Cette page a été traduite automatiquement et l'exactitude de la traduction n'est pas garantie. Veuillez vous référer au version anglaise pour un texte source.

Steroids Combined With Ruxolitinib as First-Line Therapy for Grade II Acute Graft-versus-Host Disease

11 juin 2026 mis à jour par: Daihong Liu

An Exploratory Clinical Study of Low-Dose Steroids Combined With Ruxolitinib as First-Line Therapy for Grade II Acute Graft-versus-Host Disease

This study aims to evaluate the efficacy and safety of low-dose corticosteroids combined with ruxolitinib in the treatment of grade II acute graft-versus-host disease (aGVHD) after allogeneic hematopoietic stem cell transplantation.

Aperçu de l'étude

Statut

Actif, ne recrute pas

Intervention / Traitement

Description détaillée

Allogeneic hematopoietic stem cell transplantation (hereinafter referred to as transplantation) is the most effective and even the only curative approach for malignant hematologic diseases. Over the past decade, the cure rate for acute leukemia using transplants from HLA-matched sibling donors has reached 50%-75%. Although transplantation techniques have been continuously improving, the development of graft-versus-host disease (GVHD) after transplantation remains one of the most significant and severe complications, particularly acute GVHD (aGVHD). It reduces the success rate of transplantation and post-transplant disease-free survival, and is also one of the leading causes of non-relapse mortality (NRM). Acute GVHD typically occurs within the first 100 days post-transplant, with an incidence of 35% to 64%, and a mortality rate of 15% to 40% among allogeneic transplant recipients. Despite advances in transplantation techniques and GVHD prophylaxis in recent years, the incidence of acute GVHD remains as high as 30% to 60%, and treatment outcomes remain unsatisfactory. Among these, grade II acute GVHD, although less severe than grades III and IV, has a high incidence, a tendency to progress to severe GVHD, and often leads to long-term dependence on immunosuppressive therapy, imposing a heavy medical burden on patients.

Currently, the standard first-line therapy for grade II acute GVHD is systemic corticosteroids. However, approximately 40% of patients progress to severe (grade III-IV) acute GVHD, leading to a significant increase in non-relapse mortality (1-year overall mortality reaching 35.2%). Long-term high-dose corticosteroid therapy not only readily causes side effects such as infections and metabolic disorders, but also results in treatment failure or steroid dependence in up to 44.4% of patients. Nevertheless, there is currently no standard second-line treatment option for patients with steroid-refractory acute GVHD, and commonly used combination strategies lack robust evidence-based support. Therefore, there is an urgent need to explore more effective and safer early intervention strategies for the treatment of grade II acute GVHD.

In recent years, ruxolitinib (a JAK inhibitor) has brought new hope for the treatment of acute GVHD. Ruxolitinib is a selective JAK1/2 inhibitor that has been approved for the treatment of steroid-refractory acute GVHD. Studies have shown that in the early stage of GVHD, neutrophils migrate to mesenteric lymph nodes and promote disease progression, and ruxolitinib can effectively inhibit this process while reducing MHC-II expression, thereby blocking the early pathogenesis of GVHD. Furthermore, hyperactivation of the JAK-STAT signaling pathway exacerbates GVHD, and early intervention with ruxolitinib may prevent disease progression and reduce the need for second-line therapy. Additionally, ruxolitinib can enhance the therapeutic effect of corticosteroids on T cells by modulating the balance of apoptotic factors to overcome steroid resistance.

In summary, the occurrence of acute GVHD is one of the most important and severe complications after allogeneic hematopoietic stem cell transplantation, reducing transplant success rates and post-transplant disease-free survival. Grade II acute GVHD has a high incidence, a tendency to progress to severe disease, and long-term steroid dependence leads to complications such as infections and metabolic disorders, severely affecting patients' quality of life and transplant outcomes. Currently, approximately 40% of patients receiving standard first-line therapy (systemic corticosteroids) progress to grade III-IV aGVHD, and the rate of steroid resistance or dependence is as high as 44.4%. Therefore, more effective early intervention strategies are urgently needed for patients with grade II GVHD. We plan to conduct a prospective, randomized, single-arm study in patients undergoing allogeneic hematopoietic stem cell transplantation to explore a new treatment strategy for grade II acute GVHD. By introducing an innovative regimen of "ruxolitinib combined with corticosteroids", we aim to prospectively and randomly observe the therapeutic efficacy and safety of low-dose corticosteroids combined with ruxolitinib in patients with grade II acute GVHD, with the goal of improving the treatment response rates, reducing the dose and duration of corticosteroid use, and decreasing the risk of disease progression and long-term complications. This study is expected not only to improve the prognosis of patients with grade II acute GVHD and increase the success rate of transplantation, but also to drive innovative advances in the field of acute GVHD therapy.

