A novel NCOR2-NTRK1 fusion detected in a patient of lung adenocarcinoma and response to larotrectinib: a case report

Abstract Background The identification of NTRK fusions in tumours has become critically important due to the actionable events predictive of response to TRK inhibitor. It is not clear whether the NTRK breakpoint location is different for response to targeted therapy and NTRK fusions affects the effi...

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Main Authors: Lei Zhang, Huanhuan Liu, Ye Tian, Huina Wang, Xueying Yang
Format: Article
Language:English
Published: BMC 2021-04-01
Series:BMC Pulmonary Medicine
Subjects:
Online Access:https://doi.org/10.1186/s12890-021-01490-x
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author Lei Zhang
Huanhuan Liu
Ye Tian
Huina Wang
Xueying Yang
author_facet Lei Zhang
Huanhuan Liu
Ye Tian
Huina Wang
Xueying Yang
author_sort Lei Zhang
collection DOAJ
description Abstract Background The identification of NTRK fusions in tumours has become critically important due to the actionable events predictive of response to TRK inhibitor. It is not clear whether the NTRK breakpoint location is different for response to targeted therapy and NTRK fusions affects the efficacy of immunotherapy. Case presentation Here we reported a 60-year-old female diagnosed with advanced lung adenocarcinoma. NGS-based molecular profiling identified a novel NCOR2-NTRK1 fusion and high tumor mutational burden (TMB) (58.58 mutations/Mb) in this case. Additionally, program death-ligand 1 (PD-L1) expression was detected in 20–30% of the tumor cells by immunohistochemical (IHC) staining. The patient received treatment with anti-PD-1 immune checkpoint inhibitor of camrelizumab. After two cycles of treatment, the CT scan showed some tumor nodules were still enlarged, indicating disease progression. She was then changed to TRK inhibitor larotrectinib. One month later, the CT scan showed the volume of some lesions started to decrease, and no metastasis lesions were found. The patient then continued the administration of larotrectinib, and some lesion sizes were significantly reduced or even disappeared in the next few months. Currently, this patient is still alive. Conclusions Altogether, this report provided a new driver of lung adenocarcinoma expanded the mutational spectrum of NTRK1 fusion variants and suggested using larotrectinib as the targeted therapy is more effective than anti-PD-1 inhibitor in lung adenocarcinoma harboring with NTRK fusion, positive PD-L1 expression, and high TMB simultaneously.
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spelling doaj.art-0e06223fb7e7491a99caeed19ac251232022-12-21T23:03:46ZengBMCBMC Pulmonary Medicine1471-24662021-04-012111510.1186/s12890-021-01490-xA novel NCOR2-NTRK1 fusion detected in a patient of lung adenocarcinoma and response to larotrectinib: a case reportLei Zhang0Huanhuan Liu1Ye Tian2Huina Wang3Xueying Yang4Department of Thoracic Surgery, The Fourth Affiliated Hospital of China Medical UniversityAcornmed Biotechnology Co., Ltd.Department of Thoracic Surgery, The Fourth Affiliated Hospital of China Medical UniversityAcornmed Biotechnology Co., Ltd.Department of Thoracic Surgery, The Fourth Affiliated Hospital of China Medical UniversityAbstract Background The identification of NTRK fusions in tumours has become critically important due to the actionable events predictive of response to TRK inhibitor. It is not clear whether the NTRK breakpoint location is different for response to targeted therapy and NTRK fusions affects the efficacy of immunotherapy. Case presentation Here we reported a 60-year-old female diagnosed with advanced lung adenocarcinoma. NGS-based molecular profiling identified a novel NCOR2-NTRK1 fusion and high tumor mutational burden (TMB) (58.58 mutations/Mb) in this case. Additionally, program death-ligand 1 (PD-L1) expression was detected in 20–30% of the tumor cells by immunohistochemical (IHC) staining. The patient received treatment with anti-PD-1 immune checkpoint inhibitor of camrelizumab. After two cycles of treatment, the CT scan showed some tumor nodules were still enlarged, indicating disease progression. She was then changed to TRK inhibitor larotrectinib. One month later, the CT scan showed the volume of some lesions started to decrease, and no metastasis lesions were found. The patient then continued the administration of larotrectinib, and some lesion sizes were significantly reduced or even disappeared in the next few months. Currently, this patient is still alive. Conclusions Altogether, this report provided a new driver of lung adenocarcinoma expanded the mutational spectrum of NTRK1 fusion variants and suggested using larotrectinib as the targeted therapy is more effective than anti-PD-1 inhibitor in lung adenocarcinoma harboring with NTRK fusion, positive PD-L1 expression, and high TMB simultaneously.https://doi.org/10.1186/s12890-021-01490-xLung adenocarcinomaNTRK fusionPD-L1LarotrectinibCase report
spellingShingle Lei Zhang
Huanhuan Liu
Ye Tian
Huina Wang
Xueying Yang
A novel NCOR2-NTRK1 fusion detected in a patient of lung adenocarcinoma and response to larotrectinib: a case report
BMC Pulmonary Medicine
Lung adenocarcinoma
NTRK fusion
PD-L1
Larotrectinib
Case report
title A novel NCOR2-NTRK1 fusion detected in a patient of lung adenocarcinoma and response to larotrectinib: a case report
title_full A novel NCOR2-NTRK1 fusion detected in a patient of lung adenocarcinoma and response to larotrectinib: a case report
title_fullStr A novel NCOR2-NTRK1 fusion detected in a patient of lung adenocarcinoma and response to larotrectinib: a case report
title_full_unstemmed A novel NCOR2-NTRK1 fusion detected in a patient of lung adenocarcinoma and response to larotrectinib: a case report
title_short A novel NCOR2-NTRK1 fusion detected in a patient of lung adenocarcinoma and response to larotrectinib: a case report
title_sort novel ncor2 ntrk1 fusion detected in a patient of lung adenocarcinoma and response to larotrectinib a case report
topic Lung adenocarcinoma
NTRK fusion
PD-L1
Larotrectinib
Case report
url https://doi.org/10.1186/s12890-021-01490-x
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