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The Efficacy of Enzalutamide plus Androgen Deprivation Therapy in Oligometastatic Hormone-sensitive Prostate Cancer: A Post Hoc Analysis of ARCHES.
Armstrong, Andrew J; Iguchi, Taro; Azad, Arun A; Villers, Arnauld; Alekseev, Boris; Petrylak, Daniel P; Szmulewitz, Russell Z; Alcaraz, Antonio; Shore, Neal D; Holzbeierlein, Jeffrey; Gomez-Veiga, Francisco; Rosbrook, Brad; Zohren, Fabian; Haas, Gabriel P; Gourgiotti, Georgia; El-Chaar, Nader; Stenzl, Arnulf.
Afiliação
  • Armstrong AJ; Center for Prostate & Urologic Cancers, Duke Cancer Institute, Durham, NC, USA. Electronic address: andrew.armstrong@duke.edu.
  • Iguchi T; Kanazawa Medical University, Ishikawa, Japan.
  • Azad AA; Monash Health, Clayton, Victoria, Australia.
  • Villers A; University Hospital Centre, Lille University, Lille, France.
  • Alekseev B; Hertzen Moscow Cancer Research Institute, Moscow, Russia.
  • Petrylak DP; Department of Medical Oncology, Yale Cancer Center, New Haven, CT, USA.
  • Szmulewitz RZ; The University of Chicago, Chicago, IL, USA.
  • Alcaraz A; Hospital Clinic de Barcelona, Barcelona, Spain.
  • Shore ND; Carolina Urologic Research Center, Myrtle Beach, SC, USA.
  • Holzbeierlein J; The University of Kansas Medical Center, Kansas City, KS, USA.
  • Gomez-Veiga F; Hospital Universitario de Salamanca, Instituto de Investigación Biomédica de Salamanca, Salamanca, Spain.
  • Rosbrook B; Pfizer Inc., San Diego, CA, USA.
  • Zohren F; Pfizer Inc., San Diego, CA, USA.
  • Haas GP; Astellas Pharma Inc., Northbrook, IL, USA.
  • Gourgiotti G; Department of Biostatistics, Oncology, Astellas Pharma Inc., London, UK.
  • El-Chaar N; Astellas Pharma Inc., Northbrook, IL, USA.
  • Stenzl A; Department of Urology, University Hospital, Eberhard Karls University of Tübingen, Tübingen, Germany.
Eur Urol ; 84(2): 229-241, 2023 08.
Article em En | MEDLINE | ID: mdl-37179240
ABSTRACT

BACKGROUND:

Few phase 3 studies have evaluated optimal systemic treatment strategies for patients with oligometastatic hormone-sensitive prostate cancer (HSPC), who may be at risk of undertreatment.

OBJECTIVE:

To evaluate outcomes for patients with oligometastatic and polymetastatic HSPC treated with enzalutamide plus androgen deprivation therapy (ADT) versus placebo plus ADT. DESIGN, SETTING, AND

PARTICIPANTS:

This was a post hoc analysis of data for 927 patients with nonvisceral metastatic HSPC in the ARCHES trial (NCT02677896). INTERVENTION Patients were randomized 11 to enzalutamide (160 mg/d orally) plus ADT or placebo plus ADT with HSPC categorized as oligometastatic (1-5 metastases) or polymetastatic (≥6 metastases). OUTCOME MEASUREMENTS AND STATISTICAL

ANALYSIS:

The treatment effect on radiographic progression-free survival (rPFS), overall survival (OS), and secondary efficacy endpoints was evaluated in terms of the number of metastases. Safety was assessed. Cox proportional hazards models were used to generate hazard ratios (HRs). The Brookmeyer and Crowley method was used to generate 95% confidence intervals (CIs) for Kaplan-Meier median values. RESULTS AND

LIMITATIONS:

Enzalutamide plus ADT improved rPFS (HR 0.27, 95% CI 0.16-0.46; p < 0.001), OS (HR 0.59, 95% CI 0.40-0.87; p < 0.005), and secondary endpoints in patients with oligometastatic or polymetastatic disease (rPFS HR 0.33, 95% CI 0.23-0.46; p < 0.001; OS HR 0.55, 95% CI 0.41-0.74; p < 0.001). Safety profiles were generally similar across subgroups. Limitations include the small numbers of patients with fewer than three metastases.

CONCLUSIONS:

This post hoc analysis demonstrated the utility of enzalutamide, irrespective of metastatic burden or type of oligometastatic disease, and suggests that earlier treatment intensification with systemic potent androgen receptor inhibition is advantageous. PATIENT

SUMMARY:

This study considered two treatment options for metastatic hormone-sensitive prostate cancer in patients with one to five metastases or six or more metastases. Treatment with enzalutamide plus ADT improved survival and other outcomes over ADT alone, whether patients had few or many metastases.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Próstata / Neoplasias de Próstata Resistentes à Castração Tipo de estudo: Clinical_trials / Diagnostic_studies Limite: Humans / Male Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Próstata / Neoplasias de Próstata Resistentes à Castração Tipo de estudo: Clinical_trials / Diagnostic_studies Limite: Humans / Male Idioma: En Ano de publicação: 2023 Tipo de documento: Article