- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT07778212
Orelabrutinib Combined With Pola-R-CHP as First-Line Treatment for Patients With Intermediate- to High-Risk DLBCL
A Translational Study of Orelabrutinib Combined With Polatuzumab Vedotin, Rituximab, Cyclophosphamide, Doxorubicin, and Prednisone (Pola-R-CHP) as First-Line Treatment for Patients With Intermediate- to High-Risk Diffuse Large B-Cell Lymphoma (DLBCL)
Aperçu de l'étude
Statut
Intervention / Traitement
Description détaillée
This study is designed to evaluate the efficacy and safety of orelabrutinib in combination with polatuzumab vedotin, rituximab, cyclophosphamide, doxorubicin, and prednisone (Pola-R-CHP) as first-line treatment for patients with intermediate- to high-risk Diffuse large B-cell lymphoma (DLBCL).
Participants will receive orelabrutinib 150 mg orally once daily on Days 1-21 of each 21-day cycle. Polatuzumab vedotin will be administered intravenously at 1.8 mg/kg once every 21 days in combination with rituximab, cyclophosphamide, doxorubicin, and prednisone (R-CHP) for 6 cycles. During Cycles 7 and 8, participants will receive rituximab in combination with orelabrutinib. Thereafter, orelabrutinib maintenance therapy will be continued for up to 1 year.
Type d'étude
Inscription (Estimé)
Phase
- N'est pas applicable
Contacts et emplacements
Coordonnées de l'étude
- Nom: Bing Xu, PhD,MD
- Numéro de téléphone: 18750918842
- E-mail: xubingzhangjian@126.com
Lieux d'étude
-
-
Fujian
-
Xiamen, Fujian, Chine
- Recrutement
- The First Affiliated Hospital of Xiamen University
-
Contact:
- Bing Xu
- Numéro de téléphone: 18750918842
- E-mail: xubingzhangjian@126.com
-
-
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
- Adulte
- Adulte plus âgé
Accepte les volontaires sains
La description
Inclusion Criteria:
- Aged ≥ 18 years;
- Pathologically confirmed diffuse large B-cell lymphoma (DLBCL) by tumor tissue, with at least one measurable lesion, including DLBCL, not otherwise specified (GCB and non-GCB subtypes), DLBCL with MYC and BCL-2 rearrangements, and high-grade B-cell lymphoma;
- No prior receipt of other anti-tumor treatments;
- ECOG performance status 0-2;
- IPI score 2-5, and patients with stage III-IV disease;
- Life expectancy ≥ 6 months;
- Voluntarily sign a written informed consent form.
Exclusion Criteria:
- Lymphoma involving the central nervous system or leptomeningeal metastasis;
- Transformed lymphoma, i.e., transformed from other types of lymphoma, such as follicular lymphoma, marginal zone lymphoma, chronic lymphocytic leukemia, or small B-cell lymphoma;
- Primary mediastinal large B-cell lymphoma;
- Burkitt lymphoma;
- Left ventricular ejection fraction < 50%;
Laboratory test values at screening: (unless caused by lymphoma);
- Neutrophils < 1.5×10⁹/L;
- Platelets < 75×10⁹/L;
- ALT or AST higher than 2 times the upper limit of normal, AKP and bilirubin higher than 1.5 times the upper limit of normal;
- Creatinine level higher than 1.5 times the upper limit of normal;
- Patients with psychiatric disorders or other patients who are known or suspected to be unable to fully comply with the study protocol;
- Pregnant or lactating women;
- Known infection with human immunodeficiency virus (HIV), or active hepatitis B or C virus infection (positive result by polymerase chain reaction [PCR]). If a patient has a positive HBsAg test result, HBV DNA testing is required. If HBV DNA < 10³ IU/ml, the patient can be enrolled. If the HBsAg test result is negative, but the HBcAb test is positive (regardless of HBsAb status), HBV DNA testing is also required. If HBV DNA < 10³ IU/ml, the patient can be enrolled. If a patient is HCV antibody positive, HCV RNA is detected by PCR technology, and a positive result meets the exclusion criterion;
- Need for continuous treatment with strong or moderate CYP3A inhibitors or CYP3A inducers;
- nability to swallow capsules or presence of diseases that significantly affect gastrointestinal function, such as malabsorption syndrome, bariatric surgery, inflammatory bowel disease, or partial or complete intestinal obstruction;
- Other concurrent and uncontrolled medical conditions that the investigator deems will affect the patient's participation in the study.
Plan d'étude
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: Orelabrutinib Plus Pola-R-CHP Regimen
Orelabrutinib in combination with polatuzumab vedotin, rituximab, cyclophosphamide, doxorubicin, and prednisone (Pola-R-CHP)
|
Participants will receive orelabrutinib 150 mg orally once daily on Days 1-21 of each 21-day cycle.
Polatuzumab vedotin will be administered intravenously at 1.8 mg/kg once every 21 days in combination with rituximab, cyclophosphamide, doxorubicin, and prednisone (R-CHP) for 6 cycles.
During Cycles 7 and 8, participants will receive rituximab in combination with orelabrutinib.
Thereafter, orelabrutinib maintenance therapy will be continued for up to 1 year.
Autres noms:
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Complete Response Rate (CRR)
Délai: up to 12 months
|
The proportion of patients who achieve Complete Response.
|
up to 12 months
|
|
Objective Response Rate (ORR):
Délai: up to 12 months
|
The proportion of patients who achieve either a complete response (CR) or a partial response (PR, partial reduction of tumor lesions).
|
up to 12 months
|
|
Progression-Free Survival (PFS)
Délai: up to 24 months
|
The length of time during which a patient's disease does not progress (i.e., no new tumor growth or spread of existing tumors).
|
up to 24 months
|
|
Overall Survival (OS)
Délai: up to 24 months
|
The length of time from the start of treatment until a patient's death from any cause.
|
up to 24 months
|
Collaborateurs et enquêteurs
Les enquêteurs
- Chercheur principal: Bing Xu, PhD,MD, The First Affiliated Hospital of Xiamen University
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Estimé)
Achèvement primaire (Estimé)
Achèvement de l'étude (Estimé)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
- Tumeurs
- Tumeurs par type histologique
- Maladies lymphatiques
- Troubles histiocytaires, malins
- Histiocytose
- Maladies hémiques et lymphatiques
- Sarcome à cellules dendritiques, interdigité
- Acides aminés, peptides et protéines
- Protéines
- Produits chimiques organiques
- Hydrocarbures
- Hydrocarbures, cyclique
- Glucides
- Hydrocarbures aromatiques polycycliques
- Hydrocarbures, aromatique
- Composés polycycliques
- Glycosides
- Anticorps, monoclonal
- Anticorps
- Immunoglobulines
- Immunoprotéines
- Protéines sanguines
- Globulines sériques
- Globulines
- Prégnades
- Grossesse
- Stéroïdes
- Composés à anneau fusionné
- Moutards phosphoramides
- Composés de moutarde d'azote
- Composés moutarde
- Hydrocarbures, halogénés
- Phosphoramides
- Composés organophosphores
- Grossissements
- Anthracyclines
- Naphtacènes
- Aminoglycosides
- Anticorps, monoclonal et murin
- Daunorubicine
- Rituximab
- Prednisone
- Cyclophosphamide
- Doxorubicine
- Polatuzumab Vedotin
- orelabrutinib
Autres numéros d'identification d'étude
- XMDYYYXYK-18
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
Étudie un produit d'appareil réglementé par la FDA américaine
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 .