- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT07594899
AI-Driven Treatment Strategy vs Pola-R-CHP in Untreated LBCL (GUIDANCE-10)
17. mai 2026 oppdatert av: Zhao Weili, Ruijin Hospital
A Study to Evaluate the Efficacy and Safety of an AI-Driven Treatment Strategy Versus Pola-R-CHP in Patients With Previously Untreated Large B-Cell Lymphoma
This is a prospective, open-label, multicenter, randomized controlled study in participants with previously untreated large B-cell lymphoma.
Participants will be stratified into different risk groups using an AI-based multimodal model.
Those classified as intermediate- or high-risk will be randomized in a 1:1 ratio to receive either an AI-guided treatment strategy or Pola-R-CHP.
In the experimental arm, participants will receive either genotype-guided targeted agents in combination with Pola-R-CHP or Pola-R-CHP combined with glofitamab, according to their AI-defined risk group and molecular features.
Participants in the control arm will receive Pola-R-CHP.
The study will evaluate the efficacy and safety of the AI-guided treatment strategy compared with Pola-R-CHP.
Studieoversikt
Status
Har ikke rekruttert ennå
Forhold
Studietype
Intervensjonell
Registrering (Antatt)
178
Fase
- Fase 2
Kontakter og plasseringer
Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.
Studiekontakt
- Navn: Weili Zhao
- Telefonnummer: +862164370045 Ext. 610707
- E-post: zwl_trial@163.com
Studer Kontakt Backup
- Navn: Pengpeng Xu
- Telefonnummer: +862164370045 Ext. 610707
- E-post: pengpeng_xu@126.com
Studiesteder
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Shanghai Municipality
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Shanghai, Shanghai Municipality, Kina, 200020
- Ruijin Hospital, Shanghai Jiao Tong University School of Medicine
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Ta kontakt med:
- Weili Zhao
- Telefonnummer: 64370045
- E-post: zwl_trial@163.com
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Deltakelseskriterier
Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
- Voksen
- Eldre voksen
Tar imot friske frivillige
Nei
Beskrivelse
Inclusion Criteria:
- Age 18-75 years with comprehensive geriatric assessment stratified as fit
- Previously untreated participants with CD20-positive LBCL (without central nervous system involvement)
- ECOG Performance Status of 0, 1, or 2
- After 1 cycle of Pola-R-CHP, classified as intermediate-risk or high-risk by AI-based multimodal stratification
- Life expectancy ≥ 3 months
- At least 1 measurable site of disease (defined as lymph nodes with the long diameters longer than 1.5cm, or extra-nodal sites with the long diameters longer than 1.0cm; meanwhile, any lesion site with at least 2 measurable vertical diameters)
- The patient or his or her legal representative must provide written informed consent prior to any special examination or procedure for the research.
- Anti-lymphoma drugs have not been used before (except glucocorticoids)
Exclusion Criteria:
- Prior solid organ transplantation or SCT
- Significant or extensive history of cardiovascular disease such as New York Heart Association Class III or IV cardiac disease or Objective Assessment Class C or D, myocardial infarction within the last 6 months prior to the start of Cycle 1, unstable arrhythmias, or unstable angina
- History or presence of an abnormal ECG that is clinically significant in the investigator's opinion
Any of the following abnormal laboratory values (unless any of these abnormalities are due to underlying lymphoma):
- Absolute neutrophil count <1.0 × 10⁹/L.
- Platelet count <75 × 10⁹/L
- Serum AST and ALT ≥ 2.5 x ULN
- Total bilirubin ≥ 1.5 x ULN
- Serum creatinine clearance < 30 mL/min (using Cockcroft-Gault formula)
- Any active infection within 7 days prior to Cycle 1 Day 1 that would impact participant safety
- Positive test results for chronic hepatitis B infection (defined as positive hepatitis B surface antigen [HBsAg] serology):Participants with occult or prior hepatitis B infection (defined as positive total hepatitis B core antibody and negative HbsAg) may be included if hepatitis B virus (HBV) DNA is undetectable at the time of screening. Such participants must be willing to undergo HBV DNA testing every month and appropriate antiviral therapy as indicated
- Positive test results for hepatitis C (hepatitis C virus [HCV] antibody serology testing):Participants positive for HCV antibody are eligible only if PCR is negative for HCV RNA
- Participants with a history of progressive multifocal leukoencephalopathy
- Pregnancy or breastfeeding, or intention of becoming pregnant during the study or within 12 months after final dose of treatment
- Participants with uncontrolled coagulation disorders, connective tissue diseases, severe infectious diseases
- Other concurrent and uncontrolled medical conditions that, in the opinion of the investigator, would affect the patient's participation in the study
Studieplan
Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
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Eksperimentell: Genotype-guided targeted agents or glofitamab in combination with Pola-R-CHP
Participants will receive polatuzumab vedotin 1.8 milligrams per kilogram (mg/kg) intravenously (IV) on Day 2, rituximab 375 milligrams per square meter (mg/m²) IV on Day 1, cyclophosphamide 750 mg/m² IV on Day 2, doxorubicin 50 mg/m² IV on Day 2, and prednisone 100 milligrams per day (mg/day) orally (PO) on Days 2-6 of the first 21-day cycle.
