- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT07565532
Establishment of a Prospective Clinical Cohort of Small Cell Lung Cancer Patients Receiving Radiotherapy-Involved Comprehensive Treatment
연구 개요
상태
연구 유형
등록 (추정된)
연락처 및 위치
연구 연락처
- 이름: Xuwei Cai, Ph.D
- 전화번호: 02122200000
- 이메일: birdhome2000@163.com
연구 장소
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Shanghai Municipality
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Shanghai, Shanghai Municipality, 중국, 200030
- 모병
- Shanghai Chest Hospital
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연락하다:
- Xuwei Cai, Ph.D
- 전화번호: 86+021-22200000
- 이메일: chestgcp@126.com
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참여기준
자격 기준
공부할 수 있는 나이
- 성인
- 고령자
건강한 자원 봉사자를 받아들입니다
샘플링 방법
연구 인구
설명
Inclusion Criteria:
Inclusion Criteria for Limited-Stage Small Cell Lung Cancer (LS-SCLC):
1. Voluntary signed informed consent according to clinical routine practice. 2. Histologically and radiologically confirmed, previously untreated limited-stage SCLC (according to the Veterans Administration Lung Study Group staging system).
3. Age ≥ 18 years. 4. Life expectancy ≥ 8 weeks. 5. Eastern Cooperative Oncology Group performance status (ECOG PS) of 0 or 1. 6. At least one documented efficacy assessment. 7. At least one measurable lesion as confirmed by the investigator according to RECIST (iRECIST 2017) criteria.
8. Adequate organ and bone marrow function, with laboratory tests performed within 7 days prior to the first dose meeting the following criteria (without receiving any blood components, hematopoietic growth factors, albumin, or other corrective therapies considered by the investigator within 14 days prior to laboratory assessments):
- Hematology: Hemoglobin (Hb) ≥ 90 g/L, absolute neutrophil count (ANC) ≥ 1.5 × 10⁹/L, platelet count (PLT) ≥ 90 × 10⁹/L.
- Biochemistry: Serum creatinine (Cr) ≤ 1.5 × upper limit of normal (ULN); serum total bilirubin (TBIL) ≤ 1.5 × ULN; alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤ 3.0 × ULN in patients without liver metastases, or ≤ 5.0 × ULN in patients with liver metastases; serum albumin (ALB) ≥ 25 g/L.
- Coagulation: International normalized ratio (INR) ≤ 1.5 × ULN; prothrombin time (PT) and activated partial thromboplastin time (APTT) ≤ 1.5 × ULN (for patients receiving prophylactic anticoagulation, the INR and APTT values should be judged by the treating physician or investigator to be within a safe and effective therapeutic range).
9. Pulmonary function test showing FEV₁ > 0.75 L. 10. No evidence of severe interstitial lung disease confirmed by CT or PET/CT prior to treatment.
11. No prior or concurrent primary malignancy at other sites. 12. No requirement for PD-L1 expression level.
Inclusion Criteria for Extensive-Stage Small Cell Lung Cancer (ES-SCLC):
1. Voluntary signed informed consent according to clinical routine practice. 2. Histologically confirmed SCLC with complete staging workup showing extensive-stage disease (according to the Veterans Administration Lung Study Group staging system).
3. Age ≥ 18 years. 4. Life expectancy ≥ 8 weeks. 5. At least one documented efficacy assessment. 6. Eastern Cooperative Oncology Group performance status (ECOG PS) of 0-2. 7. Adequate organ and bone marrow function, with laboratory tests performed within 7 days prior to the first dose meeting the following criteria (without receiving any blood components, hematopoietic growth factors, albumin, or other corrective therapies considered by the investigator within 14 days prior to laboratory assessments):
- Hematology: Hemoglobin (Hb) ≥ 90 g/L, absolute neutrophil count (ANC) ≥ 1.5 × 10⁹/L, platelet count (PLT) ≥ 90 × 10⁹/L.
