Outcomes following mycophenolate mofetil versus cyclophosphamide induction treatment for proliferative juvenile-onset lupus nephritis

Background Juvenile-onset systemic lupus erythematosus (JSLE) is more severe than adult-onset disease, including more lupus nephritis (LN). Despite differences in phenotype/pathogenesis, treatment is based upon adult trials. This study aimed to compare treatment response, damage accrual, time to ina...

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Veröffentlicht in:Lupus 2019-04, Vol.28 (5), p.613-620
Hauptverfasser: Smith, EMD, Al-Abadi, E, Armon, K, Bailey, K, Ciurtin, C, Davidson, J, Gardner-Medwin, J, Haslam, K, Hawley, D, Leahy, A, Leone, V, McErlane, F, Mewar, D, Modgil, G, Moots, R, Pilkington, C, Ramanan, A, Rangaraj, S, Riley, P, Sridhar, A, Wilkinson, N, Beresford, M W, Hedrich, C M
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container_end_page 620
container_issue 5
container_start_page 613
container_title Lupus
container_volume 28
creator Smith, EMD
Al-Abadi, E
Armon, K
Bailey, K
Ciurtin, C
Davidson, J
Gardner-Medwin, J
Haslam, K
Hawley, D
Leahy, A
Leone, V
McErlane, F
Mewar, D
Modgil, G
Moots, R
Pilkington, C
Ramanan, A
Rangaraj, S
Riley, P
Sridhar, A
Wilkinson, N
Beresford, M W
Hedrich, C M
description Background Juvenile-onset systemic lupus erythematosus (JSLE) is more severe than adult-onset disease, including more lupus nephritis (LN). Despite differences in phenotype/pathogenesis, treatment is based upon adult trials. This study aimed to compare treatment response, damage accrual, time to inactive LN and subsequent flare, in JSLE LN patients treated with mycophenolate mofetil (MMF) versus intravenous cyclophosphamide (IVCYC). Methods UK JSLE Cohort Study participants, ≤16 years at diagnosis, with ≥4 American College of Rheumatology criteria for SLE, with class III or IV LN, were eligible. Mann–Whitney U tests, Fisher's exact test and Chi-squared tests were utilized for statistical analysis. Results Of the patients, 34/51 (67%) received MMF, and 17/51 (33%) received IVCYC. No significant differences were identified at 4–8 and 10–14 months post-renal biopsy and last follow-up, in terms of renal British Isles Lupus Assessment Grade scores, urine albumin/creatinine ratio, serum creatinine, ESR, anti-dsDNA antibody, C3 levels and patient/physician global scores. Standardized Damage Index scores did not differ between groups at 13 months or at last follow-up. Inactive LN was attained 262 (141–390) days after MMF treatment, and 151 (117–305) days following IVCYC (p = 0.17). Time to renal flare was 451 (157–1266) days for MMF, and 343 (198–635) days for IVCYC (p = 0.47). Conclusion This is the largest study to date investigating induction treatments for proliferative LN in children, demonstrating comparability of MMF and IVCYC.
