Quantifying the Value of the Molecular Tumor Board: Discordance Recommendation Rate and Drug Cost Avoidance
- PMID: 36265115
- DOI: 10.1200/PO.22.00132
Quantifying the Value of the Molecular Tumor Board: Discordance Recommendation Rate and Drug Cost Avoidance
Abstract
Purpose: Molecular tumor boards (MTBs) provide interventions that assist the patient's primary oncologist's interpretation and application of precision oncology and avoid clinical and financial toxicities of prescribing inappropriate targeted therapy. In this article, we describe a novel method for illustrating MTBs value and recommendation discordance rate and report associated drug cost avoidance data.
Methods: From January 1, 2021, to December 31, 2021, patients assessed by our program's MTB were retrospectively evaluated. Recommendation discordance was defined as any disagreement between MTB therapeutic recommendations and those provided in the next-generation sequencing vendor's report.
Results: In 2021, our program processed 1,119 next-generation sequencing orders via external vendors for 1,029 unique patients with a variety of solid tumor and hematologic malignancies. During this period, 962 patients were reviewed through our MTB process. MTB recommendation discordance rate was high (229 of 502; 45.6%) and varied across test vendors. Rationales for discordance included the following: low level of evidence (88% of patients), alternative standard of care available (60%), and tolerability concerns (42%), among others. Discordance was highest for Vendor C (30%), followed by Vendor A (24%) and Vendor B (8%). The most common drug classes not supported were mTOR, PARP, MEK, and PIK3CA inhibitors when recommended by vendors in off-label settings. MTB interventions accounted for $3,209,070 in US dollars in potential drug cost avoidance.
Conclusion: Therapeutic recommendation discordance rates can provide quantitative insight into the benefit of MTB. Discordance-associated drug cost avoidance further demonstrates MTB's financial value. These measures may be used as part of the justification for this service line within a cancer care program.
Conflict of interest statement
<b>James L. Weese</b><b>Consulting or Advisory Role:</b> Via Oncology<b>Other Relationship:</b> Elsevier <b>Antony Ruggeri</b><b>Leadership:</b> Elsevier<b>Honoraria:</b> Astellas Scientific and Medical Affairs Inc <b>Michael A. Thompson</b><b>Employment:</b> Tempus, Aurora Health Care<b>Stock and Other Ownership Interests:</b> Doximity, Tempus<b>Consulting or Advisory Role:</b> Celgene, VIA Oncology, Takeda, Syapse, Adaptive Biotechnologies, AbbVie, GRAIL, Epizyme, Janssen Oncology, Sanofi<b>Research Funding:</b> Takeda (Inst), Bristol Myers Squibb (Inst), TG Therapeutics (Inst), AbbVie (Inst), PrECOG (Inst), Strata Oncology (Inst), Lynx Biosciences (Inst), Denovo Biopharma (Inst), ARMO BioSciences (Inst), GlaxoSmithKline (Inst), Amgen (Inst)<b>Patents, Royalties, Other Intellectual Property:</b> UpToDate, Peer Review for Plasma Cell Dyscrasias (Editor: Robert Kyle)<b>Other Relationship:</b> Doximity<b>Open Payments Link:</b> https://openpaymentsdata.cms.gov/physician/192826No other potential conflicts of interest were reported.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Miscellaneous
