Clinical outcomes of volume of disease on patients receiving enzalutamide

abiraterone acetate enzalutamide metastatic castration-resistant prostate cancer overall survival volume of disease

Journal

Therapeutic advances in medical oncology
ISSN: 1758-8340
Titre abrégé: Ther Adv Med Oncol
Pays: England
ID NLM: 101510808

Informations de publication

Date de publication:
2023
Historique:
received: 25 10 2022
accepted: 21 01 2023
entrez: 10 3 2023
pubmed: 11 3 2023
medline: 11 3 2023
Statut: epublish

Résumé

Androgen receptor signaling inhibitors (ARSis) abiraterone acetate (AA) plus prednisone and enzalutamide (Enza), are currently the most administered first-line treatments for metastatic castration-resistant prostate cancer (mCRPC). AA and Enza have shown similar overall survival (OS) benefits and there is no consensus upon the best option for mCRPC first-line treatment. Volume of disease may represent a useful biomarker to predict response to therapy in such patients. In this study, we seek to evaluate the impact of volume of disease on patients treated with first-line AA We retrospectively evaluated a cohort of consecutive patients with mCRPC categorized by volume of disease [high volume (HV) or low volume (LV) per E3805 criteria] at ARSi onset and treatment type (AA or Enza), assessing OS and radiographic progression-free survival (rPFS), from therapy start, as co-primary endpoints. Of the 420 patients selected, 170 (40.5%) had LV and received AA (LV/AA), 76 (18.1%) LV and had Enza (LV/Enza), 124 (29.5%) HV and were given AA (HV/AA), and 50 (11.9%) HV and received Enza (HV/Enza). Among patients with LV, OS was significantly longer when treated with Enza [57.2 months; 95% confidence interval (CI): 52.1-62.2 months] Within the intrinsic limitations of a retrospective design and small population, our report suggests that volume of disease could be a useful predictive biomarker for patients starting first-line ARSi for mCRPC.

Sections du résumé

Background UNASSIGNED
Androgen receptor signaling inhibitors (ARSis) abiraterone acetate (AA) plus prednisone and enzalutamide (Enza), are currently the most administered first-line treatments for metastatic castration-resistant prostate cancer (mCRPC). AA and Enza have shown similar overall survival (OS) benefits and there is no consensus upon the best option for mCRPC first-line treatment. Volume of disease may represent a useful biomarker to predict response to therapy in such patients.
Objectives UNASSIGNED
In this study, we seek to evaluate the impact of volume of disease on patients treated with first-line AA
Design and methods UNASSIGNED
We retrospectively evaluated a cohort of consecutive patients with mCRPC categorized by volume of disease [high volume (HV) or low volume (LV) per E3805 criteria] at ARSi onset and treatment type (AA or Enza), assessing OS and radiographic progression-free survival (rPFS), from therapy start, as co-primary endpoints.
Results UNASSIGNED
Of the 420 patients selected, 170 (40.5%) had LV and received AA (LV/AA), 76 (18.1%) LV and had Enza (LV/Enza), 124 (29.5%) HV and were given AA (HV/AA), and 50 (11.9%) HV and received Enza (HV/Enza). Among patients with LV, OS was significantly longer when treated with Enza [57.2 months; 95% confidence interval (CI): 52.1-62.2 months]
Conclusion UNASSIGNED
Within the intrinsic limitations of a retrospective design and small population, our report suggests that volume of disease could be a useful predictive biomarker for patients starting first-line ARSi for mCRPC.

Identifiants

pubmed: 36895852
doi: 10.1177/17588359231156147
pii: 10.1177_17588359231156147
pmc: PMC9989439
doi:

Types de publication

Journal Article

Langues

eng

Pagination

17588359231156147

Commentaires et corrections

Type : ErratumIn

Informations de copyright

© The Author(s), 2023.

Déclaration de conflit d'intérêts

Loana Bueno Valenca received consulting fees from Janssen and travel grants from Janssen, Astellas, Bayer. The other authors report no conflict of interest.

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Auteurs

Pier Vitale Nuzzo (PV)

Department of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, NY, USA.

Francesco Ravera (F)

Department of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, NY, USA.
Department of Internal Medicine, University of Genoa, Genova, Italy.

Calogero Saieva (C)

Cancer Risk Factors and Lifestyle Epidemiology Unit-ISPRO, Florence, Italy.

Elisa Zanardi (E)

Medical Oncology Unit 1, IRCCS Ospedale Policlinico San Martino, Genova, Italy.

Giuseppe Fotia (G)

Medical Oncology Department, Fondazione IRCCS Istituto Nazionale Tumori, Milano, Italy.

Andrea Malgeri (A)

Division of Medical Oncology, Policlinico Universitario Campus Bio-Medico, Rome, Italy.

Sabrina Rossetti (S)

Department of Urology and Gynecology, Istituto Nazionale Tumori IRCCS Fondazione G. Pascale, Naples, Italy.

Loana Bueno Valença (LB)

Instituto D'Or de Pesquisa e Ensino (IDOR), Salvador, Brazil.
Hospital Sao Rafael, Salvador, Brazil.

Thiago Martins Oliveira (TM)

Instituto D'Or de Pesquisa e Ensino (IDOR), Salvador, Brazil.
Hospital Sao Rafael, Salvador, Brazil.

Charles Vauchier (C)

Thoracic Oncology Unit, Bichat-Claude Bernard Hospital, Paris, France.

Ricardo Pereira Mestre (R)

Istituto Oncologico della Svizzera Italiana, Bellinzona, Switzerland.

Mikol Modesti (M)

Istituto Oncologico della Svizzera Italiana, Bellinzona, Switzerland.

Anna Patrikidou (A)

Department of Medical Oncology, Gustave Roussy Institute, Villejuif, France.

Sandro Pignata (S)

Department of Urology and Gynecology, Istituto Nazionale Tumori IRCCS Fondazione G. Pascale, Naples, Italy.

Giuseppe Procopio (G)

Oncology Unit, ASST Cremona, Cremona, CR, Italy.

Giuseppe Fornarini (G)

Medical Oncology Unit 1, IRCCS Ospedale Policlinico San Martino, Genova, Italy.

Ugo De Giorgi (U)

Department of Medical Oncology, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST), Meldola, Italy.

Antonio Russo (A)

Department of Surgical, Oncological and Oral Sciences, Section of Medical Oncology, University of Palermo, Palermo, Italy.

Edoardo Francini (E)

Department of Experimental and Clinical Medicine, University of Florence, Largo Brambilla 3, Florence 50134, Italy.

Classifications MeSH