Nurse Navigator Reference Guide

Supporting Patients Through Post-Surgical Molecular Risk Assessment for Early-Stage Lung Cancer

With early-stage lung cancer, we always hope that a resection will offer the patient a complete cure. Unfortunately, for many patients, this is not the case. Even in stages IA-IIA, cancer returns in about 30-45% of patients, and the results are devastating.
Now, they are also preventable.
RiskReveal is the only test that helps give low-risk patients peace of mind and that offers high-risk patients a pathway to real curative treatment based on highly validated, randomized predictive data.

Overview

RiskReveal is a 14-gene RNA expression assay performed on surgically resected tumor tissue that stratifies early-stage NSCLC patients into low-risk and high-risk groups for cancer recurrence. As a nurse navigator, you play a central role in ensuring patients are offered this testing, understand their results, and are guided through the appropriate care pathway.

This guide gives you the clinical background, workflow integration points, patient communication tools, and reimbursement information you need to support RiskReveal at every step of their journey.
The Problem

The Clinical Problem RiskReveal Solves

Approximately one-third of patients with very-early-stage (stage IA) NSCLC who undergo curative-intent resection will experience disease recurrence. The outcomes in stages IB and IIA are even worse. Conventional TNM staging relies on visual cues such as tumor size, location, and lymph node involvement, and cannot reliably differentiate which patients harbor residual micrometastatic disease from those who are truly cured.
As a result, many patients who would benefit from adjuvant chemotherapy are not identified. Despite a high risk for recurrence and 5-year mortality, these patients are not offered potentially life-saving adjuvant treatment because of outdated, now obsolete, data from studies that were unable to document a benefit of post-operative chemotherapy in stage I NSCLC patients because these patients were not segregated according to actual risk. New randomized data are now available that dispel the myth that adjuvant therapy is not appropriate for stage I, and especially for stage IA, NSCLC.

The Clinical Gap RiskReveal Addresses:

Two tumors with identical pathological staging can have very different molecular behavior. One will recur; the other will not. Standard TNM staging cannot distinguish them. RiskReveal’s 14-gene expression signature identifies the molecular phenotype that reflects a high risk of recurrence, enabling treatment decisions based on definitive randomized predictive data made with personalized genetic evidence rather than population-level risk estimates.

How RiskReveal Works

RiskReveal analyzes gene expression patterns from FFPE tumor tissue already collected at the time of surgical resection. No additional biopsy, blood draw, or patient visit is required.
The assay measures the activity of 14 specific genes and generates a risk score that classifies the tumor as:

Low Risk

Surgical resection is likely curative.

Routine surveillance with standard follow-up intervals is appropriate.

Adjuvant chemotherapy is not indicated based on molecular profile.

High Risk

A pattern of tumor gene expression indicates an elevated likelihood of recurrence.

Referral to medical oncology for adjuvant chemotherapy discussion is recommended.

With treatment, clinical study data show ~96% of high-risk patients are cancer-free at 2 years, compared to only 79% of untreated high-risk patients.

Key Clinical Data Points

When speaking with patients or multidisciplinary team members, the following data from the RiskReveal clinical validation study are relevant:
  • High-risk patients in stages I-IIA who received adjuvant chemotherapy enjoyed a 78% reduction in risk of recurrence or death (96% DFS) at a 24-month endpoint
  • The stage IA subset of high-risk patients also enjoyed an 85% reduction in risk of recurrence or death (98% DFS) at the same 24-month endpoint
  • Results returned within 10 business days of tissue receipt, most often sooner
  • The dramatic improvement in DFS was achieved with 3-4 cycles of simple platinum doublet chemotherapy, with complication rates consistent with known platinum-doublet chemotherapy profiles

Navigator Note:

When patients express concern about adjuvant chemotherapy, these data provide meaningful context: mortality risk from chemotherapy is only about 1%, while a molecular high-risk designation by RiskReveal entails at least a 20-times or higher risk of recurrence and death without this treatment. Frame the risk-benefit conversation around what is known, not what is assumed.

Dispelling Confusion About Other Prognostic Tests in NSCLC

Some doctors are considering using blood based Minimal Residual Disease (MRD) circulating tumor DNA testing as a part of post-operative decision making in NSCLC. This approach is not supported by available data, and should not distract from definitive, predictive 14-gene risk assessment with RiskReveal.

Workflow Integration: When and How to Order

RiskReveal is most effectively integrated at two points in the surgical care pathway:

Point 1: Pre-Operative Discussion

This is the ideal time to introduce patients to the full breadth of modern integration of molecular technology into the management of early-stage NSCLC. Avoid a sudden, disconcerting introduction of the high risk of recurrence (even for stage IA patients) during the post-operative period by explaining up front that although surgery for lung cancer was traditionally associated with high recurrence rates, recurrence in stage IA-IIA can now be dramatically lowered by taking a two-stage approach when necessary: gold-standard surgery followed by molecular analysis of the resected tumor and a short course of well-tolerated post-operative chemotherapy when necessary to raise survival rates from the 60s to 70s into the high 90s.

