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Status unknownNCT04053725Updated Sep 9, 2019

Prediction of the Efficacy of ctDNA in Immunotherapy for Advanced Gastric Cancer

An observational study in Stomach Neoplasms, sponsored by Sun Yat-sen University. Status unknown at 1 site in China. Open to participants aged 18 Years to 80 Years. Per ClinicalTrials.gov, last updated 2019-09-09.

Sponsored by Sun Yat-sen University · Observational

The sponsor has not verified this record recently (last verified Sep 2019), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Case-only
Time perspective
Prospective
Enrollment
200
Ages
18 Years to 80 Years
Sex
All
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Study summary

Gastric cancer is one of the common malignant tumors in China, with relatively high incident rate and mortality among the population. Surgery is the conventional treatment option for early and intermediate-stage stage gastric cancer, but postoperative relapse is the major issue. Circulating tumor DNA (ctDNA) is tumor-derived fragmented DNA with an average size of 166 bp, mixed with cell free DNA (cfDNA) of other sources in blood circulation.ctDNA is reflecting the most up-to-date status of tumor genome. Hence, it is considered as a new biomarker for tumor, which can be qualitative, quantitative and used for disease monitoring. The present clinical trial aims to explore the possibility of clinical utility of serum ctDNA as a clinical index to predict the efficacy in immunotherapy for advanced gastric cancer.

Read the detailed description

Gastric cancer is one of the most common malignant tumors in China, with the second highest incidence and the third highest mortality.Adenocarcinoma accounts for 95% of gastric malignancies and is the most common malignancy of the digestive tract. Seventy percent of the patients with early gastric cancer had no obvious symptoms, and a few had nausea, vomiting or ulcer-like upper gastrointestinal symptoms.

Surgical treatment is the first choice for the treatment of early gastric cancer, but postoperative recurrence and metastasis are prone to occur. At the same time, there are relatively few chemotherapy drugs for gastric cancer, only a few chemotherapy drugs of Paclitaxel and platinum drugs are selected, and the chemotherapy regimen is relatively single. Meanwhile, the prognosis of gastric cancer in different parts is significantly different, and its molecular heterogeneity is strong. Studies have shown that about 13% of gastric cancer has HER2 gene variation, and there is no other specific driver gene mutation except HER2. Currently, only two targeted drugs, trastuzumab and apatinib, are approved for the treatment of gastric cancer in China.

CtDNA is the body's endogenous tumor DNA free of cells in circulating blood. It is generally believed that ctDNA in the blood of tumor patients is mainly derived from tumor cell necrosis and proliferation after apoptosis, as well as the release of proliferative and active tumor cells. At present, most studies have proved that the DNA of tumor cells has consistent genetic changes with ctDNA, and the same genetic changes may be detected in the plasma free DNA of patients with driver gene mutations in the primary or metastatic lesions. Therefore, ctDNA is a characteristic tumor biomarker and can be qualitatively, quantitatively and dynamically tracked.

Immunoassay point inhibitors, including pd-1 inhibitors, pd-l1 inhibitors and ctla-4 inhibitors, have achieved significant efficacy in a variety of tumors and are expected to change the treatment status of tumors. In the case of gastric cancer, recently the Lancet Oncology published the final results and review of the KEYNOTE 012 study that investigated the efficacy of Pembrolizumab in patients with advanced pd-l1 positive gastric cancer. Results showed that 53% of patients had tumor regression, 22% had partial imaging remission, and the median duration of remission was 40 weeks. Pembrolizumab is also superior to standard second-line chemotherapy. However, currently there is no recognized indicator that can predict the efficacy of immunotherapy for gastric cancer, and relevant research is urgently needed.

The purpose of this study was to investigate the correlation between the dynamic changes of ctDNA during surgery and the effect of immunotherapy on gastric cancer patients and its effect as a hematological index for the prognosis of advanced gastric cancer. Meanwhile, molecular markers related to the prognosis of advanced gastric cancer were screened out by comparing the differences in the molecular characteristics of gastric cancer tissues among patients with different prognosis.

