- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT07778745
A Prospective Phase II Clinical Trial Evaluating the Efficacy and Safety of Adebrelimab in Combination With Trastuzumab Rezetecan for Patients With Stage III Unresectable HER2-Positive NSCLC
19. august 2026 opdateret af: Tianjin Medical University Cancer Institute and Hospital
This is a single-arm, open-label, multicenter phase II investigator-initiated trial.
The study aims to explore the efficacy and safety of Adebrelimab plus Trastuzumab rezetecan induction therapy in patients with stage III unresectable HER2-altered non-small cell lung cancer (NSCLC).
Eligible patients receive 3-4 cycles Q3W induction combination therapy.
After induction, patients will receive radical surgery or concurrent chemoradiotherapy via MDT evaluation, followed by consolidation therapy and long-term survival follow-up.
The primary endpoint is objective response rate (ORR) assessed per RECIST v1.1.
Secondary endpoints include surgical conversion rate, major pathological response (MPR), event-free survival (EFS), overall survival (OS), and safety profiles.
Studieoversigt
Status
Ikke rekrutterer endnu
Betingelser
Intervention / Behandling
Undersøgelsestype
Interventionel
Tilmelding (Anslået)
37
Fase
- Fase 2
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiekontakt
- Navn: Meng Wang Meng Wang
- Telefonnummer: 18622221623
- E-mail: 18622221623@pm.com
Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Ingen
Beskrivelse
Inclusion Criteria:
- Aged 18-75 years, male or female.
- Histologically or cytologically confirmed stage III unresectable NSCLC per AJCC 9th edition, judged unresectable by institutional MDT team.
- Confirmed HER2 alteration: HER2 mutation/amplification detected by tissue NGS, or HER2 protein overexpression (IHC 2+ or 3+).
- No prior systemic anti-tumor therapy for NSCLC; prior anti-tumor Chinese herbal medicine allowed if ≥2 weeks washout before first dose.
- At least 1 measurable target lesion per RECIST v1.1.
- ECOG performance status 0 or 1.
- Able to provide tumor tissue specimen (archival ≤6 months or newly biopsied non-irradiated lesion).
- FEV1 >1.0 L and FEV1% predicted >40% within past 3 months.
Adequate organ function within 7 days before first dose (no blood product/G-CSF support within 14 days):
- Hematology: WBC ≥3.0×10⁹/L, ANC ≥1.5×10⁹/L, PLT ≥100×10⁹/L, Hb ≥90g/L
- Liver: AST/ALT ≤2.5×ULN (≤5×ULN for liver metastasis), TBIL ≤1.5×ULN
- Renal: Serum Cr ≤1.5×ULN or CrCl ≥50 mL/min
- Cardiac: LVEF ≥50% by echocardiogram
- Fertile male/female participants must use effective contraception during treatment and 6 months after last dose; female participants non-lactating, negative serum HCG within 14 days pre-first dose.
- Voluntarily sign written informed consent, good compliance for follow-up.
Exclusion Criteria:
- Mixed small cell/large cell neuroendocrine/sarcomatoid NSCLC histology.
- Concurrent other actionable driver gene alterations (EGFR, ALK, MET, BRAF, RET etc.) besides HER2.
- Past or concurrent other malignant tumor (except fully resected cancer ≥5 years without active treatment).
- Prior thoracic radiotherapy.
- Major surgery within 28 days or minor invasive surgery within 7 days before first dose.
- HIV infection, active hepatitis B/C, organ transplant history, congenital/acquired immunodeficiency.
- Systemic immune modulators (thymosin, interferon, IL-2) within 4 weeks pre-enrollment.
- Uncontrolled severe cardiovascular disease, unstable angina or intervention-required ventricular arrhythmia within 1 month.
- Confirmed or suspected interstitial lung disease, severe baseline pulmonary dysfunction interfering with lung toxicity monitoring.
- Active uncontrolled ≥2 grade infection within 2 weeks before enrollment.