Point 2: Ordering the Test Prior to the First Post-Operative Visit (14 days after operative admission)

Tumor tissue is in the pathology lab, results can return before the post-operative visit, and the patient has not yet begun surveillance-only follow-up. Coordinate with the surgical team.
Process overview:

Surgical resection complete

Navigator initiates discussion with surgical team about RiskReveal ordering

Physician places test order

Simple requisition submitted to Razor Genomics. Tissue is requested from pathology; no patient action required.

Results returned in ≤10 business days, generally within 2-3 days of tissue receipt

Razor Genomics delivers a clear low-risk or high-risk report to the ordering physician.

Navigator facilitates care pathway

Navigator initiates discussion with surgical team about RiskReveal ordering
Preop discussion Learn More
Resection
Tumor block
sent for testing
High risk
Low risk
Discuss results Learn More
Discuss results Learn More
Adjuvant
chemotherapy
No
chemotherapy
Preop discussion Learn More
Resection
Tumor block
sent for testing
High risk
Discuss results Learn More
Adjuvant
chemotherapy
Low risk
Discuss results Learn More
No
chemotherapy

Dispelling Confusion About Other Prognostic Tests in NSCLC

Some doctors are considering using blood based Minimal Residual Disease (MRD) circulating tumor DNA testing as a part of post-operative decision making in NSCLC. This approach is not supported by available data, and should not distract from definitive, predictive 14-gene risk assessment with RiskReveal.

PATIENT COMMUNICATION

Patient Communication: Key Messages by Scenario

Use these conversation guides to introduce the test, explain results clearly, and support patients through the next decision.

When the Ordering Physician Is Unfamiliar with RiskReveal

Although RiskReveal has been helping to save lives for over a decade, the most definitive, prospective randomized predictive data only became available in 2025. Some surgeons and oncologists may not yet be familiar with it. As a navigator, you may be the one to bring it to their attention. Suggested language:

For Surgeons:

“I’ve been reviewing options for post-surgical molecular risk stratification in early-stage lung cancer patients. There’s one test that has actually completed a Phase 3 prospective randomized study and therefore has definitive predictive data that will allow oncologists to treat high-risk stage I-IIA patients with simple adjuvant chemotherapy and dramatically reduce their otherwise very high risk of recurrence. The test is called RiskReveal, and it analyzes RNA expression from the resected tumor tissue. Would you like me to pull the clinical data for your review?”

For Medical Oncologists:

“The patient’s surgical team mentioned RiskReveal for molecular risk assessment. It’s a 14-gene mRNA expression profile that is run on the resected tissue. Phase 3 prospective randomized data were published in Lancet Respiratory Medicine in 2025 documenting definitive predictive data that stage I-IIA patients identified by the test as molecular high-risk do have a dramatic positive response to adjuvant platinum doublet chemotherapy. These surgeons are now referring all their high-risk stage IA-IIA patients for adjuvant therapy.”

Reimbursement & Patient Financial Support

Razor Genomics manages billing directly. As a navigator, your role is to ensure patients know that cost should not be a barrier to testing or treatment.

Medicare Patients

No out-of-pocket cost. RiskReveal is covered for eligible Medicare beneficiaries.

Commercial Insurance

Razor Genomics bills insurance directly. Coverage varies by plan. Patients do not need to manage claims.

Financial Assistance

A Patient Assistance Program is available.
For any patient with coverage uncertainty, contact Razor Genomics directly to request pre-authorization support or patient financial assistance enrollment. Do not let reimbursement ambiguity delay testing.

Phone: 1-844-662-6298
Secure Fax: (949) 271-5753

For coverage verification, prior authorization questions, or patient financial assistance.

Care Transition Checklist

Questions to Prompt at Key Care Transitions

Use these at care team handoffs or patient check-ins to ensure nothing is missed:

At Surgical Discharge / Post-Op Follow-Up

At Results Discussion

For High-Risk Patients Entering Adjuvant Treatment

Reset Checklist

Insurance Coverage & Resources

Razor Genomics, Clinical and Patient Support:

Billing: 1-844-662-6298 
Secure Fax: (949) 271-5753

Materials available from Razor Genomics:

Patient-facing low-risk and high-risk result explanation guides

RiskReveal® is a product of Razor Genomics. This reference guide is intended for use by clinical nurse navigators supporting RiskReveal in the post-surgical care pathway for early-stage NSCLC.