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Conditions studied

  • Stomach Neoplasms

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03

In context

Stomach Neoplasms

2,851 studies on the registry are indexed under Stomach Neoplasms; 864 are open to participants now.

This study's planned enrollment of 200 is below the median of 274 across 670 observational studies indexed under Stomach Neoplasms.

Browse Stomach Neoplasms studies →

Lead sponsor

Sun Yat-sen University is the lead sponsor of 1,644 studies on the registry; 602 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 80 Years
Sexes eligible
All
Sampling method
Probability sample

Study population

This prospective clinical study program enrolled 80 patients. Patients should be treated with second- or third-line chemotherapy and combined with immunoassay inhibitors. The pre-treatment plasma ctDNA sample mutation information of each patient was compared with the tissue sample mutation information. The pre-treatment ctDNA dynamic monitoring results were compared with the ctDNA mutation information after treatment initiation. The post-treatment ctDNA dynamic monitoring results and imaging comparison analysis.

Inclusion criteria

  1. Male or female ≥ 18 years of age at first visit.
  2. Patients must have histologically confirmed gastric cancer .
  3. Patients were surgically assessed to be inoperable.
  4. Patients received second-line or third-line chemotherapy and were treated with immunoassay point inhibitors.
  5. Patients' early pathological information was complete, including tumor site and pathological type.
  6. Patients must be able to provide sufficient fresh tissue/biopsies or minimum 5-10 FFPE sections for NGS analysis.
  7. Patients must be able to follow the study visit schedule and willing to provide peripheral blood samples at the indicated time point.
  8. Written informed consent must be obtained from patient or patient's legal representative and ability for patient to comply with the requirements of the study.

Exclusion criteria

Exclusion Criteria:

  1. Patients who cannot provide peripheral blood samples prior to the surgical treatment will be excluded.
  2. Patients with severe infection will be excluded.
  3. Patients with other serious disease besides gastric cancer will be excluded.
  4. Pregnant women will be excluded.
  5. Patients who are alcoholic or drug abusers will be excluded.
  6. Patients with a condition or abnormality that in the opinion of the Investigator would compromise the safety of the patient or the quality of the data will be excluded.
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Study design

Observational model
Case-only
Time perspective
Prospective
Enrollment
200 participants (estimated)
Patient registry
No
Biospecimen retention
Samples with dna
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What researchers measure

Primary outcomes

  1. the proportions of patients with positive serum ctDNA that have postoperative relapse

    the proportions of patients with positive serum ctDNA (in any follow-up) that have postoperative relapse

    Time frame: through study completion, an average of 2 years

Secondary outcomes

  1. The proportion of ctDNA content decreased in patients with good therapeutic effect

    The proportion of patients with good therapeutic effect whose serum ctDNA content decreased (in any follow-up)

    Time frame: through study completion, an average of 2 years

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Study locations

1 of 1 sites recruiting
  • Cancer center of Sun Yat-sen University
    Guangzhou, Guangdong 510060, China
    • Rui-Hua Xu, MD, PhD · Contact · lvzd@sysucc.org.cn · +862087342635
    • Rui-hua Xu, MD, PhD · Principal investigator
    • Dongsheng Zhang, MD, PhD · Sub investigator
    Recruiting
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References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 9, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT04053725
Lead sponsor
Sun Yat-sen University
Responsible party
Ruihua Xu (president, Sun Yat-sen University) — Principal investigator
First posted
Aug 12, 2019
Start date
Feb 1, 2019
Primary completion
May 2020 (estimated)
Completion
Nov 2021 (estimated)
Last update
Sep 9, 2019

Study contacts

Dongsheng Zhang, MD.,PhD.
Contact
Zhangdsh@sysucc.org.cn
86-2087343804
Zhida Lv, BS.
Contact
lvzd@sysucc.org.cn
86-2087343795
Rui-hua Xu
principal investigator · Sun Yat-sen University

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Sep 2019. You cannot join it, but the record below documents what was studied.

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