TY - JOUR
T1 - Lupus nephritis trials network (LNTN) repeat kidney biopsy-based definitions of treatment response
T2 - A systematic literature review-based proposal
AU - Parodis, Ioannis
AU - Cetrez, Nursen
AU - Palazzo, Leonardo
AU - Alberton, Valeria
AU - Anders, Hans Joachim
AU - Bajema, Ingeborg M.
AU - Costedoat-Chalumeau, Nathalie
AU - Malvar, Ana
AU - Rovin, Brad H.
AU - Sanchez-Guerrero, Jorge
AU - Zhao, Ming Hui
AU - Weinmann-Menke, Julia
AU - Tektonidou, Maria G.
AU - Houssiau, Frédéric A.
N1 - Publisher Copyright:
© 2025 The Authors
PY - 2025/6/24
Y1 - 2025/6/24
N2 - Within the frame of the Lupus Nephritis Trials Network (LNTN), we conducted a systematic literature review (SLR) to propose kidney tissue-based definitions of treatment outcomes in lupus nephritis (LN). Given the limitations of clinical markers like proteinuria in predicting immunological, histological, and long-term outcomes, our work emphasises the importance of repeat kidney biopsies. Such biopsies help identify discordance between clinical and histological response, which has implications for long-term kidney outcomes. The research objectives of this SLR focused on defining repeat biopsy-based treatment response and histological remission, and their associations with long-term outcomes. The SLR reviewed studies published from 2000 to 2022, identifying 20 eligible works. Histological response was commonly defined by changes in the National Institutes of Health (NIH) Activity Index (AI), with response indicated by a decrease of ≥50 % and to ≤3. Remission was most commonly defined as an AI score of 0. These benchmarks were associated with improved long-term renal outcomes, such as reduced flare rates and preserved kidney function. Conversely, NIH AI scores ≥4 and NIH Chronicity Index (CI) scores ≥4 were associated with poor prognosis, highlighting their predictive utility. Consensus definitions were established through expert panel deliberation, setting a foundation for standardising LN treatment evaluation in clinical trials and observational studies. These definitions are not intended for routine clinical decisions but aim to enhance uniformity and comparability in research, especially when repeat kidney biopsies are performed, an approach strongly advocated by our work. Further validation through ongoing initiatives and molecular characterisation efforts will refine these criteria, fostering advances in LN management and patient outcomes.
AB - Within the frame of the Lupus Nephritis Trials Network (LNTN), we conducted a systematic literature review (SLR) to propose kidney tissue-based definitions of treatment outcomes in lupus nephritis (LN). Given the limitations of clinical markers like proteinuria in predicting immunological, histological, and long-term outcomes, our work emphasises the importance of repeat kidney biopsies. Such biopsies help identify discordance between clinical and histological response, which has implications for long-term kidney outcomes. The research objectives of this SLR focused on defining repeat biopsy-based treatment response and histological remission, and their associations with long-term outcomes. The SLR reviewed studies published from 2000 to 2022, identifying 20 eligible works. Histological response was commonly defined by changes in the National Institutes of Health (NIH) Activity Index (AI), with response indicated by a decrease of ≥50 % and to ≤3. Remission was most commonly defined as an AI score of 0. These benchmarks were associated with improved long-term renal outcomes, such as reduced flare rates and preserved kidney function. Conversely, NIH AI scores ≥4 and NIH Chronicity Index (CI) scores ≥4 were associated with poor prognosis, highlighting their predictive utility. Consensus definitions were established through expert panel deliberation, setting a foundation for standardising LN treatment evaluation in clinical trials and observational studies. These definitions are not intended for routine clinical decisions but aim to enhance uniformity and comparability in research, especially when repeat kidney biopsies are performed, an approach strongly advocated by our work. Further validation through ongoing initiatives and molecular characterisation efforts will refine these criteria, fostering advances in LN management and patient outcomes.
KW - Autoimmunity
KW - Kidney biopsy
KW - Lupus nephritis
KW - Rheumatology
KW - Systemic lupus erythematosus
UR - https://www.scopus.com/pages/publications/105001682131
U2 - 10.1016/j.autrev.2025.103810
DO - 10.1016/j.autrev.2025.103810
M3 - Review article
C2 - 40180257
AN - SCOPUS:105001682131
SN - 1568-9972
VL - 24
JO - Autoimmunity reviews
JF - Autoimmunity reviews
IS - 7
M1 - 103810
ER -