4.7 Article

NCI Comparative Oncology Program Testing of Non-Camptothecin Indenoisoquinoline Topoisomerase I Inhibitors in Naturally Occurring Canine Lymphoma

期刊

CLINICAL CANCER RESEARCH
卷 24, 期 23, 页码 5830-5840

出版社

AMER ASSOC CANCER RESEARCH
DOI: 10.1158/1078-0432.CCR-18-1498

关键词

-

类别

资金

  1. National Cancer Institute, NIH [Z01-BC006161]
  2. Division of Cancer Treatment and Diagnosis of the National Cancer Institute
  3. National Cancer Institute, National Institutes of Health [HHSN261200800001E]
  4. National Cancer Institute of the NIH [K12CA138464]
  5. NCI [HHSN261201100015C, HHSN261200422002C, HHSN261201100027C]
  6. [P30CA047904]

向作者/读者索取更多资源

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/m(2) for LMP 776 and 100 mg/m(2) for LMP744; bone marrow toxicity was dose-limiting; up to 65 mg/m(2) LMP400 was well-tolerated and MTD was not reached. None of the drugs induced notable diarrhea. Sustained tumor accumulation was observed for LMP744; gamma H2AX 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 (1319 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.govComparative-Oncology-Program) for evaluating novel therapies in immunocompetent pets with cancers.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据