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Adebrelimab Combined With Chemoradiotherapy in Patients With Large Bulky Stage III Unresectable Non-Small Cell Lung Cancer

24. dubna 2026 aktualizováno: Zhijie Wang, Cancer Institute and Hospital, Chinese Academy of Medical Sciences

A Randomized Controlled Clinical Study of Adebrelimab Combined With Chemoradiotherapy in Patients With Large Bulky Stage III Unresectable Non-Small Cell Lung Cancer

This is a randomized, controlled, multicenter clinical study that enrolled patients with unresectable bulky stage III NSCLC, with PFS as the primary endpoint. The study aims to investigate the efficacy and safety of adebrelimab combined with chemoradiotherapy in the treatment of locally advanced/unresectable stage III non-small cell lung cancer.

Přehled studie

Typ studie

Intervenční

Zápis (Odhadovaný)

204

Fáze

  • Fáze 3

Kontakty a umístění

Tato část poskytuje kontaktní údaje pro ty, kteří studii provádějí, a informace o tom, kde se tato studie provádí.

Studijní kontakt

  • Jméno: Zhijie Wang, MD
  • Telefonní číslo: +86 13466323860
  • E-mail: jie_969@163.com

Studijní místa

    • Beijing Municipality
      • Beijing, Beijing Municipality, Čína, 100021
        • National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College

Kritéria účasti

Výzkumníci hledají lidi, kteří odpovídají určitému popisu, kterému se říká kritéria způsobilosti. Některé příklady těchto kritérií jsou celkový zdravotní stav osoby nebo předchozí léčba.

Kritéria způsobilosti

Věk způsobilý ke studiu

  • Dospělý
  • Starší dospělý

Přijímá zdravé dobrovolníky

Ne

Popis

Inclusion Criteria:

  • Aged between 18 and 75 years;
  • ECOG performance status score of 0 or 1;
  • Histologically or cytologically confirmed non-small cell lung cancer (NSCLC);
  • Unresectable stage III NSCLC (per AJCC 9th edition staging), with primary tumor diameter T ≥ 5 cm or regional metastatic lymph node short-axis diameter N ≥ 2 cm;
  • Expected survival time of at least 3 months;
  • No prior anti-tumor treatment before enrollment, including radiotherapy, chemotherapy, surgery and targeted therapy;
  • Adequate function of major organs;
  • Female subjects must have a negative pregnancy test result and be willing to use effective contraception;
  • Subjects voluntarily participate in the study, sign the informed consent form, with good compliance and willingness to complete follow-up.

Exclusion Criteria:

  • Subjects with known positive EGFR mutation or positive ALK fusion.
  • Histologically or cytologically confirmed mixed SCLC and NSCLC, large cell neuroendocrine carcinoma, and sarcomatoid carcinoma.
  • Participation in another clinical trial within 4 weeks prior to the first study dose or within 5 half-lives of the study drug, whichever is shorter.
  • Subjects who have received systemic immunosuppressive therapy within 2 weeks before the first dose, or those who are expected to require systemic immunosuppressive drugs during the study treatment period.
  • Subjects with congenital or acquired immunodeficiency, such as HIV infection; or with a history of autoimmune diseases.
  • Active hepatitis B, hepatitis C, or co-infection with both hepatitis B and hepatitis C.
  • Uncontrolled third-space effusions, such as massive pleural effusion, ascites or pericardial effusion.
  • History of other malignant tumors (other than NSCLC) within 5 years prior to screening.
  • Subjects with prior interstitial lung disease requiring hormone therapy.
  • Subjects with severe cardiovascular and cerebrovascular diseases.
  • History of severe bleeding events or arterial/venous thromboembolic events.
  • Severe infection within 4 weeks before the first dose; evidence of active tuberculosis infection within 1 year prior to the first dose; active fungal, bacterial and/or viral infections requiring systemic treatment.
  • Subjects with prior or planned allogeneic bone marrow transplantation or solid organ transplantation.
  • History of live attenuated vaccination within 28 days before the first dose, or planned live attenuated vaccination during the study period; pregnant or lactating women; fertile patients who are unwilling or unable to adopt effective contraceptive measures.
  • Known hypersensitivity, anaphylactic reaction or intolerance to adebrelimab, chemotherapy agents, or their excipients.
  • Subjects with a known history of psychoactive substance abuse, alcoholism or drug addiction.

