Early infectious risk in patients with anti-neutrophil cytoplasmic antibody-associated vasculitis according to remission-induction therapy

被引:4
|
作者
Gerard, M. [1 ]
de Boysson, H. [1 ,2 ]
Morello, R. [3 ]
Martin-Silva, N. [1 ]
Leroux, A-c [4 ]
Dumont, A. [1 ,2 ]
Maigne, G. [1 ]
Boutemy, J. [1 ]
Khoy, K. [5 ]
Mariotte, D. [5 ]
Lobbedez, T. [6 ]
Aouba, A. [1 ,2 ]
Deshayes, S. [1 ,2 ]
机构
[1] CHU Caen Normandie, Dept Internal Med, Caen, France
[2] Univ Caen Normandie UNICAEN, Fac Caen, Caen, France
[3] CHU Caen Normandie, Funct Unit Biostat & Clin Res, Caen, France
[4] Ctr Hosp Mem, Dept Nephrol, St Lo, France
[5] CHU Caen Normandie, Dept Immunol, Caen, France
[6] CHU Caen Normandie, Dept Nephrol, Caen, France
关键词
SYSTEMIC-NECROTIZING-VASCULITIDES; ANCA-ASSOCIATED VASCULITIS; MAINTENANCE THERAPY; JAPANESE PATIENTS; RITUXIMAB; GRANULOMATOSIS; CYCLOPHOSPHAMIDE; RECOMMENDATIONS; COMPLICATIONS; FVSG;
D O I
10.1080/03009742.2021.2001929
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective Few comparative data exist on early infections secondary to remission-induction therapy (RIT) with rituximab (RTX) versus cyclophosphamide (CYC) in newly diagnosed anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) patients. We compared and analysed the rates and predictors of severe infection in such patients within the first 6 months following RIT. Method From the Caen University Hospital databases, we included all consecutive adults newly diagnosed with ANCA-positive granulomatosis with polyangiitis or microscopic polyangiitis between January 2006 and December 2019. We compared rates of survival without severe infection and survival without infections of any severity within 6 months of RIT and used a multivariate Cox analysis to identify predictors of infection. Results We included 145 patients, 27 in the RTX and 118 in the CYC group. Patients in the RTX group more frequently had pneumococcal vaccination (p < 0.01) and creatinine < 150 mu mol/L; other characteristics were comparable between the two groups. Overall, 37 severe infections and 65 infections of any severity were recorded. Rates of survival without severe infection were similar in both groups (p = 0.69), but survival without infections of any severity was lower in the RTX group (p = 0.005). In multivariate analysis, risk factors at diagnosis for severe infections included chronic urinary tract disease, dialysis, and absence of trimethoprim-sulfamethoxazole prophylaxis (p < 0.01 each). Conclusions Within 6 months of RIT, rates of survival without severe infection were similar in newly diagnosed ANCA-positive AAV patients treated with RTX or CYC, but survival rates without infections of any severity appeared to be lower with RTX treatment.
引用
收藏
页码:161 / 173
页数:13
相关论文
共 50 条
  • [1] OUTCOME OF ANTI-NEUTROPHIL CYTOPLASMIC ANTIBODY-ASSOCIATED VASCULITIS DURING REMISSION MAINTENANCE THERAPY IN JAPAN
    Hara, Akinori
    Wada, Takashi
    Sada, Ken-ei
    Ito, Satoshi
    Arimura, Yoshihiro
    [J]. RHEUMATOLOGY, 2017, 56 : 156 - 156
  • [2] Pathogenesis of anti-neutrophil cytoplasmic antibody-associated vasculitis
    Sun, Xiao-Jing
    Li, Zhi-Ying
    Chen, Min
    [J]. RHEUMATOLOGY AND IMMUNOLOGY RESEARCH, 2023, 4 (01): : 11 - 21
  • [3] Rituximab as Maintenance Therapy for Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis
    Rhee, Eugene P.
    Laliberte, Karen A.
    Niles, John L.
    [J]. CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2010, 5 (08): : 1394 - 1400
  • [4] Clonal hematopoiesis in patients with anti-neutrophil cytoplasmic antibody-associated vasculitis
    Arends, Christopher Maximilian
    Weiss, Marlene
    Christen, Friederike
    Eulenberg-Gustavus, Claudia
    Rousselle, Anthony
    Kettritz, Ralph
    Eckardt, Kai-Uwe
    Chan, Willy
    Hoyer, Kaja
    Frick, Mareike
    Bullinger, Lars
    Bieringer, Markus
    Schreiber, Adrian
    Damm, Frederik
    [J]. HAEMATOLOGICA, 2020, 105 (06) : E264 - E267
  • [5] Immunoglobulin levels and infection risk with rituximab induction for anti-neutrophil cytoplasmic antibody-associated vasculitis
    Shah, Shivani
    Jaggi, Khushleen
    Greenberg, Keiko
    Geetha, Duvuru
    [J]. CLINICAL KIDNEY JOURNAL, 2017, 10 (04): : 470 - 474
  • [6] A glance into the future of anti-neutrophil cytoplasmic antibody-associated vasculitis
    Moura, Marta Casal
    Branco, Carolina
    Martins-Martinho, Joana
    Ferraro, Jose Luis
    Berti, Alvise
    Nogueira, Estela
    Ponte, Cristina
    [J]. THERAPEUTIC ADVANCES IN MUSCULOSKELETAL DISEASE, 2022, 14
  • [7] Influenza vaccination and anti-neutrophil cytoplasmic antibody-associated vasculitis
    Wiwanitkit, Viroj
    [J]. NEPHROLOGY, 2015, 20 (07) : 511 - 512
  • [8] Novel Therapies for Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis
    Richard W. Lee
    David P. D’Cruz
    [J]. Drugs, 2008, 68 : 747 - 770
  • [9] Novel therapies for anti-neutrophil cytoplasmic antibody-associated vasculitis
    Tervaert, JWC
    Stegeman, CA
    Kallenberg, CGM
    [J]. CURRENT OPINION IN NEPHROLOGY AND HYPERTENSION, 2001, 10 (02): : 211 - 217
  • [10] Renal transplantation in anti-neutrophil cytoplasmic antibody-associated vasculitis
    Hruskova, Zdenka
    Geetha, Duvuru
    Tesar, Vladimir
    [J]. NEPHROLOGY DIALYSIS TRANSPLANTATION, 2015, 30 : i159 - i163