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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

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.

Studieoversikt

Status

Har ikke rekruttert ennå

Forhold

Studietype

Intervensjonell

Registrering (Antatt)

37

Fase

  • Fase 2

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiekontakt

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:

  • 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

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: N/A
  • Intervensjonsmodell: Enkeltgruppeoppdrag
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: 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.

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
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
Tiltaksbeskrivelse
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.

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

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)

20. august 2026

Primær fullføring (Antatt)

30. august 2027

Studiet fullført (Antatt)

30. august 2029

Datoer for studieregistrering

Først innsendt

6. august 2026

Først innsendt som oppfylte QC-kriteriene

19. august 2026

Først lagt ut (Faktiske)

21. august 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

21. august 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

19. august 2026

Sist bekreftet

1. august 2026

Mer informasjon

Begreper knyttet til denne studien

Andre studie-ID-numre

  • NSCLC-HER2-II-001

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

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