TY - JOUR
T1 - Mesothelioma
T2 - Scientific clues for prevention, diagnosis, and therapy
AU - Carbone, Michele
AU - Adusumilli, Prasad S.
AU - Alexander, H. Richard
AU - Baas, Paul
AU - Bardelli, Fabrizio
AU - Bononi, Angela
AU - Bueno, Raphael
AU - Felley-Bosco, Emanuela
AU - Galateau-Salle, Francoise
AU - Jablons, David
AU - Mansfield, Aaron S.
AU - Minaai, Michael
AU - de Perrot, Marc
AU - Pesavento, Patricia
AU - Rusch, Valerie
AU - Severson, David T.
AU - Taioli, Emanuela
AU - Tsao, Anne
AU - Woodard, Gavitt
AU - Yang, Haining
AU - Zauderer, Marjorie G.
AU - Pass, Harvey I.
N1 - Funding Information:
Corresponding author: Michele Carbone, MD, PhD, Thoracic Oncology Program, University of Hawaii Cancer Center, 701 Ilalo St, Room 437, Honolulu, HI 96813; mcarbone@cc.hawaii.edu DISCLOSURES: This work was supported by grants from the National Institutes of Health (1U01CA214195-01 and 1R01CA198138-01). Michele Carbone reports grants from the National Institutes of Health/National Cancer Institute, the US Department of Defense, the V Foundation, and the UH Foundation (“Pathogenesis of Malignant Mesothelioma”; through donations from Honeywell International Inc, Riviera United-4-a Cure, and the Maurice and Joanna Sullivan Family Foundation) during the conduct of the study; has a patent pending application for BAP1, a patent issued for “Using Anti-HMGB1 Monoclonal Antibody or other HMGB1 Antibodies as a Novel Mesothelioma Therapeutic Strategy,” and a patent issued for “HMGB1 As a Biomarker for Asbestos Exposure and Mesothelioma Early Detection”; and is a board-certified pathologist who provides consultation for mesothelioma expertise and diagnosis, including paid medical-legal consulting. Paul Baas reports grants and personal fees from Bristol-Myers Squibb and Merck Sharp & Dohme and personal fees from Aldeyra Therapeutics, Pfizer, and AstraZeneca, all outside the submitted work. Raphael Bueno reports grants from the National Cancer Institute, Roche-Genentech, Gritsone Oncology, Siemens, Merck, Epizyme, and the US Department of Defense and holds equity in and patents with Navigation Sciences, all outside the submitted work. David Jablons holds equity in Razor Genomics. Aaron Mansfield reports research funding to his institution from Verily and Novartis and from AbbVie, Genentech, and Bristol-Myers Squibb for participation on advisory boards, all outside the submitted work. Marc de Perrot reports personal fees and nonfinancial support from Bayer and personal fees from Actelion and Merck outside the submitted work. Valerie Rusch reports grants supporting institutional clinical trials from Genelux Inc and Genentech; travel support for teaching sessions from DaVinci Surgery; travel support for advisory meetings from Bristol-Myers Squibb; and personal fees from the National Institutes of Health/Coordinating Center for Clinical Trials for Thoracic Malignancy Staging Committee meetings and preparation for clinical trial review, all outside the submitted work. Anne Tsao reports grants, personal fees, and research support from Eli Lilly; personal fees and research support from Bristol-Myers Squibb, Genentech, Ariad, Merck, AstraZeneca, Boehringer-Ingelheim, and Takeda; research support from Seattle Genetics, Polaris, and Millennium Pharmaceuticals; and personal fees from Roche, Novartis, EMD Serono, and Epizyme, all outside the submitted work. Haining Yang reports grants from the National Institutes of Health/National Cancer Institute, the US Department of Defense, the V Foundation, and Riviera United-4 a Cure during the conduct of the study; a patent issued for “HMGB1 As a Biomarker for Asbestos Exposure and Mesothelioma Early Detection,” a patent issued for “Using Anti-HMGB1 Monoclonal Antibody or Other HMGB1 Antibodies as a Novel Mesothelioma Therapeutic Strategy,” a patent pending for “BAP1 Regulates IP3R3-Mediated Ca2+ Flux to Mitochondria Preventing Cellular Transformation and Regulating Gene-Environment Interaction,” and a patent pending for “Germline BAP1 Mutations Induce a Warburg Effect.” Marjorie Zauderer reports grants from the US Department of Defense, the National Cancer Institute, MedImmune, Polaris, Bristol-Myers Squibb, and Millennium Pharmaceuticals; grants and personal fees from Epizyme and Sellas Life Sciences; and personal fees from Aldeyra Therapeutics, all outside the submitted work. Harvey Pass reports funding from the National Cancer Institute, the Department of Defense, the Center for Disease Control, Genentech, and Belluck and Fox. The remaining authors made no disclosures.
