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Early Post-treatment Prostate-specific Antigen at 4 Weeks and Abiraterone and Enzalutamide Treatment for Advanced Prostate Cancer: An International Collaborative Analysis.
Rescigno, Pasquale; Dolling, David; Conteduca, Vincenza; Rediti, Mattia; Bianchini, Diletta; Lolli, Cristian; Ong, Michael; Li, Haoran; Omlin, Aurelius G; Schmid, Sabine; Caffo, Orazio; Zivi, Andrea; Pezaro, Carmel J; Morley, Courtney; Olmos, David; Romero-Laorden, Nuria; Castro, Elena; Saez, Maria I; Mehra, Niven; Smeenk, Stella; Sideris, Spyridon; Gil, Thyerry; Banks, Patricia; Sandhu, Shaneen K; Sternberg, Cora N; De Giorgi, Ugo; De Bono, Johann S.
  • Rescigno P; The Institute of Cancer Research, Sutton, UK; The Royal Marsden NHS Foundation Trust, Sutton, UK; University of Naples Federico II, Naples, Italy.
  • Dolling D; Clinical Trials and Statistics Unit, The Institute of Cancer Research, London, UK.
  • Conteduca V; Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori (IRST), IRCCS, Meldola, Italy.
  • Rediti M; The Institute of Cancer Research, Sutton, UK; Jules Bordet Institut, Brussels, Belgium.
  • Bianchini D; The Royal Marsden NHS Foundation Trust, Sutton, UK.
  • Lolli C; Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori (IRST), IRCCS, Meldola, Italy.
  • Ong M; The Ottawa Hospital Cancer Centre, Ottawa, Canada.
  • Li H; The Ottawa Hospital Cancer Centre, Ottawa, Canada.
  • Omlin AG; Department of Medical Oncology and Haematology, Cantonal Hospital St. Gallen, University of Bern, Bern, Switzerland.
  • Schmid S; Department of Medical Oncology and Haematology, Cantonal Hospital St. Gallen, University of Bern, Bern, Switzerland.
  • Caffo O; Santa Chiara Hospital, Trento, Italy.
  • Zivi A; Ospedale dell'Angelo Mestre, AULSS3 Serenissima, UOC Oncologia, Venice, Italy.
  • Pezaro CJ; Monash University and Eastern Health, Box Hill, Australia.
  • Morley C; Monash University and Eastern Health, Box Hill, Australia.
  • Olmos D; Spanish National Cancer Research Center, Madrid, Spain.
  • Romero-Laorden N; Spanish National Cancer Research Center, Madrid, Spain.
  • Castro E; Spanish National Cancer Research Center, Madrid, Spain.
  • Saez MI; Hospital Virgen de la Victoria, Malaga, Spain.
  • Mehra N; Department of Medical Oncology, Radboud University Nijmegen Medical Center, Nijmegen, The Netherlands.
  • Smeenk S; Department of Medical Oncology, Radboud University Nijmegen Medical Center, Nijmegen, The Netherlands.
  • Sideris S; Jules Bordet Institut, Brussels, Belgium.
  • Gil T; Jules Bordet Institut, Brussels, Belgium.
  • Banks P; Division of Medical Oncology, Peter MacCallum Cancer Centre, Melbourne, Australia.
  • Sandhu SK; Division of Medical Oncology, Peter MacCallum Cancer Centre, Melbourne, Australia.
  • Sternberg CN; Englander Institute for Precision Medicine, Weill Cornell Medicine, New York-Presbyterian, New York, NY, USA.
  • De Giorgi U; Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori (IRST), IRCCS, Meldola, Italy.
  • De Bono JS; The Institute of Cancer Research, Sutton, UK; The Royal Marsden NHS Foundation Trust, Sutton, UK. Electronic address: johann.de-bono@icr.ac.uk.
Eur Urol Oncol ; 3(2): 176-182, 2020 04.
Article en En | MEDLINE | ID: mdl-31307958
ABSTRACT

BACKGROUND:

Declines in prostate-specific antigen (PSA) levels at 12wk are used to evaluate treatment response in metastatic castration-resistant prostate cancer (mCRPC). PSA fall by ≥30% at 4wk (PSA4w30) has been reported to be associated with better outcome in a single-centre cohort study.

OBJECTIVE:

To evaluate clinical relevance of early PSA decline in mCRPC patients treated with next-generation hormonal treatments (NGHTs) such as abiraterone and enzalutamide. DESIGN, SETTING, AND

PARTICIPANTS:

This was a retrospective multicentre analysis. Eligible patients received NGHT for mCRPC between 6 January 2006 and 31 December 2017 in 13 cancer centres worldwide, and had PSA levels assessed at baseline and at 4 and/or 12wk after treatment. PSA response was defined as a ≥30% decline (progression as a ≥25% increase) from baseline. OUTCOME MEASUREMENTS AND STATISTICAL

ANALYSIS:

Association with overall survival (OS) was analysed using landmark multivariable Cox regression adjusting for previous chemotherapy, including cancer centre as a shared frailty term. RESULTS AND

LIMITATIONS:

We identified 1358 mCRPC patients treated with first-line NGHT (1133 had PSA available at 4wk, and 948 at both 4 and 12wk). Overall, 583 (52%) had a PSA4w30; it was associated with longer OS (median 23; 95% confidence interval [CI] 21-25) compared with no change (median 17; 95% CI 15-18) and progression (median 13; 95% CI 10-15). A PSA12w30 was associated with lower mortality (median OS 22 vs 14; hazard ratio=0.57; 95% CI=0.48-0.67; p<0.001). PSA4w30 strongly correlated with PSA12w30 (ρ=0.91; 95% CI=0.90-0.92; p<0.001). In total, 432/494 (87%) with a PSA4w30 achieved a PSA12w30. Overall, 11/152 (7%) patients progressing at 4wk had a PSA12w30 (1% of the overall population).

CONCLUSIONS:

PSA changes in the first 4wk of NGHT therapies are strongly associated with clinical outcome from mCRPC and can help guide early treatment switch decisions. PATIENT

SUMMARY:

Prostate-specific antigen changes at 4wk after abiraterone/enzalutamide treatment are important to determine patients' outcome and should be taken into consideration in clinical practice.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Feniltiohidantoína / Antígeno Prostático Específico / Neoplasias de la Próstata Resistentes a la Castración / Androstenos Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans / Male Idioma: En Año: 2020 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Feniltiohidantoína / Antígeno Prostático Específico / Neoplasias de la Próstata Resistentes a la Castración / Androstenos Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans / Male Idioma: En Año: 2020 Tipo del documento: Article