Evidence map›Paper›PMID 26285571›Full record

ArticleActa neuropathologica communications2015

Histological criteria for atypical pituitary adenomas - data from the German pituitary adenoma registry suggests modifications.

Christian P Miermeister, Stephan Petersenn, Michael Buchfelder, Rudolf Fahlbusch, Dieter K Lüdecke, Annett Hölsken, Markus Bergmann, Hans Ulrich Knappe, Volkmar H Hans, Jörg Flitsch and 2 more

Erratum issuedAbstract read
In one paragraph

Article in Acta neuropathologica communications, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 58 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed, 2 pooled it
–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

58 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors.

Christian P MiermeisterDepartments of Neuropathology, Friedrich-Alexander University Erlangen-Nürnberg (FAU), Schwabachanlage 6, 91054, Erlangen, Germany.
Stephan PetersennENDOC Center for Endocrine Tumors, Hamburg & University of Duisburg-Essen, Essen, Germany.
Michael BuchfelderDepartments of Neurosurgery, Friedrich-Alexander University Erlangen-Nürnberg (FAU), Erlangen, Germany.
Rudolf FahlbuschDepartment of Neurosurgery, International Neuroscience Institute, Hannover, Germany.
Dieter K LüdeckeDepartments of Neurosurgery, University Clinic Hamburg-Eppendorf, Hamburg, Germany.
Annett HölskenDepartments of Neuropathology, Friedrich-Alexander University Erlangen-Nürnberg (FAU), Schwabachanlage 6, 91054, Erlangen, Germany.
Markus BergmannDepartment of Neuropathology, Klinikum Bremen Mitte, Bremen, Germany.
Hans Ulrich KnappeDepartment of Neurosurgery, Johannes Wesling Hospital Minden, Minden, Germany.
Volkmar H HansDepartment of Pathology, Ruhr University Bochum, Bochum, Germany.
Jörg FlitschDepartments of Neurosurgery, University Clinic Hamburg-Eppendorf, Hamburg, Germany.
Wolfgang SaegerDepartments of Neuropathology, University Clinic Hamburg-Eppendorf, Hamburg, Germany.
Rolf BusleiDepartments of Neuropathology, Friedrich-Alexander University Erlangen-Nürnberg (FAU), Schwabachanlage 6, 91054, Erlangen, Germany. rolf.buslei@uk-erlangen.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe term atypical pituitary adenoma (APA) was revised in the 2004 World Health Organization (WHO) classification of pituitary tumors. However, two of the four parameters required for the diagnosis of APAs were formulated rather vaguely (i.e., "extensive" nuclear staining for p53; "elevated" mitotic index). Based on a case-control study using a representative cohort of typical pituitary adenomas and APAs selected from the German Pituitary Tumor Registry, we aimed to obtain reliable cut-off values for both p53 and the mitotic index. In addition, we analyzed the impact of all four individual parameters (invasiveness, Ki67-index, p53, mitotic index) on the selectivity for differentiating both adenoma subtypes.

methodsOf the 308 patients included in the study, 98 were diagnosed as APAs (incidence 2.9 %) and 10 patients suffered from a pituitary carcinoma (incidence 0.2 %). As a control group, we selected 200 group matched patients with typical pituitary adenomas (TPAs). Cut-off values were attained using ROC analysis.

resultsWe determined significant threshold values for p53 (≥2 %; AUC: 0.94) and the mitotic index (≥2 mitosis within 10 high power fields; AUC: 0.89). The most reliable individual marker for differentiating TPAs and APAs was a Ki-67-labeling index ≥ 4 % (AUC: 0.98). Using logistic regression analysis (LRA) we were able to show that all four criteria (Ki-67 (p < 0.001); OR 5.2// p53 (p < 0.001); OR 3.1// mitotic index (p < 0.001); OR 2.1// invasiveness (p < 0.001); OR 8.2)) were significant for the group of APAs. Furthermore, we describe the presence of nucleoli as a new favorable parameter for TPAs (p = 0.008; OR: 0.4; CI95 %: 0.18; 0.77).

conclusionsHere we present a proposed rectification of the current WHO classification of pituitary tumors describing an additional marker for TPA and specific threshold values for p53 and the mitotic index. This will greatly help in the reliable diagnosis of APAs and facilitate further studies to ascertain the prognostic relevance of this categorization.

Indexed as

RegistriesAdenomaAdolescentAdultAgedAged, 80 and overFemaleGermanyHumansKi-67 AntigenLogistic ModelsMaleMiddle AgedPituitary NeoplasmsRetrospective StudiesROC CurveKi-67 AntigenTumor Suppressor Protein p53

Identifiers

PMID26285571
PMCPMC4545559

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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.