Studijní plán

Tato část poskytuje podrobnosti o studijním plánu, včetně toho, jak je studie navržena a co studie měří.

Jak je studie koncipována?

Detaily designu

  • Primární účel: Léčba
  • Přidělení: Randomizované
  • Intervenční model: Paralelní přiřazení
  • Maskování: Žádné (otevřený štítek)

Zbraně a zásahy

Skupina účastníků / Arm
Intervence / Léčba
Experimentální: After chemoimmunotherapy induction followed by cCRT/sCRT, then maintenance immunotherapy.
Patients receive adebrelimab(1200 mg iv, q3w) combined with chemotherapy for 2 cycles of induction therapy, followed by sequential/concurrent chemoradiotherapy (sCRT/cCRT), and then undergo adebrelimab monotherapy for consolidation treatment.

Patients receive adebrelimab combined with chemotherapy for 2 cycles of induction therapy, followed by sequential/concurrent chemoradiotherapy (sCRT/cCRT), and then undergo adebrelimab monotherapy for consolidation treatment.

adebrelimab: 1200 mg iv, q3w Radiation therapy: Total dose of 60 Gy ± 10% (range: 54 Gy - 66 Gy). Chemotherapy: Regimens will be administered in accordance with guideline recommendations.

Subsequently, patients will receive adebrelimab monotherapy as consolidation treatment, with each treatment cycle lasting 3 weeks. Treatment will be continued until disease recurrence or metastasis, intolerable toxicity, subject's voluntary withdrawal, or investigator's decision to discontinue the subject from the study.

Aktivní komparátor: Receive cCRT/sCRT followed by maintenance immunotherapy.
Adebrelimab monotherapy consolidation is administered after sCRT/cCRT.
Receive cCRT/sCRT followed by maintenance immunotherapy. adebrelimab: 1200 mg iv, q3w Radiation therapy: Total dose of 60 Gy ± 10% (range: 54 Gy - 66 Gy). Chemotherapy: Regimens will be administered in accordance with guideline recommendations. Subsequently, patients will receive adebrelimab monotherapy as consolidation treatment, with each treatment cycle lasting 3 weeks. Treatment will be continued until disease recurrence or metastasis, intolerable toxicity, subject's voluntary withdrawal, or investigator's decision to discontinue the subject from the study.

Co je měření studie?

Primární výstupní opatření

Měření výsledku
Popis opatření
Časové okno
Progression-Free Survival (PFS)
Časové okno: From enrollment to the end of monitoring at 1.5 years.
PFS is defined as the time from the first dose of study treatment to the first documentation of disease progression according to RECIST v1.1 (as assessed by investigators) or death from any cause, whichever occurs first. Subjects who are alive without progression at the time of analysis will be censored at the date of the last tumor assessment.
From enrollment to the end of monitoring at 1.5 years.

