Evidence map›Paper›PMID 29330226›Full record

ArticleEuropean journal of endocrinology2018

Mitotane treatment in patients with metastatic testicular Leydig cell tumor associated with severe androgen excess.

Vasileios Chortis, Nicholas J Johal, Irina Bancos, Matthew Evans, Kassiani Skordilis, Peter Guest, Michael H Cullen, Emilio Porfiri, Wiebke Arlt

Open access · hybridAbstract readCase Reports
In one paragraph

Article in European journal of endocrinology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 35% 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

2 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Review
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 4 institutions in 2 countries.

Vasileios ChortisInstitute of Metabolism and Systems Research, University of Birmingham, Birmingham, UK.
Nicholas J JohalInstitute of Metabolism and Systems Research, University of Birmingham, Birmingham, UK.
Irina BancosInstitute of Metabolism and Systems Research, University of Birmingham, Birmingham, UK.
Matthew EvansDepartments of Pathology, Queen Elizabeth Hospital, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
Kassiani SkordilisDepartments of Pathology, Queen Elizabeth Hospital, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
Peter GuestRadiology and Cancer Centre, Queen Elizabeth Hospital, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
Michael H CullenCancer Centre, Queen Elizabeth Hospital, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
Emilio PorfiriCancer Centre, Queen Elizabeth Hospital, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
Wiebke ArltInstitute of Metabolism and Systems Research, University of Birmingham, Birmingham, UK.
University of Birmingham · GBQueen Elizabeth Hospital · GBUniversity Hospitals Birmingham NHS Foundation Trust · GBQueen Elizabeth Hospital · GB

Funding

Cancer Research UK 15622Medical Research Council G0801473
6 · The paper itself

Abstract

Mitotane (o,p'DDD) is established in the adjuvant and advanced-stage treatment of adrenocortical carcinoma and counteracts both tumor growth and tumor-related steroid production. Both the adrenal glands and the gonads are steroidogenically active organs and share a common embryogenic origin. Here, we describe the effects of mitotane in two patients with metastatic Leydig cell tumor (LCT) of the testes and associated severe androgen excess (serum testosterone 93 and 88 nmol/L, respectively; male reference range 7-27 nmol/L). Both men suffered from severe restlessness, insomnia and irritability, which they described as intolerable and disrupting normal life activities. Urinary steroid profiling by gas chromatography-mass spectrometry (GC-MS) confirmed excess androgen production and revealed concurrent overproduction of glucocorticoids and glucocorticoid precursors, which under physiological conditions are produced only by the adrenal glands but not by the gonads. In a palliative approach, they were commenced on mitotane, which achieved swift control of the hormone excess and the debilitating clinical symptoms, restoring normal quality of life. GC-MS demonstrated normalization of steroid production and decreased 5α-reductase activity, resulting in decreased androgen activation, and imaging demonstrated disease stabilization for 4-10 months. In conclusion, mitotane can be highly effective in controlling steroid excess in metastatic LCTs, with anti-tumor activity in some cases.

Indexed as

3-Oxo-5-alpha-Steroid 4-DehydrogenaseAndrogensAntineoplastic Agents, HormonalGas Chromatography-Mass SpectrometryHumansHyperandrogenismLeydig Cell TumorMaleMiddle AgedMitotaneNeoplasm MetastasisQuality of LifeTesticular NeoplasmsTreatment Outcome3-Oxo-5-alpha-Steroid 4-DehydrogenaseAndrogensAntineoplastic Agents, HormonalMitotane

Identifiers

PMID29330226
PMCPMC5811932
OpenAlexW2783595812

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.