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Pilot study comparing the childhood arthritis and rheumatology research alliance consensus treatment plans for induction therapy of juvenile proliferative lupus nephritis.
Cooper, Jennifer C; Rouster-Stevens, Kelly; Wright, Tracey B; Hsu, Joyce J; Klein-Gitelman, Marisa S; Ardoin, Stacy P; Schanberg, Laura E; Brunner, Hermine I; Eberhard, B Anne; Wagner-Weiner, Linda; Mehta, Jay; Haines, Kathleen; McCurdy, Deborah K; Phillips, Thomas A; Huang, Zhen; von Scheven, Emily.
Afiliación
  • Cooper JC; University of California, San Francisco, 550 16th Street, 5th Floor, San Francisco, CA, 94158, USA. jennifer.cooper@childrenscolorado.org.
  • Rouster-Stevens K; Emory University School of Medicine/Children's Healthcare of Atlanta, 2015 Uppergate Dr, Atlanta, GA, 30322, USA.
  • Wright TB; Texas Scottish Rite Children's Hospital, 5323 Harry Hines Blvd, Dallas, TX, 75390, USA.
  • Hsu JJ; Stanford University, 725 Welch Rd, Palo Alto, CA, 94304, USA.
  • Klein-Gitelman MS; Ann & Robert H. Lurie Children's Hospital of Chicago, 225 E. Chicago Ave, Chicago, IL, 60611, USA.
  • Ardoin SP; Ohio State University College of Medicine, 480 Medical Center Dr. S-2056, Columbus, OH, 43210, USA.
  • Schanberg LE; Duke University Medical Center, 2100 Erwin Rd, Durham, NC, 27705, USA.
  • Brunner HI; Cincinnati Children's Hospital Medical Center, 3333 Burnet Ave, Cincinnati, OH, 45229, USA.
  • Eberhard BA; Cohen Children's Hospital Medical Center, 1991 Marcus Ave, Lake Success, NY, 11042, USA.
  • Wagner-Weiner L; University of Chicago Hospitals, 5841 S. Maryland Ave, MC 5044, Chicago, IL, 60637, USA.
  • Mehta J; Children's Hospital at Montefiore/Albert Einstein College of Medicine, 111 E 210th St, Bronx, NY, 10467, USA.
  • Haines K; Hackensack University Medical Center, 30 Prospect Ave, Hackensack, NJ, 07601, USA.
  • McCurdy DK; University of California, 200 UCLA Medical Plaza, Los Angeles, 90095, CA, USA.
  • Phillips TA; Duke University Medical Center, 2400 Pratt, St. Durham, NC, 27705, USA.
  • Huang Z; Duke University Medical Center, 2400 Pratt, St. Durham, NC, 27705, USA.
  • von Scheven E; University of California, San Francisco, 550 16th Street, 5th Floor, San Francisco, CA, 94158, USA.
Pediatr Rheumatol Online J ; 16(1): 65, 2018 Oct 22.
Article en En | MEDLINE | ID: mdl-30348175
ABSTRACT

BACKGROUND:

To reduce treatment variability and facilitate comparative effectiveness studies, the Childhood Arthritis and Rheumatology Research Alliance (CARRA) published consensus treatment plans (CTPs) including one for juvenile proliferative lupus nephritis (LN). Induction immunosuppression CTPs outline treatment with either monthly intravenous (IV) cyclophosphamide (CYC) or mycophenolate mofetil (MMF) in conjunction with one of three corticosteroid (steroid) CTPs primarily oral, primarily IV or mixed oral/IV. The acceptability and in-practice use of these CTPs are unknown. Therefore, the primary aims of the pilot study were to demonstrate feasibility of adhering to the LN CTPs and delineate barriers to implementation in clinical care in the US. Further, we aimed to explore the safety and effectiveness of the treatments for induction therapy.

METHODS:

Forty-one patients were enrolled from 10 CARRA sites. Patients had new-onset biopsy proven ISN/RPS class III or IV proliferative LN, were starting induction therapy with MMF or IV CYC and high-dose steroids and were followed for up to 24 months. Routine clinical data were collected at each visit. Provider reasons for CTP selection were assessed at baseline. Adherence to the CTPs was evaluated by provider survey and medication logs. Complete and partial renal responses were reported at 6 months.

RESULTS:

The majority of patients were female (83%) with a mean age of 14.7 years, SD 2.8. CYC was used more commonly than MMF for patients with ISN/RPS class IV LN (vs. class III), those who had hematuria, and those with adherence concerns. Overall adherence to the immunosuppression induction CTPs was acceptable with a majority of patients receiving the target MMF (86%) or CYC (63%) dose. However, adherence to the steroid CTPs was poor (37%) with large variability in dosing. Renal response endpoints were exploratory and did not show a significant difference between CYC and MMF.

CONCLUSIONS:

Overall, the immunosuppression CTPs were followed as intended in the majority of patients however, adherence to the steroid CTPs was poor indicating revision is necessary. In addition, our pilot study revealed several sources of treatment selection bias that will need to be addressed in for future comparative effectiveness research.
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Texto completo: 1 Colección: 01-internacional Asunto principal: Nefritis Lúpica / Adhesión a Directriz / Ciclofosfamida / Glucocorticoides / Inmunosupresores / Ácido Micofenólico Tipo de estudio: Clinical_trials / Etiology_studies / Guideline / Incidence_studies / Observational_studies / Risk_factors_studies Límite: Adolescent / Child / Female / Humans / Male Idioma: En Revista: Pediatr Rheumatol Online J Año: 2018 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Asunto principal: Nefritis Lúpica / Adhesión a Directriz / Ciclofosfamida / Glucocorticoides / Inmunosupresores / Ácido Micofenólico Tipo de estudio: Clinical_trials / Etiology_studies / Guideline / Incidence_studies / Observational_studies / Risk_factors_studies Límite: Adolescent / Child / Female / Humans / Male Idioma: En Revista: Pediatr Rheumatol Online J Año: 2018 Tipo del documento: Article País de afiliación: Estados Unidos