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A Multicenter, Open-label, Randomized, Prospective Clinical Study of Adebrelimab Consolidation Therapy for Limited-Stage Small-Cell Lung Cancer (LS-SCLC) Without Progression After Concurrent Chemoradiotherapy (ARL-LS-SCLC)

2026年7月17日 更新者:Qiming Wang、Henan Cancer Hospital
This study aims to evaluate the efficacy and safety of adebrelimab consolidation therapy after progression-free response of concurrent chemoradiotherapy in patients with limited-stage small cell lung cancer. This study plans to enroll patients with untreated limited-stage small cell lung cancer who meet the inclusion criteria. The eligible patients will be randomly divided 1:1 into two groups to receive treatment regimens for residual lymph nodes and involved irradiated areas. That is, carboplatin AUC 5, D1 + etoposide 100 mg/m…^2 on days 1, 2, and 3 + thoracic radiotherapy (residual lymph nodes or involved irradiated areas), with each 3-week cycle. After 4 cycles of concurrent chemoradiotherapy, the non-progressing subjects will continue to receive adebrelimab (1200 mg, IV, Q3W) maintenance therapy.

研究概览

研究类型

介入性

注册 (估计的)

200

阶段

  • 阶段2

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

学习地点

    • Henan
      • Zhengzhou、Henan、中国、450000
        • 招聘中
        • Henan Cancer Hospital
        • 接触:
      • Zhengzhou、Henan、中国、450000
        • 尚未招聘
        • Henan Cancer Hospital
        • 接触:

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 成人
  • 年长者

接受健康志愿者

不

描述

Inclusion Criteria:

1.Age ≥ 18 and ≤ 75 years, regardless of gender. 2.Histopathologically confirmed, untreated limited-stage small cell lung cancer (LS-SCLC) (stage I-III per AJCC 8th edition, with all lesions encompassed in a tolerable radiation plan).

3.Clinically staged T1-2N0, operable LS-SCLC patients who are ineligible for surgery or refuse surgery.

4.ECOG performance status 0-1. 5.Expected survival ≥ 3 months. 6.At least one measurable lesion per RECIST 1.1. 7.Pulmonary function: FEV1 > 70% of predicted value. 8.Adequate hematologic and end-organ function, with laboratory results obtained within 7 days before first study treatment:

  1. Hematology: Absolute neutrophil count (ANC) ≥ 1.5×10⁹/L without G-CSF support within 14 days before first treatment; lymphocyte count (LC) ≥ 0.5×10⁹/L; platelet count (PLT) ≥ 90×10⁹/L without transfusion, G-CSF, or other hematopoietic stimulants within 14 days before first treatment.
  2. Hepatic function: Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 3 × ULN; total bilirubin (TBIL) ≤ 1.5 × ULN (≤3.0 mg/dL for patients with confirmed Gilbert syndrome).
  3. Renal function: Serum creatinine ≤ 1.5 × ULN or creatinine clearance (CrCl) ≥ 50 mL/min (calculated by Cockcroft-Gault, CKD-EPI, or MDRD equation); urine protein < 2+ (if urine protein ≥ 2+, 24-hour urine protein must be < 1 g for eligibility).
  4. Coagulation: International normalized ratio (INR) ≤ 1.5; activated partial thromboplastin time (APTT) ≤ 1.5 × ULN.
  5. Echocardiography: Left ventricular ejection fraction (LVEF) ≥ 50%. 9.Sexually active subjects of reproductive potential (non-sterilized) must agree to use at least one medically accepted contraceptive method during study treatment and for 6 months after treatment completion. For females of reproductive potential: serum pregnancy test (HCG) must be negative within 7 days before first dosing.

10.Subjects are voluntarily enrolled, provide written informed consent, have good compliance, and agree to follow-up.

Exclusion Criteria:

  1. Histologically confirmed combined small cell lung cancer (SCLC) or non-small cell lung cancer (NSCLC).
  2. Prior systemic anti-tumor therapy or immune checkpoint inhibitor therapy for SCLC.
  3. Extensive-stage SCLC.
  4. Presence of malignant pleural effusion. If aspiratable pleural effusion is present during screening, at least one thoracentesis must be performed to confirm the presence or absence of malignant cells.
  5. Subjects with known or suspected interstitial lung disease (ILD); other moderate-to-severe pulmonary diseases that may interfere with the detection or management of drug-related pulmonary toxicity and severely impair respiratory function, including but not limited to idiopathic pulmonary fibrosis, organizing pneumonia/bronchiolitis obliterans, etc.
  6. History of active, known or suspected autoimmune disease, including but not limited to myasthenia gravis, autoimmune hepatitis, systemic lupus erythematosus, rheumatoid arthritis, inflammatory bowel disease, etc.

