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- Essai clinique NCT07680933
Orelabrutinib Combined With Standard Immunochemotherapy With or Without Autologous Hematopoietic Stem Cell Transplantation (Auto-HSCT) for Newly Diagnosed Diffuse Large B-cell Lymphoma (DLBCL)
A Prospective, Phase II Clinical Study Protocol of Orelabrutinib Combined With Standard Immunochemotherapy With or Without Autologous Hematopoietic Stem Cell Transplantation (Auto-HSCT) for Newly Diagnosed Diffuse Large B-cell Lymphoma (DLBCL)
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Description détaillée
Type d'étude
Inscription (Estimé)
Phase
- Phase 2
Contacts et emplacements
Coordonnées de l'étude
- Nom: Feng Zhu
- Numéro de téléphone: 0516-85806985
- E-mail: frankfeng_2004@126.com
Lieux d'étude
-
-
Jiangsu
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Xuzhou, Jiangsu, Chine, 221000
- Recrutement
- The Affiliated Hospital of Xuzhou Medical University
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Contact:
- Feng Zhu
- Numéro de téléphone: 0516-85806985
- E-mail: frankfeng_2004@126.com
-
-
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
- Adulte
- Adulte plus âgé
Accepte les volontaires sains
La description
Inclusion Criteria:
Signed informed consent;
Age 18-80 years at the time of signing informed consent, and willingness to comply with the study protocol procedures;
Pathologically confirmed CD20-positive DLBCL;
④ IPI score of 2-5;
⑤ ECOG performance status of 0-2;
⑥ Life expectancy ≥12 months;
⑦ Left ventricular ejection fraction (LVEF) ≥50% as assessed by multigated acquisition (MUGA) scan or echocardiography (ECHO);
Adequate hematologic function (unless due to underlying disease, e.g., extensive bone marrow involvement, or hypersplenism secondary to splenic involvement attributed to DLBCL as determined by the investigator; transfusion of blood products is permitted), defined as follows:
- Hemoglobin ≥90 g/L within 7 days prior to enrollment without packed red blood cell transfusion;
- Absolute neutrophil count (ANC) ≥1.0 × 10⁹/L;
Platelet count ≥75 × 10⁹/L.
⑨ Adequate organ function.
Exclusion Criteria:
Presence of uncontrolled cardiovascular or cerebrovascular disease, coagulation disorders, autoimmune diseases, severe infectious diseases, etc.;
Abnormal laboratory values at screening (unless attributable to lymphoma):
- Coagulation function: INR > 1.5× the upper limit of normal (ULN); PT and APTT > 1.5× ULN;
- Liver function: ALT or AST > 2× ULN; ALP and bilirubin > 1.5× ULN;
Renal function: Creatinine > 1.5× ULN; creatinine clearance < 60 mL/min (estimated by the Cockcroft-Gault formula);
③ HIV-infected patients;
④ For HBsAg-positive patients, HBV DNA must be negative prior to enrollment. In addition, if a patient is HBsAg-negative but HBcAb-positive (regardless of HBsAb status), HBV DNA testing is still required. If the result is positive, antiviral therapy is needed, and HBV DNA must be negative prior to enrollment;
⑤ Requiring continuous treatment with strong or moderate CYP3A inhibitors or CYP3A inducers. Patients who have taken strong or moderate CYP3A inhibitors or CYP3A inducers within 7 days prior to the first dose of study drug (or have not completed at least 5 half-lives since the last dose) are not eligible for enrollment;
Inability to swallow capsules or presence of gastrointestinal conditions that significantly affect gastrointestinal function, such as malabsorption syndrome, gastric or small bowel resection, symptomatic inflammatory bowel disease, or partial or complete intestinal obstruction;
- Other concurrent and uncontrolled medical conditions that, in the investigator's opinion, may affect the patient's participation in the study, including patients with psychiatric disorders or other known or suspected inability to fully comply with the study protocol.
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 combined with standard immunochemotherapy with or without auto-HSCT
In the induction phase, patients receive 4 cycles of orelabrutinib combined with standard chemotherapy.
