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- Publisher Website: 10.1016/j.amjmed.2005.08.045
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- PMID: 16564783
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Article: Long-term outcome of diffuse proliferative lupus glomerulonephritis treated with cyclophosphamide
Title | Long-term outcome of diffuse proliferative lupus glomerulonephritis treated with cyclophosphamide |
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Authors | |
Keywords | Cytotoxic Glomerulonephritis Immunosuppressive Prognosis Renal Toxicity |
Issue Date | 2006 |
Publisher | Excerpta Medica, Inc. The Journal's web site is located at http://www.elsevier.com/locate/amj |
Citation | American Journal Of Medicine, 2006, v. 119 n. 4, p. 355.e25-355.e33 How to Cite? |
Abstract | PURPOSE: To report the long-term outcome of diffuse proliferative lupus nephritis (DPLN) treated with cyclophosphamide (CYC) in Chinese patients. METHODS: Patients with biopsy-proven DPLN treated with prednisolone and CYC were identified. The long-term renal outcome and treatment-related toxicities were reported. RESULTS: A total of 212 patients were studied (89% women; mean age 30.9 ± 10.9 years; mean system lupus erythematosus [SLE] duration 36.7 ± 55.1 months). At renal biopsy, 148 (70%) patients were nephrotic, and 78 (37%) had impaired serum creatinine. One hundred and three (49%) patients received daily oral CYC, whereas 109 (51%) received intravenous bolus CYC. At last dose of CYC, 126 (59%) patients responded completely, and 56 (26%) responded partially. In a logistic regression model, the cumulative CYC dose and histologic chronicity score predicted complete response. One hundred fifty-five (73%) patients received maintenance immunosuppression for at least 3 years (88% azathioprine). After a follow-up of 1873 patient-years, 66 patients experienced renal flares, 30 had doubling of serum creatinine, 18 developed end-stage renal failure, and 14 died. The renal survival rates were 88.7%, 82.8% and 70.7% at 5, 10 and 15 years, respectively. Failure to respond completely to CYC and the absence of maintenance immunosuppression were independent predictors of a poor renal outcome. Ovarian toxicity was more frequent with the oral CYC regimen. Increasing age and higher cumulative doses of CYC were independent risk factors. CONCLUSIONS: In Chinese patients with DPLN, the cumulative dose, rather than the route of CYC administration, determines the initial treatment response and ovarian toxicity. Maintenance immunosuppression is associated with a better long-term prognosis. The oral CYC regimen is more toxic and should be reserved for high-risk patients. © 2006 Elsevier Inc. All rights reserved. |
Persistent Identifier | http://hdl.handle.net/10722/162954 |
ISSN | 2023 Impact Factor: 5.1 2023 SCImago Journal Rankings: 1.063 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
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dc.contributor.author | Mok, CC | en_US |
dc.contributor.author | Ying, KY | en_US |
dc.contributor.author | Ng, WL | en_US |
dc.contributor.author | Lee, KW | en_US |
dc.contributor.author | To, CH | en_US |
dc.contributor.author | Lau, CS | en_US |
dc.contributor.author | Wong, RWS | en_US |
dc.contributor.author | Au, TC | en_US |
dc.date.accessioned | 2012-09-05T05:25:50Z | - |
dc.date.available | 2012-09-05T05:25:50Z | - |
dc.date.issued | 2006 | en_US |
dc.identifier.citation | American Journal Of Medicine, 2006, v. 119 n. 4, p. 355.e25-355.e33 | en_US |
dc.identifier.issn | 0002-9343 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/162954 | - |
