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Long-Term Outcome of ABO-Incompatible Kidney Transplantation in Patients Treated With Low-Dose Rituximab Regimen.
Sasaki, Hajime; Hotta, Kiyohiko; Mitsuke, Akihiko; Fukasawa, Yuichiro; Tanabe, Tatsu; Higuchi, Haruka; Takada, Yusuke; Harada, Hiroshi.
Afiliação
  • Sasaki H; Departments of Kidney Transplant Surgery, Sapporo City General Hospital, Sapporo, Japan.
  • Hotta K; Department of Urology, Hokkaido University Hospital, Sapporo, Japan. Electronic address: hotta1125@mac.com.
  • Mitsuke A; Departments of Kidney Transplant Surgery, Sapporo City General Hospital, Sapporo, Japan.
  • Fukasawa Y; Department of Surgical Pathology, Sapporo City General Hospital, Sapporo, Japan.
  • Tanabe T; Department of Urology, Hokkaido University Hospital, Sapporo, Japan.
  • Higuchi H; Departments of Kidney Transplant Surgery, Sapporo City General Hospital, Sapporo, Japan.
  • Takada Y; Department of Urology, Sapporo City General Hospital, Sapporo, Japan.
  • Harada H; Departments of Kidney Transplant Surgery, Sapporo City General Hospital, Sapporo, Japan.
Transplant Proc ; 53(3): 989-994, 2021 Apr.
Article em En | MEDLINE | ID: mdl-33272650
ABSTRACT

BACKGROUND:

Introduction of rituximab in the desensitization protocols for ABO-incompatible (ABOI) kidney transplantation (KTX) has afforded excellent results. However, the acceptability of minimal dosage of rituximab in these protocols remains to be defined.

METHODS:

Sixty-three patients who underwent ABOI KTX were included in this study. The desensitization protocol consisted of plasmapheresis, tacrolimus, mycophenolate mofetil, methylprednisolone, intravenous immunoglobulin, basiliximab, and low-dose rituximab (100 mg/body). We evaluated the efficacy, safety, and long-term outcome of this protocol (group R, n = 39) and compared them with those of patients who underwent splenectomy (group S, n = 24).

RESULTS:

Graft and patient survival at 10 years after KTX were comparable between the groups (94.4% [group R] vs 95.4% [group S] and 94.6% [group R] vs 95.8% [group S], respectively). The incidence of acute antibody-mediated rejection (AAMR) was similar in the 2 groups (10.2% vs 12.5%). There were no significant differences in the incidence of chronic active antibody-mediated rejection. Of the patients, 7 developed AAMR and 3 of these patients (1 in group R and 2 in group S) lost their grafts. There were no significant differences in the incidence of chronic active antibody-mediated rejection. The incidence of postoperative cytomegalovirus infection in group R was significantly lower than that in group S. Furthermore, the incidence of postoperative late-onset neutropenia was low in group R.

CONCLUSIONS:

A low-dose rituximab regimen for ABOI KTX is acceptable for preventing AAMR with a low incidence of delayed adverse events.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Complicações Pós-Operatórias / Incompatibilidade de Grupos Sanguíneos / Transplante de Rim / Rituximab / Rejeição de Enxerto Tipo de estudo: Etiology_studies / Incidence_studies / Prognostic_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Complicações Pós-Operatórias / Incompatibilidade de Grupos Sanguíneos / Transplante de Rim / Rituximab / Rejeição de Enxerto Tipo de estudo: Etiology_studies / Incidence_studies / Prognostic_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2021 Tipo de documento: Article