Evidence map›Paper›PMID 32154490›Full record

ArticleJournal of the Endocrine Society2020

Leptomeningeal Metastasis from Adrenocortical Carcinoma: A Case Report.

Anna R Schreiber, Adwitiya Kar, Andrew E Goodspeed, Nikita Pozdeyev, Hilary Somerset, Christopher D Raeburn, Aik-Choon Tan, Stephen Leong, Margaret E Wierman, Katja Kiseljak-Vassiliades

Open access · goldAbstract readCase Reports
In one paragraph

Article in Journal of the Endocrine Society, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
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

10 authors at 4 institutions in 1 country.

Anna R SchreiberDepartment of Medicine, University of Colorado, Aurora, Colorado.
Adwitiya KarDivision of Endocrinology, Metabolism and Diabetes, Department of Medicine, University of Colorado, Aurora, Colorado.
Andrew E GoodspeedDepartment of Pharmacology, University of Colorado, Aurora, Colorado.
Nikita PozdeyevDivision of Endocrinology, Metabolism and Diabetes, Department of Medicine, University of Colorado, Aurora, Colorado.
Hilary SomersetDepartment of Pathology, University of Colorado Anschutz Medical Campus, Aurora Colorado.
Christopher D RaeburnDepartment of Surgery, University of Colorado Anschutz Medical Campus, Aurora Colorado.
Aik-Choon TanDivision of Medical Oncology, Department of Medicine, University of Colorado Anschutz Medical Campus, Aurora Colorado.
Stephen LeongUniversity of Colorado Cancer Center, Aurora, Colorado.
Margaret E WiermanDivision of Endocrinology, Metabolism and Diabetes, Department of Medicine, University of Colorado, Aurora, Colorado.
Katja Kiseljak-VassiliadesDivision of Endocrinology, Metabolism and Diabetes, Department of Medicine, University of Colorado, Aurora, Colorado.ORCID 0000-0003-3341-582X
University of Colorado Anschutz Medical Campus · USUniversity of Colorado Cancer Center · USVeterans Health Administration · USMoffitt Cancer Center · US

Funding

Identifying and Characterizing Therapeutic Targets in Adrenal CancerK08CA222620 · NCI · UNIVERSITY OF COLORADO DENVER · PI KISELJAKVASSILIADES, KATJA · 2018 to 2022
$1.0M
Role of the Sterile20 (Ste20)-like kinase MST4 in Pituitary TumorigenesisI01BX001876 · VA · VA EASTERN COLORADO HEALTH CARE SYSTEM · PI WIERMAN, MARGARET E · 2014 to 2017
–
Targeting Kinases in Novel Preclinical Models of Adrenocortical CarcinomaI01BX004665 · VA · VA EASTERN COLORADO HEALTH CARE SYSTEM · PI KISELJAKVASSILIADES, KATJA, WIERMAN, MARGARET E · 2019 to 2024
–
BLRD VA I01 BX001876BLRD VA I01 BX004665NCI NIH HHS K08 CA222620
6 · The paper itself

Abstract

Adrenocortical carcinoma (ACC) is an uncommon endocrine malignancy with limited treatment options. While the overall 5-year survival rate in patients with ACC is 35%, the disease is often rapidly progressive with long-term survival in only 5% of patients. Although tumor stage, grade, and excess hormonal activity predict unfavorable prognosis, additional biomarkers are needed to identify patients with aggressive disease. A 23-year-old woman presented with rapidly progressing signs and symptoms of Cushing's syndrome, with associated abdominal pain and fullness. Evaluation revealed a large left adrenal mass which had developed over 8 months. En bloc surgical resection was performed by an endocrine surgeon, and pathology revealed adrenocortical carcinoma with Ki67 of 60%. Despite adjuvant treatment with mitotane and etoposide-doxorubicin-carboplatin chemotherapy, the patient had rapid disease progression with metastatic spread to liver, lung, bone, brain, and leptomeningies, and she died 11 months after the initial diagnosis. Subsequent analysis of the patient's tumor revealed mutations in

Indexed as

adrenocortical carcinomaleptomeningeal metastasis

Identifiers

PMID32154490
PMCPMC7053406
OpenAlexW3009780197

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.