4.7 Article

Randomized Double-Blind Placebo-Controlled Trial of Acetyl-L-Carnitine for the Prevention of Taxane-Induced Neuropathy in Women Undergoing Adjuvant Breast Cancer Therapy

Journal

JOURNAL OF CLINICAL ONCOLOGY
Volume 31, Issue 20, Pages 2627-+

Publisher

AMER SOC CLINICAL ONCOLOGY
DOI: 10.1200/JCO.2012.44.8738

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Funding

  1. Advanced Clinical Research Award from the American Society of Clinical Oncology Conquer Cancer Foundation
  2. Avon Foundation
  3. National Cancer Institute Division of Cancer Prevention [CA037429]
  4. Clinical and Translational Science Awards [ULR000040]
  5. Medical Research Council [G0701870] Funding Source: researchfish
  6. MRC [G0701870] Funding Source: UKRI

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Purpose Chemotherapy-induced peripheral neuropathy (CIPN) is common and leads to suboptimal treatment. Acetyl-L-carnitine (ALC) is a natural compound involved in neuronal protection. Studies have suggested ALC may be effective for the prevention and treatment of CIPN. Patients and Methods A 24-week randomized double-blind trial comparing ALC (3,000 mg per day) with placebo in women undergoing adjuvant taxane-based chemotherapy was conducted. The primary objective was to determine if ALC prevents CIPN as measured by the 11-item neurotoxicity (NTX) component of the Functional Assessment of Cancer Therapy (FACT) -Taxane scale at 12 weeks. Secondary objectives included changes in 24-week end points, functional status (FACT-Trial Outcome Index [TOI]), fatigue (Functional Assessment of Chronic Illness Therapy [FACIT]-Fatigue), and NTX grade. Results A total of 409 patients were evaluable (208 received ALC; 201, placebo). In a multivariate linear regression, week-12 scores were 0.9 points lower (more CIPN) with ALC than placebo (95% CI, -2.2 to 0.4; P=.17), whereas week-24 scores were 1.8 points lower with ALC (95% CI, -3.2 to -0.4; P=.01). Patients receiving ALC were more likely to have a > 5-point decrease in FACT-NTX scores (38% v 28%; P=.05), and FACT-TOI scores were 3.5 points lower with ALC (P=.03). Grade 3 to 4 neurotoxicity was more frequent in the ALC arm (eight v one). No differences between arms were observed for FACIT-Fatigue or other toxicities. Serum carnitine level increased with ALC but remained stable with placebo. Conclusion There was no evidence that ALC affected CIPN at 12 weeks; however, ALC significantly increased CIPN by 24 weeks. This is the first study to our knowledge showing that a nutritional supplement increased CIPN. Patients should be discouraged from using supplements without proven efficacy. (C) 2013 by American Society of Clinical Oncology

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