doi_str_mv 10.1177/0961203319836712
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Despite differences in phenotype/pathogenesis, treatment is based upon adult trials. This study aimed to compare treatment response, damage accrual, time to inactive LN and subsequent flare, in JSLE LN patients treated with mycophenolate mofetil (MMF) versus intravenous cyclophosphamide (IVCYC). Methods UK JSLE Cohort Study participants, ≤16 years at diagnosis, with ≥4 American College of Rheumatology criteria for SLE, with class III or IV LN, were eligible. Mann–Whitney U tests, Fisher's exact test and Chi-squared tests were utilized for statistical analysis. Results Of the patients, 34/51 (67%) received MMF, and 17/51 (33%) received IVCYC. No significant differences were identified at 4–8 and 10–14 months post-renal biopsy and last follow-up, in terms of renal British Isles Lupus Assessment Grade scores, urine albumin/creatinine ratio, serum creatinine, ESR, anti-dsDNA antibody, C3 levels and patient/physician global scores. Standardized Damage Index scores did not differ between groups at 13 months or at last follow-up. Inactive LN was attained 262 (141–390) days after MMF treatment, and 151 (117–305) days following IVCYC (p = 0.17). Time to renal flare was 451 (157–1266) days for MMF, and 343 (198–635) days for IVCYC (p = 0.47). Conclusion This is the largest study to date investigating induction treatments for proliferative LN in children, demonstrating comparability of MMF and IVCYC.</description><identifier>ISSN: 0961-2033</identifier><identifier>EISSN: 1477-0962</identifier><identifier>DOI: 10.1177/0961203319836712</identifier><identifier>PMID: 30871425</identifier><language>eng</language><publisher>London, England: SAGE Publications</publisher><subject>Anti-DNA antibodies ; Biopsy ; Clinical trials ; Creatinine ; Cyclophosphamide ; Intravenous administration ; Kidneys ; Lupus ; Lupus nephritis ; Mycophenolate mofetil ; Mycophenolic acid ; Nephritis ; Phenotypes ; Statistical analysis ; Systemic lupus erythematosus ; Urine</subject><ispartof>Lupus, 2019-04, Vol.28 (5), p.613-620</ispartof><rights>The Author(s) 2019</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c407t-891f9c6ae96ab5f18624a8b41b962bb974b108c1638d65c2fd66e8e40fa974443</citedby><cites>FETCH-LOGICAL-c407t-891f9c6ae96ab5f18624a8b41b962bb974b108c1638d65c2fd66e8e40fa974443</cites><orcidid>0000-0002-8911-4113 ; 0000-0002-8371-7597</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.1177/0961203319836712$$EPDF$$P50$$Gsage$$H</linktopdf><linktohtml>$$Uhttps://journals.sagepub.com/doi/10.1177/0961203319836712$$EHTML$$P50$$Gsage$$H</linktohtml><link.rule.ids>314,776,780,21798,27901,27902,43597,43598</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30871425$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Smith, EMD</creatorcontrib><creatorcontrib>Al-Abadi, E</creatorcontrib><creatorcontrib>Armon, K</creatorcontrib><creatorcontrib>Bailey, K</creatorcontrib><creatorcontrib>Ciurtin, C</creatorcontrib><creatorcontrib>Davidson, J</creatorcontrib><creatorcontrib>Gardner-Medwin, J</creatorcontrib><creatorcontrib>Haslam, K</creatorcontrib><creatorcontrib>Hawley, D</creatorcontrib><creatorcontrib>Leahy, A</creatorcontrib><creatorcontrib>Leone, V</creatorcontrib><creatorcontrib>McErlane, F</creatorcontrib><creatorcontrib>Mewar, D</creatorcontrib><creatorcontrib>Modgil, G</creatorcontrib><creatorcontrib>Moots, R</creatorcontrib><creatorcontrib>Pilkington, C</creatorcontrib><creatorcontrib>Ramanan, A</creatorcontrib><creatorcontrib>Rangaraj, S</creatorcontrib><creatorcontrib>Riley, P</creatorcontrib><creatorcontrib>Sridhar, A</creatorcontrib><creatorcontrib>Wilkinson, N</creatorcontrib><creatorcontrib>Beresford, M W</creatorcontrib><creatorcontrib>Hedrich, C M</creatorcontrib><title>Outcomes following mycophenolate mofetil versus cyclophosphamide induction treatment for proliferative juvenile-onset lupus nephritis</title><title>Lupus</title><addtitle>Lupus</addtitle><description>Background Juvenile-onset systemic lupus erythematosus (JSLE) is more severe than adult-onset disease, including more lupus nephritis (LN). Despite differences in phenotype/pathogenesis, treatment is based upon adult trials. This study aimed to compare treatment response, damage accrual, time to inactive LN and subsequent flare, in JSLE LN patients treated with mycophenolate mofetil (MMF) versus