Pirtobrutinib+Pola-R-CHP for Newly Diagnosed Non-GCB DLBCL
A Prospective, Multicenter Clinical Study of Pirtobrutinib Combined With Polatuzumab Vedotin, Rituximab, Cyclophosphamide, Doxorubicin and Prednisone (Pola-R-CHP) for Newly Diagnosed Non-GCB Diffuse Large B-Cell Lymphoma (DLBCL)
Studienübersicht
Status
Status
Bedingungen
Bedingungen
Intervention / Behandlung
Intervention / Behandlung
Studientyp
Studientyp
Einschreibung (Geschätzt)
Einschreibung
Phase
Phase
- Phase 2
Kontakte und Standorte
Studienkontakt
Studienkontakt
- Name: Jianyong Li, PhD
- E-Mail: lijianyonglm@126.com
Studienorte
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Jiangsu
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Nanjing, Jiangsu, China
- Jiangsu Province Hospital The First Affiliated Hospital with Nanjing Medical University
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Kontakt:
- Jianyong Li, PhD
- E-Mail: lijianyonglm@126.com
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Teilnahmekriterien
Zulassungskriterien
Zulassungskriterien
Studienberechtigtes Alter
- Erwachsene
- Älterer Erwachsener
Akzeptiert gesunde Freiwillige
Beschreibung
Inclusion Criteria:
- Histologically confirmed Non-GCB DLBCL (per 2016 WHO diagnostic criteria);
- Whole-body PET/CT performed within 28 days prior to study enrollment demonstrating at least one measurable lesion (per 2014 Lugano criteria);
- Age 18-65 years, with expected survival >3 months;
- No prior anti-lymphoma treatment;
- Signed written informed consent and ability to comply with protocol-required visits and procedures;
- ECOG performance status 0-2;
Adequate organ and bone marrow function, defined as follows:
- Hematology: Absolute neutrophil count (ANC) ≥1×10⁹/L, platelet count (PLT) ≥50×10⁹/L, hemoglobin (HGB) ≥8.0 g/dL; no granulocyte colony-stimulating factor, platelet transfusion, or red blood cell transfusion within 7 days prior to testing;
- Hepatic function: Total bilirubin (TBIL) ≤1.5×upper limit of normal (ULN); Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤2.5×ULN;
- Renal function: Serum creatinine (Cr) ≤1.5×ULN or creatinine clearance (CCR) ≥50 mL/min;
- Cardiac function: NYHA Class III or below; left ventricular ejection fraction ≥50% by echocardiography;
- Coagulation: International normalized ratio (INR) ≤1.5×ULN, activated partial thromboplastin time (APTT) ≤ULN +10s, and prothrombin time (PT) ≤ULN +3s;
- Women of childbearing potential or male subjects with partners of childbearing potential must use effective contraception throughout the treatment period and for 90 days after the last dose.
Exclusion Criteria:
- Central nervous system involvement;
- History of hypersensitivity to the study drug, drugs of the same class, or excipients;
- Concurrent malignancy requiring treatment or intervention;
- Major surgery within 4 weeks prior to treatment (excluding vascular access catheter placement or biopsy);
- Presence of any life-threatening disease, medical condition, or organ system dysfunction that, in the investigator's opinion, may affect patient safety or compliance with study procedures;
- Uncontrolled cardiac symptoms or disease, including: i. NYHA Class II or higher heart failure; ii. Unstable angina; iii. Myocardial infarction within 1 year; iv. Clinically significant supraventricular or ventricular arrhythmias requiring treatment or intervention;
- Active bleeding;
- Active, uncontrolled systemic bacterial, viral, fungal, or parasitic infection (excluding onychomycosis), or other clinically significant active disease process that, in the investigator's opinion, renders the patient unsuitable for clinical trial participation;
- Known history of human immunodeficiency virus (HIV) infection and/or acquired immunodeficiency syndrome;
- Exclusion of patients with active chronic hepatitis B or active hepatitis C. Patients with positive hepatitis B surface antigen, hepatitis B core antibody, or hepatitis C virus antibody at screening must undergo further HBV-DNA and HCV-RNA testing. Patients with stable hepatitis B (HBV-DNA <2500 copies/mL or 500 IU/mL) on antiviral therapy and cured hepatitis C patients (below the limit of detection) may be enrolled;
- Definitive history of neurological or psychiatric disorder, including epilepsy or dementia;
- Pregnant or lactating women;
- Receipt of other investigational agents within 1 month prior to first dose;
- Any other factors that, in the investigator's opinion, may affect the evaluation of efficacy or safety in this study.
