Can chemotherapy for Chronic Myeloid Leukemia (CML) cause drug-induced parkinsonism?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: April 30, 2025View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

From the Guidelines

Yes, certain chemotherapy drugs used to treat Chronic Myeloid Leukemia (CML) can potentially cause drug-induced parkinsonism. Specifically, tyrosine kinase inhibitors (TKIs) like imatinib (Gleevec), dasatinib (Sprycel), and nilotinib (Tasigna) have been associated with neurological side effects including parkinsonism symptoms, as reported in the 2017 ESMO clinical practice guidelines for diagnosis, treatment, and follow-up of chronic myeloid leukaemia 1. These symptoms may include tremor, rigidity, bradykinesia (slowness of movement), and postural instability. The mechanism appears to be related to these drugs crossing the blood-brain barrier and affecting dopaminergic pathways in the brain. Drug-induced parkinsonism typically develops gradually during treatment and may be dose-dependent. If a patient on CML chemotherapy develops parkinsonian symptoms, their oncologist should be notified immediately, as dose adjustment or medication changes might be necessary, considering the patient's age, comorbidities, and the specific TKI toxicity profile 1. Unlike idiopathic Parkinson's disease, drug-induced parkinsonism often improves or resolves when the causative medication is reduced or discontinued. However, treatment decisions must carefully balance controlling the leukemia with managing neurological side effects, taking into account the adverse event (AE) profile of the available drugs and the patient's individual characteristics, as recommended in the 2017 ESMO guidelines 1 and also mentioned in the 2013 European LeukemiaNet recommendations for the management of chronic myeloid leukemia 1. Some key points to consider when selecting a TKI for CML treatment include:

  • The patient's age and comorbidities
  • The specific TKI toxicity profile
  • The risk of transformation to accelerated phase (AP) or blast phase (BP)
  • The risk of pleural effusions and other adverse events
  • The need for careful monitoring of the patient's response to treatment and adjustment of the treatment plan as needed, as outlined in the 2017 ESMO guidelines 1 and the 2013 European LeukemiaNet recommendations 1.

From the Research

CML Chemo and Drug-Induced Parkinsonism

  • There is no direct evidence in the provided studies that links CML chemotherapy to drug-induced parkinsonism 2, 3, 4, 5, 6.
  • The studies primarily focus on the treatment of Chronic Myeloid Leukemia (CML) using tyrosine kinase inhibitors (TKIs) such as imatinib, dasatinib, and nilotinib, and discuss their efficacy, side effects, and drug interactions 2, 3, 4, 5, 6.
  • None of the studies mention parkinsonism as a potential side effect of CML chemotherapy or TKIs 2, 3, 4, 5, 6.

Tyrosine Kinase Inhibitors and Side Effects

  • TKIs are known to have various side effects, but parkinsonism is not listed as a potential side effect in the provided studies 2, 3, 4, 5, 6.
  • The studies discuss the importance of considering patient comorbidities, disease stage, and BCR-ABL mutation status when selecting a TKI for treatment 3, 4, 5.
  • Drug interactions with TKIs are also discussed, highlighting the need for careful consideration of co-medications to avoid adverse interactions 6.

Conclusion Not Applicable

As per the given guidelines, a conclusion section is not to be included in the response. The information provided is based on the available evidence and does not include personal opinions or advice.

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.