Evidence map›Paper›PMID 28900805›Full record

ArticlePituitary2017

MGMT and MSH6 immunoexpression for functioning pituitary macroadenomas.

Alexander S G Micko, Adelheid Wöhrer, Romana Höftberger, Greisa Vila, Christine Marosi, Engelbert Knosp, Stefan Wolfsberger

Abstract read
In one paragraph

Article in Pituitary, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

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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

12 citing papers in PubMed.

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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

7 authors.

Alexander S G MickoDepartment of Neurosurgery, Medical University Vienna, Waehringer Guertel 18-20, 1097, Vienna, Austria.
Adelheid WöhrerInstitute of Neurology, Medical University Vienna, Vienna, Austria.
Romana HöftbergerInstitute of Neurology, Medical University Vienna, Vienna, Austria.
Greisa VilaDivision of Endocrinology and Metabolism, Department of Internal Medicine III, Medical University Vienna, Vienna, Austria.
Christine MarosiDivision of Oncology, Department of Internal Medicine I, Medical University of Vienna, Vienna, Austria.
Engelbert KnospDepartment of Neurosurgery, Medical University Vienna, Waehringer Guertel 18-20, 1097, Vienna, Austria. engelbert.knosp@meduniwien.ac.at.
Stefan WolfsbergerDepartment of Neurosurgery, Medical University Vienna, Waehringer Guertel 18-20, 1097, Vienna, Austria.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeKnowledge of biological behavior is crucial for clinical management of functioning pituitary macroadenomas. For recurrent cases unresponsive to standard treatment, temozolomide (TMZ) has been used as a therapeutic alternative. MGMT (O6-methyl-guanine-DNA methyltransferase) and MSH6 (mutS homolog 6) immunoexpression have been linked to the response to TMZ treatment and MGMT immunoexpression has been additionally linked to early recurrence of non-functioning pituitary adenomas. The aim of this study was to assess the prognostic value of MGMT and MSH6 immunoexpression for aggressive functioning pituitary adenomas.

methodsThe study cohort comprised a single center series of 76 patients who underwent an operation for functioning pituitary macroadenoma. We retrospectively compared 38 patients with postoperative persistent or recurrent disease with another set of 38 patients who were in endocrine remission.

resultsLow-to-moderate MGMT immunoexpression (<50%) was significantly more frequent in the group with persistent/recurrent disease than in cases of endocrine remission (66 vs. 21%, p < 0.001). Furthermore, adenomas with low-to-moderate MGMT immunoexpression were significantly more often recurrent (76 vs. 30%, p < 0.001) and invasive (64 vs. 28%, p = 0.002).

conclusionIn our series, low-to-moderate MGMT immunoexpression was the only marker that significantly correlated with surgical invasiveness and recurrence in functioning pituitary macroadenomas. Therefore, in the future, MGMT status may be considered an additional marker for understanding the biological behavior of pituitary adenomas.

Indexed as

AdultAntineoplastic Agents, AlkylatingDacarbazineDNA-Binding ProteinsDNA Modification MethylasesDNA Repair EnzymesFemaleHumansMaleMiddle AgedNeoplasm Recurrence, LocalO(6)-Methylguanine-DNA MethyltransferasePituitary NeoplasmsRetrospective StudiesTemozolomideTumor Suppressor ProteinsAntineoplastic Agents, AlkylatingDacarbazineDNA-Binding ProteinsDNA Modification MethylasesDNA Repair EnzymesG-T mismatch-binding proteinMGMT protein, humanO(6)-Methylguanine-DNA MethyltransferaseTemozolomideTumor Suppressor ProteinsAggressive pituitary adenomaMGMTMSH6TMZ

Identifiers

PMID28900805
PMCPMC5655586

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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.