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A phase I open-label dose-escalation study of the anti-HER3 monoclonal antibody LJM716 in patients with advanced squamous cell carcinoma of the esophagus or head and neck and HER2-overexpressing breast or gastric cancer.
Reynolds, Kerry Lynn; Bedard, Philippe L; Lee, Se-Hoon; Lin, Chia-Chi; Tabernero, Josep; Alsina, Maria; Cohen, Ezra; Baselga, José; Blumenschein, George; Graham, Donna M; Garrido-Laguna, Ignacio; Juric, Dejan; Sharma, Sunil; Salgia, Ravi; Seroutou, Abdelkader; Tian, Xianbin; Fernandez, Rose; Morozov, Alex; Sheng, Qing; Ramkumar, Thiruvamoor; Zubel, Angela; Bang, Yung-Jue.
Afiliação
  • Reynolds KL; Massachusetts General Hospital, 55 Fruit Street, Boston, MA, 02114, USA. kreynolds7@partners.org.
  • Bedard PL; Princess Margaret Cancer Centre, Toronto, ON, Canada.
  • Lee SH; Seoul National University College of Medicine, Seoul, Republic of Korea.
  • Lin CC; National Taiwan University Hospital, Taipei, Taiwan.
  • Tabernero J; Vall d'Hebron University Hospital and Institute of Oncology (VHIO), Universitat Autònoma de Barcelona, Barcelona, Spain.
  • Alsina M; Vall d'Hebron University Hospital and Institute of Oncology (VHIO), Universitat Autònoma de Barcelona, Barcelona, Spain.
  • Cohen E; Moores Cancer Center, University of California at San Diego, La Jolla, CA, USA.
  • Baselga J; Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Blumenschein G; Department of Thoracic/Head and Neck Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
  • Graham DM; Princess Margaret Cancer Centre, Toronto, ON, Canada.
  • Garrido-Laguna I; Huntsman Cancer Institute, Salt Lake City, UT, USA.
  • Juric D; Massachusetts General Hospital, 55 Fruit Street, Boston, MA, 02114, USA.
  • Sharma S; Huntsman Cancer Institute, Salt Lake City, UT, USA.
  • Salgia R; University of Chicago, Chicago, IL, USA.
  • Seroutou A; City of Hope, Department of Medical Oncology and Therapeutics Research, Duarte, CA, USA.
  • Tian X; Novartis Pharma AG, Basel, Switzerland.
  • Fernandez R; Novartis Pharmaceuticals Corporation, East Hanover, NJ, USA.
  • Morozov A; Novartis Pharmaceuticals Corporation, East Hanover, NJ, USA.
  • Sheng Q; Novartis Pharmaceuticals Corporation, East Hanover, NJ, USA.
  • Ramkumar T; Pfizer Inc., New York, NY, USA.
  • Zubel A; Novartis Institutes for BioMedical Research, Cambridge, MA, USA.
  • Bang YJ; Novartis Pharmaceuticals Corporation, East Hanover, NJ, USA.
BMC Cancer ; 17(1): 646, 2017 Sep 12.
Article em En | MEDLINE | ID: mdl-28899363
ABSTRACT

BACKGROUND:

Human epidermal growth factor receptor 3 (HER3) is important in maintaining epidermal growth factor receptor-driven cancers and mediating resistance to targeted therapy. A phase I study of anti-HER3 monoclonal antibody LJM716 was conducted with the primary objective to identify the maximum tolerated dose (MTD) and/or recommended dose for expansion (RDE), and dosing schedule. Secondary objectives were to characterize safety/tolerability, pharmacokinetics, pharmacodynamics, and preliminary antitumor activity.

METHODS:

This open-label, dose-finding study comprised dose escalation, followed by expansion in patients with squamous cell carcinoma of the head and neck or esophagus, and HER2-overexpressing metastatic breast cancer or gastric cancer. During dose escalation, patients received LJM716 intravenous once weekly (QW) or every two weeks (Q2W), in 28-day cycles. An adaptive Bayesian logistic regression model was used to guide dose escalation and establish the RDE. Exploratory pharmacodynamic tumor studies evaluated modulation of HER3 signaling.

RESULTS:

Patients received LJM716 3-40 mg/kg QW and 20 mg/kg Q2W (54 patients; 36 patients at 40 mg/kg QW). No dose-limiting toxicities (DLTs) were reported during dose-escalation. One patient experienced two DLTs (diarrhea, hypokalemia [both grade 3]) in the expansion phase. The RDE was 40 mg/kg QW, providing drug levels above the preclinical minimum effective concentration. One patient with gastric cancer had an unconfirmed partial response; 17/54 patients had stable disease, two lasting >30 weeks. Down-modulation of phospho-HER3 was observed in paired tumor samples.

CONCLUSIONS:

LJM716 was well tolerated; the MTD was not reached, and the RDE was 40 mg/kg QW. Further development of LJM716 is ongoing. TRIAL REGISTRATION Clinicaltrials.gov registry number NCT01598077 (registered on 4 May, 2012).
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Gástricas / Neoplasias da Mama / Neoplasias Esofágicas / Carcinoma de Células Escamosas / Antineoplásicos Imunológicos / Neoplasias de Cabeça e Pescoço Tipo de estudo: Prognostic_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Gástricas / Neoplasias da Mama / Neoplasias Esofágicas / Carcinoma de Células Escamosas / Antineoplásicos Imunológicos / Neoplasias de Cabeça e Pescoço Tipo de estudo: Prognostic_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2017 Tipo de documento: Article