Evidence map›Paper›PMID 41760838›Full record

ArticleChild's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery2026

Evaluating temozolomide for pediatric adamantinomatous craniopharyngiomas using microspheroid-based drug screening.

Sérgio Cavalheiro, Lorena Favaro Pavon, Caroline Brunetto de Farias, Nasjla Saba da Silva, Flávia Borelli Nascimento, Tatiana Tais Sibov, Jessica Benigno Rodrigues, Patrícia Alesssandra Dastoli, Fernando Seiji Suzuki, Rodrigo Akira Watanabe and 5 more

Abstract read
In one paragraph

Article in Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors.

Sérgio CavalheiroTranslacional Neurosurgery Laboratory, Department of Neurology and Neurosurgery, Universidade Federal de Sao Paulo (UNIFESP), São Paulo, SP, Brazil.
Lorena Favaro PavonTranslacional Neurosurgery Laboratory, Department of Neurology and Neurosurgery, Universidade Federal de Sao Paulo (UNIFESP), São Paulo, SP, Brazil.
Caroline Brunetto de FariasNational Science and Technology Institute for Children's Cancer Biology and Pediatric Oncology - INCT BioOncoPed, Porto Alegre, Brazil.
Nasjla Saba da SilvaPediatric Oncology Institute, Grupo de Apoio Ao Adolescente E À Criança Com Câncer (GRAACC), Universidade Federal de Sao Paulo (UNIFESP), São Paulo, SP, Brazil.
Flávia Borelli NascimentoTranslacional Neurosurgery Laboratory, Department of Neurology and Neurosurgery, Universidade Federal de Sao Paulo (UNIFESP), São Paulo, SP, Brazil.
Tatiana Tais SibovTranslacional Neurosurgery Laboratory, Department of Neurology and Neurosurgery, Universidade Federal de Sao Paulo (UNIFESP), São Paulo, SP, Brazil.
Jessica Benigno RodriguesPediatric Oncology Institute, Grupo de Apoio Ao Adolescente E À Criança Com Câncer (GRAACC), Universidade Federal de Sao Paulo (UNIFESP), São Paulo, SP, Brazil.
Patrícia Alesssandra DastoliTranslacional Neurosurgery Laboratory, Department of Neurology and Neurosurgery, Universidade Federal de Sao Paulo (UNIFESP), São Paulo, SP, Brazil.
Fernando Seiji SuzukiTranslacional Neurosurgery Laboratory, Department of Neurology and Neurosurgery, Universidade Federal de Sao Paulo (UNIFESP), São Paulo, SP, Brazil.
Rodrigo Akira WatanabeTranslacional Neurosurgery Laboratory, Department of Neurology and Neurosurgery, Universidade Federal de Sao Paulo (UNIFESP), São Paulo, SP, Brazil.
Isaque Hyung Tong KimTranslacional Neurosurgery Laboratory, Department of Neurology and Neurosurgery, Universidade Federal de Sao Paulo (UNIFESP), São Paulo, SP, Brazil.
Martina LichtenfelsDepartment of Translational Research, Ziel Biosciences, Porto Alegre, Rio Grande Do Sul, Brazil.
Camila Alves da SilvaDepartment of Translational Research, Ziel Biosciences, Porto Alegre, Rio Grande Do Sul, Brazil.
Andrea CappellanoPediatric Oncology Institute, Grupo de Apoio Ao Adolescente E À Criança Com Câncer (GRAACC), Universidade Federal de Sao Paulo (UNIFESP), São Paulo, SP, Brazil.
Marcos Devanir Silva da CostaPediatric Oncology Institute, Grupo de Apoio Ao Adolescente E À Criança Com Câncer (GRAACC), Universidade Federal de Sao Paulo (UNIFESP), São Paulo, SP, Brazil. marcoscostaneuro@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposePediatric adamantinomatous craniopharyngioma (ACP) is the most common tumor of the diencephalic-pituitary axis in children. Although histologically benign, pediatric ACP is frequently associated with substantial endocrine dysfunction and neurological complications. The gold-standard treatment is complete surgical resection; however, because of the tumor's location, total removal is often not feasible. Consequently, several authors recommend radiotherapy as an adjuvant option. Nevertheless, partial resections are frequently followed by recurrence, and repeated surgical interventions increase morbidity and impair quality of life. Thus, adjuvant therapeutic strategies capable of controlling this tumor should be encouraged.

methodsWe analyzed seven fresh tumor specimens ACP from patients < 18 years of age using a chemoresistance platform (Bioverso Test, Ziel Biosciences, São Paulo, Brazil). These cases demonstrated widespread resistance to most chemotherapeutic agents tested. Temozolomide (500 µM) was the only drug that showed consistent and significant sensitivity.

resultsBased on these findings, we initiated treatment in a 14-year-old patient with recurrent ACP who had previously undergone multiple surgical procedures and radiotherapy. The tumor involved the left cavernous sinus and extended into the sphenoid sinus. Clinically, the patient was amaurotic and presented with panhypopituitarism. The patient received temozolomide (200 mg/m

conclusionThese findings suggest that temozolomide may represent a promising therapeutic option for controlling ACP.

Indexed as

Antineoplastic Agents, AlkylatingCraniopharyngiomaPituitary NeoplasmsTemozolomideAdolescentChildChild, PreschoolDrug Screening Assays, AntitumorFemaleHumansMaleAntineoplastic Agents, AlkylatingTemozolomideChemoresistanceCraniopharyngiomasHypothalamusMGMT expressionPediatric neuro-oncology

Identifiers

PMID41760838
PMCPMC12948842

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.