- Biochemistry: Serum creatinine (Cr) ≤ 1.5 × upper limit of normal (ULN); serum total bilirubin (TBIL) ≤ 1.5 × ULN; alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤ 3.0 × ULN in patients without liver metastases, or ≤ 5.0 × ULN in patients with liver metastases; serum albumin (ALB) ≥ 25 g/L.
- Coagulation: International normalized ratio (INR) ≤ 1.5 × ULN; prothrombin time (PT) and activated partial thromboplastin time (APTT) ≤ 1.5 × ULN (for patients receiving prophylactic anticoagulation, the INR and APTT values should be judged by the treating physician or investigator to be within a safe and effective therapeutic range).
8. No severe concurrent medical illness. 9. Forced expiratory volume in one second (FEV₁) > 0.75 L. 10. For patients with prior radiotherapy to the primary lesion, the current radiotherapy target is limited to metastatic lesions.
11. No prior or concurrent primary malignancy at other sites. 12. No requirement for PD-L1 expression level. 13. For patients with limited-stage SCLC who previously received curative-intent treatment, upon recurrence or metastasis, if complete staging workup is available and this is their first use of immunotherapy, they may still be considered for inclusion in the extensive-stage cohort.
Exclusion Criteria:
Exclusion Criteria for Limited-Stage Small Cell Lung Cancer (LS-SCLC):
- Histologically confirmed non-small cell lung cancer (NSCLC).
- No efficacy assessment record, or missing efficacy assessment data.
- Presence of other primary malignancies; history of allogeneic organ transplantation.
- Major surgery (excluding diagnostic biopsy) within 4 weeks prior to the first dose.
- History of substance abuse (e.g., drug addiction), long-term alcoholism, or AIDS or HIV carrier.
- Active autoimmune disease, or history of autoimmune disease with potential for relapse.
- Current systemic corticosteroid therapy (e.g., equivalent to >10 mg prednisone daily) or use of any other form of immunosuppressive therapy within 14 days prior to the first dose.
- Prior treatment with any antibody/drug targeting T-cell co-regulatory proteins (immune checkpoints), including but not limited to PD-1, PD-L1, CTLA-4, TIM-3, and LAG-3.
- Interstitial lung disease (ILD) or history of ILD requiring corticosteroid therapy.
- History of idiopathic pulmonary fibrosis (IPF), drug-induced pneumonitis, organizing pneumonia (e.g., bronchiolitis obliterans), idiopathic pneumonia, or evidence of active pneumonitis on screening chest CT.
- Receipt of live vaccine within 28 days prior to the first dose of study drug.
- Any other disease or condition that contraindicates chemoradiotherapy, including but not limited to active infection, within 6 months post-myocardial infarction, symptomatic heart disease (including unstable angina, congestive heart failure, or uncontrolled arrhythmias), and immunosuppressive therapy.
- Unresolved toxicity of Grade 2 or higher (according to CTCAE version 5.0).
- Pregnant or breastfeeding women; men or women of childbearing potential who are unwilling to use adequate contraceptive measures.
- Evidence of inherited bleeding diathesis or coagulation disorders.
- Prior history of malignancy (excluding skin cancer, or in situ breast cancer, oral cancer, or cervical cancer with life expectancy >3 years).
Exclusion Criteria for Extensive-Stage Small Cell Lung Cancer (ES-SCLC):
- Pulmonary carcinoid or non-small cell lung cancer, unless transformed SCLC is ruled out.
- No efficacy assessment record, or missing efficacy assessment data.
- History of severe anaphylactic/allergic reaction to humanized antibodies or fusion proteins.
- Acute exacerbation of chronic obstructive pulmonary disease (COPD) or other pulmonary diseases requiring hospitalization.
- Active or prior autoimmune disease (within the past 2 years) or history of primary immunodeficiency.
- Progression after immunotherapy; prior or concurrent diagnosis of any other malignancy, excluding non-melanoma skin cancer or carcinoma in situ of the cervix.
- Any other disease or condition that contraindicates chemoradiotherapy, including but not limited to active infection, within 6 months post-myocardial infarction, symptomatic heart disease (including unstable angina, congestive heart failure, or uncontrolled arrhythmias), or immunosuppressive therapy.