    (Exceptions: Type 1 diabetes mellitus (glycemic control with insulin); residual hypothyroidism due to autoimmune thyroiditis requiring only hormone replacement therapy; conditions not expected to relapse in the absence of external trigger.

    Patients with eczema, psoriasis, lichen simplex chronicus, or vitiligo only (excluding psoriatic arthritis) may be enrolled if: rash involves <10% of body surface area; disease is well controlled at baseline with only low-potency topical steroids; and no acute exacerbation in the past 12 months (no PUVA, methotrexate, retinoids, biologics, oral calcineurin inhibitors, high-potency or oral steroids).)

  7. Concomitant malignancy diagnosed ≤3 years before first study treatment, except adequately treated papillary thyroid carcinoma, cervical carcinoma in situ, basal or squamous cell skin cancer, locally controlled prostate cancer after radical surgery, ductal carcinoma in situ after radical surgery (hormonal therapy for non-metastatic prostate or breast cancer is allowed).
  8. History of clinically significant cardiovascular disease, including but not limited to:

    Congestive heart failure (NYHA class >2); Unstable angina; Myocardial infarction within 3 months before signing ICF; Any severe supraventricular or ventricular arrhythmia requiring treatment or intervention.

  9. Severe infection within 4 weeks before first treatment, including but not limited to bacteremia requiring hospitalization, severe pneumonia, etc.; active infection of CTCAE grade ≥2 requiring systemic antibiotics within 2 weeks before first treatment.
  10. Active tuberculosis within 1 year before enrollment by history or CT scan, or history of active tuberculosis >1 year ago without standard treatment.
  11. History of immunodeficiency, including positive HIV serology.
  12. Active hepatitis B or hepatitis C.(HBsAg-positive or HBcAb-positive subjects may be enrolled if HBV DNA < upper limit of normal (ULN) of the local laboratory (if no ULN, HBV DNA <1000 copies/mL or 500 IU/mL); HCV Ab-positive subjects may be enrolled if HCV RNA < ULN of the local laboratory (if no ULN, HCV RNA <500 IU/mL).)
  13. Receipt of systemic immunosuppressive therapy within 14 days before first treatment, including but not limited to corticosteroids, cyclophosphamide, azathioprine, methotrexate, thalidomide, and anti-TNF agents.

(1)Patients receiving short-term systemic immunosuppression (e.g., corticosteroids for management/prophylaxis of nausea, vomiting, or hypersensitivity) may be enrolled at the investigator's discretion; a washout period before randomization may be required.

(2)Allowed: inhaled corticosteroids for COPD; mineralocorticoids (e.g., fludrocortisone) for orthostatic hypotension; low-dose corticosteroid replacement (≤10 mg/day prednisone or equivalent) for adrenal insufficiency.

14.Major surgery within 28 days before first treatment (except diagnostic surgery), or expected major surgery during the study (except diagnostic surgery).

15.Administration of live attenuated vaccine within 28 days before first treatment, or anticipated need during the study (live attenuated influenza vaccine is prohibited within 28 days before first treatment, during treatment, and for 5 months after the last dose of adebrelimab).

16.Prior allogeneic bone marrow transplant or solid organ transplant. 17.History of severe hypersensitivity to monoclonal antibody/fusion protein drugs.

