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

2026년 6월 4일 업데이트: 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.

연구 개요

상세 설명

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.

연구 유형

중재적

등록 (추정된)

32

단계

  • 2 단계

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 장소

    • Guangdong
      • Guangzhou, Guangdong, 중국
        • 모병
        • Southern Medical University Nanfang Hospital Department of Oncology
        • 연락하다:

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

  • 성인
  • 고령자

건강한 자원 봉사자를 받아들입니다

아니

설명

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.

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 치료
  • 할당: 해당 없음
  • 중재 모델: 단일 그룹 할당
  • 마스킹: 없음(오픈 라벨)

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: 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

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Median Progression-free survival
기간: 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

2차 결과 측정

결과 측정
측정값 설명
기간
objective response rate
기간: 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
기간: 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
기간: 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.
기간: 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.

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (실제)

2026년 5월 21일

기본 완료 (추정된)

2029년 3월 1일

연구 완료 (추정된)

2030년 3월 1일

연구 등록 날짜

최초 제출

2026년 5월 28일

QC 기준을 충족하는 최초 제출

2026년 6월 4일

처음 게시됨 (실제)

2026년 6월 9일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 6월 9일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 6월 4일

마지막으로 확인됨

2026년 6월 1일

추가 정보

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약물 및 장치 정보, 연구 문서

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아니

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .

EGFR 활성화 돌연변이에 대한 임상 시험

EGFR-TKIs Combined with PD-1 Monoclonal Antibody에 대한 임상 시험

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