Mycophenolate mofetil versus azathioprine for maintenance treatment of lupus nephritis
To compare the efficacy of mycophenolate mofetil (MMF) with that of azathioprine (AZA) drugs in the maintenance therapy of lupus nephritis (LN) patients, we studied 81 Sudanese patients with LN (32 in Class III, 34 in Class IV, and 15 in combined Class V + IV of the ISN/RPS 2003 Classification). All...
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creator | Khalid, Ismail Uthman Nur, Musa Muhammad Ahmad, Ahmad Ilyas Kaballo, Babikir Jabir Abu Ayshah, Hasan |
description | To compare the efficacy of mycophenolate mofetil (MMF) with that of azathioprine
(AZA) drugs in the maintenance therapy of lupus nephritis (LN) patients, we studied 81
Sudanese patients with LN (32 in Class III, 34 in Class IV, and 15 in combined Class V + IV of
the ISN/RPS 2003 Classification). All patients received induction therapy consisting of monthly
intravenous pulse doses of cyclophosphamide (CYC) (500 mg/m2 of body-surface area) for six
months, plus three consecutive pulses of intravenous methylprednisolone 15 mg/kg/day of body
weight (maximum 500 mg). Subsequently, 41 (50.6%) patients were randomized into a group that
received oral MMF (22 mg/kg/day), and 40 (49.4%) patients randomized to a group that received
oral AZA (2 mg/kg/day). All patients initially received oral prednisone (1 mg/kg of body weight
daily) for four weeks. The baseline characteristics of the two groups were similar. Total remission
rate was 75.3% (80.5% in MMF and 70% in AZA), complete remission rate of 54.3% (56.1%
with MMF and 52.5% with AZA), and a partial remission rate of 21% (24.4% with MMF and
17.5% with AZA) over 29 months. During maintenance therapy, six patients died (four in the
AZA group and two in the MMF group), and end-stage renal disease (ESRD) developed in five
patients (three in the AZA group and two in the MMF group). During the 36-months of the study,
both groups had comparable event-free survival rate for the composite end point of death or
ESRD and rate of relapse-free survival. Furthermore, both groups had no significant differences
in terms of frequency of hospitalization, amenorrhea, infection, nausea, and vomiting. We conclude. |
doi_str_mv | 10.4103/1319-2442.185233 |
format | Article |
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(AZA) drugs in the maintenance therapy of lupus nephritis (LN) patients, we studied 81
Sudanese patients with LN (32 in Class III, 34 in Class IV, and 15 in combined Class V + IV of
the ISN/RPS 2003 Classification). All patients received induction therapy consisting of monthly
intravenous pulse doses of cyclophosphamide (CYC) (500 mg/m2 of body-surface area) for six
months, plus three consecutive pulses of intravenous methylprednisolone 15 mg/kg/day of body
weight (maximum 500 mg). Subsequently, 41 (50.6%) patients were randomized into a group that
received oral MMF (22 mg/kg/day), and 40 (49.4%) patients randomized to a group that received
oral AZA (2 mg/kg/day). All patients initially received oral prednisone (1 mg/kg of body weight
daily) for four weeks. The baseline characteristics of the two groups were similar. Total remission
rate was 75.3% (80.5% in MMF and 70% in AZA), complete remission rate of 54.3% (56.1%
with MMF and 52.5% with AZA), and a partial remission rate of 21% (24.4% with MMF and
17.5% with AZA) over 29 months. During maintenance therapy, six patients died (four in the
AZA group and two in the MMF group), and end-stage renal disease (ESRD) developed in five
patients (three in the AZA group and two in the MMF group). During the 36-months of the study,
both groups had comparable event-free survival rate for the composite end point of death or
