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)
Studieoversikt
Status
Status
Forhold
Forhold
Intervensjon / Behandling
Intervensjon / Behandling
Studietype
Studietype
Registrering (Antatt)
Registrering
Fase
Fase
- Fase 2
Kontakter og plasseringer
Studiekontakt
Studiekontakt
- Navn: Jianyong Li, PhD
- E-post: lijianyonglm@126.com
Studiesteder
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Jiangsu
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Nanjing, Jiangsu, Kina
- Jiangsu Province Hospital The First Affiliated Hospital with Nanjing Medical University
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Ta kontakt med:
- Jianyong Li, PhD
- E-post: lijianyonglm@126.com
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Deltakelseskriterier
Kvalifikasjonskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
- Voksen
- Eldre voksen
Tar imot friske frivillige
Beskrivelse
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.
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: N/A
- Intervensjonsmodell: Enkeltgruppeoppdrag
- Masking: Ingen (Open Label)
Antall våpen
Våpen og intervensjoner
Deltakergruppe / ArmDeltakergruppe / Arm |
Intervensjon / BehandlingIntervensjon / Behandling |
|---|---|
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Eksperimentell: 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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Hva måler studien?
Primære resultatmål
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
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2-year progression-free survival (PFS) rate
Tidsramme: 2 years
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2 years
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Sekundære resultatmål
Sekundære resultatmål
Resultatmål |
Tidsramme |
|---|---|
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Objective Response Rate (ORR) after 6 cycles of induction therapy
Tidsramme: 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
Tidsramme: 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)
Tidsramme: 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
Tidsramme: up to 4 years
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up to 4 years
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Samarbeidspartnere og etterforskere
Sponsor
Sponsor
Studierekorddatoer
Studer hoveddatoer
Studiestart (Antatt)
Studiestart
Primær fullføring (Antatt)
Primær fullføring
Studiet fullført (Antatt)
Studiet fullført
Datoer for studieregistrering
Først innsendt
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Faktiske)
Først lagt ut
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Sist oppdatering lagt ut
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
Andre studie-ID-numre
- 2026CELH025-01
Legemiddel- og utstyrsinformasjon, studiedokumenter
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Studerer et amerikansk FDA-regulert enhetsprodukt
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