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Behandlung
- Zuteilung: N / A
- Interventionsmodell: Einzelgruppenzuweisung
- Maskierung: Keine (Offenes Etikett)
Anzahl der Arme
Waffen und Interventionen
Teilnehmergruppe / ArmTeilnehmergruppe / Arm |
Intervention / BehandlungIntervention / Behandlung |
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Experimental: Pirtobrutinib+Pola-R-CHP for newly diagnosed non GCB DLBCL
This is a single-arm, open-label, multicenter clinical study evaluating the efficacy and safety of pirtobrutinib combined with Pola-R-CHP in previously untreated Non-GCB DLBCL.
PET/CT assessment will be performed after 3 cycles of combination therapy.
Patients achieving CR/PR will continue treatment for another 3 cycles, while those with PD/SD will be discontinued from the study.
Patients achieving CR/PR after 6 cycles of treatment will undergo follow-up with PET/CT or contrast-enhanced CT every 3 months during the first year and every 6 months thereafter, until disease progression, death, withdrawal of informed consent, or study completion, whichever occurs first.
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Pirtobrutinib 200 mg once daily Polatuzumab vedotin 1.8 mg/kg intravenously on Day 1 Rituximab 375 mg/m² on Day 1 Cyclophosphamide 750 mg/m² on Day 1 Doxorubicin 50 mg/m² on Day 1 Prednisone 100 mg on Days 1 to 5 Each cycle lasts 21 days.
PET/CT evaluation is conducted after 3 treatment cycles.
Subjects who attain CR or PR will receive an additional 3 cycles of therapy.
Subjects with PD or SD will be withdrawn from the study.
Subjects who do not achieve CR or PR upon completion of 6 cycles will be withdrawn from the study.
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Was misst die Studie?
Primäre Ergebnismessungen
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Zeitfenster |
|---|---|
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2-year progression-free survival (PFS) rate
Zeitfenster: 2 years
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2 years
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Sekundäre Ergebnismessungen
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Zeitfenster |
|---|---|
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Objective Response Rate (ORR) after 6 cycles of induction therapy
Zeitfenster: week 18,at the end of 6 cycles of induction therapy(each cycle is 21 days)
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week 18,at the end of 6 cycles of induction therapy(each cycle is 21 days)
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Complete Response Rate (CRR) after 6 cycles of induction therapy
Zeitfenster: week 18, at the end of 6 cycles of induction therapy(each cycle is 21 days)
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week 18, at the end of 6 cycles of induction therapy(each cycle is 21 days)
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Overall Survival(OS)
Zeitfenster: up to 4 years
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up to 4 years
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Number of participants with treatment-related adverse events (TRAEs) as assessed by CTCAE v5.0
Zeitfenster: up to 4 years
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up to 4 years
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Mitarbeiter und Ermittler
Sponsor
Sponsor
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn (Geschätzt)
Studienbeginn
Primärer Abschluss (Geschätzt)
Primärer Abschluss
Studienabschluss (Geschätzt)
Studienabschluss
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Tatsächlich)
Zuerst gepostet
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
Letztes Update gepostet
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Zusätzliche relevante MeSH-Bedingungen
Andere Studien-ID-Nummern
Andere Studien-ID-Nummern
- 2026CELH025-01
Arzneimittel- und Geräteinformationen, Studienunterlagen
Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt
Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt
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