FDA Approval Summary: Repotrectinib for Locally Advanced or Metastatic ROS1-Positive Non-Small Cell Lung Cancer.
Michael I BarbatoDiana BradfordYi RenStephanie L AungstClaudia P MillerLili PanJeanne F ZirkelbachYangbing LiYouwei BiJianghong FanManuela GrimsteinSarah E DorffAnup K AmatyaPallavi S Mishra-KalyaniBarbara ScepuraPeter SchotlandOpeyemi UdokaIdara OjofeitimiJohn K LeightonNam Atiqur RahmanRichard PazdurHarpreet SinghPaul G KluetzNicole DreznerPublished in: Clinical cancer research : an official journal of the American Association for Cancer Research (2024)
On November 15, 2023, the U.S. Food and Drug Administration (FDA) granted traditional approval to repotrectinib (Augtyro, Bristol Myers Squibb Corporation) for the treatment of adult patients with locally advanced or metastatic receptor tyrosine kinase encoded by the ROS1 gene (ROS1)-positive non-small cell lung cancer (NSCLC). The approval was based on TRIDENT-1, a single-arm trial with multiple cohorts of patients with ROS1 fusion-positive (hereafter "ROS1-positive") NSCLC (NCT03093116), who were either treatment naïve or had received prior ROS1 tyrosine kinase inhibitor (TKI) and/or platinum-based chemotherapy. The primary efficacy outcome measure is objective response rate (ORR) assessed by blinded independent central review (BICR) using response evaluation criteria in solid tumors version 1.1. ORR was assessed in 71 patients who were ROS1 TKI naïve and 56 patients who had received a prior ROS1 TKI. Among the 71 patients who were ROS1 TKI naïve, the ORR was 79% (95% CI, 68-88), median duration of response was 34.1 months (95% CI, 26-NE). In patients who had received a prior ROS1 TKI and no prior chemotherapy, the ORR was 38% (95% CI, 25-52). The median duration of response was 14.8 months (95% CI, 7.6-NE); BICR-assessed responses were observed in CNS metastases in patients in both cohorts and in patients who developed resistance mutations following prior TKI therapy. The most common (>20%) adverse reactions were dizziness, dysgeusia, peripheral neuropathy, constipation, dyspnea, ataxia, fatigue, cognitive disorders, and muscular weakness. A unique feature of this ROS1 TKI approval is the inclusion of robust evidence of efficacy in patients with ROS1-positive NSCLC who had progressed on prior ROS1 TKIs.
Keyphrases
- tyrosine kinase
- cell death
- dna damage
- reactive oxygen species
- advanced non small cell lung cancer
- small cell lung cancer
- squamous cell carcinoma
- locally advanced
- epidermal growth factor receptor
- drug administration
- stem cells
- radiation therapy
- chronic kidney disease
- chronic myeloid leukemia
- end stage renal disease
- blood brain barrier
- emergency department
- rectal cancer
- mesenchymal stem cells
- lymph node
- early onset
- palliative care
- copy number
- clinical evaluation
- myasthenia gravis