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Longitudinal Changes in Serum KL-6 in IPF

Recruiting
Conditions
Idiopathic Pulmonary Fibrosis
Interventions
Diagnostic Test: Serum KL-6 level
Registration Number
NCT04268485
Lead Sponsor
Manchester University NHS Foundation Trust
Brief Summary

Idiopathic pulmonary fibrosis (IPF) is a chronic lung disease with a poor prognosis. More accurate tests to predict disease progression and response to treatment are required.

Krebs von den Lungen-6 (KL-6) is a blood marker associated with IPF. Results from previous studies have shown that levels of KL-6 are higher in patients with IPF compared to people without the disease. In addition, it is not clear what impact treatment has on KL-6 levels, and whether this could help us to monitor how effective treatment for IPF is.

The investigators plan to perform a study in which KL-6 levels in the blood of patients with a new diagnosis of IPF are measured at baseline, 3, 6 and 12 months to look for and changes in the levels of KL-6 in the blood.

Detailed Description

Idiopathic pulmonary fibrosis (IPF) is a chronic lung disease with a poor prognosis. Effective treatment which slows the progression of IPF has recently become available however, it is costly and at present is limited to patients who meet specific criteria based on their breathing tests. The breathing tests currently available to monitor progression of the disease are not always reliable and do not predict which patients will respond to treatment. More accurate tests to predict disease progression and response to treatment are required.

Krebs von den Lungen-6 (KL-6) is a blood marker associated with IPF. Results from previous studies have shown that levels of KL-6 are higher in patients with IPF compared to people without the disease. The majority of studies using KL-6 in IPF have taken place in Japan and there is limited evidence of how useful it is in a European population. In addition, it is not clear what impact treatment has on KL-6 levels, and whether this could help us to monitor how effective treatment for IPF is.

The investigators plan to perform a study in which KL-6 levels in the blood of patients with a new diagnosis of IPF are measured at baseline, 3, 6 and 12 months to look for and changes in the levels of KL-6 in the blood

The objective of this study is to assess changes in serum KL-6 levels in patients with IPF over a 12-month period and assess if this correlates with changes in lung function and if KL-6 levels change in response to treatment with antifibrotic therapy.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
60
Inclusion Criteria
  • Age 18 or older
  • Multi-disciplinary team (MDT) diagnosis of idiopathic pulmonary fibrosis as per international consensus guidelines

Exclusion criteria

  • Significant respiratory co-morbidity (i.e. where the major respiratory diagnosis is not IPF)
  • FEV1/FVC ratio < 70% on full lung function testing
  • Current smoker (within 4 week of enrollment)
  • Received treatment for acute lower respiratory tract infection with last 4 weeks
  • Use of long-term (greater than 4 weeks) oral corticosteroids or immunosuppression within 4 weeks of enrolment
  • Current participation in a double-blind placebo-controlled pharmaceutical trial
Exclusion Criteria

Not provided

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
IPF patientsSerum KL-6 levelPatients with an MDT diagnosis of idiopathic pulmonary fibrosis. Patients will be observed over a 12 month period and have serial serum samples taken for KL-6 level.
Primary Outcome Measures
NameTimeMethod
Serum KL-6 level12 months

Change in serum KL-6 level between baseline and 12 months

Secondary Outcome Measures
NameTimeMethod
KL-6 Gender Age and Physiology (GAP) stageAt baseline

Differences in KL-6 levels between Gender Age Physiology (GAP) stage at baseline

KL-6 forced vital capacity (FVC) correlation3, 6 and12 months

Correlation of KL-6 and FVC change at 3, 6 and 12 months

KL-6 diffusion capacity (DLCO)3, 6 and12 months

Correlation of KL-6 and DLCO change at 3, 6 and 12 months

KL-6 antifibrotics12 months

Change in KL-6 levels in response to antifibrotic therapy

KL-6 CPIAt baseline

Correlation between KL-6 levels and Composite Physiology Index (CPI)

Serum KL-6 level at 3, 6 months3 and 6 months

Change in serum KL-6 at 3 and 6 months compared to baseline

KL-6 CT patternAt baseline

Difference in KL-6 levels between patients with indeterminate, probable and definite usual interstitial pneumonia pattern (UIP) on HRCT

KL-6 symptoms3, 6 and12 months

Correlation of KL-6 and symptom scores at 3, 6 and 12 months

Trial Locations

Locations (1)

Manchester University hospitals NHS Foundation Trust

🇬🇧

Manchester, United Kingdom

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