- Active tuberculosis under treatment.
- Known hypersensitivity to any component of study drugs or other monoclonal antibodies/fusion proteins.
- Any condition judged by investigator to compromise participant safety or trial compliance.
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
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 |
|---|---|
|
Eksperimentel: Experimental: Adebrelimab + Trastuzumab rezetecan Induction Therapy
|
1200mg intravenous infusion on Day 1 of every 21-day cycle for 3-4 induction cycles; consolidation therapy after local treatment as physician discretion.
Infusion duration 30-60 minutes.
3.2mg/kg intravenous infusion on Day 1 of every 21-day cycle for 3-4 induction cycles; fixed dose 408mg if body weight ≥85kg.
First infusion over 90 mins, subsequent cycles 60 mins if well tolerated.
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Objective Response Rate (ORR)
Tidsramme: End of Cycle 3/Cycle 4 induction (each cycle 21 days). Surgery-eligible patients assess tumor 6-8 weeks after Cycle3 last dose; others evaluate at Cycle4 end, ±7-day imaging window.
|
Proportion of participants achieving Complete Response (CR) or Partial Response (PR) after 3-4 cycles induction therapy, assessed per RECIST v1.1 by investigators
|
End of Cycle 3/Cycle 4 induction (each cycle 21 days). Surgery-eligible patients assess tumor 6-8 weeks after Cycle3 last dose; others evaluate at Cycle4 end, ±7-day imaging window.
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Surgical Conversion Rate
Tidsramme: Within 6 to 8 weeks after the last induction study drug infusion (42-56 days post final induction dose)
|
Percentage of subjects receiving R0 radical pulmonary resection after MDT re-evaluation post induction
|
Within 6 to 8 weeks after the last induction study drug infusion (42-56 days post final induction dose)
|
|
Major Pathological Response (MPR) Rate
Tidsramme: Within 4 weeks after curative lung resection (pathology report completion window)
|
Proportion of surgical patients with ≤10% viable tumor cells in resected primary tumor specimen (central blinded pathology review)
|
Within 4 weeks after curative lung resection (pathology report completion window)
|
|
Event-Free Survival (EFS)
Tidsramme: Up to 36 months after the first dose of study treatment (3-year full survival follow-up)
|
Time from first study drug dose to disease progression, local recurrence, distant metastasis, or death from any cause
|
Up to 36 months after the first dose of study treatment (3-year full survival follow-up)
|
|
Overall Survival (OS)
Tidsramme: 12 months, 18 months, 24 months, and 36 months after the first dose of study treatment
|
OS defined as time from first dose to all-cause death; survival rate calculated at fixed time points
|
12 months, 18 months, 24 months, and 36 months after the first dose of study treatment
|
|
Safety Profile (Treatment-Related Adverse Events)
Tidsramme: From the date of signed informed consent through 30 days after the last study treatment infusion; long-term safety follow-up continues up to 36 months post first dose for delayed irAEs.
|
Incidence and grade of all adverse events, ≥3 grade AEs, serious adverse events (SAE), immune-related AEs, interstitial lung disease graded per NCI CTCAE v6.0
|
From the date of signed informed consent through 30 days after the last study treatment infusion; long-term safety follow-up continues up to 36 months post first dose for delayed irAEs.
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart (Anslået)
20. august 2026
Primær færdiggørelse (Anslået)
30. august 2027
Studieafslutning (Anslået)
30. august 2029
Datoer for studieregistrering
Først indsendt
6. august 2026
Først indsendt, der opfyldte QC-kriterier
19. august 2026
Først opslået (Faktiske)
21. august 2026
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
21. august 2026
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
19. august 2026
Sidst verificeret
1. august 2026
Mere information
Begreber relateret til denne undersøgelse
Andre undersøgelses-id-numre
- NSCLC-HER2-II-001
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Ingen
Studerer et amerikansk FDA-reguleret enhedsprodukt
Ingen
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .