Evidence map›Paper›PMID 40074342›Full record

ArticleEndocrine journal2025

Status of temozolomide use without insurance coverage in patients with aggressive pituitary neuroendocrine tumors.

Atsushi Ishida, Naoko Inoshita, Noriaki Tanabe, Koji Takano, Hideki Shiramizu, Haruko Yoshimoto, Masataka Kato, Go Matsuoka, Shozo Yamada

Abstract read
In one paragraph

Article in Endocrine journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Atsushi IshidaHypothalamic & Pituitary Center, Moriyama Memorial Hospital, Tokyo 134-0081, Japan.ORCID http://orcid.org/0000-0003-3492-4845
Naoko InoshitaDepartment of Pathology, Moriyama Memorial Hospital, Tokyo 134-0081, Japan.ORCID http://orcid.org/0000-0002-5459-3388
Noriaki TanabeDepartment of Pathology, Moriyama Memorial Hospital, Tokyo 134-0081, Japan.
Koji TakanoDepartment of Endocrinology, Moriyama Memorial Hospital, Tokyo 134-0081, Japan.
Hideki ShiramizuHypothalamic & Pituitary Center, Moriyama Memorial Hospital, Tokyo 134-0081, Japan.
Haruko YoshimotoHypothalamic & Pituitary Center, Moriyama Memorial Hospital, Tokyo 134-0081, Japan.
Masataka KatoHypothalamic & Pituitary Center, Moriyama Memorial Hospital, Tokyo 134-0081, Japan.
Go MatsuokaHypothalamic & Pituitary Center, Moriyama Memorial Hospital, Tokyo 134-0081, Japan.ORCID http://orcid.org/0000-0003-0417-1432
Shozo YamadaHypothalamic & Pituitary Center, Moriyama Memorial Hospital, Tokyo 134-0081, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The 2017 World Health Organization classification described aggressive pituitary neuroendocrine tumor (PitNET) as "a tumor with strong invasiveness and rapid growth, which is difficult to treat with surgery, radiation therapy, or drug therapy," which remains a challenge in the treatment of pituitary tumors. Currently, temozolomide (TMZ) is the first-line treatment for aggressive PitNET. However, it is not yet covered by insurance in Japan. Additionally, O6-Methylguanine-DNA Methyltransferase (MGMT) expression can lead to treatment resistance, further complicating treatment selection. We previously demonstrated the effectiveness of combination therapy with capecitabine (CAPTEM) in several cases of aggressive PitNETs. The present study described our experiences with TMZ in 13 patients with aggressive PitNETs (including four patients administered CAPTEM). Pathological examination revealed eight corticotroph, four lactotroph, and one somatotroph tumors. Of these, seven patients are still receiving treatment, and six patients have terminated treatment. The reasons for discontinuation were poor efficacy (three patients), financial reasons (two patients), and patient preference (one patient). No patients required treatment discontinuation owing to adverse events. Furthermore, one case of a lactotroph tumor, which achieved remission with CAPTEM but was discontinued after three years for financial reasons, remains in remission on imaging and maintained normal PRL levels for 15 months after discontinuation. The most significant issue is off-label use. Concern exists that financial constraints may prevent future patients from using TMZ.

Indexed as

Antineoplastic Agents, AlkylatingInsurance CoverageNeuroendocrine TumorsPituitary NeoplasmsTemozolomideAdultAgedFemaleHumansJapanMaleMiddle AgedTreatment OutcomeAntineoplastic Agents, AlkylatingTemozolomideAggressive pituitary neuroendocrine tumorCapecitabineO6 methylguanine DNA methyltransferaseTemozolomide

Identifiers

PMID40074342
PMCPMC12260192

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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 OpenQuestion graph.