Abstract:The monitoring of MPA trough levels with EMIT appears to be a poor predictor of efficacy or toxicity. In contrast, it is a useful tool to evaluate the degree of therapeutic compliance.
“…Mycophenolic acid reversibly blocks the de novo synthesis of guanine nucleotides and thus preferentially affects both B and T lymphocytes 18 . Numerous reports have described the utility of MMF for the treatment of psoriasis with promising results 9–12 . The effectiveness of MMF in our study is in agreement with those of earlier studies 9–12 .…”
Section: Discussionsupporting
confidence: 89%
“…It is the pro‐drug of mycophenolic acid, which was originally used to treat psoriasis in the 1970s but was associated with a relatively high incidence of gastrointestinal and infectious adverse effects 5,6 . Although there are no double‐blind randomized trials of MMF in the treatment of psoriasis, it has been used in several uncontrolled studies 7–10 . An open‐label study of 23 patients with moderate to severe psoriasis demonstrated a mean PASI reduction of 47% at 12 weeks of therapy when dosed at 2 to 3 g daily, 11 whereas another smaller open‐label study of four patients demonstrated a 62.5–90% reduction in PASI after 3 months of therapy (2 g/day) 12 .…”
No significant differences in efficacy were found between MTX and MMF groups. MMF may represent a good alternative for the treatment of psoriasis in patients who are unable to take MTX or other available drugs due to contraindication or toxicity.
“…Mycophenolic acid reversibly blocks the de novo synthesis of guanine nucleotides and thus preferentially affects both B and T lymphocytes 18 . Numerous reports have described the utility of MMF for the treatment of psoriasis with promising results 9–12 . The effectiveness of MMF in our study is in agreement with those of earlier studies 9–12 .…”
Section: Discussionsupporting
confidence: 89%
“…It is the pro‐drug of mycophenolic acid, which was originally used to treat psoriasis in the 1970s but was associated with a relatively high incidence of gastrointestinal and infectious adverse effects 5,6 . Although there are no double‐blind randomized trials of MMF in the treatment of psoriasis, it has been used in several uncontrolled studies 7–10 . An open‐label study of 23 patients with moderate to severe psoriasis demonstrated a mean PASI reduction of 47% at 12 weeks of therapy when dosed at 2 to 3 g daily, 11 whereas another smaller open‐label study of four patients demonstrated a 62.5–90% reduction in PASI after 3 months of therapy (2 g/day) 12 .…”
No significant differences in efficacy were found between MTX and MMF groups. MMF may represent a good alternative for the treatment of psoriasis in patients who are unable to take MTX or other available drugs due to contraindication or toxicity.
“…The patient's Psoriasis Area and Severity Index (PASI) score decreased from 22.0 to 11.4 over 5 weeks. 15 Numerous reports since have described the utility of MMF in treating psoriasis as either monotherapy or adjuvant therapy with promising results [16][17][18][19][20] (Table II). Two of these studies reported a 75% reduction in PASI in at least 50% of subjects.…”
“…The normal dose of EC-MPS (1440 mg daily) appeared to be more effective than the low dose, because the psoriasis worsened in several patients after dose reduction. Some case reports and small series of patients have reported the efficacy of MMF in the treatment of moderateto-severe psoriasis (8)(9)(10)(11)(12)(13)(14). At usual doses, MMF is generally well tolerated.…”
EC-MPS does not seem effective as monotherapy for moderate to severe psoriasis, but might be used at a dosage of 1440 mg daily in well-selected patients with treatment-resistant psoriasis.
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