This is the material for the clinical literature reading meeting held in our department.
Update information: November 20, 2024 No. 130 to No. 135 have been posted.
update date | theme | |
November 20, 2024 | No.135|2024.11.14|Lancet Rheumatol|Pre RA TREAT EARLIER | |
---|---|---|
No.134|2024.10.29|A&R|SLE_UPA+Elusubrutinib | ||
No.133|2024.10.22|JAMA network open|Efficacy of MMF in SLE without major organ involvement | ||
No.132│2024.10.15│ARD│ Still disease EULAR PReS reccomendations | ||
No.131│2024.10.08│ARD│BLISS-Believe | ||
No.130|2024.09.24|Lancet|SS iscalimab RCT phase2b (TWINSS) | ||
November 14, 2024 | No.129|2024.09.17|ARD|Apremilast-min for Oligoarticular PsA | |
No.128|2024.09.10|Nature|AMP-SLE TpH CXCL13 | ||
No.127|2024.09.03|NEJM|CAR-T SLE Summary | ||
No.125|2024.07.23|ARD|AAV post-RTX B cell analysis | ||
July 24, 2024 | No.124|2024.07.16|NatMed|RA BiTE Pilot Study | |
No.123│2024.07.09│ARD│VEXAS Treatment outcomes Retrospective cohort | ||
No.122│2024.07.02│ARD│MAINRITSAN Examination | ||
No.121│2024.06.25│ARD│ARS cluster analysis | ||
November 18, 2024 | No.120│2024.06.11│ARD│EULAR recommendation of PsA, 2023 | |
No.119|2024.06.04|Rheumatology|Anti-RibP antibodies and SLE | ||
No.118|2024.05.27|ARD|Anifrolumab Type I IFN signature | ||
June 4, 2024 | No.117│2024.05.21│ACR Open Rheumatol│bDMARD tapering and predictors of RA flare-ups | |
No.116|2024.05.14|Science Immunol|ThA | ||
No.115│2024.05.07│A&R│RA-related LPD Japanese multicenter cohort | ||
No.114│2024.04.30│Lancet Rheumatol│preRA, ABT, RCT (APIPPRA study) | ||
No.113│2024.04.23│Lancet Rheumatol│csDMARDs halving/gradual tapering/discontinuation (ARCTIC REWIND) | ||
May 7, 2024 | No.112│2024.04.09│NEJM│Sarilumab for recurrent PMR (SAPHYR trial) | |
No.111|2024.04.02|ARD|Reduction of GC and immunosuppressants in maintenance IgG4-RD | ||
No.110|2024.03.26|NEJM|EGPA Benralizumab vs Mepolizumab (MANDARA) | ||
No.109|2024.03.19|Kidney Int|KDIGO LN guideline 2024 | ||
March 19, 2020 | No.108|2024.03.12|Lancet Rheumatol|Remission SLE MMF withdrawal non-inferiority study | |
No.107│2024.03.05│ARD│AAV RTX mainenance Long term | ||
No.106│2024.02.27│ARD│Telitacicept phase 2b in SLE | ||
No.105|2024.02.20|ARD|Avacopan+RTX ADVOCATE subgroup analysis | ||
March 18, 2020 | No.104|2024.02.13|Nat Med|Anti-TRBV9 AS | |
No.103│2024.01.30│A&R│SS-A antibody titer and fetal AVB | ||
No.102|2024.01.23|A&R|Long-term results of VOC against LN (AURORA 2) | ||
No.101|2024.01.16|Nature|RA-SF scRNA-seq AMP phase II | ||
No.100|2024.01.09|ARD|JAKi review | ||
November 24, 2020 | No.99|2023.11.21|ARD|Long-term remission RA TNFi tapering non-inferiority study | |
No.98|2023.11.14|A&R|Relational analysis of HCQ adherence and SLE | ||
