Aller au contenu
Retour à la recherche

NCT07840456Pas encore en recrutement

Safety and Efficacy of Ruxolitinib in Patients With HNSCC and High NLR Treated With Pembrolizumab - The Phase 2 InflammaSTOP Trial

Résumé

The goal of this Phase 2 clinical trial is to learn if adding ruxolitinib to pembrolizumab may improve treatment outcomes in patients with head and neck squamous cell carcinoma (HNSCC) who have increased levels of systemic inflammation before treatment, as measured by the neutrophil-to-lymphocyte ratio (NLR). The investigational drug will be used outside of its approved indication (off-label use) based on its known pharmacologic mechanism and prior clinical experience in patients with myeloproliferative neoplasms and graft-versus-host disease. The main questions it aims to answer are: Is treatment with ruxolitinib in combination with pembrolizumab safe and well tolerated? Can the addition of ruxolitinib improve treatment outcomes compared with historical data? How does ruxolitinib affect the immune system and inflammation when given together with pembrolizumab? How does the combination treatment affect patients' quality of life? Participants will: Receive treatment with pembrolizumab and intermittent ruxolitinib. Undergo blood tests to assess immune responses and inflammation. Attend study visits for safety assessments and treatment monitoring. Complete quality-of-life questionnaires, where applicable. The results of this study will help researchers better understand how inflammation and the body's immune system affect treatment outcomes in people with head and neck cancer. The findings may also help improve the design of future studies investigating new treatment combinations for this disease.

Critères d'inclusion

• Histologically confirmed diagnosis of R/M HNSCC without local treatment options planned for treatment with pembrolizumab monotherapy (R/M cohort) or locally advanced HNSCC planned for perioperative treatment with pembrolizumab (neoadjuvant cohort) • PD-L1 CPS≥1 • ECOG-performance score 0-2 • NLR \>4 before start of pembrolizumab treatment • Signed and dated written informed consent

Critères d'exclusion

• Participation in another interventional study simultaneously and within the last 30 days prior to inclusion • Concurrent malignancies other than disease under study within 5 years prior to inclusion, with the exception of those with a negligible risk of metastasis or death treated with expected curative outcome • Active, known, or suspected autoimmune disease requiring systemic treatment, a concomitant therapy with systemic immune suppression, up to 5 mg/d prednisolone equivalent is allowed • Patients with severely reduced liver function (Child-Pugh Class C) • Known allergy or hypersensitivity reaction to ruxolitinib • Pregnancy and lactation • Any other serious or unstable medical condition that, in the Investigator's judgment, would compromise participant safety or interfere with study conduct; an active infection requiring systemic antimicrobial, antiviral, or antifungal therapy within 14 days before enrolment; or known HIV infection, active hepatitis B (HBsAg positive or detectable HBV DNA), or active hepatitis C (detectable HCV RNA) • Thrombocytopenia (platelet count \<100,000/microL) or neutropenia (absolute neutrophil count \<1000/mcroL) • Any condition that would require postponement of the planned curative surgical resection to accommodate the neoadjuvant ruxolitinib period (neoadjuvant cohort) • Anticipated inability to observe the minimum treatment-free interval of at least 48 hours between the last ruxolitinib dose and surgery (neoadjuvant cohort)

Contacts

Les coordonnées de l'équipe de l'essai s'affichent sur demande.

Voir la fiche officielle de l'essai
Statut
Pas encore en recrutement
Phase
Phase 2
Type d'étude
Interventionnelle
Pays
Suisse, Allemagne
Promoteur
University Hospital, Basel, Switzerland(Autre)
N° de protocole
th24Brandt; 2026-01363
Pathologies
Carcinoma, Squamous Cell of Head and Neck HNSCC
Interventions
Médicament

Traitements évalués

  • Ruxolitinib
  • Pembrolizumab

Collaborateurs

Clinical Trial Unit, University Hospital Basel, Switzerland

Lieux · 10

  • Basel, SuisseUniversity Hospital BaselRecrutement pas encore ouvert dans ce centre
  • Biel/Bienne, SuisseSeeland Cancer Center BielRecrutement pas encore ouvert dans ce centre
  • Sankt Gallen, SuisseHOCH Health OstschweizRecrutement pas encore ouvert dans ce centre
  • Zurich, SuisseUniversitätsspital ZürichRecrutement pas encore ouvert dans ce centre
  • Bellinzona, SuisseEnte Ospedaliero CantonaleRecrutement pas encore ouvert dans ce centre
  • Würzburg, AllemagneUniversitätslklinikum WürzburgRecrutement pas encore ouvert dans ce centre
  • Greifswald, AllemagneUniversitätsmedizin GreifswaldRecrutement pas encore ouvert dans ce centre
  • Cologne, AllemagneUniklinik KölnRecrutement pas encore ouvert dans ce centre
  • Hagen, AllemagneKatholisches Krankenhaus HagenRecrutement pas encore ouvert dans ce centre
  • Hamburg, AllemagneAsklepios Klinik St. Georg HamburgRecrutement pas encore ouvert dans ce centre

Au total, dans le monde, les 10 centres listés au registre sont prévus ; le recrutement n'est pas encore ouvert.

Statut par centre selon le registre ClinicalTrials.gov (dernière mise à jour publiée : 20 octobre 2026).

Ce statut peut avoir changé et ne dit rien de votre éligibilité : avant toute démarche, vérifiez avec votre oncologue ou le centre.

Voir aussi

Autres versions

Ces résultats sont indicatifs et ne remplacent pas un avis médical — à discuter avec votre médecin.