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Trastuzumab Rezetecan and Adebrelimab, Alone or in Combination, After Chemoradiotherapy for HER2-Altered Unresectable Stage III Lung Cancer

17. September 2026 aktualisiert von: Ming Chen

A Randomized, Open-label, Multicenter, Phase II Study of Trastuzumab Rezetecan With Adebrelimab, Trastuzumab Rezetecan Alone and Adebrelimab Alone as Consolidation Therapy in Patients With Unresectable Stage III Non-Small Cell Lung Cancer Harboring HER2 Alterations Without Progression After Definitive Chemoradiotherapy

A randomized phase II study to assess the efficacy and safety of Trastuzumab Rezetecan and/or Adebrelimab as consolidation therapy following chemoradiotherapy in patients with unresectable stage III HER2-altered NSCLC.

Studienübersicht

Detaillierte Beschreibung

This is a randomized, open-label, multi-center phase II study evaluating the efficacy and safety of consolidation therapy with Trastuzumab Rezetecan combined with Adebrelimab versus Trastuzumab Rezetecan monotherapy versus Adebrelimab monotherapy in patients with unresectable stage III NSCLC harboring HER2 alterations (mutation or overexpression) who have not progressed after definitive concurrent or sequential chemoradiotherapy. Eligible patients will be randomized in a 1:1:1 ratio to receive either combination therapy, SHR-A1811 alone, or Adebrelimab alone for up to 12 months. The primary endpoint is progression-free survival (PFS) per RECIST v1.1.

Studientyp

Interventionell

Einschreibung (Geschätzt)

105

Phase

  • Phase 2

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienkontakt

Studieren Sie die Kontaktsicherung

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

18 Jahre und älter (Erwachsene, Älterer Erwachsener)

Akzeptiert gesunde Freiwillige

Nein

Studienberechtigte Geschlechter

Alle

Beschreibung

Inclusion Criteria:

  1. Age ≥18 years.
  2. ECOG performance status 0-1.
  3. Histologically or cytologically confirmed Non-Small Cell Lung Cancer (NSCLC).
  4. Radiologically confirmed unresectable Stage III NSCLC per AJCC 9th edition.
  5. Pathologically confirmed HER2 mutation or HER2 overexpression (IHC 2+ or 3+).
  6. Life expectancy ≥3 months.
  7. Completed at least two cycles of platinum-based chemotherapy (concurrent or sequential) with definitive radiotherapy. Consolidation chemotherapy after radiotherapy is not permitted; chemotherapy with or without immunotherapy before concurrent chemoradiotherapy is permitted.
  8. Total radiotherapy dose 60 Gy ± 10% (54-66 Gy) using IMRT (preferred) or 3D-CRT, with acceptable dosimetric constraints.
  9. Adequate organ and bone marrow function.
  10. Negative pregnancy test for women of childbearing potential within 7 days prior to first dose. Willing to use effective contraception during the study and for 180 days after the last dose.
  11. Signed informed consent form (ICF).

Exclusion Criteria:

  1. Known EGFR-activating mutations or ALK fusions.
  2. Presence of other driver gene mutations with approved targeted therapies available.
  3. Mixed SCLC and NSCLC, large cell neuroendocrine carcinoma, or sarcomatoid carcinoma.
  4. Prior treatment with HER2-targeted ADCs or HER2 TKIs.
  5. Malignant pleural effusion, pericardial effusion, or ascites.
  6. Participation in another clinical trial within 4 weeks or 5 half-lives prior to first dose.
  7. Systemic immunosuppressive therapy within 2 weeks prior to first dose.
  8. Known HIV infection.
  9. Active hepatitis B (HBsAg positive with detectable HBV-DNA and ALT > ULN) or active hepatitis C.
  10. Active autoimmune disease requiring systemic treatment.
  11. Other malignancies within 5 years, except adequately treated cervical carcinoma in situ, basal/squamous cell skin carcinoma, localized prostate cancer, or ductal carcinoma in situ.
  12. Active or history of Grade ≥2 radiation pneumonitis per RTOG/EORTC, or symptomatic interstitial lung disease. Participants with grade 2 radiation pneumonitis that resolves to grade 1 or lower within 14 days without systemic glucocorticoid treatment may undergo screening if the investigator considers there to be no risk of recurrence.
  13. Significant cardiovascular disease.
  14. Severe infection within 4 weeks prior to first dose.
  15. Prior or planned allogeneic bone marrow or solid organ transplantation.
  16. Live attenuated vaccine within 28 days prior to first dose or planned during study. Pregnancy or breastfeeding.
  17. Known hypersensitivity to Adebrelimab, Trastuzumab Rezetecan, or any excipients.
  18. Known history of psychotropic substance abuse, alcohol abuse, or illicit drug use.
  19. Any condition that might impair the subject's ability to comply with study requirements.

