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Efficacy of Daflon 500 mg in the Treatment of Lymphedema (Secondary to Conventional Therapy of Breast Cancer)Department of Nuclear Medicine, Centre Rene Huguenin 35, Rue Daily 92210, Saint Cloud, France
IRIS, Courbevoie, France
IRIS, Courbevoie, France
IRIS, Courbevoie, France To assess the activity of a purified, micronized, flavonoidic fraction (Dios; Daflon® 500 mg*) on upper limb lymphedema occurring after breast cancer therapy, a monocenter, randomized, double-blind, parallel group vs placebo (Plac) trial was carried out. One hundred and four women with lymphedema were included; 94 completed the study (46 Dios, 48 Plac). A subset of 24 patients with more severe lymphedema (10 Dios, 14 Plac) was subjected to a separate analysis. Treatment consisting of Dios or Plac was given two tablets daily over a six-month period. A radionuclide lymphoscintigraphy using technetium-99m was performed at inclusion and at the end of the treatment. The upper limb volume was measured every two months.
In the overall population the evolution of parameters was not different between Dios and Plac. In the 24 patients with a more severe lymphedema, the lymphoscintigraphic parameters (m ±sd) were as follows: lymphatic migration speed was significantly improved by Dios in comparison with Plac ( In conclusion, these results suggest a beneficial therapeutic activity of Dios at the usual dose of two tablets/day in patients affected with more severe lymphedema. The clear improvement of the lymphatic speed illustrates its known lymphokinetic activity. Further studies with a higher dosage could confirm the beneficial activity of this drug in secondary lymphedema.
Angiology, Vol. 48, No. 1,
93-98 (1997) |
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Speed cm/minute: 0.84 ±0.6 vs 0.14 ± 0.26, P = 0.005). The half-life of the colloidal compound was significantly improved over time in the Dios group (