18.Known psychiatric disorder, alcoholism, drug abuse or substance abuse. 19.Any other condition that, in the investigator's judgment, may prematurely terminate the study, e.g., poor protocol compliance, other severe diseases requiring concurrent treatment, significant laboratory abnormalities, or family/social factors affecting subject safety or data/sample collection.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:Arm A: Employed residual field irradiation
Carboplatin + Etoposide plus thoracic residual-field radiotherapy (employed residual field irradiation,RFI), followed by maintenance therapy with adebrelimab in patients without progressive disease (non-PD)
Carboplatin AUC 5 d1 + Etoposide 100 mg/m² d1-3 + thoracic radiotherapy(employed residual field irradiation, RFI), q3w × 4 cycles. Post-concurrent CCRT, non-PD subjects receive maintenance adebrelimab 1200 mg IV q3w.
实验性的:Arm B:Nodal involved-field radiotherapy group
Carboplatin + Etoposide plus thoracic involved-field radiotherapy (Nodal involved-field radiotherapy group, IFRT), followed by maintenance therapy with adebrelimab in patients without progressive disease
Carboplatin AUC 5 d1 + Etoposide 100 mg/m² d1-3 + thoracic involved-field radiotherapy (IFRT), q3w × 4 cycles. Post-concurrent CCRT, non-PD subjects receive maintenance adebrelimab 1200 mg IV q3w.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
PFS
大体时间:From date of the first treatment to the first documented disease progression, assessed up to 18 months
progression-free survival: Time from the date of initiating concurrent chemoradiotherapy at enrollment to the first occurrence of objective tumor progression after starting maintenance therapy or all-cause death, whichever comes first.
From date of the first treatment to the first documented disease progression, assessed up to 18 months

次要结果测量

结果测量
措施说明
大体时间
L-PFS
大体时间:From date of the first treatment to the first documented disease progression, assessed up to 18 months
local progression-free survival: Time from start of concurrent CCRT to first local progression post-maintenance or all-cause death, whichever occurs first
From date of the first treatment to the first documented disease progression, assessed up to 18 months
M-PFS
大体时间:From date of the first treatment to the first documented disease progression, assessed up to 18 months
Metastasis-Progression Free Survival (M-PFS): Defined as the time from the date of initiating concurrent chemoradiotherapy at enrollment to the first occurrence of objective distant tumor progression after starting maintenance therapy or all-cause death, whichever comes first.
From date of the first treatment to the first documented disease progression, assessed up to 18 months
OS
大体时间:From date of the first treatment to death due to any cause, assessed up to 18 months
Overall Survival (OS): The time from the date of initiating study treatment at enrollment to death from any cause. Subjects who are alive at the time of analysis will be censored at the date of last known alive.
From date of the first treatment to death due to any cause, assessed up to 18 months
DCR
大体时间:From date of the first treatment to18 months
Disease Control Rate (DCR): The proportion of patients with tumor shrinkage or stabilization maintained for a specified duration, including subjects with Complete Response (CR), Partial Response (PR), and Stable Disease (SD).
From date of the first treatment to18 months
DoR
大体时间:from the date of first documented CR or PR to disease progression or death, censored at last evaluable assessment; maximum follow-up of 18 months
Duration of Response (DoR): The time from the date of confirmed CR or PR by imaging to the occurrence of disease progression or death without progression
from the date of first documented CR or PR to disease progression or death, censored at last evaluable assessment; maximum follow-up of 18 months
ORR
大体时间:Confirmed objective response observed within 18 months from start of treatment
Objective Response Rate (ORR): The proportion of subjects with tumor reduction achieving a predefined magnitude and maintained for a specified duration, including those with Complete Response (CR) and Partial Response (PR). Tumor objective response will be assessed using the Response Evaluation Criteria in Solid Tumors (RECIST version 1.1).
Confirmed objective response observed within 18 months from start of treatment
AE
大体时间:From signing of informed consent through 30 days after last dose (or 90 days for serious AEs), assessed at the end of every cycle (each cycle = 21 days)
Incidence of adverse events assessed by CTCAE v5.0
From signing of informed consent through 30 days after last dose (or 90 days for serious AEs), assessed at the end of every cycle (each cycle = 21 days)

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (估计的)

2026年7月17日

初级完成 (估计的)

2029年7月17日

研究完成 (估计的)

2029年7月17日

研究注册日期

首次提交

2026年3月13日

首先提交符合 QC 标准的

2026年4月27日

首次发布 (实际的)

2026年4月30日

研究记录更新

最后更新发布 (实际的)

2026年7月21日

上次提交的符合 QC 标准的更新

2026年7月17日

最后验证

2026年7月1日

更多信息

与本研究相关的术语

其他相关的 MeSH 术语

其他研究编号

  • ARL-LS-SCLC

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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