Oncology · United States · In-Market

US NSCLC Patient Flow Model

Incidence-to-eligible NSCLC funnel by cohort with sourced conversion assumptions and a share waterfall.

NSCLC · US MarketPatient Flow Model72-Hour DeliveryEditable Excel Model100% Live-Sourced
Market United States Stage
The Landscape

Your addressable market is a chain of conversion assumptions. If one step is wrong, the launch forecast is wrong — and it is usually the testing step.

Every NSCLC opportunity estimate is a funnel: incidence → advanced/metastatic → biomarker-tested → eligible → treated in your line. Each step is an assumption that has to be sourced, not guessed.

The biggest single driver of variance is biomarker testing penetration — the gap between patients who are eligible and those who are identified as eligible. A forecast that assumes full testing overstates the near-term addressable pool every time.

Below, we build the funnel the way your commercial analyst will have to defend it in the first forecast review.

5
conversion steps from incidence to your eligible cohort
~57%
of NSCLC presents at advanced/metastatic stage
3
assumptions that drive the majority of estimate variance
Y1·Y3·Y5
horizons modelled with testing-rate sensitivity
Sample Output

Exhibit 4 — NSCLC patient funnel, US (illustrative).

Diagnosed NSCLC (US/yr) ~200,000 · 100%
Illustrative base
Advanced / metastatic ~114,000 · 57%
Stage III–IV at dx
Biomarker-tested ~80,000 · 40%
Testing penetration — variance driver
Your-cohort eligible ~24,000 · 12%
By proposed biomarker/label
[YOUR ASSET] 1L-treated Scope-set · 7%
[Client] · confirmed at intake

Sources: Funnel percentages are typical-range and illustrative for this sample page. On a commissioned model, each conversion step is cited to a live SEER, NCCN, FDA, or peer-reviewed source and verified at point of writing; testing-penetration inputs are sourced and editable.

Commercial Questions

Five questions. Each section is built to answer one of them.

Every section answers a named commercial question your team is asking, scoped to your asset.

01
How many patients enter the funnel, and at what stage?

Delivers

  • Incidence base · stage distribution · advanced/metastatic entry pool
02
How many are biomarker-tested and identified as eligible?

Delivers

  • Testing penetration by biomarker · identification gap · trajectory
03
How many reach your line of therapy?

Delivers

  • Line-of-therapy attrition · treated-share assumptions · sourcing
04
Which assumptions drive the variance?

Delivers

  • Ranked driver list · sensitivity table · break-points
05
What does the funnel look like at Y1, Y3, Y5?

Delivers

  • Three-horizon projection · testing-rate scenarios · cohort splits

Scoped to your cohort and line of therapy — not the market in aggregate.

Scope Your Work
Contents

What's inside

Oncology · 24–32 pp · In-Market · Analyst report + Excel model + PowerPoint readout

01 The Funnel Frame pp. 1–3
  • The five conversion steps and why each is an assumption
  • Where your cohort enters the funnel
  • What is sourced vs. modelled
02 Incidence Base pp. 4–6
  • Incidence and stage distribution
  • Advanced/metastatic entry pool
  • Demographic skew that moves the base
03 The Testing Step pp. 7–11
  • Biomarker testing penetration — the variance driver
  • Diagnosed vs. identified gap
  • Testing-rate trajectory and its forecast impact
04 Eligibility & Line pp. 12–16
  • Eligibility funnel by cohort
  • Line-of-therapy attrition
  • Treated-share assumptions and their sources
05 Scenario Build pp. 17–21
  • Conservative, base, aggressive funnels
  • Testing-rate and staging-mix sensitivity
  • Where the model breaks
06 Driver Ranking pp. 22–25
  • The assumptions that drive 80% of variance
  • Sensitivity table by driver
  • Decision levers your team controls
07 Y1·Y3·Y5 Output pp. 26–28
  • Patient volume by horizon and cohort
  • Revenue translation inputs
  • Confidence bands
08 Client Alignment Questions pp. 29–30
  • Which conversion steps need primary validation
  • Assumptions that will be challenged in forecast review
  • Decisions contingent on testing-rate evolution
Appendix and source ledger included · 45-minute analyst readout included with delivery
Formats

Included with every brief

PDF
PDF Brief
Intelligence Brief
Structured for sequential reading by your launch lead, medical affairs director, and market access team. Every exhibit sourced.
XLS
Excel Model
Patient Flow Model (Excel)
The core deliverable — a live, editable funnel your commercial analyst can run sensitivities on without rebuilding. Every conversion step is labelled and sourced.
PPT
PowerPoint
Executive Readout — PowerPoint
12–15 slide readout deck for commercial team presentations, formatted to AXLRx design standards.
Methodology

Every figure is live-sourced before delivery. If a number cannot be verified, it does not appear.

Prepared by MoatRx analysts.

This is a field where AI confidently reproduces outdated epidemiology, superseded payer policy, and retracted analyses. AXLRx uses none of its own memory as a source. Every figure your team receives is verified against a live document at the time of writing.

A wrong number in front of your payer or your leadership team is not recoverable in the same meeting.

  • Every claim cited to a live PMID, ClinicalTrials.gov ID, or URL at point of writing — uncited claims are dropped, not estimated
  • PubMed metadata fetched live during authoring — model memory produces incorrect author and journal data even on correct PMIDs
  • Numeric cross-check: the specific figure must appear in the cited source, not merely be consistent with its topic
  • Independent audit pass after generation — broken links, unsourced claims, and numeric inconsistencies flagged before delivery
  • Drop gate: any figure that cannot clear the above is removed. No confidence tiers. No exceptions.
FAQ

Frequently asked questions

Scope
Is the model editable?
Yes — the Excel funnel is fully editable with labelled, sourced assumptions, so your analyst can run sensitivities and re-scope without rebuilding it.
Sourcing
Are the conversion rates sourced?
Every conversion step cites a live source at the point of writing and is cross-checked against it. The testing-penetration step, the biggest variance driver, is sourced and shown as a sensitivity, not a point estimate.
Delivery
How fast?
72 hours from scope confirmation, with a 30-minute readout call. A 48-hour track is available.
Format
What do we receive?
The editable Excel model is the core deliverable, plus a PDF brief walking through the funnel logic and an optional executive deck.
Process
Can you model a specific cohort only?
Yes. Tell us the biomarker, line, and geography at intake and we scope the funnel to exactly that cohort.
Get Started

Tell us your asset. Your team has the intelligence in 72 hours.

We build from your asset's clinical profile — mechanism, biomarker strategy, proposed label, and target cohort. Scope confirmation takes one call.

01
Submit your asset profile

Drug, mechanism, proposed indication, target cohort, geography. Five minutes via the intake form.

02
Scope confirmed in 24 hours

We confirm scope with your team, clarify ambiguities, and lock delivery timing.

03
Your patient flow model, delivered in 72 hours

PDF intelligence document, Excel model, and optional executive deck — with a 30-minute readout call included.