Provider Collaborations
The Problem

The Regulatory Moat Keeps Promising Treatments from Your Patients

Since 2011—over 14 years ago—research has clearly shown that triple-negative breast cancer is not a single disease, but rather diverse molecular subtypes. Yet the standard of care remains largely unchanged. We don't even routinely subtype TNBC patients, despite a myriad of promising targeted treatments that work differentially across subtypes.

Years Since TNBC Research Breakthrough 14+
Standard of Care Changes Minimal
Targeted Treatments in Routine Use None
Patient Reality

Patients Want Whole-Person Care, Not Generic Protocols

Patients don't want old and simplistic treatments that apply to the "mythical average patient" when in reality each patient is very unique. They don't want to be kept from accessing what is new and up-and-coming when they're running out of options. They want to be treated as the complex biological system they really are.

Generic Treatment Targets Mythical Average
Your Patients Are Unique Systems
What They Want Personalized Care
The Catch-22

Naturopathic Approaches Get Dismissed as 'Non-Evidence-Based'

Natural interventions that treat the patient as a complex system don't fit the reductionist A/B testing model. Because they're not patentable for profit and rarely justify the millions required for clinical trials, they're never adequately studied and therefore dismissed as "non-evidence-based" with no way of becoming standard of care.

Complex systems approach
Doesn't fit A/B testing model
Can't afford clinical trials
Dismissed as "non-evidence-based"
The Solution

CEtHI Provides Research-Grade Data to Support Your Clinical Decisions

Using standard bioinformatics pipelines like GATK with MuTect2 and Funcotator, we generate comprehensive tumor profiling reports from full exome sequencing. Each patient receives their complete mutational catalog, clonal architecture analysis, mutational signatures, and therapeutic implications—plus six weeks of education to understand their data.

DNA
Full Exome Sequencing
Complete mutational catalog + clonal architecture
EDU
Patient Education
6 weeks of support + raw data ownership
RWD
Living Documents
Updates as new methodologies emerge
Partnership

Cohort Analysis + Real-World Evidence Generation

Refer a cohort of 10-15 patients and receive specialized cohort analysis at no additional cost. We'll provide gene ontology pathway analysis, identify patterns of disruption in key cellular processes, and generate publishable real-world evidence that can inform integrative approaches—without waiting years for conventional research.

10-15
Patient Cohort
$1,500
Per Individual Report
Free
Cohort Analysis

Transform Your Practice with Scientific Rigor That Serves Whole-Person Care

Together, we can generate the evidence needed to support complex, systems-based interventions while putting patients at the center of both care and research. The future of evidence generation lies not in randomized trials that strip away context, but in sophisticated analyses of real-world data that embraces complexity.

Watch the following video for more details...

Let's Partner in Patient-Centered Care

Ready to provide your patients with research-grade molecular insights while generating real-world evidence for your integrative approaches?

Schedule a consultation to discuss detailed report examples, explore cohort analysis opportunities, and brainstorm the types of analyses that would best serve your practice.

Schedule Partnership Discussion
Paola Raska, PhD
Founder & CEO, CEtHI - Community Empowerment Through Health Information
✓ See detailed examples of comprehensive tumor profiling reports
✓ Discuss cohort analysis and real-world evidence generation
✓ Explore partnership opportunities tailored to your practice
Patient Empowerment. Patient Dignity. Patient Flourishing.
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