November 9, 2020 | No.97|2023.11.07|ARD|SLE 2023 reccomendation | |
No.96|2023.10.31|Lancet Rheumatol|FcgR2B+CD19 Obexelimab IgG4RD | ||
October 27, 2020 | No.95|2023.10.24|A&R|CAR-T SSc mouse model | |
No.94│2023.10.17│ARD│APS 2023 classification criteria | ||
No.93|2023.10.03|ARD|Safety of MTX for men who wish to have children | ||
September 29, 2020 | No.92|2022.09.26|ARD|Anti-GM-CSF otilimab vs TOFA SAR contRAst | |
No.91│2023.09.19│Lancet│JIA Baricitinib | ||
No.90|2023.09.12|Forehead osteonecrosis position paper 2023 | ||
September 12, 2020 | No.89|2023.08.01|ARD|ICI-myositis transcriptome | |
No.88|2023.07.25|Lancet Rheumatol|GCA-SEC (TitAIN) | ||
No.87│2023.07.11│Lancet Rheumatol│BILAG-BR, infection risk│ | ||
No.86 | 2023.07.04 | Lancet Rheum | ICI for cancer-bearing patients with RA | ||
No.85|2022.06.27|NEJM|PD-1 agonist Ab for RA | ||
June 27, 5th year of Reiwa | No.84|2023.06.20|Mod Rheumatol|HCQ for RA | |
No.83|2023.06.13|Lancet Rheumatol|RTX for PMR | ||
June 7, 2020 | No.82|2023.06.06|A&R|Deucravacitinib for SLE P2 | |
No.81|2023.05.23|ARD|TULIP-LLDAS Analysis | ||
June 6, 2023 | No.80│2023.05.09│ARD│2022 AAV Recommendation | |
No.79|2023.05.02|ARD|RITAZAREM | ||
No.78|2023.04.18|A&R|MDA5 3-group clustering | ||
No.77|2023.04.11|Lancet|BARI for SLE P3 | ||
No.76│2023.03.28│ARD│ax-SpA bimekizumab phaseⅢ RCT | ||
April 10, 2020 | No.75│2023.03.07│A&R│MTX withdrawal after influenza vaccine | |
No.74|2023.02.28|ARD|Treatment selection after JAKi falure | ||
No.73|2023.02.21|ARD|BEL and Pregnancy | ||
No.72|2023.02.14|ARD|anti-IFNa autoAb SLE Covid severe | ||
No.71│2023.02.07│ARD│LUPIL-2, low dose IL-2 therapy, SLE | ||
No.70│2023.01.31│Rheumatology│SSc-ILD framework | ||
March 6, 2023 | No.69│2023.01.24│ARD│GCA US score(OGUS)│ | |
No.68|2023.01.17|A&R|TULIP LTE test | ||
No.67│2023.01.10│ARD│RA Management Recommendation | ||
No.66|2022.12.13|Lancet Rheumatol|SLE LLDAS mortality | ||
No.65|2022.12.06|ARD|Summary of LVV classification criteria | ||
November 30, 2020 | No.64│2022.11.22│ARD│axial SpA recommendation | |
No.63│2022.11.15│ARD│Recommendations for Screening and Prevention of Opportunistic Infections in Rheumatic Diseases | ||
No.62│2022.11.08│Mod Rheumatol│MTXsc RA | ||
No.61|2022.11.01|NEJM|IVIg for DM (ProDERM) | ||
November 4, 2020 | No.60|2022.10.25|Lancet Rheumatol|PGA | |
No.59│2022.10.18│A&R│Ozoralizumab RCT | ||
No.58│2022.10.11│JAMA│TCZ for GC-dependent PMR | ||
October 5, 2020 | No.57│2022.10.04│Nat Med│Anti-CD19 CAR-T SLE | |
No.56|2022.09.27|ARD|SLE Bari cytokine | ||
No.55│2022.09.13│ARD│GLORIA trial (65+RA, low dose PSL add on) | ||
September 12, 2020 | No.54│2022.09.06│NEJM│CLE-Litifilimab | |
August 4, 2020 | No.53│2022.07.26│ARD│LN Dose reduction in remission RCT | |
