Enhanced metastatic risk assessment in cutaneous squamous cell carcinoma with the 40-gene expression profile test

Author:

Ibrahim Sherrif F12,Kasprzak Julia M3,Hall Mary A4ORCID,Fitzgerald Alison L4,Siegel Jennifer J4,Kurley Sarah J4ORCID,Covington Kyle R4,Goldberg Matthew S45,Farberg Aaron S6,Trotter Shannon C7,Reed Kenneth8,Brodland David G9,Koyfman Shlomo A10,Somani Ally-Khan11,Arron Sarah T12,Wysong Ashley13

Affiliation:

1. Rochester Dermatologic Surgery, Victor, NY 14564, USA

2. Department of Dermatology, University of Rochester Medical Center, Rochester, NY 14620, USA

3. Department of Dermatology, Medical College of Wisconsin, Milwaukee, WI 53226, USA

4. Castle Biosciences, Inc., Friendswood, TX 77546, USA

5. Department of Dermatology, Icahn School of Medicine at Mount Sinai, New York, NY 10025, USA

6. Department of Dermatology, Baylor University Medical Center, Dallas, TX 75246, USA

7. Oakview Dermatology, Springfield, OH 45504, USA

8. DermASAP, Quincy, MA 02169, USA

9. Zitelli & Brodland, P.C., Pittsburgh, PA 15232, USA

10. Department of Radiation Oncology, Cleveland Clinic, Cleveland, OH 44106, USA

11. Department of Dermatology, Indiana University School of Medicine, Indianapolis, IN 46202, USA

12. Sarah Arron, P.C., San Mateo, CA 94115, USA

13. Department of Dermatology, University of Nebraska Medical Center, Omaha, NE 68198, USA

Abstract

Aim: To clinically validate the 40-gene expression profile (40-GEP) test for cutaneous squamous cell carcinoma patients and evaluate coupling the test with individual clinicopathologic risk factor-based assessment methods. Patients & methods: In a 33-site study, primary tumors with known patient outcomes were assessed under clinical testing conditions (n = 420). The 40-GEP results were integrated with clinicopathologic risk factors. Kaplan–Meier and Cox regression analyses were performed for metastasis. Results: The 40-GEP test demonstrated significant prognostic value. Risk classification was improved via integration of 40-GEP results with clinicopathologic risk factor-based assessment, with metastasis rates near the general cutaneous squamous cell carcinoma population for Class 1 and ≥50% for Class 2B. Conclusion: Combining molecular profiling with clinicopathologic risk factor assessment enhances stratification of cutaneous squamous cell carcinoma patients and may inform decision-making for risk-appropriate management strategies.

Funder

Castle Biosciences, Inc.

Publisher

Future Medicine Ltd

Subject

Cancer Research,Oncology,General Medicine

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