ESRD and rate of relapse-free survival. Furthermore, both groups had no significant differences
in terms of frequency of hospitalization, amenorrhea, infection, nausea, and vomiting. We conclude.</description><identifier>ISSN: 1319-2442</identifier><identifier>EISSN: 2320-3838</identifier><identifier>DOI: 10.4103/1319-2442.185233</identifier><identifier>PMID: 27424688</identifier><language>eng</language><publisher>Riyadh, Saudi Arabia: Saudi Center for Organ Transplantation</publisher><subject>Azathioprine ; Comparative analysis ; Cyclophosphamide ; Diagnosis ; Dosage and administration ; Drug therapy ; Humans ; Immunosuppressive Agents ; Lupus Nephritis ; Mycophenolate mofetil ; Mycophenolic Acid ; Nephritis ; Systemic lupus erythematosus ; Treatment ; Treatment Outcome ; التشخيص ; التهاب الكلى الذئبي ; حمض الميكوفينوليك ; علم المداواة</subject><ispartof>Saudi journal of kidney diseases and transplantation, 2016-07, Vol.27 (4), p.717-725</ispartof><rights>COPYRIGHT 2016 Medknow Publications and Media Pvt. Ltd.</rights><rights>Copyright Medknow Publications & Media Pvt Ltd Jul-Aug 2016</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c548n-21cd432989c83f4f579c3914f4d6fe727a642c959faf94f78077ef4149282a8e3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,864,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27424688$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Khalid, Ismail Uthman</creatorcontrib><creatorcontrib>Nur, Musa Muhammad</creatorcontrib><creatorcontrib>Ahmad, Ahmad Ilyas</creatorcontrib><creatorcontrib>Kaballo, Babikir Jabir</creatorcontrib><creatorcontrib>Abu Ayshah, Hasan</creatorcontrib><title>Mycophenolate mofetil versus azathioprine for maintenance treatment of lupus nephritis</title><title>Saudi journal of kidney diseases and transplantation</title><addtitle>Saudi J Kidney Dis Transpl</addtitle><description>To compare the efficacy of mycophenolate mofetil (MMF) with that of azathioprine
(AZA) drugs in the maintenance therapy of lupus nephritis (LN) patients, we studied 81
Sudanese patients with LN (32 in Class III, 34 in Class IV, and 15 in combined Class V + IV of
the ISN/RPS 2003 Classification). All patients received induction therapy consisting of monthly
intravenous pulse doses of cyclophosphamide (CYC) (500 mg/m2 of body-surface area) for six
months, plus three consecutive pulses of intravenous methylprednisolone 15 mg/kg/day of body
weight (maximum 500 mg). Subsequently, 41 (50.6%) patients were randomized into a group that
received oral MMF (22 mg/kg/day), and 40 (49.4%) patients randomized to a group that received
oral AZA (2 mg/kg/day). All patients initially received oral prednisone (1 mg/kg of body weight
daily) for four weeks. The baseline characteristics of the two groups were similar. Total remission
rate was 75.3% (80.5% in MMF and 70% in AZA), complete remission rate of 54.3% (56.1%
with MMF and 52.5% with AZA), and a partial remission rate of 21% (24.4% with MMF and
17.5% with AZA) over 29 months. During maintenance therapy, six patients died (four in the
AZA group and two in the MMF group), and end-stage renal disease (ESRD) developed in five
patients (three in the AZA group and two in the MMF group). During the 36-months of the study,
both groups had comparable event-free survival rate for the composite end point of death or
ESRD and rate of relapse-free survival. Furthermore, both groups had no significant differences
