Evidence map›Paper›PMID 40796146›Full record

SynthesisThe Journal of clinical endocrinology and metabolism2025

Efficacy and Safety of Radiotherapy and Systemic Treatments in Adrenocortical Carcinoma: Systematic Review and Meta-Analysis.

Anita Pfeffer, Nóra Beke, Dorottya Bakó, Márk Hernádfői, Tamás Kói, András Fogarasi, Andrea Párniczky, Péter Hegyi, Miklós Garami

Abstract readSystematic ReviewMeta-Analysis
In one paragraph

Synthesis in The Journal of clinical endocrinology and metabolism, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. 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

9 authors.

Anita PfefferPediatric Center, Tűzoltó Street Department, Semmelweis University, Budapest 1094, Hungary.
Nóra BekeCentre for Translational Medicine, Semmelweis University, Budapest 1085, Hungary.
Dorottya BakóCentre for Translational Medicine, Semmelweis University, Budapest 1085, Hungary.
Márk HernádfőiCentre for Translational Medicine, Semmelweis University, Budapest 1085, Hungary.
Tamás KóiCentre for Translational Medicine, Semmelweis University, Budapest 1085, Hungary.
András FogarasiCentre for Translational Medicine, Semmelweis University, Budapest 1085, Hungary.
Andrea PárniczkyCentre for Translational Medicine, Semmelweis University, Budapest 1085, Hungary.
Péter HegyiCentre for Translational Medicine, Semmelweis University, Budapest 1085, Hungary.
Miklós GaramiPediatric Center, Tűzoltó Street Department, Semmelweis University, Budapest 1094, Hungary.ORCID 0000-0003-4298-2746

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

contextAdrenocortical carcinoma (ACC) is a rare, aggressive malignancy with a high recurrence and mortality rate even after complete resection. Therefore, intensification of adjuvant therapies is crucial, although their effectiveness remains controversial.

objectiveThis study aimed to determine the efficacy and safety of available treatments by considering the prognostic factors affecting disease outcomes.

methodsThe search was conducted across 3 databases (PubMed, Embase, and CENTRAL) in October 2024. Eligible studies compared overall survival (OS) and recurrence-free survival (RFS) in patients with ACC treated with and without systemic (mitotane, cytotoxic chemotherapy) or localized (radiotherapy) nonsurgical treatments. In total, 86 studies met the inclusion criteria for the systematic review, and 62 for the meta-analysis. Two reviewers extracted data independently. Adjusted hazard ratios (aHR) with 95% CI were calculated for survival outcomes.

resultsMitotane significantly improves OS (aHR: 0.54; CI: 0.41-0.70) and RFS (aHR: 0.60; CI: 0.43-0.84), even in stage I-III disease (OS aHR: 0.71; CI: 0.52-0.98; RFS aHR: 0.65; CI: 0.50-0.85). Radiotherapy showed a trend toward improved OS (aHR: 0.66; CI: 0.38-1.15) and RFS (aHR: 0.65; CI: 0.35-1.23), with significant benefits in stage I-III (OS aHR: 0.68; CI: 0.50-0.93; RFS aHR: 0.71; CI: 0.63-0.81). The impact of cytotoxic chemotherapy on OS remains uncertain (aHR: 0.61; CI: 0.08-4.78).

conclusionMitotane significantly improves survival outcomes in patients with ACC, while radiotherapy exhibits potential benefits, particularly in localized disease. Further research is needed to verify the efficacy of cytotoxic chemotherapy, and randomized controlled trials are required to provide robust evidence of different treatment approaches.

Indexed as

Adrenal Cortex NeoplasmsAdrenocortical CarcinomaAntineoplastic Agents, HormonalHumansMitotanePrognosisTreatment OutcomeAntineoplastic Agents, HormonalMitotaneadrenocortical carcinomacytotoxic chemotherapyirradiationmitotaneradiotherapytargeted therapy

Identifiers

PMID40796146
PMCPMC12623036

What Socratic 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 Socratic graph.