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Implantation and Monitoring by PET/CT of an Orthotopic Model of Human Pleural Mesothelioma in Athymic Mice
Published on: December 21, 2019
Experience with peritoneal mesothelioma at the Milan National Cancer Institute
Marcello Deraco1, Dario Baratti, Antonello Domenico Cabras
1Marcello Deraco, Dario Baratti, Maria Rosaria Balestra, Shigeki Kusamura, Barbara Laterza, Department of Surgery, National Cancer Institute, 20133 Milan, Italy.
Abstract:
Diffuse malignant peritoneal mesothelioma (DMPM) is an uncommon and rapidly fatal tumor. Therapeutic options have traditionally been limited and ineffective. The biologic and molecular events correlated with poor responsiveness to therapy are still poorly understood. In recent years, an innovative treatment approach involving aggressive cytoreductive surgery (CRS) and perioperative intraperitoneal chemotherapy has reportedly resulted in improved outcome, as compared to historical controls. Since 1995, at the National Cancer Institute (NCI) of Milan (Italy), patients with DMPM have been treated with CRS and hyperthermic intra-peritoneal chemotherapy (HIPEC). In the present paper, clinical experiences and basic science investigations on DMPM at Milan NCI are reviewed. Peri-operative and long-term outcome results with CRS and HIPEC are presented. Clinico-pathological prognostic factors were investigated by multivariate analysis. The pathologic features and immunohistochemical markers related to DMPM biologic behavior were assessed in a large case-series uniformly treated at our institution. The prevalence and prognostic role of telomere maintenance mechanisms, which account for the limitless cell replicative potential of many malignancies, were studied. The dysregulation of the apoptotic pathways may play a role in the relative chemo-resistance of DMPM and a better understanding of apoptosis-related mechanisms could result in novel targeted therapeutic strategies. On this basis, the expression of survivin and other IAP family members (IAP-1, IAP-2, and X-IAP), the pro-apoptotic protein Smac/DIABLO, and antigens associated with cell proliferation (Ki-67) and apoptosis (caspase-cleaved cytokeratin-18) were analyzed. Finally, analyses of EGFR, PDGFRA and PDGFRB were performed to ascertain if deregulation of RTK could offer useful alternative therapeutic targets.
Insights
Cytoreductive surgery (CRS) combined with hyperthermic intraperitoneal chemotherapy (HIPEC) offers improved outcomes for diffuse malignant peritoneal mesothelioma (DMPM). Further research into molecular pathways like apoptosis and RTK signaling may reveal new therapeutic targets.
Area of Science:
- Oncology
- Surgical Oncology
- Molecular Biology
Background:
- Diffuse malignant peritoneal mesothelioma (DMPM) is a rare, aggressive cancer with limited treatment options.
- Understanding the molecular basis of DMPM chemoresistance is crucial for developing effective therapies.
Purpose of the Study:
- To review clinical experiences and basic science investigations of DMPM treated with CRS and HIPEC at the National Cancer Institute (NCI) of Milan.
- To investigate clinico-pathological prognostic factors and molecular markers associated with DMPM biologic behavior and treatment response.
Main Methods:
- Review of clinical data and outcomes for DMPM patients treated with CRS and HIPEC since 1995.
- Multivariate analysis of clinico-pathological prognostic factors.
- Assessment of immunohistochemical markers including telomere maintenance mechanisms, apoptosis-related proteins (survivin, IAP family, Smac/DIABLO), proliferation markers (Ki-67), and apoptosis markers (caspase-cleaved cytokeratin-18).
- Analysis of receptor tyrosine kinases (EGFR, PDGFRA, PDGFRB).
Main Results:
- CRS and HIPEC demonstrate improved outcomes for DMPM compared to historical controls.
- Specific pathologic features and immunohistochemical markers correlate with DMPM biologic behavior.
- Telomere maintenance mechanisms and dysregulation of apoptotic pathways may contribute to chemoresistance.
- Expression levels of survivin, IAP family members, Smac/DIABLO, Ki-67, and caspase-cleaved cytokeratin-18 were analyzed.
- RTK deregulation was investigated as a potential therapeutic target.
Conclusions:
- CRS and HIPEC represent a viable and effective treatment strategy for DMPM.
- Further understanding of molecular mechanisms, particularly apoptosis and RTK signaling, is essential for developing novel targeted therapies for DMPM.
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