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Pembrolizumab Plus Docetaxel and Prednisone in Patients with Metastatic Castration-resistant Prostate Cancer: Long-term Results from the Phase 1b/2 KEYNOTE-365 Cohort B Study.
Yu, Evan Y; Kolinsky, Michael P; Berry, William R; Retz, Margitta; Mourey, Loic; Piulats, Josep M; Appleman, Leonard J; Romano, Emanuela; Gravis, Gwenaelle; Gurney, Howard; Bögemann, Martin; Emmenegger, Urban; Joshua, Anthony M; Linch, Mark; Sridhar, Srikala; Conter, Henry J; Laguerre, Brigitte; Massard, Christophe; Li, Xin Tong; Schloss, Charles; Poehlein, Christian H; de Bono, Johann S.
Affiliation
  • Yu EY; Department of Medicine, Division of Oncology, University of Washington and Fred Hutchinson Cancer Research Center, G4-830, Seattle, WA, USA. Electronic address: evanyu@u.washington.edu.
  • Kolinsky MP; Department of Oncology, Cross Cancer Institute, Edmonton, AB, Canada.
  • Berry WR; Department of Medical Oncology, Duke Cancer Center Cary, Cary, NC, USA.
  • Retz M; Department of Urology, Rechts der Isar Medical Center, Technical University of Munich, Munich, Germany.
  • Mourey L; Department of Medical Oncology, Institut Universitaire du Cancer de Toulouse - Oncopole, Toulouse, France.
  • Piulats JM; Department of Medical Oncology, Catalan Institute of Oncology, Barcelona, Spain.
  • Appleman LJ; Department of Hematology/Oncology, Department of Medicine, University of Pittsburgh, Pittsburgh, PA, USA.
  • Romano E; Department of Medical Oncology, Center for Cancer Immunotherapy, Institut Curie, Paris, France.
  • Gravis G; Department of Medical Oncology, Institut Paoli Calmettes, Aix-Marseille Université, Marseille, France.
  • Gurney H; Department of Medical Oncology, Macquarie University, Sydney, NSW, Australia.
  • Bögemann M; Department of Urology, University Hospital Münster, Münster, Germany.
  • Emmenegger U; Division of Medical Oncology, Odette Cancer Centre and Sunnybrook Research Institute, Toronto, ON, Canada.
  • Joshua AM; Department of Medical Oncology, Kinghorn Cancer Centre, St Vincent's Hospital, Sydney, NSW, Australia.
  • Linch M; Department of Oncology, University College London Hospital and UCL Cancer Institute, London, UK.
  • Sridhar S; Cancer Clinical Research Unit, UHN Princess Margaret Cancer Centre, Toronto, ON, Canada.
  • Conter HJ; Department of Medical Oncology, University of Western Ontario, Brampton, ON, Canada.
  • Laguerre B; Department of Medical Oncology, Centre Eugene Marquis, Rennes, France.
  • Massard C; Department of Drug Development, Gustave Roussy Cancer Campus and Université Paris-Sud, Villejuif, France; Department of Medical Oncology, Gustave Roussy Cancer Campus and Université Paris-Sud, Villejuif, France.
  • Li XT; Department of Medical Oncology, Merck & Co., Inc., Kenilworth, NJ, USA.
  • Schloss C; Department of Medical Oncology, Merck & Co., Inc., Kenilworth, NJ, USA.
  • Poehlein CH; Department of Medical Oncology, Merck & Co., Inc., Kenilworth, NJ, USA.
  • de Bono JS; Division of Clinical Studies, The Royal Marsden Hospital and The Institute of Cancer Research, London, UK.
Eur Urol ; 82(1): 22-30, 2022 07.
Article in En | MEDLINE | ID: mdl-35397952
ABSTRACT

BACKGROUND:

Patients with metastatic castration-resistant prostate cancer (mCRPC) frequently receive docetaxel after they develop resistance to abiraterone or enzalutamide and need more efficacious treatments.

OBJECTIVE:

To evaluate the efficacy and safety of pembrolizumab plus docetaxel and prednisone in patients with mCRPC. DESIGN, SETTING, AND

PARTICIPANTS:

The trial included patients with mCRPC in the phase 1b/2 KEYNOTE-365 cohort B study who were chemotherapy naïve and who experienced failure of or were intolerant to ≥4 wk of abiraterone or enzalutamide for mCRPC with progressive disease within 6 mo of screening. INTERVENTION Pembrolizumab 200 mg intravenously (IV) every 3 wk (Q3W), docetaxel 75 mg/m2 IV Q3W, and prednisone 5 mg orally twice daily. OUTCOME MEASUREMENTS AND STATISTICAL

ANALYSIS:

The primary endpoints were safety, the prostate-specific antigen (PSA) response rate, and the objective response rate (ORR) according to Response Evaluation Criteria in Solid Tumors version 1.1 (RECIST v1.1) by blinded independent central review (BICR). Secondary endpoints included time to PSA progression; the disease control rate (DCR) and duration of response (DOR) according to RECIST v1.1 by BICR; ORR, DCR, DOR, and radiographic progression-free survival (rPFS) according to Prostate Cancer Working Group 3-modified RECIST v1.1 by BICR; and overall survival (OS). RESULTS AND

LIMITATIONS:

Among 104 treated patients, 52 had measurable disease. The median time from allocation to data cutoff (July 9, 2020) was 32.4 mo, during which 101 patients discontinued treatment, 81 (78%) for disease progression. The confirmed PSA response rate was 34% and the confirmed ORR (RECIST v1.1) was 23%. Median rPFS and OS were 8.5 mo and 20.2 mo, respectively. Treatment-related adverse events (TRAEs) occurred in 100 patients (96%). Grade 3-5 TRAEs occurred in 46 patients (44%). Seven AE-related deaths (6.7%) occurred (2 due to treatment-related pneumonitis). Limitations of the study include the single-arm design and small sample size.

CONCLUSIONS:

Pembrolizumab plus docetaxel and prednisone demonstrated antitumor activity in chemotherapy-naïve patients with mCRPC treated with abiraterone or enzalutamide for mCRPC. Safety was consistent with profiles for the individual agents. Further investigation is warranted. PATIENT

SUMMARY:

We evaluated the efficacy and safety of the anti-PD-1 antibody pembrolizumab combined with the chemotherapy drug docetaxel and the steroid prednisone for patients with metastatic prostate cancer resistant to androgen deprivation therapy , and who never received chemotherapy. The combination showed antitumor activity and manageable safety in this patient population. This trial is registered on ClinicalTrials.gov as NCT02861573.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Antineoplastic Combined Chemotherapy Protocols / Prostatic Neoplasms, Castration-Resistant Type of study: Etiology_studies / Risk_factors_studies Limits: Humans / Male Language: En Journal: Eur Urol Year: 2022 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Antineoplastic Combined Chemotherapy Protocols / Prostatic Neoplasms, Castration-Resistant Type of study: Etiology_studies / Risk_factors_studies Limits: Humans / Male Language: En Journal: Eur Urol Year: 2022 Document type: Article