This project is focused on improving the treatment of pediatric sarcoma, a malignant neoplasm that arises in soft tissue and bone, comprising approximately 15% of all childhood cancers. These tumors are usually treated with multi-agent chemotherapy prior to surgical resection, and doxorubicin (DOX) is among the most commonly used agents. The cumulative dose limiting toxicity of DOX is irreversible damage to the heart muscle, which is a particular concern in children. Recently, thermosensitive liposomes (TSLs) containing DOX have been developed for directing the drug to a particular site in the body. When the liposomes pass through a heated region of tissue they release DOX very rapidly resulting in a local delivery of the drug. In parallel, a technology has been developed to precisel heat a region of tissue within the body using magnetic resonance imaging-guided high-intensity focused ultrasound therapy (referred to as MR-HIFU). MR-HIFU is well-suited for children because it is non-invasive and does not utilize ionizing radiation. Our hypothesis is that mild heating produced with MR-HIFU can be delivered safely in bone and soft tissue, and when combined with thermosensitive liposomes containing DOX will improve the therapeutic index of DOX. The project is divided into four aims that will evaluate important clinical issues including toxicity, safety, and local tumor control.
In Aim 1, image-guided drug delivery will be performed using a clinical MR-HIFU system, and the influence of heating duration on the therapeutic index of DOX will be evaluated.
In Aim 2 the reduction in DOX concentration achieved within the heart and other vital organs using this image-guided drug delivery method will be quantified.
In Aim 3 a tumor growth delay experiment will be performed in a rodent model of a human pediatric sarcoma to evaluate the local control using MR-HIFU and TSLs. Finally, in Aim 4, the capability to safely heat bone and soft tissue targets using a clinical MR-HIFU system will be evaluated. A comprehensive multi-disciplinary team has been assembled to execute this research project comprised of experts in MR-HIFU, pediatric oncologists and radiologists, pharmaceutical scientists, imaging physicists, veterinary pathologists, and biostatisticians. Further, a research partnership has been formed with Philips Healthcare, a manufacturer of MR-HIFU systems, and Celsion Corporation, the manufacturer of Thermodox(r). The research team will have access to the software, hardware, and drugs necessary for delivering hyperthermia and TSLs. This innovative technology should enable the safe delivery of high-dose chemotherapy to pediatric sarcomas prior to surgical or radiation therapy, representing a significant advance in the management of this disease. If successful, this project will lead to the development of a first in kids clinical trial of MR-HIFU targeted doxorubicin delivery for pediatric sarcomas.

Public Health Relevance

Chemotherapeutic treatments for pediatric sarcomas are still limited by the debilitating side effects to vital organs, especially the heart. This project will evaluate a novel image-guided delivery method to increase the local delivery of doxorubicin in sarcomas without increasing the dose to surrounding organs. If successful, this technology would enable the safe delivery of high-dose doxorubicin to pediatrics sarcomas prior to surgical or radiation therapy, representing a significant advance in the management of this disease.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
1R01CA199937-01
Application #
8973071
Study Section
Special Emphasis Panel (ZRG1-SBIB-Z (58))
Program Officer
Tandon, Pushpa
Project Start
2015-07-08
Project End
2020-06-30
Budget Start
2015-07-08
Budget End
2016-06-30
Support Year
1
Fiscal Year
2015
Total Cost
$554,651
Indirect Cost
$209,956
Name
University of Texas Sw Medical Center Dallas
Department
Radiation-Diagnostic/Oncology
Type
Schools of Medicine
DUNS #
800771545
City
Dallas
State
TX
Country
United States
Zip Code
75390
Munaweera, Imalka; Shaikh, Sumbul; Maples, Danny et al. (2018) Temperature-sensitive liposomal ciprofloxacin for the treatment of biofilm on infected metal implants using alternating magnetic fields. Int J Hyperthermia 34:189-200
Rosenzweig, Mark; Ali, Siraj M; Wong, Victor et al. (2017) A case of advanced infantile myofibromatosis harboring a novel MYH10-RET fusion. Pediatr Blood Cancer 64:
Staruch, Robert M; Nofiele, Joris; Walker, Jamie et al. (2017) Assessment of acute thermal damage volumes in muscle using magnetization-prepared 3D T2 -weighted imaging following MRI-guided high-intensity focused ultrasound therapy. J Magn Reson Imaging 46:354-364
Wardlow, Rachel; Bing, Chenchen; VanOsdol, Joshua et al. (2016) Targeted antibiotic delivery using low temperature-sensitive liposomes and magnetic resonance-guided high-intensity focused ultrasound hyperthermia. Int J Hyperthermia 32:254-64
Bing, Chenchen; Staruch, Robert M; Tillander, Matti et al. (2016) Drift correction for accurate PRF-shift MR thermometry during mild hyperthermia treatments with MR-HIFU. Int J Hyperthermia 32:673-87
Shim, Jenny; Staruch, Robert M; Koral, Korgun et al. (2016) Pediatric Sarcomas Are Targetable by MR-Guided High Intensity Focused Ultrasound (MR-HIFU): Anatomical Distribution and Radiological Characteristics. Pediatr Blood Cancer 63:1753-60
Ramsay, Elizabeth; Mougenot, Charles; Kazem, Mohammad et al. (2015) Temperature-dependent MR signals in cortical bone: potential for monitoring temperature changes during high-intensity focused ultrasound treatment in bone. Magn Reson Med 74:1095-102
Huisman, Merel; Staruch, Robert M; Ladouceur-Wodzak, Michelle et al. (2015) Non-Invasive Targeted Peripheral Nerve Ablation Using 3D MR Neurography and MRI-Guided High-Intensity Focused Ultrasound (MR-HIFU): Pilot Study in a Swine Model. PLoS One 10:e0144742
Bing, Chenchen; Nofiele, Joris; Staruch, Robert et al. (2015) Localised hyperthermia in rodent models using an MRI-compatible high-intensity focused ultrasound system. Int J Hyperthermia 31:813-22