A Theragnostic AI Platform for Precision NSCLC Treatment

K2 Think powers a scalable platform to identify tumor-specific molecular networks, assess inhibitor effects, and predict outcomes before treatment begins.

Demo Video Presentation
Illustration of a molecular network

The Problem: Critical Gaps in NSCLC Care

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Target Users & Scope

For oncologists, researchers, and developers in the fight against NSCLC, a disease fueled by complex genetic mutations and molecular networks.

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Critical Pain Points

Care is hindered by blind spots in druggable mutations, tumor resistance to inhibitors like osimertinib, and toxicity from off-target effects.

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Importance & Urgency

NSCLC claims 1.8M lives annually. Patients demand personalized therapies tailored to their unique tumor networks, as every delay costs lives.

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Current Limitations

Today’s tools analyze single genes, missing the dynamic interplay of mutations and tumor biology that truly drives patient outcomes.

What You'll Build: The K2 Think Platform

Core Offering

  • Integrates patient, sample, and molecular data to decode each tumor's landscape.
  • Analyzes mutations, gene expression, and copy number variations (CNVs).
  • Identifies driver genes (e.g., EGFR, KRAS) and simulates inhibitor interactions.
  • Predicts drug response, resistance risks, and optimal therapy combinations.
  • Generates onco-specific safety alerts
See The Workflow

Tech Stack

  • Native iOS & Android app powered by Firestore (NoSQL).
  • Secure user management with Firebase Authentication.
  • k2 Think API integration
  • Backend automation using Node.js & Objective-C Cloud Functions.
  • Interactive visualizations generated directly from cloud collections.
See The Workflow

Workflow

Tap to expand

Patient
ID: PAT001
Name: John Doe
Age: 63
Sex: Male
Diagnosis: NSCLC
Subtype: Adenocarcinoma
Notes: High-risk patient
Sample
Sample ID: SMP001
Type: Tumor
Tissue: Lung
Stage: IIIA
Grade: Moderately differentiated
Notes: RNA-seq prepared
Molecular Profile ID: MP001
Molecular Profile
Mutations
EGFR: L858R
TP53: R273H
KRAS: G12C
Expression
EGFR: 2.4
TP53: 1.0
KRAS: 1.8
CNV
EGFR: Amplified
TP53: Normal
KRAS: Normal
K2 Think Analysis
Genes Analyzed
EGFR: Oncogene, L858R
Predicted Response: Sensitive
Inhibitors: Erlotinib, Osimertinib

TP53: Tumor Suppressor, R273H
Predicted Response: Unknown
Summary
Primary Targets: EGFR, KRAS
Best Candidate: EGFR
Confidence Score: 0.87

Explore the Data

Tap a chip to view the data

Why K2 Think

K2 Think’s ultra-fast reasoning (≈2,000 tokens/sec) enables real-time genomic interpretation and interactive molecular modeling. Its superior mathematical and analytical precision empowers the system to decode complex oncogenic networks, simulate molecular interactions, and recommend optimal drug strategies — capabilities essential for advancing personalized NSCLC treatment beyond current computational limits.

K2 Think
High-Speed Processing ~2,000 tokens/sec enables entirely new product experiences.
Superior Reasoning Advanced math and systems logic for complex biological problems.
Data Integration Parses genomics, drug libraries, and clinical data simultaneously.
Causal Inference Decodes tangled molecular networks to find the true drivers of disease.
Predictive Outcomes Forecasts treatment response, resistance, and toxicity pre-prescription.

Demo (MVP)

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1. Data Input

The patient's molecular profile data is fed into the native iOS/Android app and securely linked to our Firestore (NoSQL) database.

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2. K2 Think Analysis

Node.js Cloud Functions trigger the K2 Think API to analyze the profile, simulate drug responses, and predict resistance risks.

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3. Actionable Results

Actionable therapeutic recommendations are generated in real-time and presented in the app, ready for clinical decision-making.

Real-Time Voice Analysis

Talk with k2 Think. Ask complex questions in natural language and receive immediate, audible responses from the K2 Think engine. Analyze molecular profiles, simulate treatments, and explore hypotheses, all through a fluid, lively conversation.

K2 Vynce Voice Assistant
mic "What are the combination suggestions for the KRAS G12C mutation?"
volume_up "The combination of a KRAS G12C inhibitor with an EGFR inhibitor has the greatest therapeutic potential. Should I detail the predicted response data?"
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Listening...

Our Motivations

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Prior Diagnosis

By analyzing complex molecular signals, K2 Think helps identify lung cancer subtypes earlier and more accurately, opening a crucial window for timely and more effective intervention.

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Increase Treatment Effectiveness

Our analyses aim to increase treatment success rates. By predicting a tumor's response to different therapies, we can help oncologists select the most effective treatment plan, improving patient outcomes.

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Building a Knowledge Base

Each analysis contributes to an interconnected and growing database. This resource becomes increasingly powerful, uncovering new patterns and insights that can benefit the entire oncology community.

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Accelerating Cancer Research

Our platform serves as a powerful research tool, allowing scientists to virtually test hypotheses and analyze molecular interactions in seconds, dramatically reducing the time and cost of discovering new therapeutic targets.

Our Team

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Zhasmin

Clinical and Pharmacology Research Lead

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Aibarly

K2 Logic and Verification Engineer, Researcher, and Team Leader

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Luther

Project Manager, Developer, Data Integration & Backend Engineer

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Axel

UI/UX Designer, and Demo Engineer

"At the intersection of data and biology, we don't just find insights. We find hope."
— K2 Vynce Team