| Literature DB >> 30289572 |
Hayakazu Sumida1, Yoshihide Asano1, Zenshiro Tamaki1, Naohiko Aozasa1, Takashi Taniguchi1, Tetsuo Toyama1, Takehiro Takahashi1, Yohei Ichimura1, Shinji Noda1, Kaname Akamata1, Ryosuke Saigusa1, Miki Miyazaki1, Yoshihiro Kuwano1, Koichi Yanaba1, Ayumi Yoshizaki1, Shinichi Sato1.
Abstract
There have been no established parameters to predict responsiveness to i.v. cyclophosphamide (IVCY) pulse therapy in combination with corticosteroids in patients with interstitial lung disease (ILD) related to systemic sclerosis (SSc). This retrospective study was conducted to determine predictive factors for efficacy of IVCY at the time of before and during the treatment. Thirty-two Japanese SSc patients, ever treated for ILD with IVCY in combination with prednisolone, were analyzed retrospectively. We performed detailed time-course analyses of parameters derived from blood samples and pulmonary function tests. With the exclusion of eight unclassified patients, 24 patients were classified into 14 good responders (GR) or 10 poor responders (PR) on the basis of changes in percent predicted diffusing capacity for carbon monoxide (DLco). Pretreatment percent predicted DLco was significantly reduced in PR compared with GR. In addition, serum parameters such as Krebs von den Lungen-6 (KL-6), surfactant protein D (SP-D) and C-reactive protein were significantly higher in PR than in GR. Furthermore, our time-course analyses revealed a transient increase in serum KL-6 levels with a peak at 3 months after the first infusion of cyclophosphamide, which showed no relation to therapeutic efficacy. Moreover, continuously high serum KL-6 levels (>2000 U/mL) and rapid decrease in SP-D levels (<200 ng/mL) during IVCY were remarkably characteristic of PR and GR, respectively. ILD severity/activity before treatment and variability of serum KL-6 and SP-D levels during treatment may be useful to predict therapeutic effects of IVCY on SSc-ILD.Entities:
Keywords: Krebs von den Lungen-6; cyclophosphamide; interstitial lung disease; surfactant protein D; systemic sclerosis
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Year: 2018 PMID: 30289572 DOI: 10.1111/1346-8138.14669
Source DB: PubMed Journal: J Dermatol ISSN: 0385-2407 Impact factor: 4.005