AI Article Synopsis

  • Researchers have developed liposomal formulations of doxorubicin to reduce severe side effects of standard treatments, with thermosensitive versions enhancing tumor targeting and drug release through localized mild hyperthermia.
  • The study proposed combining this thermosensitive treatment with radiation therapy to improve anti-tumor effects, using a breast cancer model in mice.
  • Results showed that the multi-modal treatment strategy significantly delayed tumor growth and had a similar toxicity level as lower doses of individual therapies, suggesting promise for better breast cancer management with reduced adverse effects.

Article Abstract

Liposome formulations of the cancer drug doxorubicin have been developed to address the severe side effects that result from administration of this drug in a conventional formulation. Among them, thermosensitive liposomal doxorubicin presents enhanced tumor targeting and efficient drug release when combined with mild hyperthermia localized to the tumor site. Exploiting the radiosensitizing benefits of localized thermal therapy, the integration of radiation therapy with the thermally activated liposomal system is posited to amplify the anti-tumor efficacy. This study explored a synergistic therapeutic strategy that combines thermosensitive liposomal doxorubicin, mild hyperthermia, and radiotherapy, using an orthotopic murine model of breast cancer. The protocol of sequential multi-modal treatment, incorporating low-dose chemotherapy and radiotherapy, substantially postponed the progression of primary tumor growth in comparison to the application of monotherapy at elevated dosages. Improvements in unheated distant lesions were also observed. Furthermore, the toxicity associated with the combination treatment was comparable to that of either thermosensitive liposome treatment or radiation alone at low doses. These outcomes underscore the potential of multi-modal therapeutic strategies to refine treatment efficacy while concurrently diminishing adverse effects in the management of breast cancer, providing valuable insight for the future refinement of thermosensitive liposomal doxorubicin applications.

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http://dx.doi.org/10.1007/s13346-024-01654-2DOI Listing

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