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利妥昔单抗在维持足细胞病成人缓解中的应用。

Rituximab in maintaining remission in adults with podocytopathy.

机构信息

Department of Nephrology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.

Department of Histopathology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.

出版信息

Nephrology (Carlton). 2020 Aug;25(8):616-624. doi: 10.1111/nep.13717. Epub 2020 Jun 14.

Abstract

UNLABELLED

Rituximab is currently used after the conventional agents have failed in the management of steroid-dependent (SD)/ steroid-resistant (SR) podocytopathies and have a safer toxicity profile. We report 53 adults with podocytopathies who were managed effectively with CD19-targeted rituximab therapy.

METHODS

This was a prospective study carried out at a tertiary care centre in India between January 2014 and June 2019. Adults between 16 and 60 years with SD, frequently relapsing (FR), and SR nephrotic syndrome (NS) due to podocytopathy received rituximab in a CD19-targeted approach.

PRIMARY OUTCOME

Percentage of patients who were in remission at 6 and 12 months. Secondary outcome: Percentage of patients in remission at the last follow-up, rituximab dose and adverse events of rituximab therapy.

RESULTS

Fifty-three adults with SD/FR/SR NS received CD19-targeted rituximab. The median age at the time of first rituximab injection was 30.09 ± 13.21 (16.53) years. At the time of first rituximab infusion, all patients were in remission with steroids and/or calcineurin inhibitors (CNIs). Fifty (94.33%) patients were in remission at the end of 6 and 12 months and the last follow-up (median: 36 months). The mean total dose of rituximab at 1 year was 788.7 ± 128.1 (6 001 100) mg. At last follow-up (median 36 months), 42 (79%) patients did not require any additional CNI or steroids therapy. No serious adverse events to rituximab were noted.

CONCLUSION

CD19-targeted rituximab therapy is safe and efficacious in the management of SD/SR adult podocytopathy. Also, rituximab is effective in maintaining remission in treatment naïve adult SD or FR podocytopathy.

摘要

目的

目前,在常规药物治疗失败后,利妥昔单抗被用于治疗依赖激素(SD)/激素抵抗(SR)足细胞病患者,且具有更安全的毒性特征。我们报告了 53 例接受 CD19 靶向利妥昔单抗治疗的足细胞病患者。

方法

这是一项在印度一家三级医疗中心进行的前瞻性研究,时间为 2014 年 1 月至 2019 年 6 月。16-60 岁的 SD、频繁复发(FR)和 SR 肾病综合征(NS)患者,由于足细胞病变,接受 CD19 靶向利妥昔单抗治疗。

主要结局

6 个月和 12 个月时缓解的患者比例。次要结局:最后一次随访时缓解的患者比例、利妥昔单抗剂量和利妥昔单抗治疗的不良反应。

结果

53 例 SD/FR/SR NS 患者接受了 CD19 靶向利妥昔单抗治疗。首次利妥昔单抗注射时的中位年龄为 30.09±13.21(16.53)岁。首次利妥昔单抗输注时,所有患者均因激素和/或钙调磷酸酶抑制剂(CNI)而缓解。50 例(94.33%)患者在 6 个月和 12 个月以及最后一次随访(中位时间:36 个月)时缓解。1 年时利妥昔单抗的总剂量平均为 788.7±128.1(6001100)mg。在最后一次随访(中位时间 36 个月)时,42 例(79%)患者无需额外使用 CNI 或激素治疗。未观察到与利妥昔单抗相关的严重不良反应。

结论

CD19 靶向利妥昔单抗治疗 SD/SR 成人足细胞病安全有效。此外,利妥昔单抗在维持初治成人 SD 或 FR 足细胞病缓解方面有效。

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