Identifying Predictors Of Response To Mepolizumab In CRSwNP

Trial statusRecruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age18+
SponsorCentre hospitalier de l'Université de Montréal (CHUM)

About this trial

The investigators propose a real-world study to assess the mechanism of action of long-lasting response to mepolizumab in patients with chronic rhinosinusitis with nasal polyposis (CRSwNP) and identify clinically useful predictors of response.

Mepolizumab is a monoclonal antibody targeting IL-5 and is approved for use in asthma and CRSwNP. In clinical studies, 12 months of treatment with mepolizumab improved signs and symptoms of CRSwNP and reduced the need for surgery. While several biologic medications targeting facets of the Type 2 mechanism are currently indicated for chronic rhinosinusitis with nasal polyps mepolizumab alone appears capable of modifying the disease's biological behaviour and producing long-standing improvements after the cessation of treatment. In the mepolizumab for CRSwNP regulatory trial (SYNAPSE), a subset of patients experienced dramatic and long-lasting, which is over 48 months after cessation of administration of the investigational medicinal product (IMP) in our experience. This has been partially captured in a follow-on study to the registration trail, which showed that a subset of patients followed for 24 weeks after cessation of biologic therapy (with continued use of mometasone furoate) demonstrated persistent improvements over baseline.

However, the mechanism of the long-lasting effect in a subset of patients is not well understood, and it is impossible currently to identify patients who will derive this maximal benefit. The mechanism for the prolonged improvements in CRSwNP seen in certain patients with mepolizumab remains to be established but suggests that effects beyond eosinophil trafficking are implicated.

The investigators believe that mepolizumab has IL-5-mediated pleiotropic effects which contribute to disease modification with effects extending beyond eosinophil activation and trafficking. This may include the following primary or secondary effects:

i) Improving epithelial barrier function ii) Altering mast cell dynamics iii) Reversing epigenetic modifications iv) Altering the immune response to better clear pathogenic bacteria or viruses.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Bilateral NP, as diagnosed by endoscopy or historical CT scan

At least one NP surgery* within the last 10 years.

Severe NP symptoms consistent with a need for surgery (obstruction VAS symptom score>5, overall, VAS symptom score >7, endoscopic bilateral NP score ≥4 [with a score ≥2 in each nasal cavity]).

Ongoing treatment with INCS (via spray or intranasal liquid steroid wash/douching) for ≥4 weeks prior to screening

Disqualifiers

If as a result of a medical interview, physical examination, or screening investigation the physician responsible considers the participant unfit for the study.

Cystic fibrosis

Eosinophilic granulomatosis with polyangiitis (also known as Churg Strauss syndrome), Young's, Kartagener's or dyskinetic ciliary syndromes

Antrochoanal polyps

Trial design

Design model

Single group

Treatments tested in this trial

  • Mepolizumab 100 MG Injection

    Drug

    Patients will receive Mepolizumab 100mg SC once every 4 weeks for 48 weeks (twelve injections, no placebo) at the hospital. The IMP will be administered following clinic procedures and blood collection. Patients will be monitored at the study site for at least 30 minutes after injections for signs of hypersensitivity reaction. Subcutaneous injection sites should be alternated among the 4 quadrants of the abdomen (avoiding navel and waist areas) or the upper arms. Background therapy will be assured with mometasone furoate nasal spray (200µg BID) daily throughout the study.

Treatment groups

36 Participants
are divided into 1 treatment group
Group A: Mepolizumab 100mg injectionExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Persistent clinical response to mepolizumab after cessation off mepoluzimab treatment

Percentage (%) of participants demonstrating persistent clinical response to mepolizumab following cessation of treatment will be defined as persistence of improvement in Nasal Polyp size greater than 1 six months after cessation of a twelve-month treatment course of mepoluzimab.

Time frame
18 months

Secondary outcomes

Other outcomes

1

Determine effect of mepolizumab on trafficking of individual immune and structural cell types present in the epithelium in CRSwNP

Single-cell transcriptomic techniques will be used to identify cell types present in CRSwNP biopsy samples. Relative proportion identified cell types will be defined, and compared at pre-treatment and after 6 months of treatment with mepolizumab.

Time frame
6 months
2

Effect on epithelial function in vitro

In vitro wound repair speed will be measured in primary epithelial cell (PEC) cultures raised from the patients, before and at 6-month time point of mepolizumab treatment.

Time frame
6 months
3

Effect on epithelial function in vivo

Impact of mepolizumab on In vivo epithelial development and differentiation will be verified by gene expression profiling. Endoscopically-collected epithelial brushings will be collected before and after mepoluzimab treatment. Samples will be processed to undergo expression proofing to assess activity of genes associated with epithelial proliferation and differentiation in Gene Set Ontology (GSEA) Hallmark network.

Time frame
6 months
4

Identify viruses associated with CRSwNP.

A library of frozen samples biopsies taken from CRSwNP patients undergoing ESS for inflammatory disease will be compared with control subjects undergoing access procedures to the skull base . Viruses will be defined as 'significantly present' if identified in five reads of more of bulk sequencing. Viruses associated with CRSwNP will be defined as those attaining significant levels in tissue (defined as greater than 5 'reads') and not significantly present in healthy tissue.

Time frame
6 months

Sponsors and contacts

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