For the remaining five cycles, participants will receive standard Pola-R-CHP in combination with one of the following: zanubrutinib 160 mg BID PO on Days 1-21, lenalidomide 25 mg/day PO on Days 2-11, decitabine 10 mg/m²/day IV on Days -5 to -1, or glofitamab administered IV with step-up dosing of 2.5 mg on Cycle 2 Day 8, 10 mg on Cycle 2 Day 15, and 30 mg on Day 8 of Cycles 3-6.
Each treatment cycle is 21 days.
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Polatuzumab vedotin IV infusjon vil bli administrert i henhold til planen spesifisert i den respektive armen.
Cyklofosfamid IV-infusjon vil bli administrert i henhold til planen spesifisert i den respektive armen.
Doxorubicin IV infusjon vil bli administrert i henhold til planen spesifisert i den respektive armen.
Prednison PO vil bli administrert i henhold til planen spesifisert i den respektive armen.
Lenalidomid PO vil bli administrert i henhold til planen spesifisert i den respektive armen.
Decitabin IV-infusjon vil bli administrert i henhold til planen spesifisert i den respektive armen.
Zanubrutinib Po vil bli administrert i henhold til planen som er spesifisert i den respektive armen.
Glofitamab IV-infusjon vil bli administrert i henhold til timeplanen som er spesifisert i den respektive armen.
Rituximab IV infusion will be administered as per the schedule specified in the respective arm.
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Aktiv komparator: Pola-R-CHP
Participants will receive polatuzumab vedotin 1.8 milligrams per kilogram (mg/kg) intravenously (IV) on Day2, rituximab 375 milligrams per square meter (mg/m²) IV on Day 1, cyclophosphamide 750 mg/m² IV on Day 2, doxorubicin 50 mg/m² IV on Day 2, and prednisone 100 milligrams per day (mg/day) orally (PO) on Days 2-6 of every 21-day cycle for 6 cycles.
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Polatuzumab vedotin IV infusjon vil bli administrert i henhold til planen spesifisert i den respektive armen.
Cyklofosfamid IV-infusjon vil bli administrert i henhold til planen spesifisert i den respektive armen.
Doxorubicin IV infusjon vil bli administrert i henhold til planen spesifisert i den respektive armen.
Prednison PO vil bli administrert i henhold til planen spesifisert i den respektive armen.
Rituximab IV infusion will be administered as per the schedule specified in the respective arm.
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Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
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Progression-free survival
Tidsramme: From randomization to the first occurrence of disease progression or relapse, or death from any cause, whichever occurs earlier (up to 24 months)
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PFS, defined as the time from randomization to the first occurrence of disease progression or relapse using the 2014 Lugano Response Criteria or death due to any cause, whichever occurs first.
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From randomization to the first occurrence of disease progression or relapse, or death from any cause, whichever occurs earlier (up to 24 months)
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Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
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Antall deltakere med behandlingsrelaterte bivirkninger vurdert ved CTCAE v6.0
Tidsramme: Fra opptak til studiens fullførelse, maksimalt 4 år
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Fra opptak til studiens fullførelse, maksimalt 4 år
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Event-free survival
Tidsramme: Up to approximately 24 months
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EFS, defined as the time from date of randomization to the earliest occurrence of any of the following: Disease progression/relapse; Death due to any cause; The primary efficacy reason that leads to initiation of NALT (other than disease progression/relapse).
If biopsy is obtained after treatment completion and is positive for residual disease regardless of whether NALT is initiated or not.
