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- Sperimentazione clinica 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)
Panoramica dello studio
Stato
Condizioni
Intervento / Trattamento
Descrizione dettagliata
Tipo di studio
Iscrizione (Stimato)
Fase
- Fase 2
Contatti e Sedi
Contatto studio
- Nome: Feng Zhu
- Numero di telefono: 0516-85806985
- Email: frankfeng_2004@126.com
Luoghi di studio
-
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Jiangsu
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Xuzhou, Jiangsu, Cina, 221000
- Reclutamento
- The Affiliated Hospital of Xuzhou Medical University
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Contatto:
- Feng Zhu
- Numero di telefono: 0516-85806985
- Email: frankfeng_2004@126.com
-
-
Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
- Adulto
- Adulto più anziano
Accetta volontari sani
Descrizione
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.
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: N / A
- Modello interventistico: Assegnazione di gruppo singolo
- Mascheramento: Nessuno (etichetta aperta)
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
|
Sperimentale: 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 |
Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Sopravvivenza libera da progressione (PFS) a 1 anno
Lasso di tempo: Dalla data della firma del consenso informato fino alla data della prima progressione documentata o alla data del decesso per qualsiasi causa, a seconda di quale si sia verificata per prima, valutata fino a 1 anno
|
La PFS è definita come il tempo trascorso dalla registrazione alla prima occorrenza di progressione o recidiva, come valutato dallo sperimentatore, o morte per qualsiasi causa.
La PFS per i pazienti senza progressione della malattia, recidiva o morte sarà censurata al momento dell'ultima valutazione tumorale.
|
Dalla data della firma del consenso informato fino alla data della prima progressione documentata o alla data del decesso per qualsiasi causa, a seconda di quale si sia verificata per prima, valutata fino a 1 anno
|
Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
ORR (Objective Response Rate)
Lasso di tempo: 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)
Lasso di tempo: 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)
|
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2-year Progression free survival (PFS)
Lasso di tempo: 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
|
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2-year overall survival (OS)
Lasso di tempo: 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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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.
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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
Lasso di tempo: At the end of whole theray (through study completion, an average of 1 year)
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At the end of whole theray (through study completion, an average of 1 year)
|
Collaboratori e investigatori
Studiare le date dei record
Studia le date principali
Inizio studio (Effettivo)
Completamento primario (Stimato)
Completamento dello studio (Stimato)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Effettivo)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
Termini MeSH pertinenti aggiuntivi
Altri numeri di identificazione dello studio
- XYFY2026-001-01
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