Addressing Challenges and Controversies in the Management of Prostate Cancer with Multidisciplinary Teams
- PMID: 36399218
- PMCID: PMC9672595
- DOI: 10.1007/s11523-022-00925-7
Addressing Challenges and Controversies in the Management of Prostate Cancer with Multidisciplinary Teams
Abstract
The diagnostic and treatment landscapes of prostate cancer are rapidly evolving. This has led to several challenges and controversies regarding optimal management of the disease that outpace guidelines and clinical data. Multidisciplinary teams (MDTs) can be used to engage the array of specialists that collaborate to treat complex malignancies such as prostate cancer. While the rationale for the use of MDTs in prostate cancer is well known, ways to optimally use MDTs to address the challenges and controversies associated with prostate cancer management are less well understood. One area of MDT care that remains undefined is how MDTs can most effectively provide guidance on clinical decision-making in situations in which information from novel diagnostic testing (genetic testing, molecular imaging) is substantially different from the established clinical risk factors. In this review, we provide a clinical perspective on ways that MDTs can be used to address this and other challenges and controversies across the prostate cancer disease continuum, from diagnosis to end-of-life considerations. Beyond clinical scenarios, we also review ways in which MDTs can mitigate disparities of care in prostate cancer. Overall, MDTs play a central role in helping to address the daily vexing issues faced by clinicians related to diagnosis, risk stratification, and treatment. Given the accelerating advances in precision medicine and targeted therapy, and the new questions and controversies these will bring, the value of MDTs for prostate cancer management will only increase in the future.
© 2022. The Author(s).
Conflict of interest statement
Neal D. Shore reports consulting fees from Abbvie, Amgen, Astellas, AstraZeneca, Bayer, BMS, Boston Scientific, Clarity, Clovis Oncology, Cold Genesys, Dendreon, Exact Imaging, Exact Sciences, FerGene, Foundation Medicine, Genesis Care, Invitae, Janssen, Lantheus, Lilly, MDxhealth, Merck, Myovant, Myriad, Nymox, Pacific Edge, Pfizer, Phosphorous, Photocure, Propella, PreView, Sanofi Genzyme, Sema4, Specialty Networks, Sesen Bio, Telix, Tempus, Tolmar, Urogen, and Vaxiion; and payment for expert testimony from Ferring. Alicia K. Morgans has received grants from Bayer, Myovant, Pfizer, and the Prostate Cancer Foundation; has received consulting fees from Advanced Accelerator Applications, Astellas, AstraZeneca, Bayer, Blue Earth Diagnostics, Exelixis, Janssen, Lantheus Medical Imaging, Merck, Myovant Sciences, Myriad Genetics, Novartis, and Sanofi; has received payment or honoraria for lectures, presentations, speaker bureaus, publication writing, or educational events from Astellas, Clovis, Janssen, Myovant, Sanofi, and Telix; has received travel support from Sanofi; has participated in a data safety monitoring board or advisory board for Bayer and Myovant; has received honoraria from Advanced Accelerator Applications, Astellas Pharma, Astellas, AstraZeneca, Bayer, Clovis Oncology, Exelixis, Genentech, Janssen, Janssen Oncology, Merck, Myovant Sciences, Pfizer, and Sanofi; and has received research funding from Astellas, AstraZeneca, Bayer, Dendreon, Genentech, Myovant Sciences, Sanofi, and Seattle Genetics. Ghassan El-Haddad is a consultant for Bayer HealthCare, Boston Scientific, Canon Medical Systems Corporation, Curium Pharma, Novartis, and Terumo Corporation. Matthew Abramowitz reports travel support from AlphaTau; honoraria from Varian Medical Systems; and grant support from Varian Medical Systems. Sandy Srinivas has no conflicts to disclose.
Figures
References
-
- Shore ND, Laliberte F, Ionescu-Ittu R, Yang L, Mahendran M, Lejeune D, et al. Real-world treatment patterns and overall survival of patients with metastatic castration-resistant prostate cancer in the US prior to PARP inhibitors. Adv Ther. 2021;38:4520–4540. doi: 10.1007/s12325-021-01823-6. - DOI - PMC - PubMed
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Medical