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Up to approximately 24 months
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Complete response rate
Tidsramme: End of treatment visit (6-8 weeks after last dose on Day 1 of Cycle 6 [Cycle length=21 days] )
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CR rate at the end of treatment by FDG-PET defined as the proportion of participants with CR at the end of treatment according to the 2014 Lugano Response Criteria
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End of treatment visit (6-8 weeks after last dose on Day 1 of Cycle 6 [Cycle length=21 days] )
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Objective response rate
Tidsramme: End of treatment visit (6-8 weeks after last dose on Day 1 of Cycle 6 [Cycle length=21 days] )
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ORR at treatment completion or discontinuation defined as the proportion of participants with partial response (PR) or CR at the end of treatment according to the 2014 Lugano Response Criteria
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End of treatment visit (6-8 weeks after last dose on Day 1 of Cycle 6 [Cycle length=21 days] )
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Overall survival
Tidsramme: Up to approximately 3 years
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OS defined as the time from randomization to death from any cause
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Up to approximately 3 years
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Duration of response
Tidsramme: From documentation of CR/PR until relapse/progression or death due to any reason without documented relapse, whichever came first, assessed up to 3 years.
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From documentation of CR/PR until relapse/progression or death due to any reason without documented relapse, whichever came first, assessed up to 3 years.
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Duration of complete response
Tidsramme: From documentation of CR until relapse/progression or death due to any reason without documented relapse, whichever came first, assessed up to 3 years.
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From documentation of CR until relapse/progression or death due to any reason without documented relapse, whichever came first, assessed up to 3 years.
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Patient reported outcome assessed by EORTC QLQ-C30 (Verison 3.0)
Tidsramme: Day 1 of Cycles 1 and 4 (Cycle length=21 days); 30 days after treatment completion
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Day 1 of Cycles 1 and 4 (Cycle length=21 days); 30 days after treatment completion
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Patient reported outcome assessed by EORTC QLQ-ELD14
Tidsramme: Day 1 of Cycles 1 and 4 (Cycle length=21 days); 30 days after treatment completion
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Day 1 of Cycles 1 and 4 (Cycle length=21 days); 30 days after treatment completion
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Patient reported outcome assessed by FACT-Lym LymS
Tidsramme: Day 1 of Cycles 1 and 4 (Cycle length=21 days); 30 days after treatment completion
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Day 1 of Cycles 1 and 4 (Cycle length=21 days); 30 days after treatment completion
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Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Sponsor
Studierekorddatoer
Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.
Studer hoveddatoer
Studiestart (Antatt)
6. mai 2026
Primær fullføring (Antatt)
31. mai 2029
Studiet fullført (Antatt)
31. desember 2029
Datoer for studieregistrering
Først innsendt
5. mai 2026
Først innsendt som oppfylte QC-kriteriene
17. mai 2026
Først lagt ut (Faktiske)
19. mai 2026
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
19. mai 2026
Siste oppdatering sendt inn som oppfylte QC-kriteriene
17. mai 2026
Sist bekreftet
1. mai 2026
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
- Aminosyrer, peptider og proteiner
- Proteiner
- Organiske kjemikalier
- Heterocykliske forbindelser, 1-ring
- Heterocykliske forbindelser
- Heterocykliske forbindelser, 2-ring
- Heterocykliske forbindelser, smeltet ringen
- Nukleinsyrer, nukleotider og nukleosider
- Hydrokarboner
- Hydrokarboner, syklisk
- Karbohydrater
- Karboksylsyrer
- Polysykliske aromatiske hydrokarboner
- Hydrokarboner, aromatisk
- Polysykliske forbindelser
- Glykosider
- Piperidines
- Antistoffer, monoklonalt
- Antistoffer
- Immunoglobuliner
- Immunoproteiner
- Blodproteiner
- Serumglobuliner
- Globuliner
- Cytidin
- Pyrimidin -nukleosider
- Pyrimidiner
- Gravadienes
- Gravaner
- Steroider
- Smeltede ringforbindelser
- Fosforamid -sennep
- Nitrogen sennepsforbindelser
- Sennepsforbindelser
- Hydrokarboner, halogenert
- Fosforamider
- Organofosforforbindelser
- AZA -forbindelser
- Nukleosider
- Ribonukleosider
- Gravadienedioler
- Antracykliner
- Naphthacenes
- Aminoglykosider
- Antistoffer, monoklonale, murine-avledede
- Daunorubicin
- Azacitidin
- Ftalimider
- Ftalsyrer
- Syrer, karbosykliske
- Piperidoner
- Isoindoles
- Decitabin
- Lenalidomid
- Rituximab
- Prednison
- Cyklofosfamid
- Doxorubicin
- Zanubrutinib
- Polatuzumab Vedotin
- Glofitamab
Andre studie-ID-numre
- GUIDANCE-10
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
NEI
Legemiddel- og utstyrsinformasjon, studiedokumenter
Studerer et amerikansk FDA-regulert medikamentprodukt
Nei
Studerer et amerikansk FDA-regulert enhetsprodukt
Nei
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