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EGFR-TKIs Plus PD-1 in EGFR-Mutant Advanced NSCLC

4 czerwca 2026 zaktualizowane przez: Nanfang Hospital, Southern Medical University

A Clinical Study Evaluating the Preliminary Antitumor Activity and Safety of EGFR-TKIs Combined With PD-1 Monoclonal Antibody as First-Line Therapy in Patients With EGFR-Mutant Advanced Non-Small Cell Lung Cancer

This study is an open-label, multicenter, single-arm clinical study.

Przegląd badań

Szczegółowy opis

This open-label, multicenter, single-arm exploratory clinical trial plans to enroll a total of 32 patients: 6 in a safety lead-in phase and the remaining 26 in an expansion phase. Eligible subjects are treatment-naïve patients with locally advanced or metastatic non-small cell lung cancer (NSCLC) harboring EGFR 19del or L858R mutations. All patients receive first-line oral therapy with standard-dose third-generation EGFR-TKIs (osimertinib, aumolertinib, or furmonertinib). Once stable disease is confirmed by two consecutive radiological assessments, sintilimab (200 mg intravenously every three weeks) is added as maintenance treatment until disease progression, unacceptable toxicity, or a maximum treatment duration of two years. The primary endpoint is progression-free survival (PFS). Secondary endpoints include objective response rate (ORR), disease control rate (DCR), overall survival (OS), and adverse events occurring throughout treatment. Exploratory analyses focus on the correlation of serum lipid profiles and the tumor immune microenvironment with the safe treatment window and mechanisms of drug resistance. The trial consists of screening, treatment, safety follow-up, and survival follow-up periods. Tumor imaging evaluations are performed every six weeks during the first 24 weeks of treatment and every nine weeks thereafter.

Typ studiów

Interwencyjne

Zapisy (Szacowany)

32

Faza

  • Faza 2

Kontakty i lokalizacje

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

Lokalizacje studiów

    • Guangdong
      • Guangzhou, Guangdong, Chiny
        • Rekrutacyjny
        • Southern Medical University Nanfang Hospital Department of Oncology
        • Kontakt:

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:

  1. Patients with histologically or cytologically confirmed, previously untreated EGFR-mutant (19del/L858R) locally advanced or metastatic (stage IIIB/IIIC or IV) non-small cell lung cancer (NSCLC), according to the 9th edition of the TNM staging system for lung cancer jointly issued by the International Association for the Study of Lung Cancer (IASLC) and the American Joint Committee on Cancer (AJCC);
  2. Male or female patients aged ≥ 18 years;
  3. Patients who are willing to receive third-generation EGFR-TKI targeted therapy, followed by maintenance therapy with a PD-1 antibody during the stable phase of the disease (defined as no further tumor shrinkage for at least two consecutive assessments based on RECIST v1.1 criteria);
  4. Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1;
  5. At least one measurable or non-measurable but evaluable lesion according to RECIST version 1.1;
  6. Adequate organ function;
  7. Female or male patients of childbearing potential must agree to use highly effective contraceptive measures throughout the study period;
  8. Willing and able to comply with scheduled visits, treatment plans, laboratory tests, and other study requirements as specified in the visit schedule.

Exclusion Criteria:

