Rituximab versus cyclophosphamide for the treatment of connective tissue disease-associated interstitial lung disease (RECITAL): study protocol for a randomised controlled trial

Trials. 2017 Jun 15;18(1):275. doi: 10.1186/s13063-017-2016-2.

Abstract

Background: Interstitial lung disease (ILD) frequently complicates systemic autoimmune disorders resulting in considerable morbidity and mortality. The connective tissue diseases (CTDs) most frequently resulting in ILD include: systemic sclerosis, idiopathic inflammatory myositis (including dermatomyositis, polymyositis and anti-synthetase syndrome) and mixed connective tissue disease. Despite the development, over the last two decades, of a range of biological therapies which have resulted in significant improvements in the treatment of the systemic manifestations of CTD, the management of CTD-associated ILD has changed little. At present there are no approved therapies for CTD-ILD. Following trials in scleroderma-ILD, cyclophosphamide is the accepted standard of care for individuals with severe or progressive CTD-related ILD. Observational studies have suggested that the anti-CD20 monoclonal antibody, rituximab, is an effective rescue therapy in the treatment of refractory CTD-ILD. However, before now, there have been no randomised controlled trials assessing the efficacy of rituximab in this treatment population.

Methods/design: RECITAL is a UK, multicentre, prospective, randomised, double-blind, double-dummy, controlled trial funded by the Efficacy and Mechanism Evaluation Programme of the Medical Research Council and National Institute for Health Research. The trial will compare rituximab 1 g given intravenously, twice at an interval of 2 weeks, with intravenously administered cyclophosphamide given monthly at a dose of 600 mg/m2 body surface area in individuals with ILD due to systemic sclerosis, idiopathic inflammatory myositis (including anti-synthetase syndrome) or mixed connective tissue disease. A total of 116 individuals will be randomised 1:1 to each of the two treatment arms, with stratification based on underlying CTD, and will be followed for a total of 48 weeks from first dose. The primary endpoint for the study will be change in forced vital capacity (FVC) at 24 weeks. Key secondary endpoints include: safety, change in FVC at 48 weeks as well as survival, change in oxygen requirements, total 48-week corticosteroid exposure and utilisation of health care resources.

Discussion: This is the first randomised control trial to study the efficacy of rituximab as first-line treatment in CTD-associated ILD. The results generated should provide important information on the treatment of a life-threatening complication affecting a rare group of CTDs.

Trial registration: ClinicalTrials.gov, NCT01862926. Registered on 22 May 2013.

Keywords: Biomarkers; Mixed connective tissue disease; Myositis; Pulmonary fibrosis; Respiratory failure; Scleroderma.

Publication types

  • Comparative Study
  • Multicenter Study
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Administration, Intravenous
  • Adrenal Cortex Hormones / administration & dosage
  • Clinical Protocols
  • Connective Tissue Diseases / diagnosis
  • Connective Tissue Diseases / drug therapy*
  • Connective Tissue Diseases / immunology
  • Connective Tissue Diseases / physiopathology
  • Cyclophosphamide / administration & dosage*
  • Cyclophosphamide / adverse effects
  • Double-Blind Method
  • Drug Administration Schedule
  • Humans
  • Immunosuppressive Agents / administration & dosage*
  • Immunosuppressive Agents / adverse effects
  • Lung / drug effects*
  • Lung / immunology
  • Lung / physiopathology
  • Lung Diseases, Interstitial / diagnosis
  • Lung Diseases, Interstitial / drug therapy*
  • Lung Diseases, Interstitial / immunology
  • Lung Diseases, Interstitial / physiopathology
  • Oxygen Inhalation Therapy
  • Prospective Studies
  • Recovery of Function
  • Research Design
  • Rituximab / administration & dosage*
  • Rituximab / adverse effects
  • Time Factors
  • Treatment Outcome
  • United Kingdom
  • Vital Capacity

Substances

  • Adrenal Cortex Hormones
  • Immunosuppressive Agents
  • Rituximab
  • Cyclophosphamide

Associated data

  • ClinicalTrials.gov/NCT01862926