- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT07836543
Trastuzumab Rezetecan and Adebrelimab, Alone or in Combination, After Chemoradiotherapy for HER2-Altered Unresectable Stage III Lung Cancer
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.
Studieoversikt
Status
Forhold
Detaljert beskrivelse
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
Registrering (Antatt)
Fase
- Fase 2
Kontakter og plasseringer
Studiekontakt
- Navn: Ming Chen, MD
- Telefonnummer: +86 020-87345647
- E-post: chenming@sysucc.org.cn
Studer Kontakt Backup
- Navn: Chenfei Wu, MD
- Telefonnummer: +86 020-87345647
- E-post: wucf@sysucc.org.cn
Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Beskrivelse
Inclusion Criteria:
- Age ≥18 years.
- ECOG performance status 0-1.
- Histologically or cytologically confirmed Non-Small Cell Lung Cancer (NSCLC).
- Radiologically confirmed unresectable Stage III NSCLC per AJCC 9th edition.
- Pathologically confirmed HER2 mutation or HER2 overexpression (IHC 2+ or 3+).
- Life expectancy ≥3 months.
- 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.
- Total radiotherapy dose 60 Gy ± 10% (54-66 Gy) using IMRT (preferred) or 3D-CRT, with acceptable dosimetric constraints.
- Adequate organ and bone marrow function.
- 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.
- Signed informed consent form (ICF).
Exclusion Criteria:
- Known EGFR-activating mutations or ALK fusions.
- Presence of other driver gene mutations with approved targeted therapies available.
- Mixed SCLC and NSCLC, large cell neuroendocrine carcinoma, or sarcomatoid carcinoma.
- Prior treatment with HER2-targeted ADCs or HER2 TKIs.
- Malignant pleural effusion, pericardial effusion, or ascites.
- Participation in another clinical trial within 4 weeks or 5 half-lives prior to first dose.
- Systemic immunosuppressive therapy within 2 weeks prior to first dose.
- Known HIV infection.
- Active hepatitis B (HBsAg positive with detectable HBV-DNA and ALT > ULN) or active hepatitis C.
- Active autoimmune disease requiring systemic treatment.
- 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.
- 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.
- Significant cardiovascular disease.
- Severe infection within 4 weeks prior to first dose.
- Prior or planned allogeneic bone marrow or solid organ transplantation.
- Live attenuated vaccine within 28 days prior to first dose or planned during study. Pregnancy or breastfeeding.
- Known hypersensitivity to Adebrelimab, Trastuzumab Rezetecan, or any excipients.
- Known history of psychotropic substance abuse, alcohol abuse, or illicit drug use.
- Any condition that might impair the subject's ability to comply with study requirements.
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Eksperimentell: 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. |
|
Eksperimentell: 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. |
|
Eksperimentell: 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. |
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Progression-Free Survival (PFS)
Tidsramme: 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.
|
Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Overall Survival (OS)
Tidsramme: 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)
Tidsramme: 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)
Tidsramme: 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)
Tidsramme: 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)
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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)
Tidsramme: Assessed up to approximately 36 months.
|
AEs graded by CTCAE version 6.0 |
Assessed up to approximately 36 months.
|
Andre resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Patients reported disease-related symptoms and HRQoL by the EORTC QLQ-C30 questionnaires
Tidsramme: 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
Tidsramme: Assessed up to approximately 36 months.
|
Assessed up to approximately 36 months.
|
Samarbeidspartnere og etterforskere
Sponsor
Studierekorddatoer
Studer hoveddatoer
Studiestart (Antatt)
Primær fullføring (Antatt)
Studiet fullført (Antatt)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Faktiske)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- MA-NSCLC-II-064
Plan for individuelle deltakerdata (IPD)
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