For transplant-eligible patients, based on response assessment after 4 cycles, those achieving PR or CR proceed to auto-HSCT, followed by either 6 cycles of orelabrutinib maintenance or no maintenance based on patient preference.
For transplant-ineligible patients, based on response assessment after 4 cycles, those achieving PR or CR receive an additional 2-4 cycles of orelabrutinib combination therapy.
Depending on the patient's performance status, each cycle lasts 21-28 days.
|
1+2.1 or 2.2 ±3 1. Orelabrutinib: 150 mg once daily, orally, Days 1-28 2.1 Pola-R-CHP Regimen: Polatuzumab vedotin: 1.8 mg/kg, intravenous infusion, Day 1 Rituximab: 375 mg/m², intravenous infusion, Day 1 Cyclophosphamide: 750 mg/m², intravenous administration, Day 2 Doxorubicin: 50 mg/m², intravenous administration or per institutional guidelines, Day 2 Prednisone: 100 mg/day, orally, Days 2-6 2.2. R-CHOP Regimen: Rituximab: 375 mg/m², intravenous infusion, Day 0 Cyclophosphamide: 750 mg/m², intravenous administration, Day 1 Doxorubicin: 40-50 mg/m², intravenous administration or per institutional guidelines, Day 1 Vincristine: 1.4 mg/m², intravenous administration, Day 1 (maximum dose 2 mg) OR Vindesine: 4 mg, intravenous administration, Day 1 Prednisone: 100 mg/day, orally, Days 1-5 3. auto-HSCT |
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Survie sans progression (PFS) à 1 an
Délai: À partir de la date de signature du consentement éclairé jusqu'à la date de la première progression documentée ou de la date de décès quelle qu'en soit la cause, selon la première éventualité, évaluée jusqu'à 1 an
|
La PFS est définie comme le temps écoulé entre l'inscription et la première occurrence de progression ou de rechute, évaluée par l'investigateur, ou le décès quelle qu'en soit la cause.
La PFS pour les patients sans progression de la maladie, sans rechute ou sans décès sera censurée au moment de la dernière évaluation tumorale. |
À partir de la date de signature du consentement éclairé jusqu'à la date de la première progression documentée ou de la date de décès quelle qu'en soit la cause, selon la première éventualité, évaluée jusqu'à 1 an
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
ORR (Objective Response Rate)
Délai: At the end of Consolidation therapy (up to 8 cycles, each cycle is 21-28 days )
|
ORR is defined as the proportion of patients with a response of CR or PR
|
At the end of Consolidation therapy (up to 8 cycles, each cycle is 21-28 days )
|
|
CRR (Complete Response Rate)
Délai: At the end of Consolidation therapy (up to 8 cycles, each cycle is 21-28 days)
|
CRR is defined as the proportion of patients with a best response of CR
|
At the end of Consolidation therapy (up to 8 cycles, each cycle is 21-28 days)
|
|
2-year Progression free survival (PFS)
Délai: From date of signing the informed consent until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 2 years
|
PFS is defined as the time from registration to the first occurrence of progression or relapse as assessed by the investigator, or death from any cause.
PFS for patients without disease progression, relapse, or death will be censored at the time of the last tumor assessment.
|
From date of signing the informed consent until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 2 years
|
|
2-year overall survival (OS)
Délai: From date of signing the informed consent until the date of death from any cause, whichever came first, assessed up to 2 years
|
Overall survival is defined as the period from the induction registration to death from any cause.
Patients who have not died until the time of the analysis will be censored at their last contact date.
|
From date of signing the informed consent until the date of death from any cause, whichever came first, assessed up to 2 years
|
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The occurrence of adverse events and serious adverse events
Délai: At the end of whole theray (through study completion, an average of 1 year)
|
At the end of whole theray (through study completion, an average of 1 year)
|
Collaborateurs et enquêteurs
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Réel)
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
Mots clés
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- XYFY2026-001-01
Informations sur les médicaments et les dispositifs, documents d'étude
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