Publisher Copyright:
© 2019 American Cancer Society
PY - 2019/9/1
Y1 - 2019/9/1
N2 - Mesothelioma affects mostly older individuals who have been occupationally exposed to asbestos. The global mesothelioma incidence and mortality rates are unknown, because data are not available from developing countries that continue to use large amounts of asbestos. The incidence rate of mesothelioma has decreased in Australia, the United States, and Western Europe, where the use of asbestos was banned or strictly regulated in the 1970s and 1980s, demonstrating the value of these preventive measures. However, in these same countries, the overall number of deaths from mesothelioma has not decreased as the size of the population and the percentage of old people have increased. Moreover, hotspots of mesothelioma may occur when carcinogenic fibers that are present in the environment are disturbed as rural areas are being developed. Novel immunohistochemical and molecular markers have improved the accuracy of diagnosis; however, about 14% (high-resource countries) to 50% (developing countries) of mesothelioma diagnoses are incorrect, resulting in inadequate treatment and complicating epidemiological studies. The discovery that germline BRCA1-asssociated protein 1 (BAP1) mutations cause mesothelioma and other cancers (BAP1 cancer syndrome) elucidated some of the key pathogenic mechanisms, and treatments targeting these molecular mechanisms and/or modulating the immune response are being tested. The role of surgery in pleural mesothelioma is controversial as it is difficult to predict who will benefit from aggressive management, even when local therapies are added to existing or novel systemic treatments. Treatment outcomes are improving, however, for peritoneal mesothelioma. Multidisciplinary international collaboration will be necessary to improve prevention, early detection, and treatment.
AB - Mesothelioma affects mostly older individuals who have been occupationally exposed to asbestos. The global mesothelioma incidence and mortality rates are unknown, because data are not available from developing countries that continue to use large amounts of asbestos. The incidence rate of mesothelioma has decreased in Australia, the United States, and Western Europe, where the use of asbestos was banned or strictly regulated in the 1970s and 1980s, demonstrating the value of these preventive measures. However, in these same countries, the overall number of deaths from mesothelioma has not decreased as the size of the population and the percentage of old people have increased. Moreover, hotspots of mesothelioma may occur when carcinogenic fibers that are present in the environment are disturbed as rural areas are being developed. Novel immunohistochemical and molecular markers have improved the accuracy of diagnosis; however, about 14% (high-resource countries) to 50% (developing countries) of mesothelioma diagnoses are incorrect, resulting in inadequate treatment and complicating epidemiological studies. The discovery that germline BRCA1-asssociated protein 1 (BAP1) mutations cause mesothelioma and other cancers (BAP1 cancer syndrome) elucidated some of the key pathogenic mechanisms, and treatments targeting these molecular mechanisms and/or modulating the immune response are being tested. The role of surgery in pleural mesothelioma is controversial as it is difficult to predict who will benefit from aggressive management, even when local therapies are added to existing or novel systemic treatments. Treatment outcomes are improving, however, for peritoneal mesothelioma. Multidisciplinary international collaboration will be necessary to improve prevention, early detection, and treatment.
KW - BRCA1-associated protein 1 (BAP1)
KW - asbestos
KW - cancer syndromes
KW - chromothripsis
KW - gene-environment interaction
KW - immunotherapy
KW - mesothelioma
UR - http://www.scopus.com/inward/record.url?scp=85068712177&partnerID=8YFLogxK
U2 - 10.3322/caac.21572
DO - 10.3322/caac.21572
M3 - Review article
C2 - 31283845
AN - SCOPUS:85068712177
SN - 0007-9235
VL - 69
SP - 402
EP - 429
JO - Ca-A Cancer Journal for Clinicians
JF - Ca-A Cancer Journal for Clinicians
IS - 5
ER -