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Real-world evidence on levodopa dose escalation in patients with Parkinson's disease treated with istradefylline.
Hattori, Nobutaka; Kabata, Daijiro; Asada, Shinji; Kanda, Tomoyuki; Nomura, Takanobu; Shintani, Ayumi; Mori, Akihisa.
Afiliação
  • Hattori N; Department of Neurology, Juntendo University School of Medicine, Tokyo, Japan.
  • Kabata D; Department of Medical Statistics, Osaka City University Graduate School of Medicine, Osaka, Japan.
  • Asada S; Kyowa Kirin Co., Ltd., Tokyo, Japan.
  • Kanda T; Kyowa Kirin Co., Ltd., Tokyo, Japan.
  • Nomura T; Kyowa Kirin Co., Ltd., Tokyo, Japan.
  • Shintani A; Department of Medical Statistics, Osaka City University Graduate School of Medicine, Osaka, Japan.
  • Mori A; Kyowa Kirin Co., Ltd., Tokyo, Japan.
PLoS One ; 18(12): e0269969, 2023.
Article em En | MEDLINE | ID: mdl-38134023
ABSTRACT

OBJECTIVE:

Istradefylline, a selective adenosine A2A receptor antagonist, is indicated in the US and Japan as adjunctive treatment to levodopa/decarboxylase inhibitors in adults with Parkinson's disease (PD) experiencing OFF time. This study aimed to observe patterns of dose escalation of levodopa over time in patients initiated on istradefylline.

METHODS:

Using Japanese electronic health record data, interrupted time series analyses were used to compare levodopa daily dose (LDD, mg/day) gradients in patients before and after initiation of istradefylline. Data were analyzed by period relative to istradefylline initiation (Month 1) pre-istradefylline (Months -72 to 0), early istradefylline (Months 1 to 24), and late istradefylline (Months 25 to 72). Subgroup analyses included LDD before istradefylline initiation (<400, ≥400 to <600, ≥600 mg/day) and treatment with or without monoamine oxidase-B (MAO-B) inhibitors, catechol-O-methyltransferase (COMT) inhibitors, or dopamine agonists before istradefylline initiation.

RESULTS:

The analysis included 4026 patients; mean (SD) baseline LDD was 419.27 mg (174.19). Patients receiving ≥600 mg/day levodopa or not receiving MAO-B inhibitors or COMT inhibitors demonstrated a significant reduction in LDD increase gradient for pre-istradefylline vs late-phase istradefylline (≥600 mg/day levodopa, -6.259 mg/day each month, p<0.001; no MAO-B inhibitors, -1.819 mg/day each month, p = 0.004; no COMT inhibitors, -1.412 mg/day each month, p = 0.027).

CONCLUSIONS:

This real-world analysis of Japanese prescription data indicated that slowing of LDD escalation was observed in patients initiated on istradefylline, particularly in those receiving ≥600 mg/day levodopa, suggesting istradefylline may slow progressive LDD increases. These findings suggest that initiating istradefylline before other levodopa-adjunctive therapies may mitigate LDD increases, potentially reducing occurrence or severity of levodopa-induced complications in long-term istradefylline treatment.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Levodopa Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Levodopa Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article