ANALYSIS OF INFLAMMATORY REACTIONS OBSERVED IN BRONCHOALVEOLAR LAVAGES (BALS) (LBA-PI)
ANALYSIS OF INFLAMMATORY REACTIONS OBSERVED IN BRONCHOALVEOLAR LAVAGES (BALS) PERFORMED FOR INFILTRATIVE LUNG DISEASE THAT COMPLICATE ANTI PD-(L)1 IMMUNOTHERAPIES
Immunological toxicities associated with immune checkpoint inhibitor (ICI) monoclonal antibodies are unpredictable autoimmune and inflammatory pathologies that can affect all treated patients. Some of these events are severe and occur in 15-20% of patients treated with Programmed Death 1 (PD-1) antibodies.
The study of cellular immunological characteristics within tissues affected by toxicities and the interactions between the different actors of these toxicities aims at improving the knowledge concerning the mechanisms of these toxicities, but also at being able to specify the unexpected effects of ICIs on cells of the immune system, outside the tumor microenvironment.
Diffuse infiltrative lung disease is one of the most frequent and severe toxicities encountered in patients treated with anti PD-(L)1; either for bronchial cancer, melanoma or any other type of cancer. Patients developing this type of complication benefit from cytological, bacteriological, mycological and molecular analyses of intra-alveolar constituents obtained by bronchoalveolar lavage (BAL) performed during bronchial fibroscopy as part of their routine care. These analyses help to confirm the diagnosis of alveolitis, to specify the cellular characteristics of alveolar inflammation and to eliminate differential diagnoses of ICI toxicity.
Studieoversigt
Status
Betingelser
Undersøgelsestype
Tilmelding (Forventet)
Fase
- Ikke anvendelig
Kontakter og lokationer
Studiekontakt
- Navn: Jérôme LE PAVEC, MD
- Telefonnummer: 01.40.94.24.30
- E-mail: J.lepavec@ghpsj.fr
Studiesteder
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Le Plessis Robinson, Frankrig, 92350
- Rekruttering
- Centre chirurgical Marie Lannelongue
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Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
Inclusion Criteria:
- Adult subject (≥ 18 years old)
- Patient having consented to the research
Group 1:
- Patient with cancer who was treated with immunotherapy
- Appearance of CT lung abnormalities during immunotherapy, not related to cancer
- With high suspicion of infiltrative lung disease:
- Pneumopathy (CTCAE version 5 classification).
- Patients requiring bronchial fibroscopy with BAL
Groups 2:
- Patient with lung cancer with peripheral tumor
- Requires surgical pulmonary lobectomy in the operating room
Exclusion Criteria:
- Patient treated or having been treated in the last 2 months with corticosteroid therapy
- Patient treated with immunosuppressant and/or cyclophosphamide, and/or Anti-TNF α in the last 12 months
- Absence of consent
- Patient under curatorship, guardianship or safeguard of justice
- Pregnant woman
- Group 1:
- Patient with respiratory failure
Groups 2:
- Patient with lung cancer with proximal or endobronchial tumor
- Patients requiring bilobectomy or pneumonectomy
- Patient who has been treated with immunotherapy
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Sundhedstjenesteforskning
- Tildeling: Ikke-randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
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Aktiv komparator: Patients treated with with immunotherapy and developing diffuse infiltrative lung disease
Group 1: Patients treated for cancer with immunotherapy and developing diffuse infiltrative lung disease
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Patients treated with with immunotherapy and developing diffuse infiltrative lung disease
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Placebo komparator: Patients not treated with immunotherapy and requiring carcinologic lobectomy
Group 2: Patients with lung cancer not treated with immunotherapy and requiring carcinologic lobectomy
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Patients requiring carcinologic lobectomy
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Tidsramme |
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Expression levels of cellular and soluble actors involved in the occurrence of pulmonary toxicities associated with antitumor immunotherapies
Tidsramme: 1 day
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1 day
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Samarbejdspartnere og efterforskere
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Primær færdiggørelse (Forventet)
Studieafslutning (Forventet)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- 2020-A01626-33
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Studerer et amerikansk FDA-reguleret enhedsprodukt
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