in terms of frequency of hospitalization, amenorrhea, infection, nausea, and vomiting. We conclude.</description><subject>Azathioprine</subject><subject>Comparative analysis</subject><subject>Cyclophosphamide</subject><subject>Diagnosis</subject><subject>Dosage and administration</subject><subject>Drug therapy</subject><subject>Humans</subject><subject>Immunosuppressive Agents</subject><subject>Lupus Nephritis</subject><subject>Mycophenolate mofetil</subject><subject>Mycophenolic Acid</subject><subject>Nephritis</subject><subject>Systemic lupus erythematosus</subject><subject>Treatment</subject><subject>Treatment Outcome</subject><subject>التشخيص</subject><subject>التهاب الكلى الذئبي</subject><subject>حمض الميكوفينوليك</subject><subject>علم المداواة</subject><issn>1319-2442</issn><issn>2320-3838</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNptks1vVCEUxYnR2Dq6d6N5iYlx80a-3gOWtfErqXGjbgkyF4eWByPwnNS_XibTjh1jWJDA75x7uQeEnhK85ASz14QR1VPO6ZLIgTJ2D51SRnHPJJP30enh-gQ9KuUS42FQ4_gQnVDBKR-lPEXfPl3btFlDTMFU6KbkoPrQ_YJc5tKZ36aufdpkH6FzKXeT8bFCNNFCVzOYOkGsXXJdmDeNj7BZZ199eYweOBMKPLnZF-jru7dfzj_0F5_ffzw_u-jtwGXsKbErzqiSykrmuBuEskwR7vhqdCCoMCOnVg3KGae4ExILAY4TrqikRgJboFd7301OP2coVU--WAjBREhz0UTiVoiTNqwFevEPepnmHFt3jWKYYMrG8S_1wwTQPrpUs7E7U33GBzFyNWLWqOV_qLZWMHmbIjjfzo8EL-8I1mBCXZcU5upTLMcg3oM2p1IyON2GP5l8rQnWu8z1LlS9C1XvM2-S5zcPm79PsDoIbkNuwJs9sE2htmCvwryFrBt7FdP2yLi_Y6wFEfr2ezSTZ3sTaObgzKHMqBgWiv0BFufDLw</recordid><startdate>20160701</startdate><enddate>20160701</enddate><creator>Khalid, Ismail Uthman</creator><creator>Nur, Musa Muhammad</creator><creator>Ahmad, Ahmad Ilyas</creator><creator>Kaballo, Babikir Jabir</creator><creator>Abu Ayshah, Hasan</creator><general>Saudi Center for Organ Transplantation</general><general>Wolters Kluwer - Medknow Publications</general><general>Medknow Publications and Media Pvt. 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(AZA) drugs in the maintenance therapy of lupus nephritis (LN) patients, we studied 81
Sudanese patients with LN (32 in Class III, 34 in Class IV, and 15 in combined Class V + IV of
the ISN/RPS 2003 Classification). All patients received induction therapy consisting of monthly
intravenous pulse doses of cyclophosphamide (CYC) (500 mg/m2 of body-surface area) for six
months, plus three consecutive pulses of intravenous methylprednisolone 15 mg/kg/day of body
weight (maximum 500 mg). Subsequently, 41 (50.6%) patients were randomized into a group that
received oral MMF (22 mg/kg/day), and 40 (49.4%) patients randomized to a group that received
oral AZA (2 mg/kg/day). All patients initially received oral prednisone (1 mg/kg of body weight
daily) for four weeks. The baseline characteristics of the two groups were similar. Total remission
rate was 75.3% (80.5% in MMF and 70% in AZA), complete remission rate of 54.3% (56.1%
with MMF and 52.5% with AZA), and a partial remission rate of 21% (24.4% with MMF and
17.5% with AZA) over 29 months. During maintenance therapy, six patients died (four in the
AZA group and two in the MMF group), and end-stage renal disease (ESRD) developed in five
patients (three in the AZA group and two in the MMF group). During the 36-months of the study,
both groups had comparable event-free survival rate for the composite end point of death or
ESRD and rate of relapse-free survival. Furthermore, both groups had no significant differences
in terms of frequency of hospitalization, amenorrhea, infection, nausea, and vomiting. We conclude.</abstract><cop>Riyadh, Saudi Arabia</cop><pub>Saudi Center for Organ Transplantation</pub><pmid>27424688</pmid><doi>10.4103/1319-2442.185233</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Azathioprine Comparative analysis Cyclophosphamide Diagnosis Dosage and administration Drug therapy Humans Immunosuppressive Agents Lupus Nephritis Mycophenolate mofetil Mycophenolic Acid Nephritis Systemic lupus erythematosus Treatment Treatment Outcome التشخيص التهاب الكلى الذئبي حمض الميكوفينوليك علم المداواة |
title | Mycophenolate mofetil versus azathioprine for maintenance treatment of lupus nephritis |
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