Evidence map›Paper›PMID 41304942›Full record

ReviewPharmaceuticals (Basel, Switzerland)2025

Recent Advances in Androgen Receptor Pathway Inhibitors for Castration-Sensitive Prostate Cancer.

Andrea Lancia, Marco Oderda, Federico Camilli, Eleonora Festa, Marta Bottero, Emanuele Alì, Salvatore La Mattina, Elisabetta Bonzano, Jessica Saddi, Beatrice Detti and 2 more

Abstract readReview
In one paragraph

Review in Pharmaceuticals (Basel, Switzerland), 2025. 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
–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. Article
  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

12 authors.

Andrea LanciaRadiation Oncology, Fondazione IRCCS Policlinico San Matteo, 27100 Pavia, Italy.ORCID 0000-0001-6106-7725
Marco OderdaDivision of Urology, Department of Surgical Sciences, Molinette Hospital, University of Turin, 10124 Turin, Italy.ORCID 0000-0003-4681-888X
Federico CamilliRadiation Oncology Section, Department of Medicine and Surgery, University of Perugia and Perugia General Hospital, 06156 Perugia, Italy.
Eleonora FestaRadiation Oncology Section, Department of Medicine and Surgery, University of Perugia and Perugia General Hospital, 06156 Perugia, Italy.
Marta BotteroRadiotherapy Unit, IRCCS Regina Elena National Cancer Institute, 00144 Rome, Italy.ORCID 0000-0001-8105-2942
Emanuele AlìRadiation Oncology Unit, Azienda Unitaria Sanitaria Locale-Istituto di Ricovero e Cura a Carattere Scientifico, 42123 Reggio Emilia, Italy.ORCID 0000-0002-6196-5864
Salvatore La MattinaRadiation Oncology, Fondazione IRCCS Policlinico San Matteo, 27100 Pavia, Italy.ORCID 0009-0008-0137-5142
Elisabetta BonzanoRadiation Oncology, Fondazione IRCCS Policlinico San Matteo, 27100 Pavia, Italy.ORCID 0000-0002-1349-5853
Jessica SaddiRadiation Oncology, Fondazione IRCCS Policlinico San Matteo, 27100 Pavia, Italy.
Beatrice DettiRadiotherapy Unit Prato, Usl Centro Toscana, Presidio Villa Fiorita, 59100 Prato, Italy.
David Alberto Santos HernandezRadiation Oncology, Fondazione IRCCS Policlinico San Matteo, 27100 Pavia, Italy.ORCID 0000-0002-6099-0195
Gianluca IngrossoRadiation Oncology Section, Department of Medicine and Surgery, University of Perugia and Perugia General Hospital, 06156 Perugia, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Prostate cancer (PCa) is the second most common cancer in men, and it is frequently diagnosed at an advanced stage of the disease. Androgen Deprivation Therapy (ADT) has traditionally represented the backbone of therapy for high-risk, recurrent, and metastatic disease; however, in the last ten years a new group of molecules known as androgen receptor pathway inhibitors (ARPIs) have been demonstrated to improve outcomes in metastatic patients when added to ADT. Developed and validated originally in the setting of castration-resistant disease, ARPIs have been implemented progressively earlier in the natural history of PCa, involving patients who have never received ADT before or that are still responsive to this treatment. Considering the strong evidence for treatment intensification in patients with high-risk features, with this review we aim to provide a complete overview of the current indications for the use of ARPIs through all the stages of castration-sensitive prostate cancer (CSPC).

Indexed as

androgen receptor pathway inhibitormetastasesprostate cancerradiotherapysurgery

Identifiers

PMID41304942
PMCPMC12655341

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.