Metastatic Prostate Cancer: Treatment Options.


Journal

Oncology
ISSN: 1423-0232
Titre abrégé: Oncology
Pays: Switzerland
ID NLM: 0135054

Informations de publication

Date de publication:
2022
Historique:
received: 03 08 2021
accepted: 20 09 2021
pubmed: 16 11 2021
medline: 15 1 2022
entrez: 15 11 2021
Statut: ppublish

Résumé

Metastatic prostate cancer (PCa) is associated with considerable diminished overall survival (OS). Standard treatment for metastatic PCa has long been androgen deprivation therapy alone, with patients initially responding to this treatment and then progressing to a castration-resistant phase. The advent of novel therapeutic agents has changed this paradigm, with high-level evidence that upfront combination therapy with either docetaxel or new hormonal agents results in improved OS for patients with metastatic hormone-sensitive PCa. In the absence of a comprehensive clinical trial investigating the comparative efficacy and safety of all agents, clinicians are responsible for choosing the most appropriate therapy in close coordination with patients. Furthermore, the same therapeutic agents are also efficient in the castration-resistant phase, leading to the issue of the best therapeutic sequence. Finally, along with systemic therapy and molecular imaging advancements, radiotherapy was investigated in the oligometastatic setting, whether it is to treat the primary tumour or metastases. Key Messages: In this complex landscape, where providers have multiple effective therapeutic options to treat metastatic PCa patients, priority must be given to determine which treatment combination and sequence is best suited to a particular patient, given his comorbidities and preferences.

Sections du résumé

BACKGROUND BACKGROUND
Metastatic prostate cancer (PCa) is associated with considerable diminished overall survival (OS). Standard treatment for metastatic PCa has long been androgen deprivation therapy alone, with patients initially responding to this treatment and then progressing to a castration-resistant phase.
SUMMARY CONCLUSIONS
The advent of novel therapeutic agents has changed this paradigm, with high-level evidence that upfront combination therapy with either docetaxel or new hormonal agents results in improved OS for patients with metastatic hormone-sensitive PCa. In the absence of a comprehensive clinical trial investigating the comparative efficacy and safety of all agents, clinicians are responsible for choosing the most appropriate therapy in close coordination with patients. Furthermore, the same therapeutic agents are also efficient in the castration-resistant phase, leading to the issue of the best therapeutic sequence. Finally, along with systemic therapy and molecular imaging advancements, radiotherapy was investigated in the oligometastatic setting, whether it is to treat the primary tumour or metastases. Key Messages: In this complex landscape, where providers have multiple effective therapeutic options to treat metastatic PCa patients, priority must be given to determine which treatment combination and sequence is best suited to a particular patient, given his comorbidities and preferences.

Identifiants

pubmed: 34781285
pii: 000519861
doi: 10.1159/000519861
doi:

Substances chimiques

Antineoplastic Agents 0
Radiopharmaceuticals 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

48-59

Informations de copyright

© 2021 S. Karger AG, Basel.

Auteurs

Vérane Achard (V)

Department of Radiation Oncology, Geneva University Hospital, Geneva, Switzerland.
Faculty of Medicine, Geneva University, Geneva, Switzerland.

Paul Martin Putora (PM)

Department of Radiation Oncology, Kantonsspital St. Gallen, St. Gallen, Switzerland.
Faculty of Medicine, University of Bern, Bern, Switzerland.

Aurelius Omlin (A)

Department of Medical Oncology and Haematology, Kantonsspital St. Gallen, St. Gallen, Switzerland.

Thomas Zilli (T)

Department of Radiation Oncology, Geneva University Hospital, Geneva, Switzerland.
Faculty of Medicine, Geneva University, Geneva, Switzerland.

Stefanie Fischer (S)

Department of Medical Oncology and Haematology, Kantonsspital St. Gallen, St. Gallen, Switzerland.

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Classifications MeSH