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Signatera-Guided De-escalation of Adjuvant Therapy in Resectable Stage II-IVa Gastric/Gastric-Esophageal Cancer (SIGNAL GEC-101)

2026年5月1日 更新者:Natera, Inc.

SIGNAL GEC-101: Signatera-Guided De-escalation of Adjuvant Therapy in Resectable Stage II-IVa Gastric/Gastric-Esophageal Cancer

The goal of this clinical trial is to assess if circulating tumor DNA, as assessed by Signatera tumor-informed MRD assay, can guide de-escalation of adjuvant therapy in patients with resectable Stage II-IVa Gastric/Gastric-Esophageal Cancer. The main question it aims to answer is:

• To demonstrate if 2-year disease-free survival (DFS) among participants with resectable clinical Stage II-IVa gastric/gastro-esophageal cancer who received neoadjuvant D-FLOT and are ctDNA negative after curative intent R0 surgery receiving adjuvant durvalumab monotherapy is non-inferior to standard of care D-FLOT.

Researchers will compare post-operative ctDNA negative participants who are receiving adjuvant durvalumab monotherapy to those who receive standard of care (D-FLOT) to see if they have similar outcomes.

Participants will be asked to:

  • Receive serial ctDNA testing
  • Visit their study doctor per their standard of care visits about every 3 months for first 2 years and then every 6 months for an additional 3 years
  • Answer 5 questionnaires about their well-being

研究概览

详细说明

This is a prospective, open-label, multi-center, ctDNA-guided study with a randomized, non-inferiority component designed to examine clinical outcomes in treatment of gastric/gastric-esophageal cancer. Specifically, a component of the study will evaluate an adjuvant treatment de-escalation strategy for participants with resectable clinical Stage II-IVa gastric/gastric-esophageal cancer who have completed neoadjuvant therapy with durvalumab plus fluorouracil, leucovorin, oxaliplatin, docetaxel (D-FLOT) and R0 curative intent surgery. Concurrently, participants with post-operative ctDNA positive results will receive standard of care (SOC) D-FLOT with blinded serial ctDNA testing.

Following R0 curative intent surgery, participants will be consented for study participation. Eligible participants will undergo treatment assignment based on post-operative MRD status at 5 weeks (+/- 2 weeks), as determined by the Signatera assay.

Participants with negative post-operative circulating tumor DNA (ctDNA) results and no radiographic evidence of disease (within 6 weeks prior to randomization) will be randomized (1:1) to either SOC vs ct-DNA guided treatment. Randomized participants will be stratified according to pathologic (yp) lymph node status and tumor staging (ypT1-3, N0 vs T4 or N+), Combined Positive Score (CPS, CPS ≥ 1 vs CPS <1), and pathological complete response (yes vs no). Assigned adjuvant treatment must start no later than 12 weeks post surgery.

  • Arm A (SOC Arm): Durvalumab for 1 year plus four 2 week cycles of FLOT with unblinded serial ctDNA testing and patient-reported outcomes (PROs) assessments.
  • Arm B (ctDNA-guided Arm): Durvalumab monotherapy for 1 year with unblinded serial ctDNA testing and PROs assessments. Participants who become ctDNA positive up through Cycle 11 Day 1 (C11D1) will receive four 2 week cycles of FLOT added to Durvalumab.

Once adjuvant therapy is completed, all randomized participants will continue with serial ctDNA testing until recurrence and followed for up to 5 years for overall survival (OS), disease-free survival (DFS), metastasis-free survival (MFS) and disease-specific survival (DSS).

Participants with post-operative ctDNA positive results at 5 weeks (+/- 2 weeks) will not be randomized. They will continue on observation and receive SOC D-FLOT with blinded serial ctDNA testing.