- Unresolved toxicity of Grade 2 or higher (according to CTCAE version 5.0).
- Current or prior history of autoimmune disease or immunodeficiency, including but not limited to myasthenia gravis, myositis, autoimmune hepatitis, systemic lupus erythematosus, and rheumatoid arthritis.
- History of idiopathic pulmonary fibrosis (IPF), organizing pneumonia (e.g., bronchiolitis obliterans), drug-induced pneumonitis, or idiopathic pneumonia; or evidence of active pneumonitis on chest CT scan. Patients with a history of radiation pneumonitis (fibrosis) within the radiation field may be enrolled.
- Pregnant or breastfeeding women; men or women of childbearing potential who are unwilling to use adequate contraceptive measures.
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
코호트 및 개입
그룹/코호트 |
개입 / 치료 |
|---|---|
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SCLC Clinical Cohort
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This is an observation study.
This study adopted different timing of radio-immunotherapy combination, fractionation schedules, radiation doses, irradiation sites, PCI, and various types of immune checkpoint inhibitors.
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연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Progression-free survival (PFS)
기간: up to 12 months after the last participant entry
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The time from the start of study treatment to the first occurrence of disease progression or death from any cause, whichever occurs first.
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up to 12 months after the last participant entry
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Overall Survival (OS)
기간: up to 12 months after the last participant entry
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The time from the start of study treatment to death from any cause or the data cut-off date.
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up to 12 months after the last participant entry
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2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Distant Metastasis-Free Survival
기간: up to 12 months after the last participant entry
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the time from the date of diagnosis to the first occurrence of distant metastasis.
For patients with extensive-stage small cell lung cancer (ES-SCLC) who already have distant metastasis at baseline, DMFS is defined as the time to new distant organ metastasis or new distant lesions.
Patients who have not developed distant metastasis by the last follow-up are censored.
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up to 12 months after the last participant entry
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Locoregional Recurrence-Free Survival (LRFS)
기간: up to 12 months after the last participant entry
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The time from the date of diagnosis to the first locoregional disease progression.
Patients who have not experienced locoregional events by the last follow-up are censored.
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up to 12 months after the last participant entry
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Objective Response Rate (ORR)
기간: up to 12 months after the last participant entry
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The percentage of patients achieving a best overall response of complete response (CR) or partial response (PR) during the study period.
The evaluable population includes patients with baseline imaging and at least one response assessment (or documented record).
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up to 12 months after the last participant entry
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Disease Control Rate (DCR)
기간: up to 12 months after the last participant entry
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The percentage of patients achieving a best overall response of CR, PR, or stable disease (SD).
The evaluable population includes patients with baseline imaging and at least one response assessment (or documented record).
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up to 12 months after the last participant entry
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Local Control Rate (LCR)
기간: up to 12 months after the last participant entry
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The start of radiotherapy to the first objective progression within the irradiated target volume, or death, or the last follow-up date.
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up to 12 months after the last participant entry
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기타 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Exploratory Endpoint
기간: up to 12 months after the last participant entry
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Correlation of tumor biomarkers (PD-L1, TMB, ctDNA) and peripheral blood inflammatory/immune indices (NLR, PLR, LMR, CRP, LDH, lymphocyte subsets) with antitumor activity (ORR/DCR) and survival (OS, PFS, DMFS, LRFS).
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up to 12 months after the last participant entry
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공동 작업자 및 조사자
연구 기록 날짜
연구 주요 날짜
연구 시작 (실제)
기본 완료 (추정된)
연구 완료 (추정된)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (실제)
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 연구와 관련된 용어
추가 관련 MeSH 약관
기타 연구 ID 번호
- IS26056
개별 참가자 데이터(IPD) 계획
개별 참가자 데이터(IPD)를 공유할 계획입니까?
약물 및 장치 정보, 연구 문서
미국 FDA 규제 의약품 연구
미국 FDA 규제 기기 제품 연구
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