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- Ensaio Clínico NCT07637448
EGFR-TKIs Plus PD-1 in EGFR-Mutant Advanced NSCLC
4 de junho de 2026 atualizado por: 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.
Visão geral do estudo
Status
Recrutamento
Condições
Intervenção / Tratamento
Descrição detalhada
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.
Tipo de estudo
Intervencional
Inscrição (Estimado)
32
Estágio
- Fase 2
Contactos e Locais
Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.
Locais de estudo
-
-
Guangdong
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Guangzhou, Guangdong, China
- Recrutamento
- Southern Medical University Nanfang Hospital Department of Oncology
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Contato:
- Professor Wang
- Número de telefone: +86 20 87150
- E-mail: doc_wang@163.com
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-
Critérios de participação
Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.
Critérios de elegibilidade
Idades elegíveis para estudo
- Adulto
- Adulto mais velho
Aceita Voluntários Saudáveis
Não
Descrição
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.
Plano de estudo
Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.
Como o estudo é projetado?
Detalhes do projeto
- Finalidade Principal: Tratamento
- Alocação: N / D
- Modelo Intervencional: Atribuição de grupo único
- Mascaramento: Nenhum (rótulo aberto)
Armas e Intervenções
Grupo de Participantes / Braço |
Intervenção / Tratamento |
|---|---|
|
Experimental: 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
|
O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Median Progression-free survival
Prazo: 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
|
Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
objective response rate
Prazo: 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.
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through study completion, an average of 3 years.
|
|
Disease Control Rate
Prazo: 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.
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through study completion, an average of 3 years.
|
|
Median Overall Survival
Prazo: 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.
Prazo: 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.
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through study completion, an average of 3 years.
|
Colaboradores e Investigadores
É aqui que você encontrará pessoas e organizações envolvidas com este estudo.
Patrocinador
Datas de registro do estudo
Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.
Datas Principais do Estudo
Início do estudo (Real)
21 de maio de 2026
Conclusão Primária (Estimado)
1 de março de 2029
Conclusão do estudo (Estimado)
1 de março de 2030
Datas de inscrição no estudo
Enviado pela primeira vez
28 de maio de 2026
Enviado pela primeira vez que atendeu aos critérios de CQ
4 de junho de 2026
Primeira postagem (Real)
9 de junho de 2026
Atualizações de registro de estudo
Última Atualização Postada (Real)
9 de junho de 2026
Última atualização enviada que atendeu aos critérios de controle de qualidade
4 de junho de 2026
Última verificação
1 de junho de 2026
Mais Informações
Termos relacionados a este estudo
Termos MeSH relevantes adicionais
Outros números de identificação do estudo
- NFEC-2026-076
Plano para dados de participantes individuais (IPD)
Planeja compartilhar dados de participantes individuais (IPD)?
NÃO
Informações sobre medicamentos e dispositivos, documentos de estudo
Estuda um medicamento regulamentado pela FDA dos EUA
Não
Estuda um produto de dispositivo regulamentado pela FDA dos EUA
Não
Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .