Safety, Tolerability and Symptom Outcomes Associated with l-Carnitine Supplementation in Patients with Cancer, Fatigue, and Carnitine Deficiency: A Phase I/II Study

Ricardo A. Cruciani, Ella Dvorkin, Peter Homel, Stephen Malamud, Bruce Culliney, Jeanne Lapin, Russell K. Portenoy, Nora Esteban-Cruciani

Research output: Contribution to journalArticle

55 Scopus citations

Abstract

Carnitine deficiency is among the many metabolic disturbances that may contribute to fatigue in patients with cancer. Administration of exogenous l-carnitine may hold promise as a treatment for this common symptom. Little is known about l-carnitine safety, tolerability, and dose-response in patients with cancer. We conducted a Phase I/II open-label trial to assess the safety and tolerability of exogenous l-carnitine and clarify the safe dose range associated with symptom effects for future controlled trials. Adult patients with advanced cancer, carnitine deficiency (free carnitine <35 for males or <25 μM/L for females, or acyl/free carnitine ratio >0.4), moderate to severe fatigue, and a Karnofsky Performance Status (KPS) score ≥50 were entered by groups of at least three into a standard maximum tolerated dose design. Each successive group received a higher dose of l-carnitine (250, 750, 1250, 1750, 2250, 2750, 3000 mg/day, respectively), administered in two daily doses for 7 days. To compare symptom outcomes before and after supplementation, patients completed validated measures of fatigue (Brief Fatigue Inventory [BFI]), depressed mood (Center for Epidemiologic Studies Depression Scale [CES-D]), quality of sleep (Epworth Sleeplessness Scale [ESS]), and KPS at baseline and 1 week later. Of the 38 patients screened for carnitine levels, 29 were deficient (76%). Twenty-seven patients participated ("intention to treat, ITT") (17 males, 10 females), and 21 completed the study ("completers"); 17 of these patients ("responders," mean ± [SD] age = 57.9 ± 15) had increased carnitine levels at the end of the supplementation period. The highest dose achieved was 3000 mg/day. No patient experienced significant side effects and no toxicities were noted. Analysis of all the patients accrued (ITT, n = 27) showed a total carnitine increase from 32.8 ± 10 to 54.3 ± 23 μM/L (P < 0.001) and free carnitine increase from 26.8 ± 8 to 44.1 ± 17 μM/L (P < 0.001). BFI decreased significantly, from 66 ± 12 to 39.7 ± 26 (P < 0.001); ESS decreased from 12.9 ± 12 to 9 ± 6 (P = 0.001); and CES-D decreased from 29.2 ± 12 to 19 ± 12 (P < 0.001). A separate analysis of the 17 "responders" showed a dose-response relationship for total- (r = 0.54, P = 0.03), free-carnitine (r = 0.56, P = 0.02) levels, and fatigue (BFI) scores (r = -0.61, P = 0.01). These findings suggest that l-carnitine may be safely administered at doses up to 3000 mg/day and that positive effects may be more likely at relatively higher doses in this range. This study provides the basis for the design of future placebo-controlled studies of l-carnitine supplementation for cancer-related fatigue.

Original languageEnglish (US)
Pages (from-to)551-559
Number of pages9
JournalJournal of Pain and Symptom Management
Volume32
Issue number6
DOIs
StatePublished - Dec 1 2006

Keywords

  • cancer-related fatigue
  • l-carnitine deficiency
  • l-carnitine supplementation

ASJC Scopus subject areas

  • Nursing(all)
  • Clinical Neurology
  • Anesthesiology and Pain Medicine

Fingerprint Dive into the research topics of 'Safety, Tolerability and Symptom Outcomes Associated with l-Carnitine Supplementation in Patients with Cancer, Fatigue, and Carnitine Deficiency: A Phase I/II Study'. Together they form a unique fingerprint.

  • Cite this