Enzalutamide in patients with castration-resistant prostate cancer: retrospective, multicenter, real life study.


Journal

Minerva urology and nephrology
ISSN: 2724-6442
Titre abrégé: Minerva Urol Nephrol
Pays: Italy
ID NLM: 101777299

Informations de publication

Date de publication:
08 2021
Historique:
pubmed: 5 8 2020
medline: 26 11 2021
entrez: 5 8 2020
Statut: ppublish

Résumé

Metastatic castration-resistant prostate cancer (mCRPC) is the final stage of pCa history and represents a clinically relevant phenotype with an elevated burden of mortality. The aim of the present study was to evaluate the efficacy and safety of enzalutamide in a "real-life" setting in mCRPC patients. Data about all mCRPC patients treated with enzalutamide from September 2017 to September 2018 were collected. Demographics, comorbidities, clinical parameters, outcomes, toxicity, overall survival and progression free survival were analyzed. Overall, 158 patients were enrolled. Mean age was 75.8 (±8.7) years with a baseline median PSA of 16.5 (IQR 7.4-47.8) ng/mL. The median follow-up lasted 7.7 (IQR 4-14.1) months. Of all the 10.1% of patients reported grade 3-4 adverse events. 43.7% of patients experienced a progression. Overall, the 6 and 12 months PFS rates were 69.5% (95% CI: 61.7-78.3%) and the 45.6% (95% CI: 36.5-57.1%); a median baseline PSA>16 ng/mL (HR:2.0, 95% CI: 1.2-3.3, P<0.005), the use of opioid (HR: 3.1, 95% CI: 1.9-5.0, P<0.001), a previous treatment (abiraterone, docetaxel or abiraterone + docetaxel) were significantly associated with higher rates of cancer progression. Conversely, a brief pain questionnaire of 0-1 (HR: 0.4, 95% CI: 0.2-0.7, P<0.001), a 12 weeks 50% PSA reduction (HR: 0.4, 95% CI: 0.2-0.8, P<0.006) and a longer time to mCRPC (HR: 0.4, 95% CI: 0.3-0.7, P<0.002) were related to lower cancer progression rates. Our data shows an effective and safe profile of enzalutamide in a "real world" perspective in patients with mcRPC.

Sections du résumé

BACKGROUND
Metastatic castration-resistant prostate cancer (mCRPC) is the final stage of pCa history and represents a clinically relevant phenotype with an elevated burden of mortality. The aim of the present study was to evaluate the efficacy and safety of enzalutamide in a "real-life" setting in mCRPC patients.
METHODS
Data about all mCRPC patients treated with enzalutamide from September 2017 to September 2018 were collected. Demographics, comorbidities, clinical parameters, outcomes, toxicity, overall survival and progression free survival were analyzed.
RESULTS
Overall, 158 patients were enrolled. Mean age was 75.8 (±8.7) years with a baseline median PSA of 16.5 (IQR 7.4-47.8) ng/mL. The median follow-up lasted 7.7 (IQR 4-14.1) months. Of all the 10.1% of patients reported grade 3-4 adverse events. 43.7% of patients experienced a progression. Overall, the 6 and 12 months PFS rates were 69.5% (95% CI: 61.7-78.3%) and the 45.6% (95% CI: 36.5-57.1%); a median baseline PSA>16 ng/mL (HR:2.0, 95% CI: 1.2-3.3, P<0.005), the use of opioid (HR: 3.1, 95% CI: 1.9-5.0, P<0.001), a previous treatment (abiraterone, docetaxel or abiraterone + docetaxel) were significantly associated with higher rates of cancer progression. Conversely, a brief pain questionnaire of 0-1 (HR: 0.4, 95% CI: 0.2-0.7, P<0.001), a 12 weeks 50% PSA reduction (HR: 0.4, 95% CI: 0.2-0.8, P<0.006) and a longer time to mCRPC (HR: 0.4, 95% CI: 0.3-0.7, P<0.002) were related to lower cancer progression rates.
CONCLUSIONS
Our data shows an effective and safe profile of enzalutamide in a "real world" perspective in patients with mcRPC.

Identifiants

pubmed: 32748613
pii: S0393-2249.20.03723-6
doi: 10.23736/S2724-6051.20.03723-6
doi:

Substances chimiques

Benzamides 0
Nitriles 0
Phenylthiohydantoin 2010-15-3
enzalutamide 93T0T9GKNU

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

489-497

Auteurs

Mauro Gacci (M)

Department of Minimally Invasive and Robotic Urologic Surgery and Kidney Transplantation, AOUC Careggi Hospital, Florence, Italy.

