesterone receptor) [NCBI Gene 5241] {aka NR3C3, PR}, POU1F1 (POU class 1 homeobox 1) [NCBI Gene 5449] {aka CPHD1, GHF-1, PIT1, POU1F1a, Pit-1}, PRL (prolactin) [NCBI Gene 5617] {aka GHA1, pPRL}, TPI1 (triosephosphate isomerase 1) [NCBI Gene 7167] {aka HEL-S-49, TIM, TPI, TPID}, POMC (proopiomelanocortin) [NCBI Gene 5443] {aka ACTH, CLIP, LPH, MSH, NPP, OBAIRH}
- **Diseases:** vomiting (MESH:D014839), thrombocytopenia (MESH:D013921), Hematological toxicity (MESH:D006402), hematologic malignancies (MESH:D019337), headache (MESH:D006261), gastrointestinal (MESH:D005767), aplastic anemia (MESH:D000741), fatigue (MESH:D005221), Prolactinomas (MESH:D015175), cutaneous reactions (MESH:D017445), ACTH-secreting tumors (MESH:D049913), neutropenia (MESH:D009503), SD (MESH:D060050), cytotoxicity (MESH:D064420), brain tumors (MESH:D001932), Crooke (MESH:C536852), asthenia (MESH:D001247), deaths (MESH:D003643), acromegaly (MESH:D000172), aggressiveness (MESH:D010554), Cancer (MESH:D009369), metastases (MESH:D009362), somatotroph tumors (MESH:D049912), Pituitary neuroendocrine tumors (MESH:D018358), Nausea (MESH:D009325), Cushing disease (MESH:D047748), APTs (MESH:D010911), PD (MESH:D018450)
- **Chemicals:** ketoconazole (MESH:D007654), cabergoline (MESH:D000077465), TMZ (MESH:D000077204), octreotide (MESH:D015282), PR (-), cortisol (MESH:D006854)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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Source: https://tomesphere.com/paper/PMC13031238