TY - JOUR
T1 - Thymic Carcinomas—A Concise Multidisciplinary Update on Recent Developments From the Thymic Carcinoma Working Group of the International Thymic Malignancy Interest Group
AU - Roden, Anja C.
AU - Ahmad, Usman
AU - Cardillo, Giuseppe
AU - Girard, Nicolas
AU - Jain, Deepali
AU - Marom, Edith M.
AU - Marx, Alexander
AU - Moreira, Andre L.
AU - Nicholson, Andrew G.
AU - Rajan, Arun
AU - Shepherd, Annemarie F.
AU - Simone, Charles B.
AU - Strange, Chad D.
AU - Szolkowska, Malgorzata
AU - Truong, Mylene T.
AU - Rimner, Andreas
N1 - Funding Information:
Disclosure: Dr. Marom received honoraria for lectures from Merck Sharp & Dohme and Boehringer Ingelheim. Dr. Moreira received consulting fees from Hoffman-La Roche and participated on a data safety monitoring board or advisory board of Olympus Corporation. Dr. Nicholson received consultation fees from Merck, Boehringer Ingelheim, Pfizer, Novartis, AstraZeneca, Bristol-Myers Squibb, Roche, AbbVie, Oncologica, and Takeda UK; a research grant from Pfizer; and payment for provision of educational materials from UpToDate, European Society of Oncology, and Liberum. Dr. Roden received honorarium for contributing educational material to UpToDate. Dr. Shepherd received support for attending meetings and travel from Memorial Sloan Kettering Cancer Center. Dr. Simone received an honorarium from Varian Medical Systems; is the chair of the NRG Oncology Particle Therapy Work Group; and is the President of the Board of Directors of the Proton Collaborative Group. Dr. Szolkowska received honoraria for lectures from Boehringer Ingelheim, AstraZeneca Pharma Poland, Roche Polska, and Merck Sharp & Dohme Polska; is the Secretary of ITMIG; Chair of a working group of the ESP; and member of the main revisory board of the Polish Society of Pathology. Dr. Rimner has grant funding for investigator-initiated trials to Memorial Sloan Kettering Cancer Center from Varian Medical Systems, AstraZeneca, Merck, Pfizer, and Boehringer Ingelheim; received consultation fees from Boehringer Ingelheim, AstraZeneca, Merck, Cybrexa, and MoreHealth; received honorarium from ResearchToPractice; received travel support from Philips/Elekta; is scientific advisory board member for KEYLYNK-012 and KEYLYNK-013 studies for Merck; and is Vice President of ITMIG, board member of IMIG, Chair of the lung track of the Annual ASTRO meeting, and member of the Board of examiners of the American Board of Radiology. The remaining authors declare no conflict of interest.
Funding Information:
This research was funded in part by the Intramural Research Program of the National Institutes of Health (NIH), National Cancer Institute (NCI), Center for Cancer Research (Dr. Rajan), and through the NIH/NCI Cancer Center Support Grant P30 CA008748 (Drs. Rimner, Shepherd, and Simone).
Publisher Copyright:
© 2022 International Association for the Study of Lung Cancer
PY - 2022/5
Y1 - 2022/5
N2 - Thymic carcinomas are rare malignancies that in general arise in the prevascular (anterior) mediastinum. These tumors are usually invasive, often present at advanced stages, and typically behave aggressively. Studies are hampered by the paucity of these tumors, the large variety of carcinoma subtypes, and the lack of unique morphologic and immunophenotypic features. Despite these challenges, advances in diagnostic imaging, surgical approaches, systemic therapies, and radiation therapy techniques have been made. The WHO classification of thymic epithelial tumors has been updated in 2021, and the eighth tumor nodal metastasis staging by the American Joint Committee on Cancer/Union for International Cancer Control included thymic carcinomas in 2017. Molecular alterations that provide more insight into the pathogenesis of these tumors and that potentially permit use of novel targeted therapies are increasingly being identified. New approaches to radiation therapy, chemotherapy, and immunotherapy are under evaluation. International societies, including the International Thymic Malignancy Interest Group, European Society of Thoracic Surgeons, and Japanese, Chinese, and Korean thymic associations, have been critical in organizing and conducting multi-institutional clinical studies. Herein, we review contemporary multidisciplinary perspectives in diagnosis and management of thymic carcinoma.
AB - Thymic carcinomas are rare malignancies that in general arise in the prevascular (anterior) mediastinum. These tumors are usually invasive, often present at advanced stages, and typically behave aggressively. Studies are hampered by the paucity of these tumors, the large variety of carcinoma subtypes, and the lack of unique morphologic and immunophenotypic features. Despite these challenges, advances in diagnostic imaging, surgical approaches, systemic therapies, and radiation therapy techniques have been made. The WHO classification of thymic epithelial tumors has been updated in 2021, and the eighth tumor nodal metastasis staging by the American Joint Committee on Cancer/Union for International Cancer Control included thymic carcinomas in 2017. Molecular alterations that provide more insight into the pathogenesis of these tumors and that potentially permit use of novel targeted therapies are increasingly being identified. New approaches to radiation therapy, chemotherapy, and immunotherapy are under evaluation. International societies, including the International Thymic Malignancy Interest Group, European Society of Thoracic Surgeons, and Japanese, Chinese, and Korean thymic associations, have been critical in organizing and conducting multi-institutional clinical studies. Herein, we review contemporary multidisciplinary perspectives in diagnosis and management of thymic carcinoma.
KW - ITMIG
KW - International Thymic Malignancy Interest Group
KW - TNM staging
KW - Thymic carcinoma
KW - WHO
UR - http://www.scopus.com/inward/record.url?scp=85126509834&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85126509834&partnerID=8YFLogxK
U2 - 10.1016/j.jtho.2022.01.021
DO - 10.1016/j.jtho.2022.01.021
M3 - Review article
C2 - 35227908
AN - SCOPUS:85126509834
SN - 1556-0864
VL - 17
SP - 637
EP - 650
JO - Journal of Thoracic Oncology
JF - Journal of Thoracic Oncology
IS - 5
ER -