Mutational Profiling in US Patients With Chronic-phase Chronic Myeloid Leukemia on Tyrosine Kinase Inhibitors.
[BACKGROUND/AIM] Widespread use of BCR::ABL1 tyrosine kinase inhibitors (TKIs) has transformed the clinical landscape of chronic myeloid leukemia (CML).
APA
Haddad FG, Jabbour EJ, et al. (2026). Mutational Profiling in US Patients With Chronic-phase Chronic Myeloid Leukemia on Tyrosine Kinase Inhibitors.. Cancer diagnosis & prognosis, 6(2), 186-198. https://doi.org/10.21873/cdp.10518
MLA
Haddad FG, et al.. " Mutational Profiling in US Patients With Chronic-phase Chronic Myeloid Leukemia on Tyrosine Kinase Inhibitors.." Cancer diagnosis & prognosis, vol. 6, no. 2, 2026, pp. 186-198.
PMID
41778234
Abstract
[BACKGROUND/AIM] Widespread use of BCR::ABL1 tyrosine kinase inhibitors (TKIs) has transformed the clinical landscape of chronic myeloid leukemia (CML). However, mutation-driven treatment resistance challenges optimal care and outcomes. The purpose of this study was to ascertain real-world practices concerning such mutational profiling in US hematology and oncology practices, which were mainly community-based.
[MATERIALS AND METHODS] This is the first chart review of kinase domain mutational profiling in the US. In this study of the Cardinal Health Oncology Provider Extended Network (OPEN), 13 hematologists and/or oncologists selected charts of adults with chronic-phase CML for approximately equal numbers of patients who underwent such testing (Cohort 1; =26) or did not (Cohort 2; =25).
[RESULTS] Across most time points, failure and warning signs by molecular testing were not significantly more frequent in patients who did or did not undergo mutational profiling. Conversely, similar frequencies of optimal milestones were observed in patients with or without testing. Patients who underwent mutational profiling were more likely to have splenomegaly (=0.0069) versus those who did not.
[CONCLUSION] There were few significant differences in failure and warning signs by molecular testing in patients who did or did not undergo mutational profiling. Patients who underwent mutational profiling were significantly more likely to have splenomegaly, which is not included in consensus guidelines as a reason to conduct such testing. Taken together, these findings raise potential concerns about consensus guideline adherence as a means to optimize CML management for TKI resistance.
[MATERIALS AND METHODS] This is the first chart review of kinase domain mutational profiling in the US. In this study of the Cardinal Health Oncology Provider Extended Network (OPEN), 13 hematologists and/or oncologists selected charts of adults with chronic-phase CML for approximately equal numbers of patients who underwent such testing (Cohort 1; =26) or did not (Cohort 2; =25).
[RESULTS] Across most time points, failure and warning signs by molecular testing were not significantly more frequent in patients who did or did not undergo mutational profiling. Conversely, similar frequencies of optimal milestones were observed in patients with or without testing. Patients who underwent mutational profiling were more likely to have splenomegaly (=0.0069) versus those who did not.
[CONCLUSION] There were few significant differences in failure and warning signs by molecular testing in patients who did or did not undergo mutational profiling. Patients who underwent mutational profiling were significantly more likely to have splenomegaly, which is not included in consensus guidelines as a reason to conduct such testing. Taken together, these findings raise potential concerns about consensus guideline adherence as a means to optimize CML management for TKI resistance.
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