研究类型

介入性

注册 (估计的)

1000

阶段

  • 不适用

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

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. Signed and dated informed consent form (ICF) obtained prior to any trial-specific enrollment procedure.
  2. Age is ≥ 18 years-old at the time of ICF signature.
  3. Able to submit adequate archival tumor tissue (eg, 6 to 10 unstained slides at 10 microns (μm) each or 12-19 unstained slides at 5-microns (μm) plus one hematoxylin and eosin slide (see study lab manual) obtained per standard of care procedures for submission to a central laboratory for Signatera testing OR prior commercial Signatera Genome test results.
  4. Histologically confirmed adenocarcinoma of the stomach, esophagus and/or gastroesophageal junction (GEJ), resectable clinical Stage II-IVa per AJCC 9th edition.
  5. Completion of full or modified course (based on Dosing and Modification Guidelines) of neoadjuvant D-FLOT therapy (ie, two 4-week cycles of durvalumab, four 2-week cycles of FLOT) .
  6. Has undergone complete surgical resection of the gastric/GEJ tumor with pathologically confirmed negative margins (R0 resection).
  7. Eligible to receive adjuvant D-FLOT treatment within 12 weeks postoperative per standard of care (SOC) as assessed by the treating clinician.
  8. Known statuses pertaining to randomization stratification factors:

    1. Post neoadjuvant, post-operative (yp) lymph node status and tumor staging (ypT1-3, N0 vs T4 or N+)
    2. Combined Positive Score ( ≥ 1 vs <1)Tumor PD-L1 status confirmed by immunohistochemistry/CPS score.
    3. Post neoadjuvant, post-operative major pathological response (MPR): Yes/No
  9. ECOG performance status 0-1.
  10. No evidence of disease by radiographic imaging.
  11. Must be willing to and able to comply with adjuvant treatment plans based on ctDNA results and other trial-mandated procedures.
  12. Women of child bearing potential must have a confirmed negative pregnancy test within 14 days of enrollment per institutional standards.

Exclusion Criteria:

  1. Histologic presence of adenosquamous cell carcinoma, squamous cell carcinoma, gastrointestinal stromal tumor, or neuroendocrine tumors.
  2. Radiographic evidence of unresectable metastatic disease (ie, IVb).
  3. Presence of peritoneal dissemination.
  4. Any prior therapy (eg, radiation, chemoradiation, chemotherapy) for gastric or gastroesophageal cancer other than neoadjuvant D-FLOT and R0 curative intent surgery.
  5. Known contradiction or hypersensitivity to durvalumab per the prescribing information; known contraindication or hypersensitivity to Fluorouracil, Leucovorin, Oxaliplatin, and Docetaxel or any of the drug excipients.
  6. Known history of active primary immunodeficiency (eg, HIV), other contraindications of immunotherapy or receiving immunosuppressive medication per approved label.
  7. Female participants who are pregnant or breastfeeding.
  8. Concurrent enrollment in another clinical trial unless the study is observational, non-interventional.
  9. Use of any commercial ctDNA or liquid biopsy monitoring outside of the study protocol during the primary 36-month monitoring period.
  10. Concurrent invasive malignancy or a prior invasive malignancy whose treatment was completed within 5 years before ICF signature. Note: Participants with prior or concurrent in situ malignancies are eligible provided that adequate curative treatment is completed prior to enrollment.
  11. Any other concurrent severe and/or uncontrolled medical condition that would, in the Investigator's judgment, cause unacceptable safety risks, contraindicate participant participation in the clinical trial or compromise compliance with the protocol (e.g., chronic pancreatitis, chronic active hepatitis, liver cirrhosis or any other significant liver disease, active untreated or uncontrolled fungal, bacterial or viral infections, active infection requiring systemic antibacterial therapy, etc.)

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:ctDNA Guided (Durvalumab monotherapy for 1 year)
Participants who become ctDNA positive up through C11D1 will receive four 2 week cycles of FLOT added to Durvalumab along with serial ctDNA testing.
Signatera Genome is intended for use as a post-surgical risk stratification tool for patients with resectable clinical Stage II-IVa gastric/gastro-esophageal cancer who are ctDNA negative after R0 curative intent surgery. The test is used to identify patients with no evidence of MRD following definitive surgery.
有源比较器:SOC (Durvalumab for 1 year plus four 2 week cycles of FLOT starting C1D1)
Participants will receive Durvalumab for 1 year plus four 2 week cycles of FLOT starting C1D1 along with serial ctDNA testing.
Signatera Genome is intended for use as a post-surgical risk stratification tool for patients with resectable clinical Stage II-IVa gastric/gastro-esophageal cancer who are ctDNA negative after R0 curative intent surgery. The test is used to identify patients with no evidence of MRD following definitive surgery.