  1. Patients who are ineligible for standard anti-tumor therapy according to routine clinical practice;
  2. Prior treatment with anti-PD-1/PD-L1 immunotherapy;
  3. Concurrent enrollment in another clinical study;
  4. Known history of allogeneic organ transplantation or allogeneic hematopoietic stem cell transplantation;
  5. Receipt of systemic corticosteroids or other immunosuppressive therapy within 2 weeks prior to the first dose of study drug;
  6. Receipt of any live vaccine within 4 weeks prior to the first dose of study drug, or planned receipt of live vaccine during the study period;
  7. Presence of brainstem, leptomeningeal, spinal cord metastasis, or spinal cord compression;
  8. Presence of uncontrolled concomitant diseases, including but not limited to decompensated cirrhosis, nephrotic syndrome, uncontrolled metabolic disorders, etc.;
  9. History of severe gastrointestinal ulcer, gastrointestinal perforation, fistula or obstruction, intra-abdominal abscess, or acute gastrointestinal bleeding within 6 months prior to the first dose, or other gastrointestinal diseases that, in the investigator's opinion, may predispose to bleeding or perforation;
  10. Presence of severe uncontrolled cardiovascular disease;
  11. Interstitial lung disease (ILD) (including pulmonary fibrosis or radiation pneumonitis) requiring corticosteroid therapy, or current ILD/non-infectious pneumonitis;
  12. Concomitant pulmonary disease resulting in clinically severe impairment of respiratory function;
  13. Chronic autoimmune disease or inflammatory disease requiring systemic therapy or receiving systemic therapy within 2 years prior to the first dose;
  14. Active or history of documented inflammatory bowel disease (e.g., Crohn's disease, ulcerative colitis, or chronic diarrhea), intestinal obstruction, or extensive bowel resection;
  15. Diagnosis of Gilbert's syndrome;
  16. Severe infection within 4 weeks prior to the first dose, including but not limited to complications requiring hospitalization, sepsis, or severe pneumonia;
  17. Known active pulmonary tuberculosis;
  18. Known active syphilis infection;
  19. Known history of immunodeficiency, or positive test for human immunodeficiency virus (HIV) antibody;
  20. Presence of active hepatitis B virus (HBV) or hepatitis C virus (HCV) infection;
  21. Known allergy to any component of any study drug, history of severe allergic reactions (e.g., anaphylactic shock), history of severe hypersensitivity to other monoclonal antibodies or recombinant protein-based substances, or history of severe infusion reactions;
  22. Women who are pregnant, breastfeeding, or planning to become pregnant or breastfeed during the study period;
  23. Any disease, medical condition, organ system dysfunction, or social circumstance (including but not limited to psychiatric illness, substance/alcohol abuse, history of drug abuse, etc.) that, in the investigator's opinion, may interfere with the subject's ability to provide informed consent, adversely affect the subject's cooperation and participation in the study, or confound the interpretation of study results.

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: Nie dotyczy
  • Model interwencyjny: Zadanie dla jednej grupy
  • Maskowanie: Brak (otwarta etykieta)

Broń i interwencje

Grupa uczestników / Arm
Interwencja / Leczenie
Eksperymentalny: EGFR-TKIs Combined with PD-1 Monoclonal Antibody
All patients receive first-line oral therapy with standard-dose third-generation EGFR-TKIs (osimertinib, aumolertinib, or furmonertinib). Once stable disease is confirmed by two consecutive radiological assessments, sintilimab (200 mg intravenously every three weeks) is added as maintenance treatment until disease progression, unacceptable toxicity, or a maximum treatment duration of two years.
EGFR-TKIs Combined with PD-1 Monoclonal Antibody

Co mierzy badanie?

Podstawowe miary wyniku

Miara wyniku
Opis środka
Ramy czasowe
Median Progression-free survival
Ramy czasowe: From date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 48 months
from randomization (or initiation of treatment) to the first occurrence of disease progression or death from any cause.
From date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 48 months

Miary wyników drugorzędnych

Miara wyniku
Opis środka
Ramy czasowe
objective response rate
Ramy czasowe: through study completion, an average of 3 years.
The proportion of patients whose tumor volume reduction meets predefined criteria (Complete Response or Partial Response) and is maintained for a certain period of time.
through study completion, an average of 3 years.
Disease Control Rate
Ramy czasowe: through study completion, an average of 3 years.
The DCR is the percentage of patients achieving CR, PR or SD per RECIST criteria at the first tumor assessment.
through study completion, an average of 3 years.
Median Overall Survival
Ramy czasowe: From date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 48 months
the time from randomization (or initiation of treatment) at which 50% of patients have died.
From date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 48 months
The incidence and severity of treatment-related adverse events (AEs) and serious adverse events (SAEs) assessed according to NCI CTCAE v5.0, as well as laboratory abnormalities.
Ramy czasowe: through study completion, an average of 3 years.
Adverse events were graded according to NCI CTCAE v5.0 and collected from the first dose to 30 days after the last dose. Serious adverse events were collected from the signing of informed consent through the end of the study.
through study completion, an average of 3 years.

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 (Rzeczywisty)

21 maja 2026

Zakończenie podstawowe (Szacowany)

1 marca 2029

Ukończenie studiów (Szacowany)

1 marca 2030

Daty rejestracji na studia

Pierwszy przesłany

28 maja 2026

Pierwszy przesłany, który spełnia kryteria kontroli jakości

4 czerwca 2026

Pierwszy wysłany (Rzeczywisty)

9 czerwca 2026

Aktualizacje rekordów badań

Ostatnia wysłana aktualizacja (Rzeczywisty)

9 czerwca 2026

Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości

4 czerwca 2026

Ostatnia weryfikacja

1 czerwca 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 .

Badania kliniczne na Mutacja aktywująca EGFR

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