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Skin rash following Administration of Apalutamide in Japanese patients with Advanced Prostate Cancer: an integrated analysis of the phase 3 SPARTAN and TITAN studies and a phase 1 open-label study.
Uemura, Hiroji; Koroki, Yosuke; Iwaki, Yuki; Imanaka, Keiichiro; Kambara, Takeshi; Lopez-Gitlitz, Angela; Smith, Andressa; Uemura, Hirotsugu.
Afiliação
  • Uemura H; Department of Urology and Renal Transplantation, Yokohama City University Medical Center, Yokohama, Japan.
  • Koroki Y; Medical Affairs, Janssen Pharmaceutical K.K., Tokyo, Japan. ykoroki@its.jnj.com.
  • Iwaki Y; Clinical Pharmacology, Janssen Pharmaceutical K.K, Tokyo, Japan.
  • Imanaka K; Clinical Science, Janssen Pharmaceutical K.K, Tokyo, Japan.
  • Kambara T; Department of Dermatology, Yokohama City University Medical Center, Yokohama, Japan.
  • Lopez-Gitlitz A; Janssen Global Research & Development, Spring House, PA, USA.
  • Smith A; Janssen Global Research & Development, Spring House, PA, USA.
  • Uemura H; Department of Urology, Kindai University Faculty of Medicine, Osaka, Japan.
BMC Urol ; 20(1): 139, 2020 Sep 02.
Article em En | MEDLINE | ID: mdl-32878613
ABSTRACT

BACKGROUND:

A higher incidence of apalutamide-related skin rash has been observed in Japanese patients with prostate cancer (PC).

METHODS:

This integrated analysis of data of Japanese patients from 2 global Phase 3 studies, SPARTAN ( NCT01946204 ; patients with non-metastatic castration-resistant PC [nmCRPC]) and TITAN ( NCT02489318 ; patients with metastatic castration-sensitive PC [mCSPC]), and the Phase 1 study 56021927PCR1008 ( NCT02162836 ; patients with metastatic CRPC [mCRPC]), assessed clinical risk factors of apalutamide-related skin rash as well as the potential correlation with plasma exposure to apalutamide. Kaplan-Meier method was used for time-to-event analyses. Clinical risk factors for skin rash were assessed using odds ratio.

RESULTS:

Data from 68 patients (SPARTAN n = 34, TITAN n = 28, 56021927PCR1008 n = 6) receiving apalutamide 240 mg orally once-daily were analyzed. Rash (13 [19.1%]) and maculo-papular rash (11 [16.2%]) were the most frequently reported skin rash. All Grade and Grade 3 skin rash occurred in 35 (51.5%) and 10 (14.7%) patients, respectively. Most (85.7%) skin rash occurred within 4 months of apalutamide initiation and resolved in a median time of 1 month following the use of antihistamines, topical or systemic corticosteroids, with/without apalutamide dose interruptions/reductions. Median time-to-remission of first incidence of rash and maximum grade incidence of rash were 1.0 month (IQR 0.36-1.81) and 1.0 month (IQR 0.30-2.43), respectively. No significant clinical risk factors for the incidence of skin rash were observed. Areas under the curve (0-24 h) (AUC0-24, ss) at steady-state of plasma apalutamide concentration were numerically slightly higher in patients with skin rash than those without.

CONCLUSIONS:

No clinical risk factors for rash could be detected. There is a potential correlation between incidence of skin rash and plasma exposure to apalutamide. In general, apalutamide-related skin rash is easily managed, with appropriate treatment with or without dose adjustment. TRIAL REGISTRATION Retrospective pooled analysis of NCT01946204 , NCT02489318 , and NCT02162836 .
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Próstata / Tioidantoínas / Toxidermias / Exantema Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Aged / Humans / Male / Middle aged País/Região como assunto: Asia Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Próstata / Tioidantoínas / Toxidermias / Exantema Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Aged / Humans / Male / Middle aged País/Região como assunto: Asia Idioma: En Ano de publicação: 2020 Tipo de documento: Article