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A phase I, dose-escalation study of PF-06650808, an anti-Notch3 antibody-drug conjugate, in patients with breast cancer and other advanced solid tumors.
Rosen, Lee S; Wesolowski, Robert; Baffa, Raffaele; Liao, Kai-Hsin; Hua, Steven Y; Gibson, Brenda L; Pirie-Shepherd, Steven; Tolcher, Anthony W.
Afiliação
  • Rosen LS; David Geffen School of Medicine, Division of Hematology-Oncology, University of California Los Angeles Medical Center, 2020 Santa Monica Blvd., Ste. 600, Santa Monica, CA, 90404, USA. LRosen@mednet.ucla.edu.
  • Wesolowski R; Ohio State University Comprehensive Cancer Center, 320 West 10th Ave., Columbus, OH, 43210, USA.
  • Baffa R; Pfizer, 10724 Science Center Drive, San Diego, CA, 92121, USA.
  • Liao KH; Pfizer, 10724 Science Center Drive, San Diego, CA, 92121, USA.
  • Hua SY; Pfizer, 10724 Science Center Drive, San Diego, CA, 92121, USA.
  • Gibson BL; Pfizer, 10724 Science Center Drive, San Diego, CA, 92121, USA.
  • Pirie-Shepherd S; Pfizer, 10724 Science Center Drive, San Diego, CA, 92121, USA.
  • Tolcher AW; START Center for Cancer Care, 4383 Medical Dr., San Antonio, TX, 78229, USA.
Invest New Drugs ; 38(1): 120-130, 2020 02.
Article em En | MEDLINE | ID: mdl-30887250
Background PF-06650808 is a novel anti-Notch3 antibody-drug conjugate (ADC) able to deliver an auristatin-based cytotoxic payload to target cells. In this first-in-human, dose-finding, phase I study (NCT02129205), we investigated safety, pharmacokinetics, immunogenicity, and preliminary antitumor activity of single-agent PF-06650808 in 40 patients with advanced breast cancer (BC) and other solid tumors unselected for Notch3 expression. Primary endpoint was dose-limiting toxicity (DLT). PF-06650808 was administered intravenously every 3 weeks at a starting dose of 0.2 mg/kg, escalated up to 6.4 mg/kg following the modified continual reassessment method. An additional dose level, 2.0 mg/kg, was evaluated in patients with advanced, estrogen receptor-positive (ER+) BC. Results The majority of patients had advanced BC (60%) and almost all (90%) had received ≥3 prior lines of anticancer therapy. Treatment with PF-06650808 was generally well tolerated at dose levels ≤2.0 mg/kg with no DLTs. The maximum tolerated dose (MTD) was estimated to be 2.4 mg/kg. The most common treatment-related AEs in all patients were fatigue (40.0%), decreased appetite (37.5%), nausea (35.0%), alopecia (32.5%), abdominal pain (25.0%), pruritus (25.0%), and vomiting (25.0%). Five patients achieved a partial response (PR), including 2 unconfirmed PRs; 4 of the responders had ER+/PR+/HER2- BC. Sixteen (51.6%) patients achieved stable disease, including 8 (57.1%) of 14 patients with ER+ BC. Tumor samples from all responders tested positive for NOTCH3 expression in a retrospective, exploratory analysis. Conclusions The anti-Notch3 ADC PF-06650808 has demonstrated a manageable safety profile and early signs of antitumor activity in patients with advanced BC.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Observational_studies / Prognostic_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Observational_studies / Prognostic_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2020 Tipo de documento: Article