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Behandlung
  • Zuteilung: Zufällig
  • Interventionsmodell: Parallele Zuordnung
  • Maskierung: Keine (Offenes Etikett)

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: Arm A (Combination Therapy)

Drug: Trastuzumab Rezetecan + Adebrelimab

Trastuzumab Rezetecan (4.8mg/kg, iv, d1, Q3W) and Adebrelimab (1200mg, iv, d1, Q3W). Treatment will continue for up to 12 months or until disease progression, unacceptable toxicity, or other criteria for treatment discontinuation are met.

Experimental: Arm B (Targeted Monotherapy)

Drug: Trastuzumab Rezetecan

Trastuzumab Rezetecan (4.8mg/kg, iv, d1, Q3W). Treatment will continue for up to 12 months or until disease progression, unacceptable toxicity, or other criteria for treatment discontinuation are met.

Experimental: Arm C (Immunotherapy Monotherapy)

Drug: Adebrelimab

Adebrelimab (1200mg, iv, d1, Q3W). Treatment will continue for up to 12 months or until disease progression, unacceptable toxicity, or other criteria for treatment discontinuation are met.

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Progression-Free Survival (PFS)
Zeitfenster: Assessed up to approximately 36 months.

Defined as the time from randomization to disease progression or death from any cause, whichever occurs first.

Assessed up to approximately 36 months.

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Overall Survival (OS)
Zeitfenster: Assessed up to approximately 60 months.

Defined as the time from randomization to death from any cause.

Assessed up to approximately 60 months.
Objective Response Rate (ORR)
Zeitfenster: Assessed up to approximately 36 months.

Defined as the proportion of participants whose best overall response (BOR) is complete response (CR) or partial response (PR), as assessed according to RECIST v1.1.

Assessed up to approximately 36 months.
Duration of Response (DoR)
Zeitfenster: Assessed up to approximately 36 months.

Defined as the time from the first documented response (CR or PR) to the first documented disease progression (PD) or death from any cause, whichever occurs first.

Assessed up to approximately 36 months.
Disease Control Rate (DCR)
Zeitfenster: Assessed up to approximately 36 months.

Defined as the proportion of participants who achieve complete response (CR), partial response (PR), or stable disease (SD) following treatment, as assessed according to RECIST v1.1.

Assessed up to approximately 36 months.
Time to Death or Distant Metastasis (TTDM)
Zeitfenster: Assessed up to approximately 36 months.

Defined as the time from randomization to the first occurrence of distant metastasis or death from any cause.

Assessed up to approximately 36 months.
Progression-Free Survival Rate at 6 Months
Zeitfenster: 6 months after randomization.

Kaplan-Meier estimate of the percentage of participants alive without disease progression at 6 months after randomization.

6 months after randomization.
Progression-Free Survival Rate at 12 Months
Zeitfenster: 12 months after randomization.

Kaplan-Meier estimate of the percentage of participants alive without disease progression at 12 months after randomization.

12 months after randomization.
Overall Survival Rate at 12 Months
Zeitfenster: 12 months after randomization.

Kaplan-Meier estimate of the percentage of participants alive at 12 months after randomization.

12 months after randomization.
Overall Survival Rate at 24 Months
Zeitfenster: 24 months after randomization.

Kaplan-Meier estimate of the percentage of participants alive at 24 months after randomization.

24 months after randomization.
Incidence of Adverse Events (AEs)
Zeitfenster: Assessed up to approximately 36 months.

AEs graded by CTCAE version 6.0

Assessed up to approximately 36 months.

Andere Ergebnismessungen

Ergebnis Maßnahme
Zeitfenster
Patients reported disease-related symptoms and HRQoL by the EORTC QLQ-C30 questionnaires
Zeitfenster: Assessed up to approximately 36 months.
Assessed up to approximately 36 months.
Patients reported disease-related symptoms and HRQoL by the EORTC QLQ-LC13 questionnaires
Zeitfenster: Assessed up to approximately 36 months.
Assessed up to approximately 36 months.

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Sponsor

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn (Geschätzt)

1. September 2026

Primärer Abschluss (Geschätzt)

1. Dezember 2029

Studienabschluss (Geschätzt)

1. Dezember 2031

Studienanmeldedaten

Zuerst eingereicht

13. September 2026

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

17. September 2026

Zuerst gepostet (Tatsächlich)

23. September 2026

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

23. September 2026

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

17. September 2026

Zuletzt verifiziert

1. August 2026

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Plan für individuelle Teilnehmerdaten (IPD)

Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?

NEIN

Arzneimittel- und Geräteinformationen, Studienunterlagen

Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt

Nein

Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt

Nein

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