PT  - JOURNAL ARTICLE
AU  - Dana C. Baiu
AU  - Ian R. Marsh
AU  - Alexander E. Boruch
AU  - Ankita Shahi
AU  - Saswati Bhattacharya
AU  - Justin J. Jeffery
AU  - Qianqian Zhao
AU  - Lance T. Hall
AU  - Jamey P. Weichert
AU  - Bryan P. Bednarz
AU  - Mario Otto
TI  - Targeted Molecular Radiotherapy of Pediatric Solid Tumors Using a Radioiodinated Alkyl-Phospholipid Ether Analog
AID  - 10.2967/jnumed.117.193748
DP  - 2018 Feb 01
TA  - Journal of Nuclear Medicine
PG  - 244--250
VI  - 59
IP  - 2
4099  - http://jnm.snmjournals.org/content/59/2/244.short
4100  - http://jnm.snmjournals.org/content/59/2/244.full
SO  - J Nucl Med2018 Feb 01; 59
AB  - External-beam radiotherapy plays a critical role in the treatment of most pediatric solid tumors. Particularly in children, achieving an optimal therapeutic index to avoid damage to normal tissue is extremely important. Consequently, in metastatic disease, the utility of external-beam radiotherapy is limited. Molecular radiotherapy with tumor-targeted radionuclides may overcome some of these challenges, but to date there exists no single cancer-selective agent capable of treating various pediatric malignancies independently of their histopathologic origin. We tested the therapeutic potential of the clinical-grade alkyl-phospholipid ether analog CLR1404, 18-(p-iodophenyl)octadecyl phosphocholine, as a scaffold for tumor-targeted radiotherapy of pediatric malignancies. Methods: Uptake of CLR1404 by pediatric solid tumor cells was tested in vitro by flow cytometry and in vivo by PET/CT imaging and dosimetry. The therapeutic potential of 131I-CLR1404 was evaluated in xenograft models. Results: In vitro, fluorescent CLR1404-BODIPY showed significant selective uptake in a variety of pediatric cancer lines compared with normal controls. In vivo tumor-targeted uptake in mouse xenograft models using 124I-CLR1404 was confirmed by imaging. Single-dose intravenous injection of 131I-CLR1404 significantly delayed tumor growth in all rodent pediatric xenograft models and extended animal survival while demonstrating a favorable side effect profile. Conclusion: 131I-CLR1404 has the potential to become a tumor-targeted radiotherapeutic drug with broad applicability in pediatric oncology. Because 131I-CLR1404 has entered clinical trials in adults, our data warrant the development of pediatric clinical trials for this particularly vulnerable patient population.