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Safety and efficacy of CDX-014, an antibody-drug conjugate directed against T cell immunoglobulin mucin-1 in advanced renal cell carcinoma.
McGregor, Bradley A; Gordon, Michael; Flippot, Ronan; Agarwal, Neeraj; George, Saby; Quinn, David I; Rogalski, Mark; Hawthorne, Thomas; Keler, Tibor; Choueiri, Toni K.
Afiliação
  • McGregor BA; Dana-Farber Cancer Institute, Lank Center for Genitourinary Oncology, Boston, MA, USA.
  • Gordon M; HonorHealth Research Institute, Scottsdale, AZ, USA.
  • Flippot R; Dana-Farber Cancer Institute, Lank Center for Genitourinary Oncology, Boston, MA, USA.
  • Agarwal N; University of Utah Huntsman Cancer Institute, Salt Lake City, UT, USA.
  • George S; Roswell Park Comprehensive Cancer Center, Buffalo, NY, USA.
  • Quinn DI; University of Southern California Norris Comprehensive Cancer Center, Los Angeles, CA, USA.
  • Rogalski M; Celldex Therapeutics, Inc., Hampton, NJ, USA.
  • Hawthorne T; Celldex Therapeutics, Inc., Hampton, NJ, USA.
  • Keler T; Celldex Therapeutics, Inc., Hampton, NJ, USA.
  • Choueiri TK; Dana-Farber Cancer Institute, Lank Center for Genitourinary Oncology, Boston, MA, USA. Toni_Choueiri@dfci.harvard.edu.
Invest New Drugs ; 38(6): 1807-1814, 2020 12.
Article em En | MEDLINE | ID: mdl-32472319
CDX-014 is an antibody-drug conjugate directed against TIM-1, a surface marker highly expressed in renal cell carcinoma (RCC) and ovarian carcinoma. This phase I, first-in-human trial was conducted to evaluate the safety and preliminary activity of CDX-014 in patients with advanced refractory RCC, following a dose-escalation and dose expansion design. CDX-014 was administered intravenously at doses ranging from 0.15 to 2.0 mg/kg every 2 or 3 weeks until progression or unacceptable toxicity. Sixteen patients received at least one dose of CDX-014. The maximum tolerated dose was not identified. Most frequent adverse grade 1 or 2 adverse events included nausea (38%), fatigue, alopecia, elevation of AST and decreased appetite (25% each). Adverse events of grade 3 or more included hyperglycemia (19%), urosepsis (6%), and one multi-organ failure (6%) responsible for one treatment-related death. Two patients discontinued therapy for adverse events including fatigue grade 2 and urosepsis grade 4. CDX-014 showed antitumor activity with one prolonged partial response and a clinical benefit rate (objective response or stable disease >6 months) of 31%. The two patients that exhibited the most marked tumor shrinkage had high TIM-1 expression on tumor tissue. Overall, CDX-014 exhibited a manageable toxicity profile and early signs of activity, supporting further evaluation of antibody-drug conjugates in patients with advanced RCC and potentially other TIM-1 expressing cancers. Trial registration https://clinicaltrials.gov/ct2/show/NCT02837991 NCT02837991; July 20, 2016.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Carcinoma de Células Renais / Imunoconjugados / Receptor Celular 1 do Vírus da Hepatite A / Neoplasias Renais / Antineoplásicos Tipo de estudo: Clinical_trials Limite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Carcinoma de Células Renais / Imunoconjugados / Receptor Celular 1 do Vírus da Hepatite A / Neoplasias Renais / Antineoplásicos Tipo de estudo: Clinical_trials Limite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2020 Tipo de documento: Article