- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg 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)
Studieoversigt
Status
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
Undersøgelsestype
Tilmelding (Anslået)
Fase
- Fase 2
Kontakter og lokationer
Studiekontakt
- Navn: Feng Zhu
- Telefonnummer: 0516-85806985
- E-mail: frankfeng_2004@126.com
Studiesteder
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Jiangsu
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Xuzhou, Jiangsu, Kina, 221000
- Rekruttering
- The Affiliated Hospital of Xuzhou Medical University
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Kontakt:
- Feng Zhu
- Telefonnummer: 0516-85806985
- E-mail: frankfeng_2004@126.com
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Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Beskrivelse
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.
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: N/A
- Interventionel model: Enkelt gruppeopgave
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
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Eksperimentel: 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.
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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 |
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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1-års progressionfri overlevelse (PFS)
Tidsramme: Fra datoen for underskrivelse af informeret samtykke indtil datoen for første dokumenterede progression eller dødsdato fra enhver årsag, alt efter hvad der kom først, vurderet op til 1 år
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PFS defineres som tiden fra registrering til første forekomst af progression eller recidiv som vurderet af undersøgeren, eller død af enhver årsag.
PFS for patienter uden sygdomsprogression, recidiv eller død vil blive censureret på tidspunktet for den sidste tumorevaluering.
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Fra datoen for underskrivelse af informeret samtykke indtil datoen for første dokumenterede progression eller dødsdato fra enhver årsag, alt efter hvad der kom først, vurderet op til 1 år
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Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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ORR (Objective Response Rate)
Tidsramme: At the end of Consolidation therapy (up to 8 cycles, each cycle is 21-28 days )
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ORR is defined as the proportion of patients with a response of CR or PR
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At the end of Consolidation therapy (up to 8 cycles, each cycle is 21-28 days )
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CRR (Complete Response Rate)
Tidsramme: At the end of Consolidation therapy (up to 8 cycles, each cycle is 21-28 days)
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CRR is defined as the proportion of patients with a best response of CR
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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)
Tidsramme: 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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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.
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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)
Tidsramme: 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
Tidsramme: 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)
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Samarbejdspartnere og efterforskere
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Primær færdiggørelse (Anslået)
Studieafslutning (Anslået)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- XYFY2026-001-01
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
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Kliniske forsøg med DLBCL - Diffust storcellet B-celle lymfom
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Memorial Sloan Kettering Cancer CenterActinium PharmaceuticalsRekrutteringDiffust storcellet B-celle lymfom | BOLD | DLBCL | DLBCL, Nos genetiske undertyper | B ALLE | Dlbcl-Ci | DLBCL Uklassificerbar | DLBCL aktiveret B-celletype | DLBCL Germinal Center B-celletype | HGBL | HGBL, nrForenede Stater
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Memorial Sloan Kettering Cancer CenterSanofi; Columbia University; Medical College of Wisconsin; University of Rochester og andre samarbejdspartnereAktiv, ikke rekrutterendeDiffust storcellet B-celle lymfom (DLBCL) | Recidiverende diffust stort B-cellet lymfom (DLBCL) | Refraktært diffust stort B-cellet lymfom (DLBCL)Forenede Stater
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Merck Sharp & Dohme LLCAktiv, ikke rekrutterendeLymfom, stor B-celle, diffus (DLBCL)Canada, Israel, Italien, Korea, Republikken, Polen, Spanien, Kalkun
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Zhejiang Teruisi Pharmaceutical Inc.Ikke rekrutterer endnuDiffust stort B-cellet lymfom (DLBCL)Kina
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Poseida Therapeutics, Inc.Roche-GenentechAktiv, ikke rekrutterendeDLBCL, diffust stort B-cellet lymfom | DLBCL | Primært mediastinalt stort B-celle lymfom (PMBCL) | Højgradigt B-celle lymfom | DLBCL - Diffust storcellet B-celle lymfom | Diffust storcellet B-celle lymfom, ikke andet specificeret | DLBCL, der opstår fra follikulært lymfom | DLBCL NOS | Follikulært lymfom... og andre forholdForenede Stater
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Neumedicines Inc.UkendtLymfom, stor B-celle, diffus (DLBCL)
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AmgenMerck Sharp & Dohme LLCAfsluttetRecidiverende eller refraktært diffust stort B-cellet lymfom (DLBCL)Forenede Stater, Tyskland, Spanien, Australien, Holland, Frankrig
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Hoffmann-La RocheAfsluttetDiffust stort B-cellet lymfom (DLBCL)Forenede Stater
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Liling ZhangRekrutteringLymfom | Recidiverende/refraktært diffust stort B-cellet lymfom (DLBCL)Kina
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Masonic Cancer Center, University of MinnesotaSuspenderetDiffust storcellet B-celle lymfom | DLBCL | Højgradigt B-celle lymfom | DLBCL, der opstår fra follikulært lymfomForenede Stater