Sekundární výstupní opatření

Měření výsledku
Popis opatření
Časové okno
Overall Survival (OS)
Časové okno: From enrollment to the end of monitoring at 1.5 years.
OS is defined as the time from the first dose of study treatment to death from any cause. Subjects who are alive at the time of analysis will be censored at the date of last follow-up.
From enrollment to the end of monitoring at 1.5 years.
Objective Response Rate (ORR)
Časové okno: From enrollment to the end of monitoring at 1.5 years.
ORR is defined as the proportion of subjects who achieve a complete response (CR) or partial response (PR) as per RECIST v1.1.
From enrollment to the end of monitoring at 1.5 years.
Duration of Response (DoR)
Časové okno: From enrollment to the end of monitoring at 1.5 years.
DoR is defined as the time from the first documentation of CR or PR to the first documentation of disease progression or death.
From enrollment to the end of monitoring at 1.5 years.
The incidence of adverse events
Časové okno: From enrollment to the end of monitoring at 1.5 years
Incidence, nature, and severity of adverse events (AEs), graded according to NCI-CTCAE v6.0, including immune-related AEs and serious AEs.
From enrollment to the end of monitoring at 1.5 years
Time to Death or Distant Metastasis(TTDM)
Časové okno: From enrollment to the end of monitoring at 1.5 years
From randomization/enrollment to the first occurrence of distant metastasis or death from any cause, whichever occurs first.
From enrollment to the end of monitoring at 1.5 years

Další výstupní opatření

Měření výsledku
Popis opatření
Časové okno
Incremental Cost-Utility Ratio (ICUR)
Časové okno: From randomization/enrollment to the end of 1.5-year follow-up.
The Incremental Cost-Utility Ratio (ICUR) is defined as the incremental total cost divided by the incremental quality-adjusted life years (QALYs) between the experimental treatment group and the control group. It reflects the additional cost required to gain one additional unit of health utility outcome (per QALY).
From randomization/enrollment to the end of 1.5-year follow-up.
Patient Quality of Life (QoL)
Časové okno: From baseline to the end of 1.5-year follow-up.
Patient Quality of Life (QoL) was assessed using validated patient-reported outcome questionnaires. Changes in health-related quality of life from baseline to scheduled follow-up time points were analyzed, including physical function, emotional function, social function and disease-related symptom domains.
From baseline to the end of 1.5-year follow-up.
Exploratory biomarker analysis
Časové okno: From enrollment to the end of 1.5-year follow-up.
Exploratory analysis of relevant biomarker characteristics and their correlation with clinical efficacy outcomes.
From enrollment to the end of 1.5-year follow-up.

Spolupracovníci a vyšetřovatelé

Zde najdete lidi a organizace zapojené do této studie.

Termíny studijních záznamů

Tato data sledují průběh záznamů studie a předkládání souhrnných výsledků na ClinicalTrials.gov. Záznamy ze studií a hlášené výsledky jsou před zveřejněním na veřejné webové stránce přezkoumány Národní lékařskou knihovnou (NLM), aby se ujistily, že splňují specifické standardy kontroly kvality.

Hlavní termíny studia

Začátek studia (Odhadovaný)

1. května 2026

Primární dokončení (Odhadovaný)

31. prosince 2029

Dokončení studie (Odhadovaný)

31. prosince 2030

Termíny zápisu do studia

První předloženo

24. dubna 2026

První předloženo, které splnilo kritéria kontroly kvality

24. dubna 2026

První zveřejněno (Aktuální)

1. května 2026

Aktualizace studijních záznamů

Poslední zveřejněná aktualizace (Aktuální)

1. května 2026

Odeslaná poslední aktualizace, která splnila kritéria kontroly kvality

24. dubna 2026

Naposledy ověřeno

1. dubna 2026

Více informací

Termíny související s touto studií

Plán pro data jednotlivých účastníků (IPD)

Plánujete sdílet data jednotlivých účastníků (IPD)?

NE

Informace o lécích a zařízeních, studijní dokumenty

Studuje lékový produkt regulovaný americkým FDA

Ne

Studuje produkt zařízení regulovaný americkým úřadem FDA

Ne

Tyto informace byly beze změn načteny přímo z webu clinicaltrials.gov. Máte-li jakékoli požadavky na změnu, odstranění nebo aktualizaci podrobností studie, kontaktujte prosím register@clinicaltrials.gov. Jakmile bude změna implementována na clinicaltrials.gov, bude automaticky aktualizována i na našem webu .

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