Type d'étude

Interventionnel

Inscription (Estimé)

30

Phase

  • La phase 1

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Lieux d'étude

    • Beijing Municipality
      • Beijing, Beijing Municipality, Chine, 100853
        • Chinese PLA General Hospital

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

  • Enfant
  • Adulte
  • Adulte plus âgé

Accepte les volontaires sains

Non

La description

Inclusion Criteria:

  • Patients with malignant hematologic diseases eligible for allogeneic hematopoietic stem cell transplantation, including MDS-RAEB, acute leukemia, and chronic phase of CML.
  • Availability of an HLA-matched sibling donor, unrelated donor, or haploidentical donor.
  • Age ≥ 14 years.
  • Liver function: ALT and AST ≤ 2.5 × upper limit of normal (ULN), total bilirubin ≤ 2 × ULN.
  • Renal function: serum creatinine ≤ ULN.
  • Absence of uncontrolled infection or severe psychiatric/psychological disorders.
  • Eastern Cooperative Oncology Group (ECOG) performance status score of 0-2.
  • Signed informed consent.
  • Diagnosis of grade II acute GVHD as assessed by the modified Glucksberg grading criteria for acute GVHD.

Exclusion Criteria:

  • Absence of an allogeneic donor.
  • Pregnancy of either the donor or the recipient.
  • Presence of psychiatric disorders or other conditions that preclude compliance with the study protocol.

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Traitement
  • Répartition: N / A
  • Modèle interventionnel: Affectation à un seul groupe
  • Masquage: Aucun (étiquette ouverte)

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: RUX+Steroids
Patients with grade II acute GVHD who receive low-dose steroids (0.5mg/kg methylprednisolone) plus ruxolitinib as first-line treatment
Patients with acute grade II GVHD are treated with a combination of methylprednisolone (0.5 mg/kg/day) and ruxolitinib.

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Graft-Versus-Host Disease-Free, Relapse-Free Survival
Délai: 1 years after treatment
Graft-versus-host disease-free, relapse-free survival (GRFS) refers to the time from the start of treatment (or from transplantation) to the first occurrence of any of the following events: grade III-IV acute graft-versus-host disease (aGVHD), chronic graft-versus-host disease (cGVHD) requiring systemic immunosuppressive therapy, disease relapse or progression, or death from any cause.
1 years after treatment

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
survie globale (OS)
Délai: 2 ans après le traitement
La survie globale (OS) correspond à la période allant du début du traitement jusqu'au décès du patient, quelle qu'en soit la raison.
2 ans après le traitement
Overall response rate
Délai: 28 day after treatment
Overall response rate (ORR) for GVHD at day 28 post treatment
28 day after treatment
Failure-free survival (FFS)
Délai: 2 years after treatment
Failure-free survival (FFS) refers to the time from the start of treatment to the first occurrence of treatment failure, including lack of response, disease progression, relapse, or death from any cause.
2 years after treatment
Transplant-related mortality (TRM)
Délai: 2 years after treatment
Transplant-related mortality (TRM) refers to death occurring from causes other than disease relapse, such as toxicity, infection, or organ failure, after hematopoietic stem cell transplantation.
2 years after treatment
disease free survival (DFS)
Délai: 2 years after treatment
Disease free survival (DFS) refers to the time from treatment to the first lymphoma recurrence.
2 years after treatment
Overall response rate (ORR) for GVHD at day 7 post treatment
Délai: 7 day after treatment
Overall response rate (ORR) for GVHD at day 7 post treatment refers to the proportion of patients achieving a complete or partial response of GVHD at day 7 after the start of treatment.
7 day after treatment
Incidence of steroid-refractory GVHD
Délai: 2 years after treatment
Incidence of steroid-refractory GVHD refers to the proportion of patients who fail to
2 years after treatment
Cumulative incidence of chronic GVHD
Délai: 2 years after treatment
Cumulative incidence of chronic GVHD refers to the probability of developing chronic graft-versus-host disease after transplantation, considering death as a competing event.
2 years after treatment
recurrence rate
Délai: 2 years after treatment
The recurrence rate refers to the proportion of transplant patients who experience recurrence after receiving treatment.
2 years after treatment

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Parrainer

Les enquêteurs

  • Chaise d'étude: Dai-Hong Liu, Dr., Chinese PLA General Hospital

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Réel)

17 janvier 2025

Achèvement primaire (Estimé)

30 décembre 2027

Achèvement de l'étude (Estimé)

30 décembre 2027

Dates d'inscription aux études

Première soumission

4 mai 2026

Première soumission répondant aux critères de contrôle qualité

4 mai 2026

Première publication (Réel)

8 mai 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

15 juin 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

11 juin 2026

Dernière vérification

1 mai 2026

Plus d'information

Termes liés à cette étude

Autres numéros d'identification d'étude

  • S2026-159-01

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

NON

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

S'abonner