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Generation and Expansion of Primary, Malignant Pleural Mesothelioma Tumor Lines
Published on: April 21, 2022
Progress in the Management of Malignant Pleural Mesothelioma in 2017
Amanda J McCambridge1, Andrea Napolitano2, Aaron S Mansfield3
1Division of Pulmonary and Critical Care Medicine, Mayo Clinic, Rochester, Minnesota.
Abstract:
Malignant pleural mesothelioma (MPM) is an uncommon, almost universally fatal, asbestos-induced malignancy. New and effective strategies for diagnosis, prognostication, and treatment are urgently needed. Herein we review the advances in MPM achieved in 2017. Whereas recent epidemiological data demonstrated that the incidence of MPM-related death continued to increase in United States between 2009 and 2015, new insight into the molecular pathogenesis and the immunological tumor microenvironment of MPM, for example, regarding the role of BRCA1 associated protein 1 and the expression programmed death receptor ligand 1, are highlighting new potential therapeutic strategies. Furthermore, there continues to be an ever-expanding number of clinical studies investigating systemic therapies for MPM. These trials are primarily focused on immunotherapy using immune checkpoint inhibitors alone or in combination with other immunotherapies and nonimmunotherapies. In addition, other promising targeted therapies, including pegylated adenosine deiminase (ADI-PEG20), which focuses on argininosuccinate synthase 1-deficient tumors, and tazemetostat, an enhancer of zeste 2 polycomb repressive complex 2 subunit inhibitor of BRCA1 associated protein 1 gene (BAP1)-deficient tumors, are currently being explored.
Insights
Advances in malignant pleural mesothelioma (MPM) treatment in 2017 focused on understanding its molecular pathogenesis and tumor microenvironment. New immunotherapies and targeted drugs like ADI-PEG20 and tazemetostat show promise for this asbestos-induced cancer.
Area of Science:
- Oncology
- Immunology
- Molecular Biology
Background:
- Malignant pleural mesothelioma (MPM) is a rare, aggressive cancer linked to asbestos exposure.
- Effective diagnostic, prognostic, and therapeutic strategies for MPM remain critical due to its poor survival rates.
- Recent epidemiological data indicate a continued rise in MPM-related deaths in the United States.
Purpose of the Study:
- To review significant advancements in malignant pleural mesothelioma research and treatment strategies reported in 2017.
- To highlight emerging insights into the molecular underpinnings and immune landscape of MPM.
- To identify promising novel therapeutic targets and clinical trial directions for MPM.
Main Methods:
- Review of epidemiological data on MPM incidence and mortality.
- Analysis of research into the molecular pathogenesis, including BRCA1 associated protein 1 (BAP1) and programmed death-receptor ligand 1 (PD-L1) expression.
- Survey of ongoing clinical trials investigating systemic therapies for MPM, including immunotherapies and targeted agents.
Main Results:
- Increased understanding of MPM's molecular pathogenesis and immunological tumor microenvironment.
- Identification of BAP1 and PD-L1 as key factors in MPM development and potential therapeutic targets.
- Active clinical investigation of immune checkpoint inhibitors, other immunotherapies, and targeted agents like ADI-PEG20 and tazemetostat.
Conclusions:
- Emerging research in 2017 provided new insights into MPM's molecular and immunological characteristics.
- Novel therapeutic strategies, including immunotherapy and targeted agents, are under active clinical investigation for MPM.
- Continued research is essential to develop more effective treatments for this challenging asbestos-induced malignancy.
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