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šŸ„ONCOLOGY CAPABILITY

Match Patients to Therapies

Mechanism-Based Drug Ranking

S/P/E fusion (Sequence/Pathway/Evidence) matches patients to therapies with 96.6% trial match accuracy. Mechanism-based matching, not just standard of care.

šŸ’ŠChemo Co‑Pilot

Turn genetics into plain, useful guidance for chemo planning: a ranked drug hypothesis, a confidence hint, and an audit‑ready summary you can share with your team

Chemo Co‑Pilot: In‑Silico Chemotherapy Guidance

Evidence-backed chemotherapy recommendations with 70-85% confidence. See which drug classes match your patient's tumor biology with transparent S/P/E reasoning. Action-ready dossiers for same-day tumor board discussions.

The Problem: Choosing chemotherapy can be unclear when biology is complex

Choosing chemotherapy can be unclear when biology is complex. We help by turning genetics into a simple, auditable starting point.

Challenge

Too many options, little clarity on fit to tumor biology.

Too many options, little clarity on fit to tumor biology.

Complex

Confidence is hard to communicate without sources and a simple story

Confidence is hard to communicate without sources and a simple story

Scattered

Data is scattered; assembling a shareable summary takes time

Data is scattered; assembling a shareable summary takes time

The Solution: Transform genetics into plain, useful guidance for chemo planning: a ranked drug hypothesis, a confidence hint, and an audit‑ready summary you can share with your team

Our live S/P/E + insights pipeline converts variants into a chemo guidance view: top drug classes, confidence, rationale, and citations—all with provenance (run ID, profile).

40% → 16-18% VUS rate

Uncertainty Reduction

Dramatically reduced variant uncertainty in chemotherapy applications through advanced AI classification

38% insufficient → consider

Classification Improvement

Enhanced variant classification accuracy with 14% consider → supported upgrades

+0.08 median improvement

Confidence Enhancement

Consistent confidence boost across all variants (range +0.05 to +0.12)

Real-World Results

Measurable outcomes from using this capability

40% → 16-18% VUS rate

Uncertainty Reduction

Dramatically reduced variant uncertainty in chemotherapy applications through advanced AI classification

38% insufficient → consider

Classification Improvement

Enhanced variant classification accuracy with 14% consider → supported upgrades

+0.08 median improvement

Confidence Enhancement

Consistent confidence boost across all variants (range +0.05 to +0.12)

0.957 (n=53,210)
Overall ClinVar AUROC
0.957 (n=14,319)
Coding SNVs AUROC
0.958 (SOTA, n=34,761)
Non-coding SNVs AUROC
0.939 (SOTA, n=1,236)
Coding non-SNVs AUROC
0.918 (n=3,894)
Non-coding non-SNVs AUROC
0.95 / 0.86 (all SNVs)
BRCA1 Supervised AUROC/AUPRC

See It In Action

Interactive demonstration of this capability

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Live Demo Coming Soon

Interactive demonstration for Chemo Co‑Pilot: In‑Silico Chemotherapy Guidance will be available here.

Request Demo →

The Chemotherapy Treatment Journey

From genetic testing confusion to precision, biology-aware chemotherapy selection with CrisPRO's Oracle & Forge Engines

Traditional Way

Genetic Testing

Patient receives genetic test results with unclear drug response predictions.

Critical Problems

  • Limited pharmacogenomic guidance for chemo selection
  • Standard protocols ignore patient-specific genetics
  • No clear drug ranking based on tumor biology
Traditional Way

Clinical Confusion

Oncologist struggles to match chemotherapy drugs to patient's genetic profile.

Critical Problems

  • Physicians rely on standard protocols, not personalized biology
  • Limited understanding of drug-gene interactions
  • Treatment decisions based on incomplete pharmacogenomic data
Traditional Way

Trial & Error Treatment

Patient undergoes chemotherapy that may not match their genetic drug response profile.

Critical Problems

  • Average 2-3 chemo attempts before finding effective therapy
  • Precious time lost during cancer progression
  • Unnecessary toxicity from ineffective drug combinations
Traditional Way

Treatment Resistance

Without precision drug matching, cancer develops resistance and becomes increasingly difficult to treat.

Critical Problems

  • Drug resistance develops from suboptimal initial selection
  • Limited treatment options once resistance occurs
  • Exponentially higher treatment costs and patient suffering
In-Silico Way

Biology-Aware Drug Ranking

CrisPRO's Oracle Engine provides MoA-aligned drug class ranking with 95.7% AUROC ClinVar validation and transparent explanations.

AI-Powered Solutions

  • 95.7% AUROC ClinVar validation for variant impact prediction
  • S/P/E fusion: Sequence, Pathway, Evidence for drug ranking
  • Real-time drug class recommendations with confidence scores
In-Silico Way

Validated Pharmacogenomic Insights

Oracle delivers peer-reviewed variant impact prediction with CrisPRO.ai embeddings and BRCA1 supervised AUROC ā‰ˆ 0.95 for drug-gene interactions.

AI-Powered Solutions

  • BRCA1 supervised AUROC ā‰ˆ 0.95 with CrisPRO.ai 40B block-20 embeddings
  • Cross-species generalization for drug response pathways
  • Transparent explanations with auditable provenance
In-Silico Way

Precision Chemo Design

Forge Engine generates personalized chemotherapy strategies with 1M token context window and guided epigenomic design.

AI-Powered Solutions

  • 1M token context window for comprehensive genomic analysis
  • Guided epigenomic design with Enformer+Borzoi scoring
  • Configurable beam width for inference-time scaling (beam width ↔ AUROC)
In-Silico Way

Research-Validated Chemo Outcomes

End-to-end chemotherapy workflow with validated performance metrics and transparent methodology.

AI-Powered Solutions

  • Research-use-only positioning with transparent methodology
  • Validated performance metrics with peer-reviewed benchmarks
  • Auditable results with complete provenance and run IDs

Journey Visualization

Traditional Approach: The Chemotherapy Treatment Journey

In-Silico Way

Biology-Aware Drug Ranking

CrisPRO's Oracle Engine provides MoA-aligned drug class ranking with 95.7% AUROC ClinVar validation and transparent explanations.

AI-Powered Solutions

  • 95.7% AUROC ClinVar validation for variant impact prediction
  • S/P/E fusion: Sequence, Pathway, Evidence for drug ranking
  • Real-time drug class recommendations with confidence scores

API Endpoints

/predict_variant_impact
/predict_gene_essentiality
/generate_therapeutic_protein