Laparoscopic Staging for Locally Advanced Gastric Cancer in Chinese Patients

NCT ID: NCT02172690

Last Updated: 2025-02-07

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

452 participants

Study Classification

INTERVENTIONAL

Study Start Date

2014-01-01

Study Completion Date

2017-09-30

Brief Summary

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RATIONALE: Laparoscopic staging may help doctors plan more effective treatment for gastric cancer, yet the efficiency have not been fully investigated in Chinese people.

PURPOSE: Study the effectiveness of laparoscopic staging in patients with pre-diagnosed as locally advanced gastric cancer.

Detailed Description

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OBJECTIVES: I. Determine the feasibility of laparoscopic staging of patients with pre-diagnosed as locally advanced gastric cancer. II. Assess the adverse effects associated with this technique.

OUTLINE: Surgery. Laparoscopy with cytologic examination.

PROJECTED ACCRUAL: Up to 450 patients will be accrued over approximately 2 years.

Conditions

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Gastric Cancer Peritoneal Metastases

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

NONE

Study Groups

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Laparoscopic Staging

For Patients diagnosed as Locally Advanced Gastric Cancer(cT2+NanyM0)by CT and EUS, undergo laparoscopic staging.

Group Type EXPERIMENTAL

Laparoscopic Staging

Intervention Type PROCEDURE

Laparoscopic Staging

Interventions

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Laparoscopic Staging

Laparoscopic Staging

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* sign written informed consent form
* age ≥ 18 years
* pathologically confirmed gastric or GEJ adenocarcinoma
* disease at clinical stage of locally advanced gastric cancer by CT/EUS(cT2+NanyM0)
* No prior antitumor treatment is allowed, including chemotherapy, radiotherapy, immune therapy or target therapy
* Adequate organ function as defined below:

Hematologic ANC ≥ 1.5\*109/l Hemoglobin ≥ 9 g/dl Platelets ≥ 100\*109/l Hepatic Albumin ≥ 30g/l Serum bilirubin ≤ 1.5×ULN AST and ALT ≤ 2.5×ULN ALP ≤ 2.5×ULN TBIL ≤ 1.5×ULN Renal Serum Creatinine \< 1.5 ULN

* KPS ≥ 70
* Adequate lung and heart function
* Negative serum or urine pregnant test within 7 days prior to randomization for child-bearing age women
* Sexually active males or females willing to practice contraception during the study until 30 days after end of study.

Exclusion Criteria

* Refuse to provide blood/tissue sample;
* With distant metastasis diagnosed by CT/EUS;
* Sexually active males or females refuse to practice contraception during the study until 30 days after end of study.
* History of organ transplantation(including autologous bone marrow transplantation and Peripheral stem cell transplantation);
* Prior long term steroid therapy (excluding short term steroid treatment which is completed prior to \> 2 weeks of study enrollment);
* Patients with central nervous system(CNS) disorder or peripheral nervous system disorder or psychiatric disease;
* Concurrent severe infection;
* Concurrent disease or condition that would make the subject inappropriate for study participation or any serious medical disorder that would interfere with the subject's safety (including current active hepatic, biliary, renal, respiratory disease, uncontrolled diabetes hypertension et al);
* History of other malignancy. However, subjects who have been disease-free for 5 years, or subjects with a history of completely resected non-melanoma skin cancer or successfully treated in situ carcinoma, are eligible;
* Known history of uncontrolled or symptomatic angina, uncontrolled arrhythmias and hypertension, or congestive heart failure, or cardiac infarction within 6 months prior to study enrollment, or cardiac insufficiency;
* Person with no capacity (legally) or inappropriate to continue study treatment for ethics/medical reasons.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Peking University

OTHER

Sponsor Role lead

Responsible Party

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Jiafu Ji

Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Jiafu Ji, MD

Role: PRINCIPAL_INVESTIGATOR

Peking University

Locations

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Peking Unicersity Cancer Hospital

Beijing, Beijing Municipality, China

Site Status

Countries

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China

References

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Li Z, Li Z, Zhang L, Liu Q, Wang Z, Zhang Z, Xiao G, Fu W, Wang X, Ye Y, Yu J, Li F, Chen L, Wang S, Ji J. Staging laparoscopy for locally advanced gastric cancer in Chinese patients: a multicenter prospective registry study. BMC Cancer. 2018 Jan 10;18(1):63. doi: 10.1186/s12885-017-3791-6.

Reference Type DERIVED
PMID: 29321007 (View on PubMed)

Other Identifiers

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D141100000414004

Identifier Type: OTHER_GRANT

Identifier Source: secondary_id

KW-LStaging-2014

Identifier Type: -

Identifier Source: org_study_id

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