Efficient Identification of Patients With NTRK Fusions Using a Supervised Tumor-Agnostic Approach

Author:

Hernandez Susana12,Conde Esther32,Molero Aida4,Suarez-Gauthier Ana5,Martinez Rebeca6,Alonso Marta1,Plaza Carlos7,Camacho Carmen8,Chantada Debora9,Juaneda-Magdalena Laura9,Garcia-Toro Enrique10,Saiz-Lopez Patricia10,Rojo Federico11,Abad Mar12,Boni Valentina13,del Carmen Sofia14,Regojo Rita Maria15,Sanchez-Frias Marina Esther16,Teixido Cristina17,Paz-Ares Luis18,Lopez-Rios Fernando3

Affiliation:

1. From the Department of Pathology, 12 de Octubre University Hospital, Research Institute 12 de Octubre University Hospital (i+12), Madrid, Spain (Hernandez, Alonso).

2. Hernandez and Conde contributed equally as co–first authors.

3. From the Department of Pathology, 12 de Octubre University Hospital, Universidad Complutense de Madrid, Research Institute 12 de Octubre University Hospital (i+12), CIBERONC, Madrid, Spain (Conde, Lopez-Rios).

4. From the Department of Pathology, Segovia General Hospital, Segovia, Spain (Molero).

5. From the Department of Pathology, Jimenez Diaz Foundation University Hospital, Madrid, Spain (Suarez-Gauthier).

6. From the Department of Pathology, Health Diagnostic-Grupo Quiron Salud, Madrid, Spain (Martinez).

7. From the Department of Pathology, Clinico San Carlos University Hospital, Madrid, Spain (Plaza).

8. From the Department of Pathology, Insular Materno-Infantil University Hospital, Las Palmas de Gran Canaria, Spain (Camacho).

9. From the Department of Pathology, Alvaro Cunqueiro Hospital, Vigo, Spain (Chantada, Juaneda-Magdalena).

10. From the Department of Pathology, Burgos University Hospital, Burgos, Spain (Garcia-Toro, Saiz-Lopez).

11. From the Institute of Health Research-Jimenez Diaz Foundation, CIBERONC, Madrid, Spain (Rojo).

12. From the Department of Pathology, Salamanca University Hospital, Salamanca, Spain (Abad).

13. From NEXT Oncology Madrid, Quiron Salud Madrid University Hospital, Madrid, Spain (Boni).

14. From the Department of Pathology, Marques de Valdecilla University Hospital, Santander, Spain (del Carmen).

15. From the Department of Pathology, La Paz University Hospital, Madrid, Spain (Regojo).

16. From the Department of Pathology, Reina Sofia University Hospital, Cordoba, Spain (Sanchez-Frias).

17. From the Department of Pathology, Thoracic Oncology Unit, Hospital Clínic of Barcelona, University of Barcelona, Barcelona, Spain (Teixido).

18. From the Department of Oncology, 12 de Octubre University Hospital, Department of Medicine, Universidad Complutense de Madrid, Research Institute 12 de Octubre University Hospital (i+12), CIBERONC, Madrid, Spain (Paz-Ares).

Abstract

Context.— The neurotrophic tropomyosin receptor kinase (NTRK) family gene rearrangements have been recently incorporated as predictive biomarkers in a “tumor-agnostic” manner. However, the identification of these patients is extremely challenging because the overall frequency of NTRK fusions is below 1%. Academic groups and professional organizations have released recommendations on the algorithms to detect NTRK fusions. The European Society of Medical Oncology proposal encourages the use of next-generation sequencing (NGS) if available, or alternatively immunohistochemistry (IHC) could be used for screening with NGS confirmation of all positive IHC results. Other academic groups have included histologic and genomic information in the testing algorithm. Objective.— To apply some of these triaging strategies for a more efficient identification of NTRK fusions within a single institution, so pathologists can gain practical insight on how to start looking for NTRK fusions. Design.— A multiparametric strategy combining histologic (secretory carcinomas of the breast and salivary gland; papillary thyroid carcinomas; infantile fibrosarcoma) and genomic (driver-negative non–small cell lung carcinomas, microsatellite instability–high colorectal adenocarcinomas, and wild-type gastrointestinal stromal tumors) triaging was put forward. Results.— Samples from 323 tumors were stained with the VENTANA pan-TRK EPR17341 Assay as a screening method. All positive IHC cases were simultaneously studied by 2 NGS tests, Oncomine Comprehensive Assay v3 and FoundationOne CDx. With this approach, the detection rate of NTRK fusions was 20 times higher (5.57%) by only screening 323 patients than the largest cohort in the literature (0.30%) comprising several hundred thousand patients. Conclusions.— Based on our findings, we propose a multiparametric strategy (ie, “supervised tumor-agnostic approach”) when pathologists start searching for NTRK fusions.

Publisher

Archives of Pathology and Laboratory Medicine

Subject

Medical Laboratory Technology,General Medicine,Pathology and Forensic Medicine

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