Evidence map›Paper›PMID 36246926›Full record

ArticleFrontiers in endocrinology2022

Prognostic factors and mitotane treatment of adrenocortical cancer. Two decades of experience from an institutional case series.

Judit Tőke, Andrea Uhlyarik, Júlia Lohinszky, Júlia Stark, Gergely Huszty, Tamás Micsik, Katalin Borka, Péter Reismann, János Horányi, Peter Igaz and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in endocrinology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
2.2field-weighted citation impact, top 12% 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 10 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Observational
  4. Perspectives on Adrenal Tumor Surgery.Medicina (Kaunas, Lithuania) · 2025
    Article
  5. Review
  6. Article
  7. 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

11 authors at 2 institutions in 1 country.

Judit TőkeDepartment of Internal Medicine and Oncology, European Reference Network on Rare Endocrine Conditions (ENDO-ERN) Health Care Provider (HCP), Faculty of Medicine, Semmelweis University, Budapest, Hungary.
Andrea UhlyarikDepartment of Internal Medicine and Oncology, European Reference Network on Rare Endocrine Conditions (ENDO-ERN) Health Care Provider (HCP), Faculty of Medicine, Semmelweis University, Budapest, Hungary.
Júlia LohinszkyDepartment of Internal Medicine and Haematology, Faculty of Medicine, Semmelweis University, Budapest, Hungary.
Júlia StarkDepartment of Internal Medicine and Oncology, European Reference Network on Rare Endocrine Conditions (ENDO-ERN) Health Care Provider (HCP), Faculty of Medicine, Semmelweis University, Budapest, Hungary.
Gergely HusztyDepartment of Surgery, Transplantation and Gastroenterology, Faculty of Medicine, Semmelweis University, Budapest, Hungary.
Tamás MicsikFirst Department of Pathology and Experimental Cancer Research, Faculty of Medicine, Semmelweis University, Budapest, Hungary.
Katalin BorkaDepartment of Pathology, Forensic and Insurance Medicine, Faculty of Medicine, Semmelweis University, Budapest, Hungary.
Péter ReismannDepartment of Internal Medicine and Oncology, European Reference Network on Rare Endocrine Conditions (ENDO-ERN) Health Care Provider (HCP), Faculty of Medicine, Semmelweis University, Budapest, Hungary.
János HorányiDepartment of Surgery, Transplantation and Gastroenterology, Faculty of Medicine, Semmelweis University, Budapest, Hungary.
Peter IgazDepartment of Internal Medicine and Oncology, European Reference Network on Rare Endocrine Conditions (ENDO-ERN) Health Care Provider (HCP), Faculty of Medicine, Semmelweis University, Budapest, Hungary.
Miklós TóthDepartment of Internal Medicine and Oncology, European Reference Network on Rare Endocrine Conditions (ENDO-ERN) Health Care Provider (HCP), Faculty of Medicine, Semmelweis University, Budapest, Hungary.
Semmelweis University · HUHungarian Academy of Sciences · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: This study aimed to characterise the clinicopathological features and prognostic factors of a large cohort of Hungarian patients with adrenocortical cancer diagnosed between 2000-2021. Patients and methods: This retrospective study included seventy-four patients (27 men and 47 women) with histologically confirmed adrenocortical cancer in a single tertiary referral endocrine centre. Descriptive statistics were performed, providing summaries of selected clinical and pathological parameters. Clinicopathological factors contributing to overall survival were analysed. Results: The median age of patients was 48,5 years (17-84 years) at diagnosis. The majority of cases were diagnosed at ENSAT stage II (39,2%) and stage IV (33,8%). At diagnosis, the median tumour size was 9,0 cm (4,5-20 cm). In 47 patients (71,6%), the tumour was hormonally active. The median overall survival and the 5-year survival rate were 23,5 months (95% CI, 17-30,5 months) and 18,3%, respectively. Primary tumour resection was performed in 68 patients (91,8%); R0 surgical resection was achieved in 30 patients. In univariate Cox regression model, tumours with stages III and IV, high proliferative activity (Ki67-index > 10%), R1-R2 surgical resection state and hormonal activity were associated with poorer survival. Cortisol excess, both isolated and combined with androgen production, was associated with poorer survival. Fifty-five patients were treated with mitotane. The overall survival of patients achieving therapeutic mitotane plasma concentration was significantly better compared to those who never reached it [27.0 (2-175) months vs 18.0 (2-83) months; p<0.05)]. The median age, the distribution of gender, ENSAT stage, resection state and Ki67-index did not differ between these two groups. The time needed to reach the therapeutic range of serum mitotane was 96.5 days (95% CI, 75-133 days). Conclusion: Our results confirm previous data that disease stage, mitotic activity, the resection state and the mitotane treatment achieving therapeutic concentration are the most critical parameters influencing the prognosis of adrenocortical cancer. Our data suggest that hormonal activity may be more frequent than described previously, and it is a strong and independent prognostic factor of overall survival. To our knowledge, this is the first single-centre study confirming the prognostic importance of achieving therapeutic mitotane concentration.

Indexed as

Adrenal Cortex NeoplasmsAdrenocortical CarcinomaAndrogensAntineoplastic Agents, HormonalFemaleHumansHydrocortisoneKi-67 AntigenMaleMitotanePrognosisRetrospective StudiesAndrogensAntineoplastic Agents, HormonalHydrocortisoneKi-67 AntigenMitotaneAdrenocortical cancermitotaneoverall survivalprognostic markerssingle centre experience

Identifiers

PMID36246926
PMCPMC9560769
OpenAlexW4298006011

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.