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Prevalence and Natural History of Non-metastatic Castrate Resistant Prostate Cancer: A Population-Based Analysis.
Hird, Amanda E; Dvorani, Erind; Saskin, Refik; Emmenegger, Urban; Herschorn, Sender; Kodama, Ronald; Kulkarni, Girish S; Nam, Robert K.
Afiliação
  • Hird AE; Division of Urology, Sunnybrook Health Sciences Center, University of Toronto, Toronto, Ontario; Institute for Health Policy, Management, and Evaluation, University of Toronto, Toronto, Ontario.
  • Dvorani E; ICES, Toronto, Ontario.
  • Saskin R; ICES, Toronto, Ontario.
  • Emmenegger U; Division of Medical Oncology and Hematology, Sunnybrook Health Sciences Center, University of Toronto, Toronto, Ontario.
  • Herschorn S; Division of Urology, Sunnybrook Health Sciences Center, University of Toronto, Toronto, Ontario.
  • Kodama R; Division of Urology, Sunnybrook Health Sciences Center, University of Toronto, Toronto, Ontario.
  • Kulkarni GS; Institute for Health Policy, Management, and Evaluation, University of Toronto, Toronto, Ontario; Division of Urology, Princess Margaret Hospital, University Health Network, University of Toronto, Toronto, Ontario.
  • Nam RK; Division of Urology, Sunnybrook Health Sciences Center, University of Toronto, Toronto, Ontario; Institute for Health Policy, Management, and Evaluation, University of Toronto, Toronto, Ontario. Electronic address: Robert.Nam@utoronto.ca.
Clin Genitourin Cancer ; 21(2): e27-e34, 2023 04.
Article em En | MEDLINE | ID: mdl-36371403
ABSTRACT

PURPOSE:

To determine the prevalence and natural history of nmCRPC prior to the adoption of novel androgen receptor axis-targeting therapies(ARAT). MATERIALS AND

METHODS:

This was a retrospective population-based cohort study of men with nmCRPC in Ontario, Canada between January 2007-March 2018. Patients with prostate cancer, castrate level of testosterone(<1.7nmol/L) and a PSA>2.0ng/mL with a subsequent rise>25% from the nadir, and without metastasis were included. Annual prevalence of nmCRPC was calculated. Crude time from nmCRPC to metastasis and all-cause death are presented as medians with interquartile range(IQR). Predictors of time from nmCRPC to death were compared using univariable and multivariable cox proportional hazard models.

RESULTS:

We identified 2045 patients with nmCRPC. Median age was 79(IQR72-84). 984 patients(48.1%) received upfront hormonal therapy while 583(28.5%) received initial radiotherapy and 478(23.4%) underwent radical prostatectomy. Median time from primary treatment to nmCRPC was 6 years(IQR3-10). The average annual prevalence of nmCRPC was 8% among men receiving ADT. Crude median time from nmCRPC to death was 37.6 months(IQR22.1-55.4). Median time from nmCRPC to metastasis and metastasis to death was 20.0 and 8.3 months, respectively. Patients who had primary surgery experienced longer crude survival. Older patients, patients who had a higher PSA at nmCRPC, and patients with grade group 4 to 5 disease had a shorter time from nmCRPC to death.

CONCLUSION:

This is the largest population-level analysis of the prevalence and natural history of nmCRPC. The current study can be used as a historical cohort to compare how novel imaging modalities and ARAT impact prevalence and disease trajectory over time.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Antígeno Prostático Específico / Neoplasias de Próstata Resistentes à Castração Tipo de estudo: Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Humans / Male Idioma: En Revista: Clin Genitourin Cancer Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Antígeno Prostático Específico / Neoplasias de Próstata Resistentes à Castração Tipo de estudo: Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Humans / Male Idioma: En Revista: Clin Genitourin Cancer Ano de publicação: 2023 Tipo de documento: Article