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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 bijgewerkt door: 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.

Studie Overzicht

Gedetailleerde beschrijving

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.

Studietype

Ingrijpend

Inschrijving (Geschat)

105

Fase

  • Fase 2

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studiecontact

Studie Contact Back-up

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

18 jaar en ouder (Volwassen, Oudere volwassene)

Accepteert gezonde vrijwilligers

Nee

Geslachten die in aanmerking komen voor studie

Allemaal

Beschrijving

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.

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Behandeling
  • Toewijzing: Gerandomiseerd
  • Interventioneel model: Parallelle opdracht
  • Masker: Geen (open label)

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Experimenteel: 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.

Experimenteel: 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.

Experimenteel: 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.

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Progression-Free Survival (PFS)
Tijdsspanne: 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.

Secundaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Overall Survival (OS)
Tijdsspanne: 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)
Tijdsspanne: 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)
Tijdsspanne: 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)
Tijdsspanne: 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)
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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)
Tijdsspanne: Assessed up to approximately 36 months.

AEs graded by CTCAE version 6.0

Assessed up to approximately 36 months.

Andere uitkomstmaten

Uitkomstmaat
Tijdsspanne
Patients reported disease-related symptoms and HRQoL by the EORTC QLQ-C30 questionnaires
Tijdsspanne: 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
Tijdsspanne: Assessed up to approximately 36 months.
Assessed up to approximately 36 months.

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Sponsor

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start (Geschat)

1 september 2026

Primaire voltooiing (Geschat)

1 december 2029

Studie voltooiing (Geschat)

1 december 2031

Studieregistratiedata

Eerst ingediend

13 september 2026

Eerst ingediend dat voldeed aan de QC-criteria

17 september 2026

Eerst geplaatst (Werkelijk)

23 september 2026

Updates van studierecords

Laatste update geplaatst (Werkelijk)

23 september 2026

Laatste update ingediend die voldeed aan QC-criteria

17 september 2026

Laatst geverifieerd

1 augustus 2026

Meer informatie

Termen gerelateerd aan deze studie

Plan Individuele Deelnemersgegevens (IPD)

Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?

NEE

Informatie over medicijnen en apparaten, studiedocumenten

Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel

Nee

Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct

Nee

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