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lüll Oral cyclophosphamide is on the verge of extinction as therapy for severe autoimmune diseases (especially lupus): should nephrologists care?Hebert LA; Rovin BHNephron Clin Pract 2011[]; 117 (1): c8-14Some day we will have powerful targeted therapies for autoimmune diseases. Remission will be induced efficiently. Side effects will be mere ripples. Unfortunately, that day is not imminent. Current therapies are powerful but with unintended targets and side effects that can be equivalent to a sea change. For SLE, the current competition to select the 'gold standard' immunosuppressant has come down to two regimens: intravenous cyclophosphamide (IVCY, standard NIH protocol or its variations) versus oral mycophenolate (MMF). Until recently, IVCY reigned as the gold standard, a title it achieved through a curious journey that did not involve rigorous head-to-head competition. Oral cyclophosphamide (POCY) has not been invited to the current competition to select the gold standard immunosuppressant despite the substantial evidence that POCY can perform at least as well as IVCY or mycophenolate, and compared to IVCY, is far less expensive, easier for the patient, and maybe more effective in African-Americans. Here, we state the case for POCY as therapy for severe autoimmune diseases. We suggest that if POCY is allowed to compete, it will not disappoint.|Autoimmune Diseases/*drug therapy[MESH]|Cyclophosphamide/*administration & dosage/adverse effects/economics[MESH]|Cyclosporine/therapeutic use[MESH]|Humans[MESH]|Immunosuppressive Agents/*administration & dosage/adverse effects/economics[MESH]|Lupus Nephritis/*drug therapy[MESH]|Mycophenolic Acid/analogs & derivatives/therapeutic use[MESH]|Tacrolimus/therapeutic use[MESH] |