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Capivasertib, an AKT Kinase Inhibitor, as Monotherapy or in Combination with Fulvestrant in Patients with AKT1 E17K-Mutant, ER-Positive Metastatic Breast Cancer.
Smyth, Lillian M; Tamura, Kenji; Oliveira, Mafalda; Ciruelos, Eva M; Mayer, Ingrid A; Sablin, Marie-Paule; Biganzoli, Laura; Ambrose, Helen J; Ashton, Jack; Barnicle, Alan; Cashell, Des D; Corcoran, Claire; de Bruin, Elza C; Foxley, Andrew; Hauser, Joana; Lindemann, Justin P O; Maudsley, Rhiannon; McEwen, Robert; Moschetta, Michele; Pass, Martin; Rowlands, Vicky; Schiavon, Gaia; Banerji, Udai; Scaltriti, Maurizio; Taylor, Barry S; Chandarlapaty, Sarat; Baselga, José; Hyman, David M.
Afiliação
  • Smyth LM; Memorial Sloan Kettering Cancer Center, New York, New York. lilsmyth@svhg.ie.
  • Tamura K; National Cancer Center Hospital, Tokyo, Japan.
  • Oliveira M; Vall d'Hebron University Hospital and Vall d'Hebron Institute of Oncology, Barcelona, Spain.
  • Ciruelos EM; Hospital Universitario 12 de Octubre, Madrid, Spain.
  • Mayer IA; Vanderbilt Breast Center, Nashville, Tennessee.
  • Sablin MP; Institut Curie, Paris, France.
  • Biganzoli L; Breast Centre, Oncology Department, Hospital of Prato, Prato, Italy.
  • Ambrose HJ; R&D Oncology, AstraZeneca, Cambridge, United Kingdom.
  • Ashton J; R&D Oncology, AstraZeneca, Cambridge, United Kingdom.
  • Barnicle A; R&D Oncology, AstraZeneca, Cambridge, United Kingdom.
  • Cashell DD; R&D Oncology, AstraZeneca, Cambridge, United Kingdom.
  • Corcoran C; R&D Oncology, AstraZeneca, Cambridge, United Kingdom.
  • de Bruin EC; R&D Oncology, AstraZeneca, Cambridge, United Kingdom.
  • Foxley A; R&D Oncology, AstraZeneca, Cambridge, United Kingdom.
  • Hauser J; R&D Oncology, AstraZeneca, Cambridge, United Kingdom.
  • Lindemann JPO; R&D Oncology, AstraZeneca, Cambridge, United Kingdom.
  • Maudsley R; R&D Oncology, AstraZeneca, Cambridge, United Kingdom.
  • McEwen R; R&D Oncology, AstraZeneca, Cambridge, United Kingdom.
  • Moschetta M; R&D Oncology, AstraZeneca, Cambridge, United Kingdom.
  • Pass M; R&D Oncology, AstraZeneca, Cambridge, United Kingdom.
  • Rowlands V; R&D Oncology, AstraZeneca, Cambridge, United Kingdom.
  • Schiavon G; R&D Oncology, AstraZeneca, Cambridge, United Kingdom.
  • Banerji U; Institute of Cancer Research and The Royal Marsden NHS Foundation Trust, London, United Kingdom.
  • Scaltriti M; Memorial Sloan Kettering Cancer Center, New York, New York.
  • Taylor BS; Memorial Sloan Kettering Cancer Center, New York, New York.
  • Chandarlapaty S; Memorial Sloan Kettering Cancer Center, New York, New York.
  • Baselga J; Memorial Sloan Kettering Cancer Center, New York, New York.
  • Hyman DM; Memorial Sloan Kettering Cancer Center, New York, New York.
Clin Cancer Res ; 26(15): 3947-3957, 2020 08 01.
Article em En | MEDLINE | ID: mdl-32312891
PURPOSE: The activating mutation AKT1 E17K occurs in approximately 7% of estrogen receptor-positive (ER+) metastatic breast cancer (MBC). We report, from a multipart, first-in-human, phase I study (NCT01226316), tolerability and activity of capivasertib, an oral AKT inhibitor, as monotherapy or combined with fulvestrant in expansion cohorts of patients with AKT1 E17K-mutant ER+ MBC. PATIENTS AND METHODS: Patients with an AKT1 E17K mutation, detected by local (next-generation sequencing) or central (plasma-based BEAMing) testing, received capivasertib 480 mg twice daily, 4 days on, 3 days off, weekly or 400 mg twice daily combined with fulvestrant at the labeled dose. Study endpoints included safety, objective response rate (ORR; RECIST v1.1), progression-free survival (PFS), and clinical benefit rate at 24 weeks (CBR24). Biomarker analyses were conducted in the combination cohort. RESULTS: From October 2013 to August 2018, 63 heavily pretreated patients received capivasertib (20 monotherapy, 43 combination). ORR was 20% with monotherapy, and within the combination cohort was 36% in fulvestrant-pretreated and 20% in fulvestrant-naïve patients, although the latter group may have had more aggressive disease at baseline. AKT1 E17K mutations were detectable in plasma by BEAMing (95%, 41/43), droplet digital PCR (80%, 33/41), and next-generation sequencing (76%, 31/41). A ≥50% decrease in AKT1 E17K at cycle 2 day 1 was associated with improved PFS. Combination therapy appeared more tolerable than monotherapy [most frequent grade ≥3 adverse events: rash (9% vs. 20%), hyperglycemia (5% vs. 30%), diarrhea (5% vs. 10%)]. CONCLUSIONS: Capivasertib demonstrated clinically meaningful activity in heavily pretreated patients with AKT1 E17K-mutant ER+ MBC, including those with prior disease progression on fulvestrant. Tolerability and activity appeared improved by the combination.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Pirimidinas / Pirróis / Neoplasias da Mama / Protocolos de Quimioterapia Combinada Antineoplásica / Proteínas Proto-Oncogênicas c-akt / Fulvestranto Tipo de estudo: Clinical_trials Limite: Adult / Aged / Female / Humans / Middle aged Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Pirimidinas / Pirróis / Neoplasias da Mama / Protocolos de Quimioterapia Combinada Antineoplásica / Proteínas Proto-Oncogênicas c-akt / Fulvestranto Tipo de estudo: Clinical_trials Limite: Adult / Aged / Female / Humans / Middle aged Idioma: En Ano de publicação: 2020 Tipo de documento: Article