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Pre-clinical Evaluation of Tyrosine Kinase Inhibitors for Treatment of Acute Leukemia
Published on: September 18, 2013
Delayed acute pancreatitis induced by nilotinib in a patient with chronic myeloid leukemia attaining sustained
Shifang Wang1, Sai Prasad Desikan1, Jay Jeffrey1
1White River Health System Batesville Arizona USA.
Abstract:
Advent of tyrosine kinase inhibitors (TKI) have revolutionized therapy of chronic myeloid leukemia. Imatinib was the first agent utilized in the therapy of CML. Nilotinib, a second generation TKI, results in an increase in number of patients achieving major molecular response at an earlier time point. Asymptomatic elevations in pancreatic enzyme is common and acute pancreatitis within weeks to months from start of therapy has been observed. Delayed onset pancreatitis has not been reported. We report a case of delayed onset pancreatitis in a patient with sustained complete molecular response. On account of the deep response, we were able to avoid starting alternate tyrosine kinase inhibitors that could also result in pancreatitis as a class effect.
Insights
Delayed pancreatitis is a rare complication of nilotinib therapy for chronic myeloid leukemia (CML). This case highlights a delayed onset in a patient with a deep molecular response, allowing avoidance of other tyrosine kinase inhibitors.
Area of Science:
- Oncology
- Pharmacology
Background:
- Tyrosine kinase inhibitors (TKIs) have transformed chronic myeloid leukemia (CML) treatment.
- Nilotinib, a second-generation TKI, enhances early major molecular response rates in CML patients.
Observation:
- Acute pancreatitis is a known side effect of TKIs, typically occurring early in treatment.
- This report details a rare case of delayed-onset pancreatitis in a CML patient on nilotinib.
Findings:
- The patient developed pancreatitis significantly later than typically observed, despite achieving a sustained complete molecular response.
- The deep molecular response enabled the discontinuation of nilotinib without switching to alternative TKIs, which share pancreatitis as a class effect.
Implications:
- This case expands the known timeline for nilotinib-induced pancreatitis.
- Careful patient monitoring for pancreatitis is crucial, even in patients with deep responses to TKIs.
- Understanding the timing of TKI-related adverse events aids in treatment management and patient safety.
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