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

24 kwietnia 2026 zaktualizowane przez: 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.

Przegląd badań

Typ studiów

Interwencyjne

Zapisy (Szacowany)

204

Faza

  • Faza 3

Kontakty i lokalizacje

Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.

Kontakt w sprawie studiów

  • Nazwa: Zhijie Wang, MD
  • Numer telefonu: +86 13466323860
  • E-mail: jie_969@163.com

Lokalizacje studiów

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

Kryteria uczestnictwa

Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.

Kryteria kwalifikacji

Wiek uprawniający do nauki

  • Dorosły
  • Starszy dorosły

Akceptuje zdrowych ochotników

Nie

Opis

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.

Plan studiów

Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.

Jak projektuje się badanie?

Szczegóły projektu

  • Główny cel: Leczenie
  • Przydział: Randomizowane
  • Model interwencyjny: Przydział równoległy
  • Maskowanie: Brak (otwarta etykieta)

Broń i interwencje

Grupa uczestników / Arm
Interwencja / Leczenie
Eksperymentalny: 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.

Aktywny komparator: 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 mierzy badanie?

Podstawowe miary wyniku

Miara wyniku
Opis środka
Ramy czasowe
Progression-Free Survival (PFS)
Ramy czasowe: 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.

Miary wyników drugorzędnych

Miara wyniku
Opis środka
Ramy czasowe
Overall Survival (OS)
Ramy czasowe: 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)
Ramy czasowe: 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)
Ramy czasowe: 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
Ramy czasowe: 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)
Ramy czasowe: 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

Inne miary wyników

Miara wyniku
Opis środka
Ramy czasowe
Incremental Cost-Utility Ratio (ICUR)
Ramy czasowe: 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)
Ramy czasowe: 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
Ramy czasowe: 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.

Współpracownicy i badacze

Tutaj znajdziesz osoby i organizacje zaangażowane w to badanie.

Daty zapisu na studia

Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.

Główne daty studiów

Rozpoczęcie studiów (Szacowany)

1 maja 2026

Zakończenie podstawowe (Szacowany)

31 grudnia 2029

Ukończenie studiów (Szacowany)

31 grudnia 2030

Daty rejestracji na studia

Pierwszy przesłany

24 kwietnia 2026

Pierwszy przesłany, który spełnia kryteria kontroli jakości

24 kwietnia 2026

Pierwszy wysłany (Rzeczywisty)

1 maja 2026

Aktualizacje rekordów badań

Ostatnia wysłana aktualizacja (Rzeczywisty)

1 maja 2026

Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości

24 kwietnia 2026

Ostatnia weryfikacja

1 kwietnia 2026

Więcej informacji

Terminy związane z tym badaniem

Plan dla danych uczestnika indywidualnego (IPD)

Planujesz udostępniać dane poszczególnych uczestników (IPD)?

NIE

Informacje o lekach i urządzeniach, dokumenty badawcze

Bada produkt leczniczy regulowany przez amerykańską FDA

Nie

Bada produkt urządzenia regulowany przez amerykańską FDA

Nie

Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .

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