Guidance of sentinel lymph node biopsy decisions in patients with T1–T2 melanoma using gene expression profiling

Author:

Vetto John T1,Hsueh Eddy C2,Gastman Brian R3,Dillon Larry D4,Monzon Federico A5,Cook Robert W5,Keller Jennifer2,Huang Xin6,Fleming Andrew6,Hewgley Preston6,Gerami Pedram789,Leachman Sancy10,Wayne Jeffrey D7811,Berger Adam C12,Fleming Martin D6

Affiliation:

1. Division of Surgical Oncology, Knight Cancer Institute, Oregon Health & Science University, Portland, OR 97239, USA

2. Department of Surgery, St Louis University, St Louis, MO 63110, USA

3. Department of Plastic Surgery, Cleveland Clinic Lerner Research Institute, Cleveland, OH 44915, USA

4. Larry D Dillon Surgical Oncology & General Surgery, Colorado Springs, CO 80907, USA

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

6. Division of Surgical Oncology, Department of Surgery, The University of Tennessee Health Science Center, Memphis, TN 38163, USA

7. Department of Dermatology, Northwestern University Feinberg School of Medicine, Chicago IL 60611, USA

8. Skin Cancer Institute, Northwestern University, Lurie Comprehensive Cancer Center, Chicago, IL 60611, USA

9. Department of Pathology, Northwestern University Feinberg School of Medicine, Chicago IL 60611, USA

10. Department of Dermatology, Knight Cancer Institute, Oregon Health & Science University, Portland, OR 97239, USA

11. Department of Surgical Oncology, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA

12. Department of Surgery, Thomas Jefferson University Hospital, Philadelphia, PA 19017, USA

Abstract

Aim: Can gene expression profiling be used to identify patients with T1–T2 melanoma at low risk for sentinel lymph node (SLN) positivity? Patients & methods: Bioinformatics modeling determined a population in which a 31-gene expression profile test predicted <5% SLN positivity. Multicenter, prospectively-tested (n = 1421) and retrospective (n = 690) cohorts were used for validation and outcomes, respectively. Results: Patients 55–64 years and ≥65 years with a class 1A (low-risk) profile had SLN positivity rates of 4.9% and 1.6%. Class 2B (high-risk) patients had SLN positivity rates of 30.8% and 11.9%. Melanoma-specific survival was 99.3% for patients ≥55 years with class 1A, T1–T2 tumors and 55.0% for class 2B, SLN-positive, T1–T2 tumors. Conclusion: The 31-gene expression profile test identifies patients who could potentially avoid SLN biopsy.

Publisher

Future Medicine Ltd

Subject

Cancer Research,Oncology,General Medicine

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