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
Disease Free Survival (DFS)
大体时间:2 years from randomization to the first occurrence of disease recurrence or death from any cause, whichever occurs first
The primary objective of this study is to evaluate if disease free survival (DFS) among patients with resectable clinical stage II-IVa gastric/gastro-esophageal cancer who are ctDNA-negative after surgery undergoing ctDNA-guided observation is non-inferior to adjuvant D-FLOT.
2 years from randomization to the first occurrence of disease recurrence or death from any cause, whichever occurs first

次要结果测量

结果测量
措施说明
大体时间
Overall Survival (OS)
大体时间:From randomization to Year 3 and randomization to Year 5
Comparison of overall survival (OS) among Arm A (SOC) and Arm B (ctDNA guided) patients and assess whether adjuvant durvalumab monotherapy is non-inferior to standard of care adjuvant D-FLOT
From randomization to Year 3 and randomization to Year 5
Molecular Recurrence
大体时间:From time of surgery up to 3 years
Compare Arm A(SOC) relative to Arm B (ctDNA guided) time from surgery (or first ctDNA negative assessment) to the detection of ctDNA positivity by the Signatera assay.
From time of surgery up to 3 years
Metastasis-Free Survival (MFS)
大体时间:From randomization at Year 2, Year 3, and Year 5
To compare Arm A (SOC) relative to Arm B (ctDNA guided) on metastasis-free survival (MFS).
From randomization at Year 2, Year 3, and Year 5
Disease-Specific Survival (DFS)
大体时间:From randomization at Year 2, Year 3, and Year 5
To compare Arm A (SOC) relative to Arm B (ctDNA guided) on disease-specific survival (DFS).
From randomization at Year 2, Year 3, and Year 5
Discontinuation due to Adverse Events
大体时间:From enrollment to Year 2
Comparison of Arm A (SOC) relative to Arm B (ctDNA guided) on treatment discontinuation due to adverse events.
From enrollment to Year 2
Quality of Life Outcomes
大体时间:From enrollment to Year 2
Comparison of Arm A (SOC) relative to Arm B (ctDNA guided) on quality of life and disease-related symptoms using patient-reported outcomes (PROs) from European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Core 30 (QLQ-C30).
From enrollment to Year 2
Quality of Life Outcomes
大体时间:From enrollment to Year 2
Comparison of Arm A (SOC) relative to Arm B (ctDNA guided) on quality of life and disease-related symptoms using patient-reported outcomes (PROs) from European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire - Stomach Cancer Module (EORTC QLQ-STO22)
From enrollment to Year 2
Quality of Life Outcomes
大体时间:From enrollment to Year 2
Comparison of Arm A (SOC) relative to Arm B (ctDNA guided) on quality of life and disease-related symptoms using patient-reported outcomes (PROs) from European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire ( EORTC-IL38).
From enrollment to Year 2
Patient Reported Treatment Tolerability
大体时间:From enrollment to Year 2
To compare Arm A (SOC) relative to Arm B (ctDNA guided) to the patient-reported tolerability of treatment using Patient Reported Outcomes of the Common Terminology Criteria for Adverse Events (PRO-CTCAE).
From enrollment to Year 2

其他结果措施

结果测量
措施说明
大体时间
Assess ctDNA Clearance Arm B (ctDNA Guided)
大体时间:From randomization to 2 years, 3 years, and 5 years
Assess ctDNA clearance patterns in participants who receive adjuvant FLOT only after molecular recurrence in Arm B (ctDNA guided).
From randomization to 2 years, 3 years, and 5 years
Assess ctDNA Clearance in Arm A (SOC)
大体时间:From randomization to 2 years, 3 years, and 5 years
Assess ctDNA clearance during and after adjuvant D-FLOT therapy in ctDNA positive cohort of Arm A (SOC).
From randomization to 2 years, 3 years, and 5 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。

赞助

调查人员

  • 研究主任:Adham Jurdi, MD、Natera, Inc.

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

一般刊物

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9月1日

初级完成 (估计的)

2028年9月1日

研究完成 (估计的)

2034年9月1日

研究注册日期

首次提交

2026年4月14日

首先提交符合 QC 标准的

2026年5月1日

首次发布 (实际的)

2026年5月4日

研究记录更新

最后更新发布 (实际的)

2026年5月4日

上次提交的符合 QC 标准的更新

2026年5月1日

最后验证

2026年4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)?

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

是的

在美国制造并从美国出口的产品

不

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