EGFR-TKIs Plus PD-1 in EGFR-Mutant Advanced NSCLC
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
Přehled studie
Postavení
Postavení
Podmínky
Podmínky
Intervence / Léčba
Intervence / Léčba
Detailní popis
Typ studie
Typ studie
Zápis (Odhadovaný)
Zápis
Fáze
Fáze
- Fáze 2
Kontakty a umístění
Studijní místa
-
-
Guangdong
-
Guangzhou, Guangdong, Čína
- Nábor
- Southern Medical University Nanfang Hospital Department of Oncology
-
Kontakt:
- Professor Wang
- Telefonní číslo: +86 20 87150
- E-mail: doc_wang@163.com
-
-
Kritéria účasti
Kritéria způsobilosti
Kritéria způsobilosti
Věk způsobilý ke studiu
- Dospělý
- Starší dospělý
Přijímá zdravé dobrovolníky
Popis
Inclusion Criteria:
- 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);
- Male or female patients aged ≥ 18 years;
- 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);
- Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1;
- At least one measurable or non-measurable but evaluable lesion according to RECIST version 1.1;
- Adequate organ function;
- Female or male patients of childbearing potential must agree to use highly effective contraceptive measures throughout the study period;
- Willing and able to comply with scheduled visits, treatment plans, laboratory tests, and other study requirements as specified in the visit schedule.
Exclusion Criteria:
- Patients who are ineligible for standard anti-tumor therapy according to routine clinical practice;
- Prior treatment with anti-PD-1/PD-L1 immunotherapy;
- Concurrent enrollment in another clinical study;
- Known history of allogeneic organ transplantation or allogeneic hematopoietic stem cell transplantation;
- Receipt of systemic corticosteroids or other immunosuppressive therapy within 2 weeks prior to the first dose of study drug;
- 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;
- Presence of brainstem, leptomeningeal, spinal cord metastasis, or spinal cord compression;
- Presence of uncontrolled concomitant diseases, including but not limited to decompensated cirrhosis, nephrotic syndrome, uncontrolled metabolic disorders, etc.;
- 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;
- Presence of severe uncontrolled cardiovascular disease;
- Interstitial lung disease (ILD) (including pulmonary fibrosis or radiation pneumonitis) requiring corticosteroid therapy, or current ILD/non-infectious pneumonitis;
- Concomitant pulmonary disease resulting in clinically severe impairment of respiratory function;
- Chronic autoimmune disease or inflammatory disease requiring systemic therapy or receiving systemic therapy within 2 years prior to the first dose;
- Active or history of documented inflammatory bowel disease (e.g., Crohn's disease, ulcerative colitis, or chronic diarrhea), intestinal obstruction, or extensive bowel resection;
- Diagnosis of Gilbert's syndrome;
- Severe infection within 4 weeks prior to the first dose, including but not limited to complications requiring hospitalization, sepsis, or severe pneumonia;
- Known active pulmonary tuberculosis;
- Known active syphilis infection;
- Known history of immunodeficiency, or positive test for human immunodeficiency virus (HIV) antibody;
- Presence of active hepatitis B virus (HBV) or hepatitis C virus (HCV) infection;
- 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;
- Women who are pregnant, breastfeeding, or planning to become pregnant or breastfeed during the study period;
- 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.
Studijní plán
Jak je studie koncipována?
Detaily designu
- Primární účel: Léčba
- Přidělení: N/A
- Intervenční model: Přiřazení jedné skupiny
- Maskování: Žádné (otevřený štítek)
Počet zbraní
Zbraně a zásahy
Skupina účastníků / ArmSkupina účastníků / Arm |
Intervence / LéčbaIntervence / Léčba |
|---|---|
|
Experimentální: 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 je měření studie?
Primární výstupní opatření
Primární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
|
Median Progression-free survival
Časové okno: 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
|
Sekundární výstupní opatření
Sekundární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
|
objective response rate
Časové okno: 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
Časové okno: 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
Časové okno: 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.
Časové okno: 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.
|
Spolupracovníci a vyšetřovatelé
Sponzor
Sponzor
Termíny studijních záznamů
Hlavní termíny studia
Začátek studia (Aktuální)
Začátek studia
Primární dokončení (Odhadovaný)
Primární dokončení
Dokončení studie (Odhadovaný)
Dokončení studie
Termíny zápisu do studia
První předloženo
První předloženo
První předloženo, které splnilo kritéria kontroly kvality
První předloženo, které splnilo kritéria kontroly kvality
První zveřejněno (Aktuální)
První zveřejněno
Aktualizace studijních záznamů
Poslední zveřejněná aktualizace (Aktuální)
Poslední zveřejněná aktualizace
Odeslaná poslední aktualizace, která splnila kritéria kontroly kvality
Odeslaná poslední aktualizace, která splnila kritéria kontroly kvality
Naposledy ověřeno
Naposledy ověřeno
Více informací
Termíny související s touto studií
Další relevantní podmínky MeSH
Další identifikační čísla studie
Další identifikační čísla studie
- NFEC-2026-076
Plán pro data jednotlivých účastníků (IPD)
Plánujete sdílet data jednotlivých účastníků (IPD)?
Informace o lécích a zařízeních, studijní dokumenty
Studuje lékový produkt regulovaný americkým FDA
Studuje produkt zařízení regulovaný americkým úřadem FDA
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 .