intravenous cyclophosphamide (IVCYC). Methods UK JSLE Cohort Study participants, ≤16 years at diagnosis, with ≥4 American College of Rheumatology criteria for SLE, with class III or IV LN, were eligible. Mann–Whitney U tests, Fisher's exact test and Chi-squared tests were utilized for statistical analysis. Results Of the patients, 34/51 (67%) received MMF, and 17/51 (33%) received IVCYC. No significant differences were identified at 4–8 and 10–14 months post-renal biopsy and last follow-up, in terms of renal British Isles Lupus Assessment Grade scores, urine albumin/creatinine ratio, serum creatinine, ESR, anti-dsDNA antibody, C3 levels and patient/physician global scores. Standardized Damage Index scores did not differ between groups at 13 months or at last follow-up. Inactive LN was attained 262 (141–390) days after MMF treatment, and 151 (117–305) days following IVCYC (p = 0.17). Time to renal flare was 451 (157–1266) days for MMF, and 343 (198–635) days for IVCYC (p = 0.47). 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Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Lupus</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Smith, EMD</au><au>Al-Abadi, E</au><au>Armon, K</au><au>Bailey, K</au><au>Ciurtin, C</au><au>Davidson, J</au><au>Gardner-Medwin, J</au><au>Haslam, K</au><au>Hawley, D</au><au>Leahy, A</au><au>Leone, V</au><au>McErlane, F</au><au>Mewar, D</au><au>Modgil, G</au><au>Moots, R</au><au>Pilkington, C</au><au>Ramanan, A</au><au>Rangaraj, S</au><au>Riley, P</au><au>Sridhar, A</au><au>Wilkinson, N</au><au>Beresford, M W</au><au>Hedrich, C M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Outcomes following mycophenolate mofetil versus cyclophosphamide induction treatment for proliferative juvenile-onset lupus nephritis</atitle><jtitle>Lupus</jtitle><addtitle>Lupus</addtitle><date>2019-04</date><risdate>2019</risdate><volume>28</volume><issue>5</issue><spage>613</spage><epage>620</epage><pages>613-620</pages><issn>0961-2033</issn><eissn>1477-0962</eissn><abstract>Background Juvenile-onset systemic lupus erythematosus (JSLE) is more severe than adult-onset disease, including more lupus nephritis (LN). Despite differences in phenotype/pathogenesis, treatment is based upon adult trials. This study aimed to compare treatment response, damage accrual, time to inactive LN and subsequent flare, in JSLE LN patients treated with mycophenolate mofetil (MMF) versus intravenous cyclophosphamide (IVCYC). Methods UK JSLE Cohort Study participants, ≤16 years at diagnosis, with ≥4 American College of Rheumatology criteria for SLE, with class III or IV LN, were eligible. Mann–Whitney U tests, Fisher's exact test and Chi-squared tests were utilized for statistical analysis. Results Of the patients, 34/51 (67%) received MMF, and 17/51 (33%) received IVCYC. No significant differences were identified at 4–8 and 10–14 months post-renal biopsy and last follow-up, in terms of renal British Isles Lupus Assessment Grade scores, urine albumin/creatinine ratio, serum creatinine, ESR, anti-dsDNA antibody, C3 levels and patient/physician global scores. Standardized Damage Index scores did not differ between groups at 13 months or at last follow-up. Inactive LN was attained 262 (141–390) days after MMF treatment, and 151 (117–305) days following IVCYC (p = 0.17). Time to renal flare was 451 (157–1266) days for MMF, and 343 (198–635) days for IVCYC (p = 0.47). Conclusion This is the largest study to date investigating induction treatments for proliferative LN in children, demonstrating comparability of MMF and IVCYC.</abstract><cop>London, England</cop><pub>SAGE Publications</pub><pmid>30871425</pmid><doi>10.1177/0961203319836712</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-8911-4113</orcidid><orcidid>https://orcid.org/0000-0002-8371-7597</orcidid><oa>free_for_read</oa></addata></record>
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source SAGE Complete A-Z List
subjects Anti-DNA antibodies
Biopsy
Clinical trials
Creatinine
Cyclophosphamide
Intravenous administration
Kidneys
Lupus
Lupus nephritis
Mycophenolate mofetil
Mycophenolic acid
Nephritis
Phenotypes
Statistical analysis
Systemic lupus erythematosus
Urine
title Outcomes following mycophenolate mofetil versus cyclophosphamide induction treatment for proliferative juvenile-onset lupus nephritis
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