Literature DB >> 35144967

Updated Integrated Analysis of the Efficacy and Safety of Entrectinib in Patients With NTRK Fusion-Positive Solid Tumors.

George D Demetri1, Filippo De Braud2,3, Alexander Drilon4, Salvatore Siena3,5, Manish R Patel6, Byoung Chul Cho7, Stephen V Liu8, Myung-Ju Ahn9, Chao-Hua Chiu10, Jessica J Lin11, Koichi Goto12, Jeeyun Lee9, Lyudmila Bazhenova13, Thomas John14, Marwan Fakih15, Sant P Chawla16, Rafal Dziadziuszko17, Takashi Seto18, Sebastian Heinzmann19, Bethany Pitcher20, David Chen21, Timothy R Wilson21, Christian Rolfo22.   

Abstract

PURPOSE: Entrectinib potently inhibits tropomyosin receptor kinases (TRKAs)/B/C and ROS1, and previously induced deep [objective response rate (ORR) 57.4%] and durable [median duration of response (DoR) 10.4 months] responses in adults with NTRK fusion-positive solid tumors from three phase I/II trials. This article expands prior reports with additional patients and longer follow-up. PATIENTS AND METHODS: Patients with locally advanced/metastatic NTRK fusion-positive solid tumors and ≥12 months' follow-up were included. Primary endpoints were ORR and DoR by blinded independent central review (BICR); secondary endpoints included progression-free survival (PFS), intracranial efficacy, and safety. The safety-evaluable populations included all patients who had received ≥1 entrectinib dose.
RESULTS: At clinical cut-off (August 31, 2020), the efficacy-evaluable population comprised 121 adults with 14 tumor types and ≥30 histologies. Median follow-up was 25.8 months; 61.2% of patients had a complete (n = 19) or partial response (n = 55). Median DoR was 20.0 months [95% confidence interval (CI), 13.0-38.2]; median PFS was 13.8 months (95% CI, 10.1-19.9). In 11 patients with BICR-assessed measurable central nervous system (CNS) disease, intracranial ORR was 63.6% (95% CI, 30.8-89.1) and median intracranial DoR was 22.1 (95% CI, 7.4-not estimable) months. The safety profile of entrectinib in adults and pediatric patients was aligned with previous reports. Most treatment-related adverse events (TRAEs) were grade 1/2 and manageable/reversible with dose modifications. TRAE-related discontinuations occurred in 8.3% of patients.
CONCLUSIONS: With additional clinical experience, entrectinib continues to demonstrate durable systemic and intracranial responses and can address the unmet need of a CNS-active treatment in patients with NTRK fusion-positive solid tumors. ©2022 The Authors; Published by the American Association for Cancer Research.

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Year:  2022        PMID: 35144967     DOI: 10.1158/1078-0432.CCR-21-3597

Source DB:  PubMed          Journal:  Clin Cancer Res        ISSN: 1078-0432            Impact factor:   12.531


  5 in total

1.  Response to entrectinib in a malignant glioneuronal tumor with ARHGEF2-NTRK fusion.

Authors:  Kazuhiko Kurozumi; Kentaro Fujii; Kana Washio; Joji Ishida; Yoshihiro Otani; Tamotsu Sudo; Makoto Tahara; Koichi Ichimura; Daisuke Ennishi; Isao Date
Journal:  Neurooncol Adv       Date:  2022-06-13

Review 2.  Predictive Biomarkers in Thyroid Cancer.

Authors:  Elisabetta Macerola; Anello Marcello Poma; Paola Vignali; Agnese Proietti; Clara Ugolini; Liborio Torregrossa; Alessio Basolo; Rossella Elisei; Ferruccio Santini; Fulvio Basolo
Journal:  Front Oncol       Date:  2022-05-06       Impact factor: 5.738

Review 3.  NTRK insights: best practices for pathologists.

Authors:  Jaclyn F Hechtman
Journal:  Mod Pathol       Date:  2021-09-16       Impact factor: 7.842

4.  Real-world survival outcomes in patients with locally advanced or metastatic NTRK fusion-positive solid tumors receiving standard-of-care therapies other than targeted TRK inhibitors.

Authors:  Derrek P Hibar; George D Demetri; Solange Peters; Jessica Davies; Olivier Humblet; Sophia L Maund; Laura Perez
Journal:  PLoS One       Date:  2022-08-08       Impact factor: 3.752

5.  TRK Inhibition with Entrectinib in Metastatic Salivary Secretory Carcinoma (SC): A Case Report.

Authors:  Matthew S Ernst; John T Lysack; Martin D Hyrcza; Shamir P Chandarana; Desiree Hao
Journal:  Curr Oncol       Date:  2022-05-31       Impact factor: 3.109

  5 in total

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