Evidence map›Paper›PMID 31043952›Full record

ArticleCase reports in oncology

Highly Aggressive and Radiation-Resistant, "Atypical" and Silent Pituitary Corticotrophic Carcinoma: A Case Report and Review of the Literature.

Laura Flores, Richard Sleightholm, Beth Neilsen, Michael Baine, Andjela Drincic, William Thorell, Nicole Shonka, David Oupicky, Chi Zhang

Open access · goldAbstract readCase Reports
In one paragraph

Article in Case reports in oncology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 33% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

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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

9 authors at 1 institution in 1 country.

Laura FloresCollege of Allied Health Professionals, University of Nebraska Medical Center, Omaha, Nebraska, USA.
Richard SleightholmDepartment of Radiation Oncology, University of Nebraska Medical Center, Omaha, Nebraska, USA.
Beth NeilsenDepartment of Radiation Oncology, University of Nebraska Medical Center, Omaha, Nebraska, USA.
Michael BaineDepartment of Radiation Oncology, University of Nebraska Medical Center, Omaha, Nebraska, USA.
Andjela DrincicDivision of Endocrinology, Department of Medicine, University of Nebraska Medical Center, Omaha, Nebraska, USA.
William ThorellDivision of Neurosurgery, Department of Surgery, University of Nebraska Medical Center, Omaha, Nebraska, USA.
Nicole ShonkaDivision of Oncology/Hematology, Department of Internal Medicine, University of Nebraska Medical Center, Omaha, Nebraska, USA.
David OupickyCenter for Drug Delivery and Nanomedicine, Department of Pharmaceutical Sciences, University of Nebraska Medical Center, Omaha, Nebraska, USA.
Chi ZhangDepartment of Radiation Oncology, University of Nebraska Medical Center, Omaha, Nebraska, USA.
University of Nebraska Medical Center · US

Funding

Discovering Vulnerabilities in Ras-driven CancersF30CA203397 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI NEILSEN, BETH · 2016 to 2019
$165k
NCI NIH HHS F30 CA203397
6 · The paper itself

Abstract

backgroundPituitary tumors typically remain silent unless interaction with nearby structures occurs. Rare subsets of pituitary tumors display aggressive phenotypes: highly mitotic, locally invasive, metastatic, chemotherapy and radiation resistant, etc. Disease progression and response to therapy is ill-defined in these subtypes, and their true prognostic potential is debated. Thus, identifying tumor characteristics with prognostic value and efficacious treatment options remains a challenge in aggressive pituitary tumors. CASE PRESENTATION: A 45-year-old female presented with a nonfunctioning corticotropic pituitary macroadenoma with biomarkers suggestive of an "atypical" subtype: Ki-67 of 8-12%, increased mitosis, and locally invasive. Despite resections and radiation, growth continued, eventually affecting her vision. Although histologically ACTH positive, the patient remained clinically asymptomatic. Twelve months later, an episode of Cushing's disease-induced psychosis prompted a PET-CT scan, identifying sites of metastasis. Temozolomide was added to her medical regimen, and her metastatic liver lesions and boney metastases were treated with radiofrequency ablation and stereotactic body radiation therapy, respectively. Systemic treatment resulted in a drop in her ACTH levels, with her most recent scans/labs at 12 months following RFA suggesting remission.

conclusionsThis is a unique presentation of a pituitary tumor, displaying characteristics of both clinically silent corticotropic and "atypical" macroadenoma subtypes. Although initially ACTH positive while clinically silent, the patient's disease ultimately recurred metastatically with manifestations of Cushing's disease and psychosis. With the addition of temozolomide to her treatment plan, her primary and metastatic sites have responded favorably to radiation therapy. Thus, the addition of temozolomide may be beneficial in the treatment of aggressive pituitary tumors.

Indexed as

Cushing's diseaseEndocrinePituitary adenomaRadiotherapyTemozolomide

Identifiers

PMID31043952
PMCPMC6477470
OpenAlexW2912308296

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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 OpenQuestion graph.