Michele Marchioni (M)

Department of Medical, Oral and Biotechnological Sciences, Laboratory of Biostatistics, G. D'Annunzio University, Chieti, Chieti-Pescara, Italy.

Piergustavo DE Francesco (P)

Department of Urology, ASL Abruzzo2, Chieti, Italy.

Clara Natoli (C)

Department of Medical, Oral and Biotechnological Sciences, Medical Oncology, G. D'Annunzio University, Chieti, Chieti-Pescara, Italy.

Fabio Calabrò (F)

Department of Medical Oncology, San Camillo-Forlanini Hospital, Rome, Italy.

Tania Losanno (T)

Department of Medical Oncology, San Camillo-Forlanini Hospital, Rome, Italy.

Cito Gianmartin (C)

Department of Minimally Invasive and Robotic Urologic Surgery and Kidney Transplantation, AOUC Careggi Hospital, Florence, Italy.

Sergio Serni (S)

Department of Minimally Invasive and Robotic Urologic Surgery and Kidney Transplantation, AOUC Careggi Hospital, Florence, Italy.

Laura Doni (L)

Department of Medical Oncology, Careggi University Hospital, Florence, Italy.

Cosimo DE Nunzio (C)

Department of Urology, Sant'Andrea Hospital, Sapienza University, Rome, Italy.

Michele DE Tursi (M)

Department of Medical, Oral and Biotechnological Sciences, Medical Oncology, G. D'Annunzio University, Chieti, Chieti-Pescara, Italy.

Maurizio Valeriani (M)

Unit of Radiation Therapy, Sant'Andrea Hospital, Sapienza University, Rome, Italy.

Silvana Giacinti (S)

Unit of Oncology, Sant'Andrea Hospital, Sapienza University, Rome, Italy.

Mario Álvarez-Maestro (M)

Department of Urology, La Paz University Hospital, Madrid, Spain.

Marcello Scarcia (M)

F. Miulli Hospital, Acquaviva delle Fonti, Bari, Italy.

Giuseppe M Ludovico (GM)

F. Miulli Hospital, Acquaviva delle Fonti, Bari, Italy.

Gabriella Del Bene (G)

Department of Medical Oncology, San Camillo-Forlanini Hospital, Rome, Italy.

Giuseppe Simone (G)

Department of Urology, Regina Elena National Cancer Institute, Rome, Italy.

Mariaconsiglia Ferriero (M)

Department of Urology, Regina Elena National Cancer Institute, Rome, Italy.

Gabriele Tuderti (G)

Department of Urology, Regina Elena National Cancer Institute, Rome, Italy.

Pierluigi Bove (P)

Department of Experimental Medicine and Surgery, Tor Vergata Polyclinic, Rome, Italy.
Unit of Urology, San Carlo di Nancy Hospital, Rome, Italy.

Anastasia Laudisi (A)

UOSD of Medical Oncology, Tor Vergata Polyclinic, Rome, Italy.

Giuseppe Carrieri (G)

Department of Urology, University of Foggia, Foggia, Italy.

Luigi Cormio (L)

Department of Urology, University of Foggia, Foggia, Italy.

Paolo Verze (P)

Unit of Urology, Department of Neurosciences, Sciences of Reproduction and Odontostomatology, Federico II University, Naples, Italy.

Roberto LA Rocca (R)

Unit of Urology, Department of Neurosciences, Sciences of Reproduction and Odontostomatology, Federico II University, Naples, Italy.

Mario Falsaperla (M)

Department of Urology, Vittorio Emanuele Polyclinic, Catania, Italy.

Viviana Frantellizzi (V)

Department of Molecular Medicine, Sapienza University, Rome, Italy.

Francesco Greco (F)

Department of Urology, Humanitas Gavazzeni Hospital, Bergamo, Italy.

Marta DI Nicola (M)

Department of Medical, Oral and Biotechnological Sciences, Laboratory of Biostatistics, G. D'Annunzio University, Chieti, Chieti-Pescara, Italy.

Luigi Schips (L)

Department of Urology, ASL Abruzzo2, Chieti, Italy.
Department of Medical, Oral and Biotechnological Sciences, Department of Urology, G. D'Annunzio University, Chieti, Chieti-Pescara, Italy.

Luca Cindolo (L)

Department of Urology, ASL Abruzzo2, Chieti, Italy - lucacindolo@virgilio.it.

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