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Adaptive Adjuvant Therapy After Neoadjuvant Therapy and Gastrectomy for Gastric or Gastroesophageal Junction Adenocarcinoma

Efficacy and Safety of Postoperative Adaptive Adjuvant Therapy After Neoadjuvant Therapy and Radical Gastrectomy for Gastric or Gastroesophageal Junction Adenocarcinoma: A Prospective, Multicenter, Open-Label Clinical Trial

The goal of this clinical trial is to evaluate postoperative adaptive adjuvant therapy in patients with gastric or gastroesophageal junction adenocarcinoma after neoadjuvant chemotherapy plus immunotherapy and radical gastrectomy.The main questions it aims to answer are:

  1. In patients with poor pathological response, does switching to a alternative postoperative treatment regimen improve survival?
  2. In patients with complete pathological response, can observation without routine postoperative treatment maintain favorable survival outcomes? Participants will be assigned to different cohorts according to their pathological response after surgery and will be followed regularly for recurrence, survival, and treatment-related side effects.

研究概览

详细说明

This prospective clinical trial will enroll patients with gastric or gastroesophageal junction adenocarcinoma who have received neoadjuvant chemotherapy plus immunotherapy followed by radical gastrectomy. Participants will be assigned to predefined cohorts according to postoperative pathological response and pathological stage.

Patients with poor pathological response, defined as TRG 3 and ypT3-4N2-3M0 disease, will be evaluated to determine whether switching to a alternative postoperative treatment regimen improves survival and remains safe compared with continuing the original treatment regimen. For patients with complete pathological response, defined as TRG 0 and ypT0N0M0 disease, will be evaluated to determine whether observation without routine postoperative treatment maintain favorable survival outcomes.

The study aims to assess whether postoperative treatment can be adapted according to pathological response after neoadjuvant therapy, rather than applying the same postoperative treatment strategy to all patients. The results may help develop more individualized postoperative management strategies for patients at very high or very low risk of recurrence after neoadjuvant therapy and radical surgery.

研究类型

介入性

注册 (估计的)

405

阶段

  • 阶段2
  • 第三阶段

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

  • 姓名:Liying Zhao, M.D., Ph.D
  • 电话号码:13430396746
  • 邮箱:zlyblue11@163.com

学习地点

    • Guangdong
      • Guangzhou、Guangdong、中国
        • Nanfang Hospital, Southern Medical University
        • 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

Key Inclusion Criteria:

  1. Voluntarily signed written informed consent.
  2. Aged 18 to 75 years, inclusive, regardless of sex.
  3. Underwent radical gastrectomy with D2 or more extended lymphadenectomy and achieved R0 resection. Surgical approaches may include open or laparoscopic surgery.
  4. Histopathologically confirmed gastric or gastroesophageal junction adenocarcinoma.
  5. Received preoperative neoadjuvant immunotherapy combined with chemotherapy, including oxaliplatin plus fluoropyrimidine-based chemotherapy. Immunotherapy may include anti-PD-1 monoclonal antibodies, anti-PD-L1 monoclonal antibodies, PD-1/CTLA-4 bispecific antibodies, and other immune checkpoint inhibitors.
  6. Eligible for one of the following predefined cohorts:

    • Cohort 1: TRG grade 3 and postoperative pathological stage ypT3-4N2-3M0.
    • Cohort 2: TRG grade 0 and postoperative pathological stage ypT0N0M0.
  7. ECOG performance status of 0 or 1.
  8. No evidence of metastasis or recurrence on postoperative imaging before enrollment.
  9. Adequate organ function, defined as hematologic, hepatic, renal, and thyroid function meeting the protocol-specified criteria based on laboratory tests performed within 14 days before randomization.
  10. Willing and able to comply with the study treatment, scheduled visits, laboratory tests, and other study procedures.
  11. Female participants of childbearing potential must have a negative pregnancy test before enrollment and agree to use effective contraception during the study and for 6 months after the last dose of study treatment. Male participants with female partners of childbearing potential must agree to use effective contraception during the study and for 6 months after the last dose of study treatment.

Key Exclusion Criteria:

  1. Presence of liver, peritoneal, or other distant metastases.
  2. Inability to take oral medications.
  3. Unresolved postoperative complications at the time of randomization, such as postoperative infection, anastomotic leakage or wound dehiscence, gastrointestinal bleeding, pancreatic fistula, or intestinal obstruction.
  4. Uncontrolled pericardial effusion, uncontrolled pleural effusion, or clinically significant moderate or greater ascites at screening, defined as any of the following: pleural effusion or ascites with clinical symptoms and detectable by physical examination; or pleural effusion or ascites requiring drainage and/or intracavitary treatment during screening.
  5. Underwent any surgery requiring general anesthesia that was not related to gastric cancer within 28 days before randomization.
  6. History of or current diagnosis of another malignancy within 5 years.
  7. Active or prior autoimmune disease that may relapse or require immunosuppressive treatment within 2 weeks or during the study period; or a history of immunodeficiency, including HIV positivity or other acquired or congenital immunodeficiency disease; or a history of organ transplantation.
  8. Participation in another clinical study, or any condition that may interfere with the interpretation of the study results.
  9. Any other severe acute or chronic disease that, in the investigator's judgment, may increase the risk associated with study participation or study treatment.
  10. Active or uncontrolled infection requiring systemic antibiotic therapy within 2 weeks before randomization or at the time of randomization.
  11. Diagnosis of interstitial pneumonia, noninfectious pneumonitis, pulmonary fibrosis, or acute lung disease.
  12. Active tuberculosis within 1 year or previous anti-tuberculosis treatment.
  13. Female participants who are pregnant, breastfeeding, or planning to become pregnant during treatment or within 6 months after the end of treatment.
  14. History of psychotropic drug abuse with inability to discontinue, or presence of a psychiatric disorder.
  15. Patients considered unsuitable for participation in this study by the investigator.

