Evidence map›Paper›PMID 31401793›Full record

ArticlePituitary2019

Clinical, pathologic, and imaging characteristics of pituitary null cell adenomas as defined according to the 2017 World Health Organization criteria: a case series from two pituitary centers.

Joao Paulo Almeida, Corbin C Stephens, Jennifer M Eschbacher, Michelle M Felicella, Kevin C J Yuen, William L White, Michael A Mooney, Anne Laure Bernat, Ozgur Mete, Gelareh Zadeh and 2 more

Abstract read
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Article in Pituitary, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
3.3field-weighted citation impact, top 7% of its field
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

29 citing papers in PubMed, 41 citations in OpenAlex.

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  7. Associations ofFrontiers in endocrinology · 2025
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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

12 authors at 4 institutions in 2 countries.

Joao Paulo AlmeidaDivision of Neurosurgery, Toronto Western Hospital, University Health Network, University of Toronto, Toronto, ON, Canada.
Corbin C StephensDepartment of Neurosurgery, Barrow Neurological Institute, Phoenix, AZ, USA.
Jennifer M EschbacherDepartment of Neuropathology, Barrow Neurological Institute, Phoenix, AZ, USA.
Michelle M FelicellaDepartment of Neuropathology, Barrow Neurological Institute, Phoenix, AZ, USA.
Kevin C J YuenDepartment of Neuroendocrinology, Barrow Neurological Institute, Phoenix, AZ, USA.
William L WhiteDepartment of Neurosurgery, Barrow Neurological Institute, Phoenix, AZ, USA.
Michael A MooneyDepartment of Neurosurgery, Barrow Neurological Institute, Phoenix, AZ, USA.
Anne Laure BernatDivision of Neurosurgery, Toronto Western Hospital, University Health Network, University of Toronto, Toronto, ON, Canada.
Ozgur MeteLaboratory Medicine Program, Department of Pathology, University Health Network, University of Toronto, Toronto, ON, Canada.
Gelareh ZadehDivision of Neurosurgery, Toronto Western Hospital, University Health Network, University of Toronto, Toronto, ON, Canada.
Fred GentiliDivision of Neurosurgery, Toronto Western Hospital, University Health Network, University of Toronto, Toronto, ON, Canada.
Andrew S LittleDepartment of Neurosurgery, Barrow Neurological Institute, Phoenix, AZ, USA. Neuropub@barrowneuro.org.
Barrow Neurological Institute · USUniversity Health Network · CAToronto Western Hospital · CAUniversity of Toronto · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe 2017 World Health Organization classification of pituitary tumors redefined pituitary null cell adenomas (NCAs) by restricting this diagnostic category to pituitary tumors that are negative for pituitary transcription factors and adenohypophyseal hormones. The clinical behavior of this redefined entity has not been widely studied, and this is a major shortcoming of the classification. This study evaluated the imaging and clinical features of NCAs from two pituitary centers and compared them with those of gonadotroph adenomas (GAs).

methodsImaging, pathologic, and clinical characteristics of NCAs and GAs were retrospectively reviewed. Tumor immunohistochemistry was performed to confirm absence of adenohypophyseal hormones and pituitary transcription factor expression.

resultsThirty-one NCAs were compared with 38 GAs. NCAs were more likely to invade the cavernous sinus (15/31 [48%] vs. 5/38 [13%], P = .003) and had a higher proliferative index (i.e., MIB-1 > 3%, 11/31 [35%] vs. 5/38 [13%], P = .04). Gross total resection was less likely in the NCA group (19/31 [61%] vs. 33/38 [87], P = .02). Progression-free survival was worse in the NCA cohort (5-year progression-free survival, 0.70 vs. 1.00; P = .011, by log-rank test).

conclusionsCompared with GAs, NCAs are more invasive at the time of presentation and have a more aggressive clinical course. This study provides evidence that NCAs represent a distinct clinicopathologic entity with behavior that differs adversely from that of GAs. This may inform clinical decision-making, including frequency of postoperative tumor surveillance and timing of adjunctive treatments.

Indexed as

FemaleHumansImmunohistochemistryKaplan-Meier EstimateLymphocytes, NullMalePituitary DiseasesPituitary GlandPituitary NeoplasmsProgression-Free SurvivalRetrospective StudiesWorld Health OrganizationGonadotroph adenomaGonadotroph tumorsNull cell adenomaNull cell pituitary tumor pituitary

Identifiers

PMID31401793
OpenAlexW2968073145

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Registered trials

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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.