Treatment‐free remission in severe systemic lupus erythematosus following synchronization of plasmapheresis with subsequent pulse cyclophosphamide

Objective. To investigate the effect of an intensified treatment protocol synchronizing plasmapheresis with subsequent pulse cyclophosphamide for severe systemic lupus erythematosus (SLE). Methods. A protocol of plasmapheresis (3 x 60 ml/kg) and subsequent high‐dose pulse cyclophosphamide (36 mg/kg)...

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Veröffentlicht in:Arthritis and rheumatism 1994-12, Vol.37 (12), p.1784-1794
Hauptverfasser: Euler, Hans H., Schroeder, Johann O., Harten, Pontus, Zeuner, Rainald A., Gutschmidt, Hans J.
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container_end_page 1794
container_issue 12
container_start_page 1784
container_title Arthritis and rheumatism
container_volume 37
creator Euler, Hans H.
Schroeder, Johann O.
Harten, Pontus
Zeuner, Rainald A.
Gutschmidt, Hans J.
description Objective. To investigate the effect of an intensified treatment protocol synchronizing plasmapheresis with subsequent pulse cyclophosphamide for severe systemic lupus erythematosus (SLE). Methods. A protocol of plasmapheresis (3 x 60 ml/kg) and subsequent high‐dose pulse cyclophosphamide (36 mg/kg) followed by 6 months of peroral immunosuppression was used to treat 14 patients with severe SLE. Results. Rapid improvement was achieved in all patients. Immunosuppressants, including corticosteroids, were withdrawn at month 6 in 12 patients. Eight patients continued without treatment for a mean observation period of 5.6 years (46–91 months). Conclusion. The results demonstrate that treatment‐free clinical remission can be achieved in some patients with severe SLE.
doi_str_mv 10.1002/art.1780371212
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To investigate the effect of an intensified treatment protocol synchronizing plasmapheresis with subsequent pulse cyclophosphamide for severe systemic lupus erythematosus (SLE). Methods. A protocol of plasmapheresis (3 x 60 ml/kg) and subsequent high‐dose pulse cyclophosphamide (36 mg/kg) followed by 6 months of peroral immunosuppression was used to treat 14 patients with severe SLE. Results. Rapid improvement was achieved in all patients. Immunosuppressants, including corticosteroids, were withdrawn at month 6 in 12 patients. Eight patients continued without treatment for a mean observation period of 5.6 years (46–91 months). Conclusion. The results demonstrate that treatment‐free clinical remission can be achieved in some patients with severe SLE.</description><identifier>ISSN: 0004-3591</identifier><identifier>EISSN: 1529-0131</identifier><identifier>DOI: 10.1002/art.1780371212</identifier><identifier>PMID: 7986225</identifier><identifier>CODEN: ARHEAW</identifier><language>eng</language><publisher>New York: John Wiley &amp; Sons, Inc</publisher><subject>Adolescent ; Adult ; Amenorrhea - physiopathology ; Biological and medical sciences ; Complement C4 - analysis ; Complement C4 - deficiency ; Creatinine - blood ; Cyclophosphamide - administration &amp; dosage ; Cyclophosphamide - therapeutic use ; Dose-Response Relationship, Drug ; Female ; Follow-Up Studies ; Humans ; Immunoglobulins - metabolism ; Immunomodulators ; Kinetics ; Leukocyte Count ; Leukopenia - etiology ; Lupus Erythematosus, Systemic - complications ; Lupus Erythematosus, Systemic - therapy ; Medical sciences ; Middle Aged ; Pharmacology. 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To investigate the effect of an intensified treatment protocol synchronizing plasmapheresis with subsequent pulse cyclophosphamide for severe systemic lupus erythematosus (SLE). Methods. A protocol of plasmapheresis (3 x 60 ml/kg) and subsequent high‐dose pulse cyclophosphamide (36 mg/kg) followed by 6 months of peroral immunosuppression was used to treat 14 patients with severe SLE. Results. Rapid improvement was achieved in all patients. Immunosuppressants, including corticosteroids, were withdrawn at month 6 in 12 patients. Eight patients continued without treatment for a mean observation period of 5.6 years (46–91 months). Conclusion. The results demonstrate that treatment‐free clinical remission can be achieved in some patients with severe SLE.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Amenorrhea - physiopathology</subject><subject>Biological and medical sciences</subject><subject>Complement C4 - analysis</subject><subject>Complement C4 - deficiency</subject><subject>Creatinine - blood</subject><subject>Cyclophosphamide - administration &amp; dosage</subject><subject>Cyclophosphamide - therapeutic use</subject><subject>Dose-Response Relationship, Drug</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Humans</subject><subject>Immunoglobulins - metabolism</subject><subject>Immunomodulators</subject><subject>Kinetics</subject><subject>Leukocyte Count</subject><subject>Leukopenia - etiology</subject><subject>Lupus Erythematosus, Systemic - complications</subject><subject>Lupus Erythematosus, Systemic - therapy</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Pharmacology. 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To investigate the effect of an intensified treatment protocol synchronizing plasmapheresis with subsequent pulse cyclophosphamide for severe systemic lupus erythematosus (SLE). Methods. A protocol of plasmapheresis (3 x 60 ml/kg) and subsequent high‐dose pulse cyclophosphamide (36 mg/kg) followed by 6 months of peroral immunosuppression was used to treat 14 patients with severe SLE. Results. Rapid improvement was achieved in all patients. Immunosuppressants, including corticosteroids, were withdrawn at month 6 in 12 patients. Eight patients continued without treatment for a mean observation period of 5.6 years (46–91 months). Conclusion. The results demonstrate that treatment‐free clinical remission can be achieved in some patients with severe SLE.</abstract><cop>New York</cop><pub>John Wiley &amp; Sons, Inc</pub><pmid>7986225</pmid><doi>10.1002/art.1780371212</doi><tpages>11</tpages></addata></record>
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source MEDLINE; Wiley Online Library Journals Frontfile Complete; Alma/SFX Local Collection
subjects Adolescent
Adult
Amenorrhea - physiopathology
Biological and medical sciences
Complement C4 - analysis
Complement C4 - deficiency
Creatinine - blood
Cyclophosphamide - administration & dosage
Cyclophosphamide - therapeutic use
Dose-Response Relationship, Drug
Female
Follow-Up Studies
Humans
Immunoglobulins - metabolism
Immunomodulators
Kinetics
Leukocyte Count
Leukopenia - etiology
Lupus Erythematosus, Systemic - complications
Lupus Erythematosus, Systemic - therapy
Medical sciences
Middle Aged
Pharmacology. Drug treatments
Plasmapheresis
Pregnancy
Pregnancy Complications - physiopathology
Pulsatile Flow
Time Factors
title Treatment‐free remission in severe systemic lupus erythematosus following synchronization of plasmapheresis with subsequent pulse cyclophosphamide
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