No.52|2022.07.19|ARD|Safety and efficacy of baricitinib for recurrent GCA | ||
July 25, 2020 | No.51|2022.07.12|ARD|TULIP-1&2 post hoc analysis | |
No.50|2022.07.05|A&R|TOFA safety | ||
No.49|2022.06.28|ARD|mavrilimumab-GCA | ||
No.48|2022.06.21|ARD|SSc-ILD module analysis and response to MMF treatment | ||
June 24, 2020 | No.47|2022.06.14|JAMAnetwork|LN Tac vs IVCY | |
No.46|2022.06.07|ARD|TCZ for PMR | ||
No.45|2022.05.31|ARD|EULAR recommendation CV risk | ||
No.44|2022.05.24|A&R|CANDLE Points to consider | ||
No.43|2022.05.17|BMJ|AAV PE systematic review | ||
No.42|2022.05.10|ARD|anifrolumab (TULIP-LN) for LN | ||
No.41|2022.04.19|NEJM|Iberdomide SLE | ||
No.40|2022.04.12|ARD|Bari safety | ||
March 8, 2020 | No.39|2022.03.02|A&R|GPA classification criteria | |
No.38|2022.02.16|ARD|MPA classification criteria | ||
No.37|2022.02.09|ARD|EGPA classification criteria | ||
No.36|2022.02.02|Lancet|SS ianalumab | ||
No.35│2022.01.26│JAMA│NOR-DRUM B trial | ||
January 26, 2020 | No.34|2022.01.19|Rheumatology|Safety of Xingrix against IMID |
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No.33|2022.01.12|ARD|NOBILITY phase2 Obinutuzumab LN | ||
No.32|2022.01.05|Lupus Sci Med|DORIS Remission | ||
No.31|2021.12.08|A&R|ACR AAV Guide | ||
January 14, 2020 | No.30|2021.11.24|Rheumatology|PET-CT evaluation of GCA during use of TCZ | |
January 5, 2020 | No.29|2021.10.06|NPSLE summary | |
No.28|2021.09.22|JCI|pDC treatment (SLE) | ||
No.27| 2021.09.15|A&R SLE-PAH prediction model | ||
November 10, 2021 | No.26|2021.09.08|A&R|RA Guidelines | |
No.25|2021.09.01|ARD|GC canceled (BeSt, IMPROVED) | ||
No.24|2021.08.25|ARD|VEXAS-UBA1 and RP | ||
August 11, 2021 | No.23|2021.07.21|A&R|LVV Guidelines | |
No.22|2021.07.14|ARD|Treatment policy for pregnant RA patients | ||
No.21|2021.07.07|Lancet|LN AURORA1 | ||
No.20|2021.06.30|ARD|JAK inhibitor selectivity | ||
No.19|2021.06.23|ARD|ACR-CRISS | ||
No.18|2021.06.23|JAMA|AAV LoVAS | ||
No.17|2021.06.02|ARD|Immunosuppressants and mRNA vaccines | ||
No.16|2021.05.27|ARD|aPL in Covid19 | ||
No.15|2021.04.28|A&R|Fraktalkine phase 2 | ||
No.14|2021.04.14|ARD|RA-SF multi-omics | ||
May 11, 2021 | No.13|2021.03.31|A&R|HCQ thrombosis | |
No.12|2021.03.24|Lancet Respir Med|Nintedanib for SSc on MMF | ||
No.11|2021.03.17|NEJM|AAV Avacopan | ||
No.10|2021.03.10|ARD|SS ABA phase III | ||
No.9|2021.03.03|A&R|ustekinumab SLE | ||
No.8|2021.02.24|Rheumatology|gout- MSUS | ||
No.7|2021.02.17|A&R|ETN withdrawal | ||
No.6|2021.02.10|ARD|EUSTAR_SSc-ILD analysis | ||
No.5|2021.02.03|ARD|D2T-RA | ||
No.4|2021.01.27|NEJM|Upadacitinib vs ABT | ||
No.3|2021.01.20|A&R|TA-AAV | ||
No.2|2021.01.13|ARD|SLE-2019 Validation | ||
No.1|2021.01.06|A&R|MTX-IP |