Bayer: Science For A Better Life

United States of America

Oncology Information for Grant Submissions

Bayer Oncology Medical Affairs Department is interested in receiving and reviewing grant applications to support appropriate programs which cover the following area of interest:

Therapeutic Areas/Disease States:

Breast Cancer including Triple Negative Breast Cancer

Intended Audience: Oncologists, Pathologists, Surgeons, Gynecologists, Radiologists, Community HCPs, Patients/Caregivers

Areas of interest based on referenced literature:

  • Treatment and management of Breast Cancer and TNBC
  • Education on biomarker driven testing strategies/appropriate testing modalities
  • Role of NTRK gene fusion and impact of TRK gene fusion/TRK testing in treatment algorithms for Breast Cancer and TNBC
  • Understanding of efficacy and safety profiles of approved TRK inhibitors in Breast Cancer and TNBC
  • Multi-disciplinary approach to precision medicine
  • Understanding and management of adverse event profiles

Proposal Requirements

All submissions for CE/CME support must be consistent with the ACCME guidelines and contain supporting documents that should include:

  • Needs assessment
  • Educational design and rationale for selection (where applicable)
  • Learning objectives
  • Proposed faculty
  • Participant recruitment plan (where applicable)
  • Outcomes strategy/plan (required on a quarterly basis)
  • Detailed budget

Provider Justification:

  • Copy of most recent accreditation letter and status
  • Sample of other program(s) in similar therapeutic area

Process

Applications/proposals which are submitted and determined to be complete are reviewed monthly. Allow a minimum of 45 days from submission for response.

Acceptance of a Bayer educational grant indicates that you will:

  • Reconcile grant funding within 60 days of completion of the educational program
  • Permit a Bayer Medical Affairs representative to audit live programs
  • Share activity data and outcomes metrics within 30 days of their availability

References

  • Drilon A, Laetsch TW, Kummar S et al. Efficacy of Larotrectinib in TRK Fusion-Positive Cancers in Adults and Children. N Engl J Med 2018; 378: 731-9. (link)
  • Hong, D et al. Long-term efficacy and safety of Larotrectinib in an integrated database of patients with TRK fusion cancer. ASCO 2021 presentation.
  • Kummar, S et al. Patient-reported outcomes from two global multicenter clinical trials of children and adults with tropomyosin receptor kinase (TRK) fusion cancers receiving larotrectinib. Journal of Clinical Oncology 37, 2019 (suppl; abstract 6602) (link)
  • National Comprehensive Cancer Network Clinical Practice Guidelines in Oncology: Breast Cancer
  • Abstract PS11-06: Efficacy and safety of Larotrectinib in patients with TRK fusion breast cancer DOI: 10.1158/1538-7445.SABCS20-PS11-06. https://cancerres.aacrjournals.org/content/81/4_Supplement/PS11-06
  • Maund SL, Sokol ES, Ang Houle A, Ross JS, Wilson TR. NTRK gene fusions are detected in both secretory and non-secretory breast cancers. Pathol Int. 2022 Jan 31. doi: 10.1111/pin.13204. Epub ahead of print. PMID: 35102630. https://pubmed.ncbi.nlm.nih.gov/35102630/
  • Westphalen CB, Krebs MG, Le Tourneau C, Sokol ES, Maund SL, Wilson TR, Jin DX, Newberg JY, Fabrizio D, Veronese L, Thomas M, de Braud F. Author Correction: Genomic context of NTRK1/2/3 fusion-positive tumors from a large real-world population. NPJ Precis Oncol. 2021 Sep 17;5(1):86. doi: 10.1038/s41698-021-00222-y. https://pubmed.ncbi.nlm.nih.gov/34535754/