Skip to main content
OpenTrials
Not Yet Recruiting

NCT Number: NCT06942663

Randomized Phase II Trial Evaluating DFS in The Absence of an Adjuvant Component of Perioperative Chemotherapy in Patients With Gastric Cancer

This single-center, open-label, randomized phase II trial (JAGC-1) will evaluate whether adjuvant chemotherapy can be safely omitted in patients with stage IB-III gastric cancer (cT2-4a and/or N+) who have achieved a pathological complete response (pCR) or TRG 4-5 on the Mandard scale, following neoadjuvant chemotherapy and surgery. The study aims to compare disease-free survival and quality of life in patients receiving or not receiving adjuvant chemotherapy after neoadjuvant treatment and surgery.

Not Yet Recruiting

Trial opening soon.

Get Notified

Key information

About this study

Population: patients with localized or locally advanced gastric cancer ( cT2-4a and/or N+ according to TNM, 8th revision, 2017) after having undergone the full extent of the planned neoadjuvant component of perioperative chemotherapy, radical surgical intervention, with a histological tumor regression grade classified as pCR or TRG 4-5 according to the Mandard scale

Study design Patients will be randomized in a ratio of approximately 1:1:

Patients who achieve pCR will be randomly assigned to one of two groups:

  • Group A (no adjuvant therapy): Patients will not receive adjuvant chemotherapy
  • Group B (adjuvant therapy): Patients will receive the adjuvant component of perioperative chemotherapy

Patients who achieve a TRG of 4-5 on the Mandard scale will be randomly assigned to one of two groups:

  • Group C (adjuvant therapy): Patients will not receive adjuvant chemotherapy.
  • Group D (no adjuvant therapy): Patients will receive the adjuvant component of perioperative chemotherapy.

Patients in the groups with adjuvant therapy will receive treatment until progression or maximal effect of therapy is detected (the longest duration of treatment is 3 months).

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • - Obtaining informed consent to participate in the study.
  • Morphologically confirmed gastric adenocarcinoma.
  • The presence of localized or locally advanced gastric cancer (cT2-4a and/or N+)
  • The full volume of the planned neoadjuvant component of perioperative chemotherapy was performed
  • Radical surgical intervention was performed for the primary tumor of gastric cancer
  • The histological degree of tumor regression after surgical resection was classified TRG1 and without metastasis to regional lymph nodes N0 or TRG 4-5 based on the Mandard tumor Regression scale.
  • ECOG score 0 - I.
  • Absence of severe uncontrolled concomitant chronic and acute diseases.
  • Adequate liver and bone marrow function
  • Neutrophils > 1.5*109/l
  • Hemoglobin >85 g/l
  • Platelets >100*109/l
  • Increased transaminases and/or bilirubin < 2 art.

Exclusion criteria

  • Lack of a neoadjuvant component of perioperative chemotherapy or insufficient number of courses
  • The time after surgical treatment is more than 12 weeks
  • Stage IV of the disease
  • Her2-positive and/or MSI\\dMMR stomach cancer
  • Severe uncontrolled concomitant chronic or acute diseases
  • The presence of a second malignant tumor (with the exception of previously cured malignant neoplasms)
  • Any conditions that, in the opinion of the doctor, interfere with the examination procedures
  • With incomplete tumor response to treatment

Treatment and study plan

Surveillance

Other

Close monitoring for disease recurrence.

Adjuvant chemotherapy

Drug

The adjuvant chemotherapy regimen will be standardized based on current clinical guidelines and may include combinations of agents such as fluoropyrimidines and oxaliplatin with or without docetaxel. Treatment until the progression of the process is detected or the maximum effect of therapy is achieved (the maximum duration of treatment is 3 months).

Primary outcomes

  1. Disease-free survival rates

    Time frame: 3 years

    Comparison of 3-year DFS in the group receiving the adjuvant component of perioperative chemotherapy and in the group without it and comparison of the indicators of 3-year DFS with TRG 4-5 on the Mandard scale in the group receiving the adjuvant component of perioperative chemotherapy and in the group without it.

Secondary outcomes

  1. Аssessment of the quality of life

    Time frame: 3 years

    Quality of life assessment by European Organisation for Research and Treatment of Cancer scale Quality of Life Questionnaire - Core 30 (QLQ-C30) by Scoring of the QLQ-C30 Summary Score using the descriptive analysis with the qlqc30 command (detailed description in manual ISBN 2-9300 64-22-6).

Study contacts

Contact information is provided by the study sponsor or research team.

MIKHAIL Anat OSIPOV, MD, PhD

CONTACT

[email protected]

89052075653

Petryakova Alex Julia, MD

CONTACT

[email protected]

79873940672

Sponsors and collaborators

Lead sponsor

Nizhny Novgorod Regional Clinical Oncology Center

Other Gov

Registry information

Official study title

Randomized Phase II Trial Evaluating DFS in the Absence of an Adjuvant Component of Perioperative Chemotherapy in Patients With Stage IB-III Gastric Cancer Who Achieved pCR or TRG4-5 on the Mandard Scale on Neoadjuvant Chemotherapy

Acronym: JAGC1

Important dates

Study start
2025
Primary completion
2027
Study completion
2030
First posted
Apr 24, 2025
Registry last updated
Apr 24, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.