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Long-term and low-dose rituximab treatment for chronic inflammatory demyelinating polyneuropathy.
Zheng, Yongsheng; Sun, Chong; Zhao, Yanyin; Meng, Quanhua; Hu, Jianian; Qiao, Kai; Sun, Jian; Xi, Jianying; Luo, Sushan; Lu, Jiahong; Zhao, Chongbo; Lin, Jie.
Affiliation
  • Zheng Y; Department of Neurology, Huashan Hospital Fudan University, Shanghai, China.
  • Sun C; National Center for Neurological Disorders (NCND), Shanghai, China.
  • Zhao Y; Huashan Rare Disease Center, Huashan Hospital Fudan University, Shanghai, China.
  • Meng Q; Department of Neurology, Huashan Hospital Fudan University, Shanghai, China.
  • Hu J; National Center for Neurological Disorders (NCND), Shanghai, China.
  • Qiao K; Huashan Rare Disease Center, Huashan Hospital Fudan University, Shanghai, China.
  • Sun J; Department of Neurology, Huashan Hospital Fudan University, Shanghai, China.
  • Xi J; National Center for Neurological Disorders (NCND), Shanghai, China.
  • Luo S; Huashan Rare Disease Center, Huashan Hospital Fudan University, Shanghai, China.
  • Lu J; Department of Neurology, Deyang People's Hospital, Deyang, China.
  • Zhao C; Department of Neurology, Huashan Hospital Fudan University, Shanghai, China.
  • Lin J; National Center for Neurological Disorders (NCND), Shanghai, China.
J Peripher Nerv Syst ; 2024 Aug 17.
Article in En | MEDLINE | ID: mdl-39152723
ABSTRACT

OBJECTIVE:

To evaluate the efficacy and safety of a low-dose, long-term rituximab regimen in the treatment of idiopathic CIDP.

METHODS:

This study included 15 CIDP patients treated with rituximab. Patients were administered 600 mg of rituximab intravenously every 6 months. Baseline evaluation was conducted before the initiation of rituximab treatment and subsequent evaluations were conducted 6 months after each rituximab infusion at on-site visits. Clinical improvement was objectively determined by improvement of scale score at least decrease ≥1 INCAT or mRS or increase ≥4 MRC or ≥8 cI-RODS after each infusion compared to baseline evaluation.

RESULTS:

Fifteen CIDP patients were included and 10 of them were typical CIDP and five were distal CIDP. Nine in 15 (60%) patients after first infusion and three in six (50%) patients after second infusion exhibited significant clinical improvement compared to baseline evaluation. Additionally, rituximab facilitated a reduction or cessation of other medications in 73% of patients at last visit. The safety profile was favorable, with no reported adverse events.

CONCLUSION:

Rituximab presents a promising therapeutic option for idiopathic CIDP, offering both efficacy and safety with a low-dose, long-term regimen.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Peripher Nerv Syst Journal subject: NEUROLOGIA Year: 2024 Document type: Article Affiliation country: China

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Peripher Nerv Syst Journal subject: NEUROLOGIA Year: 2024 Document type: Article Affiliation country: China