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利妥昔单抗治疗儿童起病的复杂性肾病综合征的多中心、双盲、随机、安慰剂对照试验的长期结果。

Long-term outcome of childhood-onset complicated nephrotic syndrome after a multicenter, double-blind, randomized, placebo-controlled trial of rituximab.

机构信息

Division of Nephrology and Rheumatology, National Center for Child Health and Development, 2-10-1, Okura, Setagaya-ku, Tokyo, 157-8535, Japan.

Division for Clinical Trials, Department of Clinical Research, Center for Clinical Research and Development, National Center for Child Health and Development, 2-10-1, Okura, Setagaya-ku, Tokyo, 157-8535, Japan.

出版信息

Pediatr Nephrol. 2017 Nov;32(11):2071-2078. doi: 10.1007/s00467-017-3718-0. Epub 2017 Jun 29.

Abstract

BACKGROUND

Although rituximab effectively prevents relapses of complicated frequently relapsing nephrotic syndrome (FRNS) and steroid-dependent nephrotic syndrome (SDNS), data of long-term outcomes and safety are limited.

METHODS

Fifty-one patients (age, 3-38 years) with childhood-onset complicated FRNS or SDNS, who received rituximab in investigator-initiated multicenter prospective trials were enrolled. Rituximab was administered at 375 mg/m once weekly for 4 weeks, and immunosuppressive agents were discontinued according to the study protocol. We investigated relapses, re-administration of immunosuppressive agents, additional rituximab treatment, body height, renal function, and late adverse events during the observation period.

RESULTS

Forty-eight patients (94%) developed relapses during the observation period (median, 59 months) and the 50% relapse-free survival was 261 days. Thirty patients (59%) developed SDNS, 44 (86%) required re-administration of immunosuppressive agents, and 22 (43%) received additional rituximab treatment. All patients who were receiving immunosuppressive agents at rituximab treatment required either immunosuppressive agents or additional rituximab treatment. On the contrary, 5 of the 13 patients without immunosuppressive agents at rituximab treatment required neither immunosuppressive agents nor additional rituximab treatment and 3 of them did not develop relapse during observation period. Growth failure due to steroid toxicity did not progress and none of the patients developed chronic renal insufficiency. None of the patients suffered from rituximab-related late adverse events.

CONCLUSIONS

As most patients suffer from relapses after B-cell recovery, long-term immunosuppressive agents or additional rituximab treatment is necessary. However, some patients who can discontinue immunosuppressive agents before rituximab treatment may achieve long-term remission after rituximab treatment without immunosuppressive agents.

摘要

背景

尽管利妥昔单抗能有效预防复杂型频复发型肾病综合征(FRNS)和激素依赖性肾病综合征(SDNS)的复发,但长期疗效和安全性的数据有限。

方法

51 例儿童起病的复杂 FRNS 或 SDNS 患者在研究者发起的多中心前瞻性研究中接受利妥昔单抗治疗。利妥昔单抗每周 1 次,每次 375mg/m2,连用 4 周,根据研究方案停用免疫抑制剂。我们在观察期内调查了复发、再次使用免疫抑制剂、额外的利妥昔单抗治疗、身高、肾功能和晚期不良事件。

结果

48 例(94%)患者在观察期内(中位数 59 个月)复发,无复发生存率为 261 天。30 例(59%)患者发展为 SDNS,44 例(86%)需要再次使用免疫抑制剂,22 例(43%)接受额外的利妥昔单抗治疗。所有在利妥昔单抗治疗时使用免疫抑制剂的患者均需要使用免疫抑制剂或额外的利妥昔单抗治疗。相反,在利妥昔单抗治疗时未使用免疫抑制剂的 13 例患者中,有 5 例既不需要免疫抑制剂,也不需要额外的利妥昔单抗治疗,其中 3 例在观察期间未复发。由于类固醇毒性引起的生长发育迟缓并未进展,且无患者发展为慢性肾功能不全。无患者发生与利妥昔单抗相关的晚期不良事件。

结论

由于大多数患者在 B 细胞恢复后仍会复发,因此需要长期使用免疫抑制剂或额外的利妥昔单抗治疗。然而,一些在利妥昔单抗治疗前能够停用免疫抑制剂的患者,在利妥昔单抗治疗后可能无需免疫抑制剂即可实现长期缓解。

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