Characterization of Pulmonary Langerhans Cell Histiocytosis

Last updated: August 16, 2020
Sponsor: Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau
Overall Status: Active - Recruiting

Phase

N/A

Condition

N/A

Treatment

N/A

Clinical Study ID

NCT03093727
IIBSP-LAN-2013-39
  • All Genders

Study Summary

Very recent studies indicate that a high percentage of HCL, about 50%, have mutations in the B-RAF oncogene. The development of ultrasensitive methodologies capable of identifying these mutations in bronchoalveolar lavage will represent a significant advance in the diagnosis and treatment of these patients. An undetermined percentage of HCL does not present mutations in B-RAF. Consequently, the deep genetic analysis, through the use of techniques of massive sequencing, can favor the identification of new alterations that contribute to the development of the disease.

We hypothesized that patients with HCL may present a different inflammatory state to healthy subjects or smokers, allowing us to identify new biomarkers.

Eligibility Criteria

Inclusion

Inclusion criteria

  • Men and women with no age limitation

  • Established histiological diagnosis of histiocytosis of langerhans cells.

  • HCLP-compatible clinical-radiological picture.

  • Signed informed consent

Exclusion criteria

  • Non-acceptance of informed consent.

  • Absence in clinical history of clinical, radiological and functional variables essential for the diagnosis of HLCP.

  • Psychiatric disorder or limitation for study compression (including language, socio-cultural problem, etc.).

  • Radiological findings suggestive of another chronic lung disease.

  • Active respiratory infection.

Study Design

Total Participants: 20
Study Start date:
September 27, 2013
Estimated Completion Date:
September 30, 2023

Study Description

The main objective of this study is to expand the genetic and pathophysiological knowledge of this disease. For this, the following points will be developed:

  • Identification of mutations in the B-RAF oncogene in Spanish patients with pulmonary LCHF.

  • Development of ultrasensitive genetic analysis methods capable of identifying mutations in B-RAF in bronchoalveolar lavage (BAL) samples.

  • To determine if patients with mutations in the B-RAF oncogene present distinct clinical, radiological and / or functional characteristics compared to those with absence of the mutation.

  • Characterization of the inflammatory profile of patients with HPCL.

Connect with a study center

  • Hospital de la Santa Creu i Sant Pau

    Barcelona, 08025
    Spain

    Active - Recruiting

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