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Impact of clinical versus radiographic progression on clinical outcomes in metastatic castration-resistant prostate cancer.
Rao, Arpit; Scher, Howard I; De Porre, Peter; Yu, Margaret K; Londhe, Anil; Qi, Keqin; Morris, Michael J; Ryan, Charles.
Afiliação
  • Rao A; Division of Hematology, Oncology and Transplantation, University of Minnesota, Minneapolis, Minnesota, USA. Electronic address: raoa@umn.edu.
  • Scher HI; Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York, New York, USA; Weill Cornell Medical College, New York, United States.
  • De Porre P; Oncology Development, Janssen Research & Development, Beerse, Belgium.
  • Yu MK; Janssen Research & Development, Los Angeles, California, USA.
  • Londhe A; Oncology Development, Janssen Research & Development, Titusville, New Jersey, USA.
  • Qi K; Oncology Development, Janssen Research & Development, Titusville, New Jersey, USA.
  • Morris MJ; Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York, New York, USA; Weill Cornell Medical College, New York, United States.
  • Ryan C; Division of Hematology, Oncology and Transplantation, University of Minnesota, Minneapolis, Minnesota, USA.
ESMO Open ; 5(6): e000943, 2020 11.
Article em En | MEDLINE | ID: mdl-33184097
ABSTRACT

OBJECTIVES:

Unequivocal clinical progression (UCP)-a worsening of clinical status with or without radiographic progression (RAD)-represents a distinct mode of disease progression in metastatic prostate cancer. We evaluated the prevalence, risk factors and the impact of UCP on survival outcomes.

METHODS:

A post-hoc analysis of the COU-AA-302, a randomised phase 3 study of abiraterone plus prednisone (AAP) versus prednisone was performed. Baseline characteristics were summarised. Cox proportional-hazards model and Kaplan-Meier method were used for survival and time to event analyses, respectively. Iterative multiple imputation method was used for correlation between clinicoradiographic progression-free survival (crPFS) and overall survival (OS).

RESULTS:

Of 736 patients with disease progression, 280 (38%) had UCP-only and 124 (17%) had UCP plus RAD. Prognostic index model high-risk group was associated with increased likelihood of UCP (p<0.0001). Median OS was 25.7 months in UCP-only and 33.0 months for RAD-only (HR 1.39; 95% CI 1.16 to 1.66; p=0.0003). UCP adversely impacted OS in both treatment groups. Lowest OS was seen in patients with prostate specific antigen (PSA)-non-response plus UCP-only progression (median OS 22.6 months (95% CI 20.7 to 24.4)). Including UCP events lowered estimates of treatment benefit-median crPFS was 13.3 months (95% CI 11.1 to 13.8) versus median rPFS of 16.5 months (95% CI 13.8 to 16.8) in AAP group. Finally, crPFS showed high correlation with OS (r=0.67; 95% CI 0.63 to 0.71).

CONCLUSIONS:

UCP is a common and clinically relevant phenomenon in patients with metastatic castration-resistant prostate cancer (mCRPC) treated with AAP or prednisone. UCP is prognostic and associated with inferior OS and post-progression survival. A combination of PSA-non-response and UCP identifies patients with poorest survival. When included in PFS analysis, UCP diminishes estimates of treatment benefit. Continued study of UCP in mCRPC is warranted.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias de Próstata Resistentes à Castração Tipo de estudo: Clinical_trials / Prognostic_studies / Risk_factors_studies Limite: Humans / Male Idioma: En Revista: ESMO Open Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias de Próstata Resistentes à Castração Tipo de estudo: Clinical_trials / Prognostic_studies / Risk_factors_studies Limite: Humans / Male Idioma: En Revista: ESMO Open Ano de publicação: 2020 Tipo de documento: Article