AI Article Synopsis

  • Clinical outcomes for peritoneal carcinomatosis (PC) remain poor, but microsphere-based intraperitoneal chemotherapy shows promise based on preclinical studies.
  • This review discusses current treatment strategies for PC, the advantages of using microspheres, the complications of peritoneal adhesions they cause, and possible solutions to these issues.
  • Future research should focus on improving microsphere formulations with biocompatible materials and optimal sizes to enhance drug distribution and tumor targeting, potentially improving treatment efficacy for PC.

Article Abstract

Introduction: Clinical outcomes for the treatment of peritoneal carcinomatosis (PC) have remained suboptimal. Microsphere-based intraperitoneal chemotherapy has shown considerable potential in preclinical studies. However, due to the complications associated with peritoneal adhesions, there has been a lack of comprehensive reviews focusing on the progress of microsphere applications in the treatment of PC.

Areas Covered: We provide an overview of the current clinical treatment strategies for PC and analyze the potential advantages of microspheres in this context. Regarding the issue of peritoneal adhesions induced by microspheres, we investigate the underlying mechanisms and propose possible solutions. Furthermore, we outline the future directions for the development of microsphere-based therapies in the treatment of PC.

Expert Opinion: Microspheres formulated with highly biocompatible materials to the peritoneum, such as sodium alginate, gelatin, or genipin, or with an optimal particle size (4 ~ 30 μm) and lower molecular weights (10 ~ 57 kDa), can prevent peritoneal adhesions and improve drug distribution. To further enhance the antitumor efficacy, enhancing the tumor penetration capability and specificity of microspheres, optimizing intraperitoneal distribution, and addressing tumor resistance have demonstrated significant potential in preclinical studies, offering new therapeutic prospects for the treatment of PC.

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Source
http://dx.doi.org/10.1080/17425247.2024.2439462DOI Listing

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