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NCI Comparative Oncology Program Testing of Non-Camptothecin Indenoisoquinoline Topoisomerase I Inhibitors in Naturally Occurring Canine Lymphoma.
Burton, Jenna H; Mazcko, Christina; LeBlanc, Amy; Covey, Joseph M; Ji, Jiuping; Kinders, Robert J; Parchment, Ralph E; Khanna, Chand; Paoloni, Melissa; Lana, Sue; Weishaar, Kristen; London, Cheryl; Kisseberth, William; Krick, Erika; Vail, David; Childress, Michael; Bryan, Jeffrey N; Barber, Lisa; Ehrhart, E J; Kent, Michael; Fan, Timothy; Kow, Kelvin; Northup, Nicole; Wilson-Robles, Heather; Tomaszewski, Joseph; Holleran, Julianne L; Muzzio, Miguel; Eiseman, Julie; Beumer, Jan H; Doroshow, James H; Pommier, Yves.
Afiliação
  • Burton JH; School of Veterinary Medicine, University of California Davis, Davis, California.
  • Mazcko C; Comparative Oncology Program, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, Maryland.
  • LeBlanc A; Comparative Oncology Program, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, Maryland.
  • Covey JM; Division of Cancer Treatment and Diagnosis, National Cancer Institute, Bethesda, Maryland.
  • Ji J; Clinical Pharmacodynamic Biomarker Program, Applied/Developmental Research Directorate, Leidos Biomedical Research, Inc., NCI Campus at Frederick, Frederick, Maryland.
  • Kinders RJ; Clinical Pharmacodynamic Biomarker Program, Applied/Developmental Research Directorate, Leidos Biomedical Research, Inc., NCI Campus at Frederick, Frederick, Maryland.
  • Parchment RE; Clinical Pharmacodynamic Biomarker Program, Applied/Developmental Research Directorate, Leidos Biomedical Research, Inc., NCI Campus at Frederick, Frederick, Maryland.
  • Khanna C; Comparative Oncology Program, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, Maryland.
  • Paoloni M; Comparative Oncology Program, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, Maryland.
  • Lana S; College of Veterinary Medicine, The Ohio State University, Columbus, Ohio.
  • Weishaar K; College of Veterinary Medicine, The Ohio State University, Columbus, Ohio.
  • London C; School of Veterinary Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
  • Kisseberth W; School of Veterinary Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
  • Krick E; School of Veterinary Medicine, University of Wisconsin-Madison, Madison, Wisconsin.
  • Vail D; College of Veterinary Medicine, Purdue University, West Lafayette, Indiana.
  • Childress M; College of Veterinary Medicine, University of Missouri-Columbia, Columbia, Missouri.
  • Bryan JN; School of Veterinary Medicine, Tufts University, North Grafton, Massachusetts.
  • Barber L; College of Veterinary Medicine, University of Illinois at Urbana-Champaign, Urbana, Illinois.
  • Ehrhart EJ; College of Veterinary Medicine, The Ohio State University, Columbus, Ohio.
  • Kent M; School of Veterinary Medicine, University of California Davis, Davis, California.
  • Fan T; College of Veterinary Medicine, University of Florida, Gainesville, Florida.
  • Kow K; College of Veterinary Medicine, University of Georgia, Athens, Georgia.
  • Northup N; College of Veterinary Medicine, Texas A&M University, College Station, Texas.
  • Wilson-Robles H; Cancer Therapeutics Program, University of Pittsburgh Cancer Institute, Pittsburgh, Pennsylvania.
  • Tomaszewski J; Division of Cancer Treatment and Diagnosis, National Cancer Institute, Bethesda, Maryland.
  • Holleran JL; Life Science Group, IIT Research Institute, Chicago, Illinois.
  • Muzzio M; Developmental Therapeutics Branch and Laboratory of Molecular Pharmacology, Center for Cancer Research, National Cancer Institute, NIH, Bethesda.
  • Eiseman J; Life Science Group, IIT Research Institute, Chicago, Illinois.
  • Beumer JH; Life Science Group, IIT Research Institute, Chicago, Illinois.
  • Doroshow JH; Division of Cancer Treatment and Diagnosis, National Cancer Institute, Bethesda, Maryland.
  • Pommier Y; Developmental Therapeutics Branch and Laboratory of Molecular Pharmacology, Center for Cancer Research, National Cancer Institute, NIH, Bethesda.
Clin Cancer Res ; 24(23): 5830-5840, 2018 12 01.
Article em En | MEDLINE | ID: mdl-30061364
PURPOSE: Only one chemical class of topoisomerase I (TOP1) inhibitors is FDA approved, the camptothecins with irinotecan and topotecan widely used. Because of their limitations (chemical instability, drug efflux-mediated resistance, and diarrhea), novel TOP1 inhibitors are warranted. Indenoisoquinoline non-camptothecin topoisomerase I (TOP1) inhibitors overcome chemical instability and drug resistance that limit camptothecin use. Three indenoisoquinolines, LMP400 (indotecan), LMP776 (indimitecan), and LMP744, were examined in a phase I study for lymphoma-bearing dogs to evaluate differential efficacy, pharmacodynamics, toxicology, and pharmacokinetics. EXPERIMENTAL DESIGN: Eighty-four client-owned dogs with lymphomas were enrolled in dose-escalation cohorts for each indenoisoquinoline, with an expansion phase for LMP744. Efficacy, tolerability, pharmacokinetics, and target engagement were determined. RESULTS: The MTDs were 17.5 mg/m2 for LMP 776 and 100 mg/m2 for LMP744; bone marrow toxicity was dose-limiting; up to 65 mg/m2 LMP400 was well-tolerated and MTD was not reached. None of the drugs induced notable diarrhea. Sustained tumor accumulation was observed for LMP744; γH2AX induction was demonstrated in tumors 2 and 6 hours after treatment; a decrease in TOP1 protein was observed in most lymphoma samples across all compounds and dose levels, which is consistent with the fact that tumor response was also observed at low doses LMP744. Objective responses were documented for all indenoisoquinolines; efficacy (13/19 dogs) was greatest for LMP744. CONCLUSIONS: These results demonstrate proof-of-mechanism for indenoisoquinoline TOP1 inhibitors supporting their further clinical development. They also highlight the value of the NCI Comparative Oncology Program (https://ccr.cancer.gov/Comparative-Oncology-Program) for evaluating novel therapies in immunocompetent pets with cancers.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Inibidores da Topoisomerase I / Linfoma / Antineoplásicos Limite: Animals Idioma: En Revista: Clin Cancer Res Assunto da revista: NEOPLASIAS Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Inibidores da Topoisomerase I / Linfoma / Antineoplásicos Limite: Animals Idioma: En Revista: Clin Cancer Res Assunto da revista: NEOPLASIAS Ano de publicação: 2018 Tipo de documento: Article
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