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:Cohort 1 Experimental Arm
Participants randomized to the cohort 1 experimental arm will switch to an alternative postoperative treatment regimen. The alternative regimen will be selected by the investigator based on the participant's preoperative treatment regimen, postoperative molecular subtype, and the 2025 CSCO and 2025 NCCN guidelines. The regimen should include taxane-based or irinotecan-based monotherapy or combination therapy that was not used before surgery. The administration schedule and dosage of adjuvant therapy will follow standard clinical practice guidelines and the relevant drug prescribing information.
Participants in this arm will switch to an alternative postoperative treatment regimen selected by the investigator according to prior neoadjuvant therapy, postoperative molecular subtype, and the 2025 CSCO and NCCN guidelines. The regimen will include taxane-based or irinotecan-based treatment that was not used before surgery, with dosage and administration based on clinical practice standards and drug prescribing information.
有源比较器:Cohort 1 Control Arm
Participants randomized to the Cohort 1 control arm will continue treatment according to the preoperative treatment regimen. The administration schedule and dosage of adjuvant therapy will follow standard clinical practice guidelines and the relevant drug prescribing information.
The original preoperative treatment regimen will be continued postoperatively. The administration schedule and dosage of adjuvant therapy will follow standard clinical practice guidelines and the relevant drug prescribing information.
实验性的:Cohort 2
Participants in Cohort 2 will undergo postoperative observation without routine antitumor drug therapy. They will receive regular follow-up monitoring according to the study protocol.
Participants will undergo postoperative observation without further antitumor drug therapy. Routine follow-up monitoring will be conducted according to the study protocol.

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
Median Event-Free Survival in Cohort 1(mEFS)
大体时间:Up to approximately 13 months
defined as the time from randomization to the first documented local, regional, or distant recurrence, or death from any cause, whichever occurs first.
Up to approximately 13 months
2-year Event-Free Survival Rate in Cohort 2(2-y EFS)
大体时间:Up to 2 years
defined as the proportion of participants in Cohort 2 who are alive without documented local, regional, or distant recurrence at 2 years after cohort assignment.
Up to 2 years

次要结果测量

结果测量
措施说明
大体时间
1-year Event-Free Survival Rate in Cohort 1(1-y EFS)
大体时间:Up to 1 year
defined as the proportion of participants in Cohort 1 who are alive without documented local, regional, or distant recurrence at 1 year after randomization.
Up to 1 year
1-Year Overall Survival Rate in Cohort 1(1-y OS)
大体时间:Up to 1 year
defined as the proportion of participants in Cohort 1 who are alive at 1 year after randomization.
Up to 1 year
Median Overall Survival in Cohort 1(mOS)
大体时间:Up to approximately 3 years
defined as the time from randomization to death from any cause. Median overall survival will be evaluated in participants in Cohort 1.
Up to approximately 3 years
2-Year Overall Survival Rate in Cohort 2(2-y OS)
大体时间:Up to 2 years
defined as the proportion of participants in Cohort 2 who are alive at 2 years after cohort assignment.
Up to 2 years
3-year Event-Free Survival Rate in Cohort 2(3-y EFS)
大体时间:Up to 3 years
defined as the proportion of participants in Cohort 2 who are alive without documented local, regional, or distant recurrence at 3 years after cohort assignment.
Up to 3 years
3-year Overall Survival Rate in Cohort 2(3-y OS)
大体时间:Up to 3 years
defined as the proportion of participants in Cohort 2 who are alive at 3 years after cohort assignment.
Up to 3 years
Incidence and Severity of Adverse Events
大体时间:Up to approximately 3 years
The incidence and severity of adverse events will be assessed according to NCI CTCAE version 5.0. Safety assessments will include adverse events, serious adverse events, vital signs, ECOG performance status, physical examination, electrocardiogram, echocardiography, and clinically significant changes from baseline in laboratory test results.
Up to approximately 3 years

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6月1日

初级完成 (估计的)

2029年8月1日

研究完成 (估计的)

2029年12月1日

研究注册日期

首次提交

2026年5月18日

首先提交符合 QC 标准的

2026年5月18日

首次发布 (实际的)

2026年5月22日

研究记录更新

最后更新发布 (实际的)

2026年5月22日

上次提交的符合 QC 标准的更新

2026年5月18日

最后验证

2026年5月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

未定

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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