AI Article Synopsis

  • Electrochemotherapy (ECT) uses electroporation alongside chemotherapeutic drugs like bleomycin (BLM) to treat colorectal liver metastases, evaluated in a rat study.
  • Three groups of rats received ECT with either intravenous (i.v.), intratumoral (i.t.), or a combination of both methods for BLM injection, and various tumor metrics were measured post-treatment.
  • Results indicated that both i.v. and i.v. + i.t. groups had significantly reduced tumor oxygen saturation compared to the i.t. group, but overall tumor necrosis and other tumor characteristics were similar across all treatments, suggesting i.v. administration may be the best option in clinical practice.

Article Abstract

Electrochemotherapy (ECT) combines the reversible electroporation (rEP) with intravenous (i.v.) or intratumoral (i.t.) administration of chemotherapeutic drugs. We conducted this study to compare the efficacy of i.v., i.t., and i.v. + i.t. injection of bleomycin (BLM) in ECT treatment of colorectal hepatic metastases in a rat model. WAG/Rij rats were randomized into three groups and underwent ECT with i.v., i.t., or i.v. + i.t. injection of BLM. Tumor volumes and oxygenation were measured by means of ultrasound and photoacoustic imaging. Moreover, liver and tumor tissue were analyzed by histology and immunohistochemistry. The i.v. and i.v. + i.t. groups exhibited a 44.0% and 46.6% reduction in oxygen saturation of the tumor tissue when compared to pretreatment values, whereas the i.t. group only showed a reduction of 35.2%. The extent of tumor tissue necrosis did not statistically differ between the groups. However, the i.t. group showed a tendency towards a lower necrosis rate. Cell proliferation, apoptotic cell death, vascularization, and immune cell infiltration were comparable in the treated tumors of the three groups. ECT with i.v. administration of BLM should be preferred in clinical practice, as the combined i.v. + i.t. therapy did not show superior oncological outcomes in the present study.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11286835PMC
http://dx.doi.org/10.1038/s41598-024-67878-xDOI Listing

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