Evidence map›Paper›PMID 42176182›Full record

ReviewAdvances in therapy2026

Therapy Optimization in mHSPC: Insights from a Multidisciplinary Uro-Oncology Expert Panel.

André Mansinho, João Carlos Gramaça, Rodrigo Ramos, Pedro Miguel Baltazar, José Palma Dos Reis, Ricardo Fernandes, Mariana Malheiro, Alina Rosinha, Sofia Amorim, Ricardo Borges and 18 more

Abstract readReview
In one paragraph

Review in Advances in therapy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

28 authors.

André MansinhoSTART Lisbon, Unidade Local de Saúde Santa Maria, Lisbon, Portugal. andre.mansinho@startlisbon.com.ORCID http://orcid.org/0000-0001-8771-0838
João Carlos GramaçaMedical Oncology Unit, Unidade Local de Saúde São José, Lisbon, Portugal.
Rodrigo RamosUrology Department, Instituto Português de Oncologia de Lisboa Francisco Gentil, Lisbon, Portugal.
Pedro Miguel BaltazariNOVA4Health, NOVA Medical School, Faculdade de Ciências Médicas, Universidade Nova de Lisboa, Lisbon, Portugal.
José Palma Dos ReisUnidade Local de Saúde Santa Maria, Lisbon, Portugal.
Ricardo FernandesUnidade Local de Saúde de Braga, Braga, Portugal.
Mariana MalheiroCUF Tejo, Lisbon, Portugal.
Alina RosinhaInstituto Português de Oncologia do Porto Francisco Gentil, Porto, Portugal.
Sofia AmorimUnidade Local de Saúde Entre Douro e Vouga, Santa Maria da Feira, Portugal.
Ricardo BorgesUnidade Local de Saúde da Região de Leiria, Leiria, Portugal.
Isaac BragaInstituto Português de Oncologia do Porto Francisco Gentil, Porto, Portugal.
Andreia CapelaUnidade Local de Saúde Gaia e Espinho, Vila Nova de Gaia, Portugal.
Diogo Nunes CarneiroUrology Department, Unidade Local de Saúde de Santo António, Porto, Portugal.
Rui DinisHospital do Espírito Santo de Évora, Unidade Local de Saúde do Alentejo Central, Évora, Portugal.
André FerreiraHospital de Santo André, Unidade Local de Saúde da Região de Leiria, Leiria, Portugal.
Arnaldo FigueiredoCoimbra Hospital and University Centre, Unidade Local de Saúde de Coimbra, Coimbra, Portugal.
Sílvia LopesUnidade Local de Saúde de Santo António, Porto, Portugal.
Pedro Silvestre MadeiraServiço de Oncologia Médica, Instituto Português de Oncologia de Coimbra Francisco Gentil, Coimbra, Portugal.
Helena MagalhãesHospital Pedro Hispano, Unidade Local de Saúde de Matosinhos, Matosinhos, Portugal.
Hélder MansinhoHospital Garcia de Orta, Unidade Local de Saúde Almada Seixal, Almada, Portugal.
Sara MeirelesUnidade Local de Saúde São João, Porto, Portugal.
Carolina PereiraServiço de Oncologia Médica, Instituto Português de Oncologia de Lisboa Francisco Gentil, Lisbon, Portugal.
Cidália PintoUnidade Local de Saúde do Algarve, Faro, Portugal.
Chiara RodriguesUnidade de Urologia, Fundação Champalimaud, Lisbon, Portugal.
Ana SpencerHospital de Cascais Dr. José de Almeida, Alcabideche, Portugal.
Carolina CarvalhoHospital de Guimarães, Unidade Local de Saúde Alto Ave, Guimarães, Portugal.
Tiago TomásHospital Prof. Dr. Fernando Fonseca, Unidade Local de Saúde Amadora/Sintra, Amadora, Portugal.
Carlos RabaçaServiço de Urologia, Instituto Português de Oncologia de Coimbra Francisco Gentil, Coimbra, Portugal.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Metastatic hormone-sensitive prostate cancer (mHSPC) is a disease state characterized by the presence of distant metastases detectable on conventional imaging while the tumor remains responsive to androgen deprivation therapy (ADT). It represents an earlier, treatment-sensitive phase that precedes the development of metastatic castration-resistant prostate cancer (mCRPC), the terminal stage of the disease. The addition of therapies beyond traditional ADT to achieve more sustained tumor regression by combining different mechanisms of action and targeting different cancer fuelling pathways has spurred the concept of treatment intensification in prostate cancer. This approach may involve the addition of androgen receptor pathway inhibitors (ARPIs) to ADT-hereafter referred to as "treatment intensification"-or the addition of ARPIs plus chemotherapy to ADT-hereafter referred to as "treatment optimization." Randomized controlled trials have consistently shown improved patient outcomes with the evolution from ADT alone to ADT plus ARPI, and more recently to ADT plus ARPI plus docetaxel, and demonstrated that treatment intensification decisions in mHSPC have clinically meaningful implications. However, in the absence of comparative efficacy data between therapy options, the treatment choice for a given patient will depend on patient- and disease-related factors, with the goal of improving outcomes while minimizing the cumulative toxicity of therapies, particularly when using combination strategies. In this article, a panel of 28 experts-8 urologists and 20 oncologists-with recognized experience and expertise in the management of advanced prostate cancer discussed the role of treatment intensification in mHSPC and which patients are more likely to benefit from each treatment strategy.

Indexed as

Androgen AntagonistsAndrogen Receptor AntagonistsAntineoplastic Combined Chemotherapy ProtocolsProstatic NeoplasmsProstatic Neoplasms, Castration-ResistantHumansMaleNeoplasm MetastasisRandomized Controlled Trials as TopicAndrogen AntagonistsAndrogen Receptor AntagonistsAndrogen deprivation therapyAndrogen receptor pathway inhibitorMetastatic hormone-sensitive prostate cancerTherapy intensificationTherapy optimizationUro-oncology

Identifiers

PMID42176182
PMCPMC13415262

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.