98%
921
2 minutes
20
To support the benefit-risk assessment and dose justification of repotrectinib for patients with c-ros oncogene 1 (ROS1) positive non-small cell lung cancer (NSCLC) or neurotrophin receptor tyrosine kinase (NTRK)-positive solid tumors, exposure-response analyses were conducted. The analysis used data from the TRIDENT-1 trial for key clinical efficacy endpoints-objective response rate (ORR) and progression-free survival (PFS), as well as 5 clinical safety endpoints: Grade 2 or higher (Gr2+) dizziness, Gr2+ anemia, Grade 3 or higher (Gr3+) treatment-emergent adverse events (AEs), Gr2+ neurologic AEs, and dose reduction or interruption due to AEs. The exposure-response relationship for ORR was characterized by logistic regression with average repotrectinib exposure over the first 56 days of dosing; PFS or safety endpoints were evaluated by Cox proportional-hazards models with time-varying cumulative half-daily average drug concentration. The model predicted efficacy and safety were compared for 160 mg QD/BID (160 mg QD for 14 days, followed by 160 mg BID) and 160 mg QD under different food statuses. The recommended dose of 160 mg QD/BID demonstrated improved ORR and PFS over 160 mg QD in both ROS1-positive NSCLC and NTRK-positive solid tumors, while the increase in AEs was minimal. Predicted efficacy and safety were comparable across food conditions, supporting the administration of 160 mg QD/BID regardless of food. This work highlighted the importance of selecting appropriate exposure measures in exposure-response analyses, particularly when dose or dose frequencies change throughout treatment. The integrated exposure-response analyses provided a robust framework to support the repotrectinib dosing strategy.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1002/psp4.70102 | DOI Listing |
CPT Pharmacometrics Syst Pharmacol
August 2025
Bristol-Myers Squibb, Princeton, New Jersey, USA.
To support the benefit-risk assessment and dose justification of repotrectinib for patients with c-ros oncogene 1 (ROS1) positive non-small cell lung cancer (NSCLC) or neurotrophin receptor tyrosine kinase (NTRK)-positive solid tumors, exposure-response analyses were conducted. The analysis used data from the TRIDENT-1 trial for key clinical efficacy endpoints-objective response rate (ORR) and progression-free survival (PFS), as well as 5 clinical safety endpoints: Grade 2 or higher (Gr2+) dizziness, Gr2+ anemia, Grade 3 or higher (Gr3+) treatment-emergent adverse events (AEs), Gr2+ neurologic AEs, and dose reduction or interruption due to AEs. The exposure-response relationship for ORR was characterized by logistic regression with average repotrectinib exposure over the first 56 days of dosing; PFS or safety endpoints were evaluated by Cox proportional-hazards models with time-varying cumulative half-daily average drug concentration.
View Article and Find Full Text PDFJ Manag Care Spec Pharm
July 2024
Department of Pharmacotherapy, College of Pharmacy, University of Utah, Salt Lake City.
Background: Neurotrophic tyrosine receptor kinase () gene fusions are rare oncogenic drivers prevalent in 0.3% of solid tumors. They are most common in salivary gland cancer (2.
View Article and Find Full Text PDFFront Oncol
April 2023
Department of Thyroid & Bariatric Metabolic Surgery, Shanxi Bethune Hospital, Shanxi Academy of Medical Sciences, Third Hospital of Shanxi Medical University, Taiyuan, Shanxi, China.
fusions are validated oncogenic drivers of various adult and pediatric tumor types, including thyroid cancer, and serve as a therapeutic target. Recently, tropomyosin receptor kinase (TRK) inhibitors, such as entrectinib and larotrectinib, display promising therapeutic efficacy in -positive solid tumors. Although some fusion partners have been identified in thyroid cancer, the spectrum of fusion is not fully characterized.
View Article and Find Full Text PDFFront Oncol
March 2023
Institute of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Background: Even though two NTRK-targeting drugs are available for the treatment of irresectable, metastatic, or progressive NTRK-positive solid tumors, less is known about the role of NTRK fusions in lymphoma. For this reason, we aimed to investigate if NTRK fusion proteins are expressed in diffuse large B-cell lymphoma (DLBCL) by systemic immunohistochemistry (IHC) screening and additional FISH analysis in a large cohort of DLBCL samples according to the ESMO Translational Research and Precision Medicine Working Group recommendations for the detection of NTRK fusions in daily practice and clinical research.
Methods: A tissue microarray of 92 patients with the diagnosis of DLBCL at the University Hospital Hamburg between 2020 and 2022 was built.
Int J Cancer
December 2023
Department of Gastrointestinal Oncology, Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Peking University Cancer Hospital and Institute, Beijing, China.
Neurotrophic tropomyosin receptor kinase (NTRK) gene fusions are rare oncogenic drivers and targets of TRK inhibitors in solid tumors. Little is known about NTRK fusion in Chinese patients with pan-cancer. Our study investigated the prevalence and genomic features of NTRK1/2/3 gene fusions in 67 883 Chinese patients with pan-cancer using next-generation sequencing (NGS) data and circulating tumor DNA (ctDNA) NGS to guide TRK inhibitor treatment and resistance monitoring.
View Article and Find Full Text PDF