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Therapeutic combination of radiolabeled CLR1404 with external beam radiation in head and neck cancer model systems.
Morris, Zachary S; Weichert, Jamey P; Saker, Jarob; Armstrong, Eric A; Besemer, Abigail; Bednarz, Bryan; Kimple, Randall J; Harari, Paul M.
Afiliação
  • Morris ZS; Department of Human Oncology, University of Wisconsin School of Medicine and Public Health, Madison, United States.
  • Weichert JP; Department of Radiology, University of Wisconsin School of Medicine and Public Health, Madison, United States.
  • Saker J; Department of Human Oncology, University of Wisconsin School of Medicine and Public Health, Madison, United States.
  • Armstrong EA; Department of Human Oncology, University of Wisconsin School of Medicine and Public Health, Madison, United States.
  • Besemer A; Department of Medical Physics, University of Wisconsin School of Medicine and Public Health, Madison, United States.
  • Bednarz B; Department of Medical Physics, University of Wisconsin School of Medicine and Public Health, Madison, United States.
  • Kimple RJ; Department of Human Oncology, University of Wisconsin School of Medicine and Public Health, Madison, United States.
  • Harari PM; Department of Human Oncology, University of Wisconsin School of Medicine and Public Health, Madison, United States. Electronic address: harari@humonc.wisc.edu.
Radiother Oncol ; 116(3): 504-9, 2015 Sep.
Article em En | MEDLINE | ID: mdl-26123834
ABSTRACT
BACKGROUND AND

PURPOSE:

CLR1404 is a phospholipid ether that exhibits selective uptake and retention in malignant tissues. Radiolabeled CLR1404 enables tumor-specific positron-emission tomography (PET) imaging ((124)I) and targeted delivery of ionizing radiation ((131)I). Here we describe the first preclinical studies of this diapeutic molecule in head and neck cancer (HNC) models. MATERIAL AND

METHODS:

Tumor-selective distribution of (124)I-CLR1404 and therapeutic efficacy of (131)I-CLR1404 were tested in HNC cell lines and patient-derived xenograft tumor models. Monte Carlo dose calculations and (124)I-CLR1404 PET/CT imaging were used to examine (131)I-CLR1404 dosimetry in preclinical HNC tumor models.

RESULTS:

HNC tumor xenograft studies including patient-derived xenografts demonstrate tumor-selective uptake and retention of (124)I-CLR1404 resulting in a model of highly conformal dose distribution for (131)I-CLR1404. We observe dose-dependent response to (131)I-CLR1404 with respect to HNC tumor xenograft growth inhibition and this effect is maintained together with external beam radiation.

CONCLUSIONS:

We confirm the utility of CLR1404 for tumor imaging and treatment of HNC. This promising agent warrants further investigation in a developing phase I trial combining (131)I-CLR1404 with reduced-dose external beam radiation in patients with loco-regionally recurrent HNC.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Éteres Fosfolipídicos / Carcinoma de Células Escamosas / Compostos Radiofarmacêuticos / Neoplasias de Cabeça e Pescoço / Iodobenzenos Tipo de estudo: Health_economic_evaluation Limite: Animals / Humans / Male Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Éteres Fosfolipídicos / Carcinoma de Células Escamosas / Compostos Radiofarmacêuticos / Neoplasias de Cabeça e Pescoço / Iodobenzenos Tipo de estudo: Health_economic_evaluation Limite: Animals / Humans / Male Idioma: En Ano de publicação: 2015 Tipo de documento: Article