AI Article Synopsis

  • Pleural mesothelioma (PM) is a rare cancer closely associated with asbestos exposure, currently lacking effective treatment options, leading to a poor prognosis.
  • The study explores using mesenchymal stromal cells (MSCs) to deliver the chemotherapy drug Paclitaxel (PTX) directly to the pleural cavity, aiming to enhance drug concentration at the tumor site while reducing side effects.
  • The PACLIMES trial assesses the safety and toxicity of this local PTX administration in patients eligible for surgery, with a goal to identify the effective dose for future studies and evaluate its anti-tumor effects.

Article Abstract

Pleural mesothelioma (PM) is a rare and aggressive neoplasm that originates from the pleural mesothelium and whose onset is mainly linked to exposure to asbestos, which cannot be attacked with truly effective therapies with consequent poor prognosis. The rationale of this study is based on the use of mesenchymal stromal cells (MSCs) as a vehicle for chemotherapy drugs to be injected directly into the pathological site, such as the pleural cavity. The study involves the use of a conventional chemotherapeutic drug, Paclitaxel (PTX), which is widely used in the treatment of different types of solid tumors, including PM, although some limitations are related to pharmacokinetic aspects. The use of PTX-loaded MSCs to treat PM should provide several potential advantages over the systemically administered drug as reduced toxicity and increased concentration of active drug in the tumor-surrounding context. The PACLIMES trial explores the safety and toxicity of the local administration of Paclimes in chemonaive patients, candidates for pleurectomy. The secondary objective is to find the effective Paclimes dose for subsequent phase II studies and to observe and record the antitumor activity. . The experimental pre-clinical background and rationale are discussed as well.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11475395PMC
http://dx.doi.org/10.3390/cancers16193391DOI Listing

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