Diagnostic testing approaches for the identification of patients with TRK fusion cancer prior to enrollment in clinical trials investigating larotrectinib.


Journal

Cancer genetics
ISSN: 2210-7762
Titre abrégé: Cancer Genet
Pays: United States
ID NLM: 101539150

Informations de publication

Date de publication:
01 2022
Historique:
received: 11 08 2021
revised: 13 10 2021
accepted: 28 11 2021
pubmed: 21 12 2021
medline: 17 2 2022
entrez: 20 12 2021
Statut: ppublish

Résumé

NTRK gene fusions are targetable oncogenic drivers independent of tumor type. Prevalence varies from highly recurrent in certain rare tumors to <1% in common cancers. The selective TRK inhibitor larotrectinib was shown to be highly active in adult and pediatric patients with tumors harboring NTRK gene fusions. We examined the techniques used by local sites to detect tumor NTRK gene fusions in patients enrolled in clinical trials of larotrectinib. We also report the characteristics of the detected fusions in different tumor types. The analysis included 225 patients with 19 different tumor types. Testing methods used were next-generation sequencing (NGS) in 196 of 225 tumors (87%); this was RNA-based in 96 (43%); DNA-based in 53 (24%); DNA/RNA-based in 46 (20%) and unknown in 1 (<1%); FISH in 14 (6%) and PCR-based in 12 (5%). NanoString, Sanger sequencing and chromosome microarray were each utilized once (<1%). Fifty-four different fusion partners were identified, 39 (72%) of which were unique occurrences. The most common local testing approach was RNA-based NGS. Many different NTRK gene fusions were identified with most occurring at low frequency. This supports the need for validated and appropriate testing methodologies that work agnostic of fusion partners.

Identifiants

pubmed: 34929613
pii: S2210-7762(21)00232-5
doi: 10.1016/j.cancergen.2021.11.006
pii:
doi:

Substances chimiques

Membrane Glycoproteins 0
NTRK1 protein, human 0
NTRK3 protein, human 0
Oncogene Proteins, Fusion 0
Pyrazoles 0
Pyrimidines 0
Receptor, trkA EC 2.7.10.1
Receptor, trkB EC 2.7.10.1
Receptor, trkC EC 2.7.10.1
tropomyosin-related kinase-B, human EC 2.7.10.1
larotrectinib PF9462I9HX

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

46-52

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2021 The Authors. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest E.R.R. reports institutional reimbursement from Bayer for time on advisory boards and as part of clinical trials. J.H. is a full-time employee of Neogenomics, and reports research funding and advisory board fees from Bayer and honoraria from WebMD. M.R., J.S., J.W., K.S. and H.N. are employees of Bayer and R.N. works for an organization that carries out contract research for Bayer. C.M.L. reports that her spouse is employed by Bayer. D.S.H. reports institutional research/grant funding from AbbVie, Adaptimmune, Aldi-Norte, Amgen, Astra-Zeneca, Bayer, BMS, Daiichi-Sankyo, Deciphera, Eisai, Erasca, Fate Therapeutics, Genentech, Genmab, Infinity, Kite, Kyowa, Lilly, LOXO, Merck, Medimmune, Mirati, Mologen, Navier, NCI-CTEP, Novartis, Numab, Pfizer, Pyramid Bio, SeaGen, Takeda, Turning Point Therapeutics, Verstatem, and VM Oncology; travel, accommodation, expenses from: Bayer, Genmab, AACR, ASCO, SITC and Telperian; consulting, speaker or advisory roles with: Adaptimmune, Alpha Insights, Acuta, Alkermes, Amgen, Aumbiosciences, Atheneum, Axiom, Barclays, Baxter, Bayer, Boxer Capital, BridgeBio, CDR-life AG, COR2ed, COG, Ecor1, Genentech, Gilead, GLG, Group H, Guidepoint, HCW Precision, Immunogen, Infinity, Janssen, Liberium, Medscape, Numab, Oncologia Brasil, Pfizer, Pharma Intelligence, POET Congress, Prime Oncology, Seattle Genetics, ST Cube, Takeda, Tavistock, Trieza Therapeutics, Turning Point, WebMD, and Ziopharm; and other ownership interests in relation to: OncoResponse (founder) and Telperian Inc (advisor). A.D. reports honoraria/advisory board roles with: Ignyta/Genentech/Roche, Loxo/Bayer/Lilly, Takeda/Ariad/Millenium, TP Therapeutics, AstraZeneca, Pfizer, Blueprint Medicines, Helsinn, Beigene, BergenBio, Hengrui Therapeutics, Exelixis, Tyra Biosciences, Verastem, MORE Health, Abbvie, 14ner/Elevation Oncology, Remedica Ltd., ArcherDX, Monopteros, Novartis, EMD Serono, Melendi, Liberum, Repare RX, Nuvalent, Merus, AXIS, Chugai Pharm, and EPG Health; associated research paid to institution from Pfizer, Exelixis, GlaxoSmithKlein, Teva, Taiho, and PharmaMar; royalties from Wolters Kluwer; other from Merck, Puma, Merus, and Boehringer Ingelheim; and CME honoraria from Medscape, OncLive, PeerVoice, Physicians Education Resources, Targeted Oncology, Research to Practice, Axis, Peerview Institute, Paradigm Medical Communications, WebMD, MJH Life Sciences, Med Learning, Imedex, Answers in CME, and Clinical Care Options. T.W.L. reports consulting roles with Bayer, Cellectis, Novartis, Deciphera, Jumo Health, Y-mAbs Therapeutics and research support from: Bayer, Pfizer and Novartis. S.R.-C. declares that he has no competing interests.

Auteurs

Erin R Rudzinski (ER)

Seattle Children's Hospital, Seattle, WA, USA. Electronic address: erin.rudzinski@seattlechildrens.org.

Jaclyn Hechtman (J)

Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Sinchita Roy-Chowdhuri (S)

The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Marion Rudolph (M)

Bayer AG Pharmaceuticals, Berlin, Germany.

Christina M Lockwood (CM)

Seattle Children's Hospital, Seattle, WA, USA; University of Washington, Seattle, WA, USA.

Josh Silvertown (J)

Bayer Healthcare Pharmaceuticals, Inc., Whippany, NJ, USA.

Justyna Wierzbinska (J)

Bayer AG Pharmaceuticals, Berlin, Germany.

Kui Shen (K)

Bayer Healthcare Pharmaceuticals, Inc., Whippany, NJ, USA.

Ricarda Norenberg (R)

Chrestos Concept GmbH & Co. KG, Essen, Germany.

Hendrik Nogai (H)

Bayer HealthCare Pharmaceuticals, Inc., Basel, Switzerland.

David S Hong (DS)

The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Alexander Drilon (A)

Memorial Sloan Kettering Cancer Center, New York, NY, USA; Weill Cornell Medical College, New York, NY, USA.

Theodore W Laetsch (TW)

The Children's Hospital of Philadelphia/University of Pennsylvania, Philadelphia, PA, USA.

Articles similaires

Genome, Chloroplast Phylogeny Genetic Markers Base Composition High-Throughput Nucleotide Sequencing

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C

Classifications MeSH