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Implementation of a Molecular Tumor Registry to Support the Adoption of Precision Oncology Within an Academic Medical Center: The Duke University Experience.

Publication ,  Journal Article
Green, MF; Bell, JL; Hubbard, CB; McCall, SJ; McKinney, MS; Riedel, JE; Menendez, CS; Abbruzzese, JL; Strickler, JH; Datto, MB
Published in: JCO Precis Oncol
2021

UNLABELLED: Comprehensive genomic profiling to inform targeted therapy selection is a central part of oncology care. However, the volume and complexity of alterations uncovered through genomic profiling make it difficult for oncologists to choose the most appropriate therapy for their patients. Here, we present a solution to this problem, The Molecular Registry of Tumors (MRT) and our Molecular Tumor Board (MTB). PATIENTS AND METHODS: MRT is an internally developed system that aggregates and normalizes genomic profiling results from multiple sources. MRT serves as the foundation for our MTB, a team that reviews genomic results for all Duke University Health System cancer patients, provides notifications for targeted therapies, matches patients to biomarker-driven trials, and monitors the molecular landscape of tumors at our institution. RESULTS: Among 215 patients reviewed by our MTB over a 6-month period, we identified 176 alterations associated with therapeutic sensitivity, 15 resistance alterations, and 51 alterations with potential germline implications. Of reviewed patients, 17% were subsequently treated with a targeted therapy. For 12 molecular therapies approved during the course of this work, we identified between two and 71 patients who could qualify for treatment based on retrospective MRT data. An analysis of 14 biomarker-driven clinical trials found that MRT successfully identified 42% of patients who ultimately enrolled. Finally, an analysis of 4,130 comprehensive genomic profiles from 3,771 patients revealed that the frequency of clinically significant therapeutic alterations varied from approximately 20% to 70% depending on the tumor type and sequencing test used. CONCLUSION: With robust informatics tools, such as MRT, and the right MTB structure, a precision cancer medicine program can be developed, which provides great benefit to providers and patients with cancer.

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Published In

JCO Precis Oncol

DOI

EISSN

2473-4284

Publication Date

2021

Volume

5

Location

United States

Related Subject Headings

  • Universities
  • Retrospective Studies
  • Registries
  • Precision Medicine
  • Neoplasms
  • Humans
  • High-Throughput Nucleotide Sequencing
  • Academic Medical Centers
  • 3211 Oncology and carcinogenesis
 

Citation

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Green, M. F., Bell, J. L., Hubbard, C. B., McCall, S. J., McKinney, M. S., Riedel, J. E., … Datto, M. B. (2021). Implementation of a Molecular Tumor Registry to Support the Adoption of Precision Oncology Within an Academic Medical Center: The Duke University Experience. JCO Precis Oncol, 5. https://doi.org/10.1200/PO.21.00030
Green, Michelle F., Jonathan L. Bell, Christopher B. Hubbard, Shannon J. McCall, Matthew S. McKinney, Jinny E. Riedel, Carolyn S. Menendez, James L. Abbruzzese, John H. Strickler, and Michael B. Datto. “Implementation of a Molecular Tumor Registry to Support the Adoption of Precision Oncology Within an Academic Medical Center: The Duke University Experience.JCO Precis Oncol 5 (2021). https://doi.org/10.1200/PO.21.00030.
Green MF, Bell JL, Hubbard CB, McCall SJ, McKinney MS, Riedel JE, Menendez CS, Abbruzzese JL, Strickler JH, Datto MB. Implementation of a Molecular Tumor Registry to Support the Adoption of Precision Oncology Within an Academic Medical Center: The Duke University Experience. JCO Precis Oncol. 2021;5.

Published In

JCO Precis Oncol

DOI

EISSN

2473-4284

Publication Date

2021

Volume

5

Location

United States

Related Subject Headings

  • Universities
  • Retrospective Studies
  • Registries
  • Precision Medicine
  • Neoplasms
  • Humans
  • High-Throughput Nucleotide Sequencing
  • Academic Medical Centers
  • 3211 Oncology and carcinogenesis