Does coasting occur in patients receiving taxane-based chemotherapy?

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Last updated: October 27, 2025View editorial policy

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Coasting Does Not Occur in Taxane-Based Chemotherapy

Unlike platinum-based chemotherapeutics, taxanes do not exhibit the "coasting" phenomenon where neuropathy worsens after treatment completion. 1

Taxane-Induced Neuropathy Characteristics

  • Paclitaxel-induced peripheral neuropathy begins improving immediately after treatment completion, unlike oxaliplatin-induced neuropathy which may worsen for 2-6 months after treatment cessation 1
  • Taxane neuropathy presents primarily as a sensory axonal neuropathy that typically begins during the first 2 months of treatment 1
  • Symptoms tend to resolve between doses and improve over several months after treatment completion 1
  • Symptoms are not worsened, on average, in subsequent cycles of treatment 1

Evidence Against Coasting in Taxanes

  • A systematic review examining coasting in taxane-induced peripheral neuropathy in breast cancer patients found only one study reporting coasting events (14.3% of patients), while eight studies reported no coasting events 2
  • Paclitaxel neuropathy follows a different recovery pattern than oxaliplatin, with improvement beginning immediately after treatment completion rather than worsening 1
  • Most patients experience improvement in symptoms over several months following treatment cessation 1

Clinical Presentation of Taxane Neuropathy

  • Primarily sensory neuropathy with a stocking-glove distribution that begins distally in fingers and toes and can progress proximally as the condition worsens 1
  • Most common symptoms include numbness, tingling, and pain 1
  • Numbness and tingling appear earlier and are generally more prominent problems than pain 1
  • Paclitaxel causes an acute pain syndrome (often labeled as arthralgia/myalgia) that typically develops within 1-3 days after administration and largely resolves within a week 1, 3
  • Taxane acute pain syndrome (TAPS) has been reported in 14-46% of patients receiving taxane-based chemotherapy 3

Risk Factors for Taxane Neuropathy

  • Diabetes mellitus, increasing age, concurrent exposure to other neurotoxic agents, pre-existing neuropathy, and conditions predisposing to neuropathy 1
  • Smoking appears to increase the risk of long-term prevalent paraesthesia 1
  • Medium to high levels of anxiety before treatment may impact the development of CIPN during and after treatment 4

Management Considerations

  • For painful taxane-induced neuropathy, duloxetine is the recommended first-line treatment option 5
  • Home-based, moderate-intensity walking and resistance exercise programs have shown benefit in reducing CIPN symptoms 5
  • Cryotherapy (cooling of hands and feet) has demonstrated a clinically meaningful impact on reducing occurrence of CIPN from taxanes 6

Clinical Pitfalls and Caveats

  • Taxane-induced neuropathy can persist as a debilitating problem for years in some patients despite the general trend of improvement 1
  • Monitoring for neuropathy should continue after treatment completion, as symptoms may persist or evolve 1
  • Taxane-induced neuropathy is often confused with other forms of neuropathic pain but has distinct pathophysiology and symptomatology 1

References

Guideline

Clinical Trajectory and Pathophysiology of Paclitaxel-Induced Peripheral Neuropathy

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Symptoms of anxiety but not depression before start of taxane-based chemotherapy are associated with peripheral neuropathy: a multicenter study in women with breast cancer.

Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer, 2022

Guideline

Management of Taxane-Induced Numbness

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

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.

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