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Durable Clinical Response to Entrectinib in NTRK1-Rearranged Non-Small Cell Lung Cancer
Anna F Farago1, Long P Le, Zongli Zheng
1*Department of Medicine, Massachusetts General Hospital, Boston, MA; †Department of Pathology, Massachusetts General Hospital, Boston, MA; ‡Memorial Sloan Kettering Cancer Center, New York, NY; ‖Sarah Cannon Research Institute/Florida Cancer Specialists, Sarasota, FL; §Sarah Cannon Research Institute/Tennessee Oncology, PLLC, Nashville, TN; ¶Department of Medicine, Georgetown University Medical Center, Washington, DC; #University of California Irving Health, Orange, CA; **Dana-Farber Cancer Institute, Boston, MA; ††Beth Israel Deaconess Medical Center, Boston, MA; and ‡‡Ignyta, Inc., San Diego, CA.
Introduction:
Chromosomal rearrangements involving neurotrophic tyrosine kinase 1 (NTRK1) occur in a subset of non-small cell lung cancers (NSCLCs) and other solid tumor malignancies, leading to expression of an oncogenic TrkA fusion protein. Entrectinib (RXDX-101) is an orally available tyrosine kinase inhibitor, including TrkA. We sought to determine the frequency of NTRK1 rearrangements in NSCLC and to assess the clinical activity of entrectinib.
Methods:
We screened 1378 cases of NSCLC using anchored multiplex polymerase chain reaction (AMP). A patient with an NTRK1 gene rearrangement was enrolled onto a Phase 1 dose escalation study of entrectinib in adult patients with locally advanced or metastatic tumors (NCT02097810). We assessed safety and response to treatment.
Results:
We identified NTRK1 gene rearrangements at a frequency of 0.1% in this cohort. A patient with stage IV lung adenocrcinoma with an SQSTM1-NTRK1 fusion transcript expression was treated with entrectinib. Entrectinib was well tolerated, with no grade 3-4 adverse events. Within three weeks of starting on treatment, the patient reported resolution of prior dyspnea and pain. Restaging CT scans demonstrated a RECIST partial response (PR) and complete resolution of all brain metastases. This patient has continued on treatment for over 6 months with an ongoing PR.
Conclusions:
Entrectinib demonstrated significant anti-tumor activity in a patient with NSCLC harboring an SQSTM1-NTRK1 gene rearrangement, indicating that entrectinib may be an effective therapy for tumors with NTRK gene rearrangements, including those with central nervous system metastases.
Insights
Entrectinib effectively treated non-small cell lung cancer with NTRK1 rearrangements. This targeted therapy showed significant anti-tumor activity, including resolving brain metastases, in a patient with NSCLC.
Area of Science:
- Oncology
- Molecular Biology
- Pharmacology
Background:
- Neurotrophic tyrosine kinase 1 (NTRK1) gene rearrangements drive oncogenesis in certain non-small cell lung cancers (NSCLCs).
- Entrectinib is an oral tyrosine kinase inhibitor targeting TrkA, the protein product of NTRK1.
- Investigating NTRK1 rearrangement frequency and entrectinib's efficacy in NSCLC is crucial for targeted therapy development.
Observation:
- A screening of 1378 NSCLC cases identified NTRK1 rearrangements in 0.1% of patients.
- A patient with stage IV lung adenocarcinoma and an SQSTM1-NTRK1 fusion transcript was treated with entrectinib in a Phase 1 study.
- The patient experienced rapid symptom relief, including resolution of dyspnea and pain, within three weeks.
Findings:
- Entrectinib was well-tolerated, with no severe adverse events.
- Radiographic assessment revealed a partial response (PR) and complete resolution of brain metastases.
- The patient maintained an ongoing PR for over six months of continuous treatment.
Implications:
- Entrectinib demonstrates significant anti-tumor activity in NSCLC with NTRK gene rearrangements.
- This suggests entrectinib's potential as an effective treatment for NTRK-rearranged tumors, including those with central nervous system involvement.
- These findings support entrectinib's role in precision oncology for specific genetic alterations in solid tumors.
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