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Virtual multi-institutional tumor board: a strategy for personalized diagnoses and management of rare CNS tumors

  • James L. Rogers,
  • Thomas Wall,
  • Alvina A. Acquaye-Mallory,
  • Lisa Boris,
  • Yeonju Kim,
  • Kenneth Aldape,
  • Martha M. Quezado,
  • John A. Butman,
  • James G. Smirniotopoulos,
  • Huma Chaudhry,
  • Christina I. Tsien,
  • Prashant Chittiboina,
  • Kareem Zaghloul,
  • Orwa Aboud,
  • Nicholas G. Avgeropoulos,
  • Eric C. Burton,
  • David M. Cachia,
  • Karan S. Dixit,
  • Jan Drappatz,
  • Erin M. Dunbar,
  • Peter Forsyth,
  • Edina Komlodi-Pasztor,
  • Jacob Mandel,
  • Byram H. Ozer,
  • Eudocia Q. Lee,
  • Surabhi Ranjan,
  • Rimas V. Lukas,
  • Margarita Raygada,
  • Michael E. Salacz,
  • Matthew A. Smith-Cohn,
  • James Snyder,
  • Ariane Soldatos,
  • Brett J. Theeler,
  • Brigitte C. Widemann,
  • Kevin A. Camphausen,
  • John D. Heiss,
  • Terri S. Armstrong,
  • Mark R. Gilbert,
  • Marta Penas-Prado

摘要

Purpose

Multidisciplinary tumor boards (MTBs) integrate clinical, molecular, and radiological information and facilitate coordination of neuro-oncology care. During the COVID-19 pandemic, our MTB transitioned to a virtual and multi-institutional format. We hypothesized that this expansion would allow expert review of challenging neuro-oncology cases and contribute to the care of patients with limited access to specialized centers.

Methods

We retrospectively reviewed records from virtual MTBs held between 04/2020–03/2021. Data collected included measures of potential clinical impact, including referrals to observational or therapeutic studies, referrals for specialized neuropathology analysis, and whether molecular findings led to a change in diagnosis and/or guided management suggestions.

Results

During 25 meetings, 32 presenters discussed 44 cases. Approximately half (n = 20; 48%) involved a rare central nervous system (CNS) tumor. In 21% (n = 9) the diagnosis was changed or refined based on molecular profiling obtained at the NIH and in 36% (n = 15) molecular findings guided management. Clinical trial suggestions were offered to 31% (n = 13), enrollment in the observational NCI Natural History Study to 21% (n = 9), neuropathology review and molecular testing at the NIH to 17% (n = 7), and all received management suggestions.

Conclusion

Virtual multi-institutional MTBs enable remote expert review of CNS tumors. We propose them as a strategy to facilitate expert opinions from specialized centers, especially for rare CNS tumors, helping mitigate geographic barriers to patient care and serving as a pre-screening tool for studies. Advanced molecular testing is key to obtaining a precise diagnosis, discovering potentially actionable targets, and guiding management.