dc.description.abstract | PURPOSE: To report the long-term outcome of diffuse proliferative lupus nephritis (DPLN) treated with cyclophosphamide (CYC) in Chinese patients. METHODS: Patients with biopsy-proven DPLN treated with prednisolone and CYC were identified. The long-term renal outcome and treatment-related toxicities were reported. RESULTS: A total of 212 patients were studied (89% women; mean age 30.9 ± 10.9 years; mean system lupus erythematosus [SLE] duration 36.7 ± 55.1 months). At renal biopsy, 148 (70%) patients were nephrotic, and 78 (37%) had impaired serum creatinine. One hundred and three (49%) patients received daily oral CYC, whereas 109 (51%) received intravenous bolus CYC. At last dose of CYC, 126 (59%) patients responded completely, and 56 (26%) responded partially. In a logistic regression model, the cumulative CYC dose and histologic chronicity score predicted complete response. One hundred fifty-five (73%) patients received maintenance immunosuppression for at least 3 years (88% azathioprine). After a follow-up of 1873 patient-years, 66 patients experienced renal flares, 30 had doubling of serum creatinine, 18 developed end-stage renal failure, and 14 died. The renal survival rates were 88.7%, 82.8% and 70.7% at 5, 10 and 15 years, respectively. Failure to respond completely to CYC and the absence of maintenance immunosuppression were independent predictors of a poor renal outcome. Ovarian toxicity was more frequent with the oral CYC regimen. Increasing age and higher cumulative doses of CYC were independent risk factors. CONCLUSIONS: In Chinese patients with DPLN, the cumulative dose, rather than the route of CYC administration, determines the initial treatment response and ovarian toxicity. Maintenance immunosuppression is associated with a better long-term prognosis. The oral CYC regimen is more toxic and should be reserved for high-risk patients. © 2006 Elsevier Inc. All rights reserved. | en_US |
dc.language | eng | en_US |
dc.publisher | Excerpta Medica, Inc. The Journal's web site is located at http://www.elsevier.com/locate/amj | en_US |
dc.relation.ispartof | American Journal of Medicine | en_US |
dc.subject | Cytotoxic | - |
dc.subject | Glomerulonephritis | - |
dc.subject | Immunosuppressive | - |
dc.subject | Prognosis | - |
dc.subject | Renal | - |
dc.subject | Toxicity | - |
dc.subject.mesh | Administration, Oral | en_US |
dc.subject.mesh | Adult | en_US |
dc.subject.mesh | Amenorrhea - Chemically Induced | en_US |
dc.subject.mesh | Analysis Of Variance | en_US |
dc.subject.mesh | Anti-Inflammatory Agents - Therapeutic Use | en_US |
dc.subject.mesh | China | en_US |
dc.subject.mesh | Cyclophosphamide - Administration & Dosage - Adverse Effects | en_US |
dc.subject.mesh | Drug Therapy, Combination | en_US |
dc.subject.mesh | Female | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Immunosuppressive Agents - Administration & Dosage - Adverse Effects | en_US |
dc.subject.mesh | Injections, Intravenous | en_US |
dc.subject.mesh | Logistic Models | en_US |
dc.subject.mesh | Lupus Nephritis - Drug Therapy - Pathology | en_US |
dc.subject.mesh | Male | en_US |
dc.subject.mesh | Ovary - Drug Effects | en_US |
dc.subject.mesh | Prednisolone - Therapeutic Use | en_US |
dc.subject.mesh | Prognosis | en_US |
dc.subject.mesh | Retrospective Studies | en_US |
dc.subject.mesh | Risk Assessment | en_US |
dc.subject.mesh | Risk Factors | en_US |
dc.subject.mesh | Time Factors | en_US |
dc.subject.mesh | Treatment Failure | en_US |
dc.subject.mesh | Treatment Outcome | en_US |
dc.title | Long-term outcome of diffuse proliferative lupus glomerulonephritis treated with cyclophosphamide | en_US |
dc.type | Article | en_US |
dc.identifier.email | Lau, CS:cslau@hku.hk | en_US |
dc.identifier.authority | Lau, CS=rp01348 | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1016/j.amjmed.2005.08.045 | en_US |
dc.identifier.pmid | 16564783 | - |
dc.identifier.scopus | eid_2-s2.0-33645241849 | en_US |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-33645241849&selection=ref&src=s&origin=recordpage | en_US |
dc.identifier.volume | 119 | en_US |
dc.identifier.issue | 4 | en_US |
dc.identifier.spage | 355.e25 | en_US |
dc.identifier.epage | 355.e33 | en_US |
dc.identifier.isi | WOS:000236311800019 | - |
dc.publisher.place | United States | en_US |
dc.identifier.scopusauthorid | Mok, CC=7102344226 | en_US |
dc.identifier.scopusauthorid | Ying, KY=7005162138 | en_US |
dc.identifier.scopusauthorid | Ng, WL=7401613401 | en_US |
dc.identifier.scopusauthorid | Lee, KW=35788977700 | en_US |
dc.identifier.scopusauthorid | To, CH=34968753300 | en_US |
dc.identifier.scopusauthorid | Lau, CS=14035682100 | en_US |
dc.identifier.scopusauthorid | Wong, RWS=34875928200 | en_US |
dc.identifier.scopusauthorid | Au, TC=7006646148 | en_US |
dc.identifier.issnl | 0002-9343 | - |