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Inflammatory myofibroblastoma (IMT) is an extremely rare mesenchymal tumor that mainly occurs in children and adolescents
Inflammatory myofibroblastoma (IMT) Inflammatory myofibroblastoma (IMT) in children
Crizotinib is a small molecule tyrosine kinase inhibitor that targets ALK, MET, ROS proto-oncogene 1 receptor tyrosine kinase (ROS1) and Recepteur d'Origine Nantais (RON)
G azole erlotinib (Crizotinib) is a small molecule tyrosine kinase inhibitors targeting ALK, MET, ROS proto-oncogene receptor tyrosine kinase (ROSl) and Recepteur d'Origine Nantais (RON) g oxazole Crizotinib is a small molecule tyrosine kinase inhibitor that targets ALK, MET, ROS proto-oncogene 1 receptor tyrosine kinase (ROS1) and Recepteur d'Origine Nantais (RON)
The CREATE trial is a prospective, multicenter, non-randomized, open-label Phase 2 basket trial that evaluates the activity and safety of crizotinib for different types of cancer, including with or without anaplastic lymphoma Advanced inflammatory myofibroblastoma with kinase (ALK) rearrangement
Lymphoma
The test patients were patients with advanced/metastatic IMT who could not be cured by surgery, radiotherapy or systemic therapy
immunity
Progression-free survival
Progression-free survivalAs of January 28, 2021, the researchers conducted a final analysis of the trial
The median follow-up was 50 months, 5 patients were still receiving crizotinib for a median follow-up of 50 months, and 5 patients were still receiving crizotinib for treatment of ALK-positive and ALK-negative patients.
Overall survival rate
Overall survival rateIn summary, the latest analysis results confirmed the results of previous studies, that is, crizotinib has a good treatment effect and lasting time for patients with locally advanced or metastatic ALK-positive IMT
Crizotinib is effective in treating patients with locally advanced or metastatic ALK-positive IMT and lasts for a long time
Original source:
Schöffski Patrick,Kubickova Michaela,Wozniak Agnieszka et al.
Long-term efficacy update of crizotinib in patients with advanced, inoperable inflammatory myofibroblastic tumour from EORTC trial 90101 CREATE https://doi.
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