duration of imatinib therapy was 9.6 years (range, 0.3-16.2 years). Estimated median overall survival time was 24.2 years, and 3-, 5-, and 10-year overall survival rates were 96.4%, 92.7%, and 88.6%, respectively. Second primary neoplasms were developed in 11 of 56 (19.6%) patients during follow-up period. Among these 11 patients, one patient developed malignant lymphoma, remaining 10 patients developed solid tumors: colorectal cancer (n = 4), gastric cancer (n = 1), pancreatic cancer (n = 1), lung cancer (n = 1), bladder cancer (n = 1), prostate cancer (n = 1), and head and neck cancer (n = 1). Surgical resection was undergone in five patients, and seven patients received chemotherapy. A total of 11 patients died during follow-up period. Most common cause of death was second primary neoplasm (n = 5), followed by cardiovascular event (n = 4). No leukemia-related deaths were recorded. In 17 patients, imatinib was switched to second generation TKIs, dasatinib (n = 10) or nilotinib (n = 7), because of intolerance (n = 7), treatment failure (n = 4), and other reasons (n = 6), including clinical trials, and patient's request. Among remaining 39 patients who were continuously treated with imatinib with median treatment duration of 11.2 years (range, 0.7-16.2 years), 35 patients achieved major molecular response (MR3.0) at last follow up. Among these 35 patients, 23 patients achieved deep molecular response (MR4.0). Therefore, 59% (23/39) of patients treated with imatinib subsequently achieved MR4.0. Nine patients, who maintained deep molecular response (MR4.0) with imatinib treatment for at least two years, discontinued imatinib. Median duration of imatinib treatment in these nine patients was 10.5 years (range, 5.7-13.8 years). Eight of nine patients are maintaining treatment-free remission with median observation period of 34 months (range, 20-42 months) at last follow up. Summary/Conclusion: By long-term imatinib treatment, substantial number of patients achieved deep molecular response, and significant number of patients may have possibility of treatment-free remission. No leukemia-related deaths were recorded in cohort of the present study. However, careful management of co-morbidity and regular screening for second primary neoplasms should be required.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
customersupport@researchsolutions.com
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.
Copyright © 2025 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.