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Preclinical Validation of a Single-Treatment Infusion Modality That Can Eradicate Extremity Melanomas
- Source :
- Cancer research. 76(22)
- Publication Year :
- 2015
-
Abstract
- Isolated limb perfusion (ILP) with the chemotherapeutic agent melphalan is an effective treatment option for extremity in-transit melanoma but is toxic and technically challenging to deliver locoregionally. CBL0137 is an experimental clinical drug with broad anticancer activity in animal models, owing to its ability to bind DNA in a nongenotoxic manner and inactivate the FACT chromatin modulator essential for tumor cell viability. Here, we report that CBL0137 delivered by ILP in a murine melanoma model is as efficacious as melphalan, displaying antitumor activity at doses corresponding to only a fraction of the systemic MTD of CBL0137. The ability to bind DNA quickly combined with a favorable safety profile made it possible to substitute CBL0137 in the ILP protocol, using an intra-arterial infusion method, to safely achieve effective tumor suppression. Our findings of a preclinical proof of concept for CBL0137 and its administration via intra-arterial infusion as a superior treatment compared with melphalan ILP allows for locoregional treatment anywhere a catheter can be placed. Cancer Res; 76(22); 6620–30. ©2016 AACR.
- Subjects :
- 0301 basic medicine
Melphalan
Drug
Cancer Research
medicine.medical_specialty
media_common.quotation_subject
Validation Studies as Topic
Article
03 medical and health sciences
Mice
0302 clinical medicine
medicine
Effective treatment
Animals
Humans
Melanoma
Infusion Pumps
media_common
Antitumor activity
Modality (human–computer interaction)
business.industry
Cancer
Extremities
medicine.disease
Surgery
Mice, Inbred C57BL
030104 developmental biology
Treatment Outcome
Oncology
030220 oncology & carcinogenesis
Cancer research
Female
business
B16 melanoma
medicine.drug
Subjects
Details
- ISSN :
- 15387445
- Volume :
- 76
- Issue :
- 22
- Database :
- OpenAIRE
- Journal :
- Cancer research
- Accession number :
- edsair.doi.dedup.....72838778b44f256037445e4cbcc3eef6