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Results From First-in-Human Phase I Dose-Escalation Study of a Novel Bicycle Toxin Conjugate Targeting EphA2 (BT5528) in Patients With Advanced Solid Tumors.
Bashir, Babar; Wang, Judy S; Falchook, Gerald; Fontana, Elisa; Arkenau, Hendrik-Tobias; Carter, Louise; Galot, Rachel; Basu, Bristi; Greystoke, Alastair; Subbiah, Vivek; Richardson, Debra L; Orr, Hanna; Bennett, Gavin; Sharma, Rajiv; Xu, Hongmei; Paganoni, Paola; Xu, Cong; Campbell, Carly; McKean, Meredith.
Afiliação
  • Bashir B; Sidney Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, PA.
  • Wang JS; Sarah Cannon Research Institute, Nashville, TN.
  • Falchook G; Sarah Cannon Research Institute, Nashville, TN.
  • Fontana E; Florida Cancer Specialists, Sarasota, FL.
  • Arkenau HT; Sarah Cannon Research Institute at HealthONE, Denver, CO.
  • Carter L; Sarah Cannon Research Institute, London, United Kingdom.
  • Galot R; Sarah Cannon Research Institute, London, United Kingdom.
  • Basu B; The University of Manchester and The Christie NHS Foundation Trust, Manchester, UK.
  • Greystoke A; Saint Luc Cliniques Universitaires Saint-Luc, Brussels, Belgium.
  • Subbiah V; University of Cambridge and Cambridge University Hospitals NHS Foundation Trust, Cambridge, United Kingdom.
  • Richardson DL; Newcastle University, Newcastle upon Tyne, United Kingdom.
  • Orr H; Sarah Cannon Research Institute, Nashville, TN.
  • Bennett G; Sarah Cannon Research Institute, Nashville, TN.
  • Sharma R; Stephenson Cancer Center, University of Oklahoma, Oklahoma City, OK.
  • Xu H; BicycleTX Ltd, Cambridge, United Kingdom.
  • Paganoni P; BicycleTX Ltd, Cambridge, United Kingdom.
  • Xu C; BicycleTX Ltd, Cambridge, United Kingdom.
  • Campbell C; Bicycle Therapeutics, Cambridge, MA.
  • McKean M; Bicycle Therapeutics, Cambridge, MA.
J Clin Oncol ; : JCO2301107, 2024 Sep 04.
Article em En | MEDLINE | ID: mdl-39231383
ABSTRACT

PURPOSE:

BT5528 is a Bicycle Toxin Conjugate, a novel class of chemically synthesized molecules, comprising a bicyclic peptide targeting EphA2 tumor antigen, linked to a cytotoxin (monomethyl auristatin E [MMAE]). EphA2 is overexpressed in many solid tumors and contributes to oncogenesis, tumor-associated angiogenesis, and metastasis. MATERIALS AND

METHODS:

The primary objectives were to investigate the safety and tolerability of BT5528 and to define the maximum-tolerated dose, if observed, and recommended phase II dose (RP2D)/expansion dose. Dose escalation exploring once every week or once every 2 weeks administration of BT5528 employed a 3 + 3 dose-escalation design for the first two dose levels, followed by a Bayesian logistic regression model. Secondary and exploratory end points included preliminary efficacy and the pharmacokinetics of BT5528 and MMAE.

RESULTS:

Forty-five patients were enrolled and received BT5528 doses between 2.2 mg/m2 once every week to 10.0 mg/m2 once every 2 weeks within the dose-escalation stage of the study. The most frequent BT5528-related adverse events (AEs) were nausea (44.4%), diarrhea (35.6%), and fatigue (33.3%), and the most common grade ≥3 BT5528-related AE was neutropenia/neutrophil count decrease (22.2%). Dose level 6.5 mg/m2 once every 2 weeks was selected as a RP2D. At 6.5 mg/m2 once every 2 weeks, the overall response rate was 6.7%, and the disease control rate was 20.0%. BT5528 and MMAE pharmacokinetics are generally dose proportional. BT5528 has a short half-life (0.4-0.7 hours), and the half-life of MMAE is longer (35-47 hours).

CONCLUSION:

BT5528 was well tolerated and demonstrated favorable and preliminary antitumor activity. We believe these data provide preliminary validation of a Bicycle Toxin Conjugate approach to EphA2 tumor antigen. The study is ongoing and is evaluating BT5528 as monotherapy at a RP2D of 6.5 mg/m2 once every 2 weeks.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article