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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)

This study is a prospective, open-label, multicenter study in previously untreated participants with CD20-positive DLBCL. Orelabrutinib combined with standard immunochemotherapy with or without autologous hematopoietic stem cell transplantation (auto-HSCT) for newly diagnosed diffuse large B-cell lymphoma (DLBCL). The primary objective is to explore the 1-year progression-free survival (PFS) of orelabrutinib combined with standard immunochemotherapy with or without auto-HSCT in newly diagnosed DLBCL.

Studieöversikt

Detaljerad beskrivning

Diffuse large B-cell lymphoma (DLBCL), as the most common type of adult lymphoma, accounts for 35%-40% of non-Hodgkin lymphoma (NHL) and is characterized by high heterogeneity. This study is a prospective, open-label, multicenter study in previously untreated participants with CD20-positive DLBCL. 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. The primary objective is to explore the 1-year progression-free survival (PFS) of orelabrutinib combined with standard immunochemotherapy with or without auto-HSCT in newly diagnosed DLBCL.

Studietyp

Interventionell

Inskrivning (Beräknad)

30

Fas

  • Fas 2

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studiekontakt

Studieorter

    • Jiangsu
      • Xuzhou, Jiangsu, Kina, 221000
        • Rekrytering
        • The Affiliated Hospital of Xuzhou Medical University
        • Kontakt:

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

  • Vuxen
  • Äldre vuxen

Tar emot friska volontärer

Nej

Beskrivning

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:

          1. Hemoglobin ≥90 g/L within 7 days prior to enrollment without packed red blood cell transfusion;
          2. Absolute neutrophil count (ANC) ≥1.0 × 10⁹/L;
          3. 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):

      1. Coagulation function: INR > 1.5× the upper limit of normal (ULN); PT and APTT > 1.5× ULN;
      2. Liver function: ALT or AST > 2× ULN; ALP and bilirubin > 1.5× ULN;
      3. 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

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Primärt syfte: Behandling
  • Tilldelning: N/A
  • Interventionsmodell: Enskild gruppuppgift
  • Maskning: Ingen (Open Label)

Vapen och interventioner

Deltagargrupp / Arm
Intervention / Behandling
Experimentell: 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

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
1-års progressionfri överlevnad (PFS)
Tidsram: Från datumet för undertecknandet av informerat samtycke till datumet för första dokumenterade progression eller dödsdatum av vilken orsak som helst, beroende på vilket som inträffade först, utvärderat upp till 1 år
PFS definieras som tiden från registrering till första förekomst av progression eller återfall som bedöms av undersökaren, eller dödsfall av vilken orsak som helst. PFS för patienter utan sjukdomsprogression, återfall eller död kommer att censureras vid tidpunkten för den senaste tumörbedömningen.
Från datumet för undertecknandet av informerat samtycke till datumet för första dokumenterade progression eller dödsdatum av vilken orsak som helst, beroende på vilket som inträffade först, utvärderat upp till 1 år

Sekundära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
ORR (Objective Response Rate)
Tidsram: 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)
Tidsram: 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)
Tidsram: 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)
Tidsram: 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
The occurrence of adverse events and serious adverse events
Tidsram: 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)

Samarbetspartners och utredare

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Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart (Faktisk)

1 mars 2026

Primärt slutförande (Beräknad)

30 juni 2027

Avslutad studie (Beräknad)

31 december 2028

Studieregistreringsdatum

Först inskickad

24 juni 2026

Först inskickad som uppfyllde QC-kriterierna

30 juni 2026

Första postat (Faktisk)

2 juli 2026

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

2 juli 2026

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

30 juni 2026

Senast verifierad

1 juni 2026

Mer information

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