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Pembrolizumab plus Olaparib in Patients with Metastatic Castration-resistant Prostate Cancer: Long-term Results from the Phase 1b/2 KEYNOTE-365 Cohort A Study.
Yu, Evan Y; Piulats, Josep M; Gravis, Gwenaelle; Fong, Peter C C; Todenhöfer, Tilman; Laguerre, Brigitte; Arranz, Jose A; Oudard, Stephane; Massard, Christophe; Heinzelbecker, Julia; Nordquist, Luke T; Carles, Joan; Kolinsky, Michael P; Augustin, Marinela; Gurney, Howard; Tafreshi, Ali; Li, Xin Tong; Qiu, Ping; Poehlein, Christian H; Schloss, Charles; de Bono, Johann S.
Afiliación
  • Yu EY; University of Washington and Fred Hutchinson Cancer Center, Seattle, WA, USA. Electronic address: evanyu@u.washington.edu.
  • Piulats JM; Catalan Institute of Oncology, Barcelona, Spain.
  • Gravis G; Institut Paoli Calmettes, Marseille, France.
  • Fong PCC; Auckland City Hospital, Auckland, New Zealand; University of Auckland, Auckland, New Zealand.
  • Todenhöfer T; Studienpraxis Urologie, Nürtingen, Germany.
  • Laguerre B; Centre Eugène Marquis, Rennes, France.
  • Arranz JA; General University Hospital Gregorio Marañón, Madrid, Spain.
  • Oudard S; Hôpital Européen Georges Pompidou, University of Paris, Paris, France.
  • Massard C; Gustave Roussy, Cancer Campus, Villejuif, France; Paris-Saclay University, Villejuif, France.
  • Heinzelbecker J; Saarland University Medical Center, Homburg, Germany; Faculty of Medicine, Saarland University, Homburg, Germany.
  • Nordquist LT; GU Research Network-Urology Cancer Center, Omaha, NE, USA.
  • Carles J; Vall d'Hebron Institute of Oncology, Vall d'Hebron, Barcelona, Spain.
  • Kolinsky MP; Cross Cancer Institute and University of Alberta, Edmonton, AB, Canada.
  • Augustin M; Paracelsus Medical University, Nuremberg, Germany.
  • Gurney H; Macquarie University, Sydney, Australia.
  • Tafreshi A; University of Wollongong, Wollongong, NSW, Australia.
  • Li XT; Merck & Co., Inc., Rahway, NJ, USA.
  • Qiu P; Merck & Co., Inc., Rahway, NJ, USA.
  • Poehlein CH; Merck & Co., Inc., Rahway, NJ, USA.
  • Schloss C; Merck & Co., Inc., Rahway, NJ, USA.
  • de Bono JS; The Institute of Cancer Research and the Royal Marsden, London, UK.
Eur Urol ; 83(1): 15-26, 2023 Jan.
Article en En | MEDLINE | ID: mdl-36055895
ABSTRACT

BACKGROUND:

Pembrolizumab and olaparib have shown single-agent activity in patients with previously treated metastatic castration-resistant prostate cancer (mCRPC).

OBJECTIVE:

To evaluate the efficacy and safety of pembrolizumab plus olaparib in mCRPC. DESIGN, SETTING, AND

PARTICIPANTS:

Cohort A of the phase 1b/2 KEYNOTE-365 study enrolled patients with molecularly unselected, docetaxel-pretreated mCRPC whose disease progressed within 6 mo of screening. INTERVENTION Pembrolizumab 200 mg intravenously every 3 wk plus olaparib 400-mg capsule or 300-mg tablet orally twice daily. OUTCOME MEASUREMENTS AND STATISTICAL

ANALYSIS:

The primary endpoints were safety, confirmed prostate-specific antigen (PSA) response rate, and objective response rate (ORR) as per Response Evaluation Criteria in Solid Tumors (RECIST), version 1.1, by blinded independent central review. The secondary endpoints included radiographic progression-free survival (rPFS) and overall survival (OS). RESULTS AND

LIMITATIONS:

Of 104 enrolled patients, 102 were treated. The median age was 70 yr (interquartile range [IQR], 65-76), and 59 patients (58%) had measurable disease as per RECIST v1.1. The median time from the first dose to database cutoff was 24 mo (IQR, 22-47). The confirmed PSA response rate was 15%. The confirmed ORR was 8.5% (five partial responses) for patients with measurable disease. The median rPFS was 4.5 mo (95% confidence interval [CI], 4.0-6.5) and median OS was 14 mo (95% CI, 10.4-18.2). Clinical activity was consistent across the programmed death ligand 1 (PD-L1)-positive and homologous recombination repair mutation subgroups. Treatment-related adverse events (TRAEs) occurred in 93 patients (91%). Grade 3-5 TRAEs occurred in 49 patients (48%). Six deaths (5.9%) were due to adverse events; two (myocardial infarction and unknown cause) were attributed to treatment. Limitations of the study include the single-arm design.

CONCLUSIONS:

Pembrolizumab plus olaparib had a safety profile consistent with the profiles of the individual agents and demonstrated antitumor activity in previously treated patients with molecularly unselected, docetaxel-pretreated mCRPC. PATIENT

SUMMARY:

Pembrolizumab plus olaparib showed antitumor activity and expected safety in patients with metastatic castration-resistant prostate cancer.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Neoplasias de la Próstata Resistentes a la Castración Tipo de estudio: Etiology_studies Límite: Aged / Humans / Male Idioma: En Revista: Eur Urol Año: 2023 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Neoplasias de la Próstata Resistentes a la Castración Tipo de estudio: Etiology_studies Límite: Aged / Humans / Male Idioma: En Revista: Eur Urol Año: 2023 Tipo del documento: Article