Standard Versus Super-extended Lymphadenectomy After Neo-adjuvant Chemotherapy for Gastric Cancer

Phase 3RecruitingNCT03961373

University of Siena539 enrolled

Overview

In this study the patients with histological evidence of adenocarcinoma of the stomach will be screened and, if eligible, submitted to neo-adjuvant chemotherapy (NAC). After conclusions of NAC and obtaining informed consent, they will be registered and randomized to receive surgical D2 vs. D2plus lymphadenectomy.

This is a prospective multi-centre phase III, two-group, randomized and controlled trial designed to prove superiority of the experimental treatment arm (neo-adjuvant chemotherapy and super-extended lymphadenectomy). The trial population consists of patients who have histologically confirmed adenocarcinoma of the stomach with locally advanced primary tumour and no evidence of distant metastases (stage IIA-IIIC gastric cancer). The lymph node clinical metastases, before neo-adjuvant chemotherapy, must be limited to the first and second compartments (stations 1-12). STANDARD GROUP: Neoadjuvant chemotherapy + surgical gastrectomy with D2 lymphadenectomy. Patients who are assigned to neoadjuvant chemotherapy+ surgical D2 treatment group will undergo either subtotal or total gastrectomy, depending on the location of the primary tumour. Standardized D2-lymph node dissection is required with specific information about lymph node stations. EXPERIMENTAL GROUP: Neoadjuvant chemotherapy + surgical gastrectomy with D2plus lymphadenectomy. Patients who are assigned to neoadjuvant chemotherapy + surgical D2plus extended lymphadenectomy treatment group will undergo either subtotal or total gastrectomy, depending on the location of the primary tumour. Standardized D2 lymph node dissection plus resection of stations 8p, 12b/p, 13, 14v, 16a2/b1 is required with specific information about lymph node stations. In both groups, surgical treatment should be performed within 4-6 weeks after the end of the last cycle of NAC. The primary objective of this study is to compare overall and cancer-related survival between D2 and D2+ lymphadenectomy following neo-adjuvant chemotherapy for resectable gastric cancer. In addition, response to chemotherapy, resection rate, quality of life, complications attributable to surgical intervention / side effects of chemotherapy and the duration of hospitalization will be evaluated. Sample size estimation was performed, to detect the minimum number of patients to be recruited in each arm. A two-sided log rank test with an overall sample size of 539 subjects, of which 270 are in group 1 and 269 are in group 2. Data will be analyzed using SPSS software. Level of significance will be defined as 5%. The trial will be open for recruitment from October 2018 to September 2023.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

NONE

Enrollment

539

Conditions

Locally Advanced Gastric Cancer

Interventions

Gastrectomy with D2 lymphadenectomyPROCEDURE

Patients who are assigned to the neoadjuvant chemotherapy+ surgical D2 treatment group will undergo either subtotal or total gastrectomy, depending on the location of the primary tumour. Standardized D2-lymph node dissection is required with specific information about lymph node stations.

Gastrectomy with D2plus lymphadenectomyPROCEDURE

Patients who are assigned to the neoadjuvant chemotherapy + surgical D2+ extended lymphadenectomy treatment group will undergo either subtotal or total gastrectomy, depending on the location of the primary tumour. Standardized D2+ lymph node dissection plus resection of stations 8p, 12p, 13, 14v, 16a2/b1 is required with specific information about lymph node stations.

Eligibility

Sex: ALLMin age: 18 YearsMax age: 80 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Age equal or greater than 18 years * IIA-IIIC histologically proven primary gastric adenocarcinoma, before the treatment with NAC. Not including gastro-oesophageal junction/cardia carcinoma but only Siewert 3, without any previous treatment (surgery and / or chemotherapy) for this diagnosis * Lack in CT scan of following: 1. Mediastinal lymph nodes 2. Lung metastases 3. Peritoneal metastases 4. Liver metastases 5. Pleural effusion, ascites 6. Metastases to para-aortic lymph nodes No 16a2/b1 7. Metastases to lymph nodes located in the "posterior" area (8p, 12 b/p, 13) 8. Extra-regional lymph node metastases * ECOG performance status ≤ 2 * No prior radio- or chemotherapy conflicting with the treatment of gastric cancer * No oesophageal invasion, or invasion \<=3cm * Negative peritoneal washing cytology findings and no peritoneal metastases in staging laparoscopy * No gastric stump cancer * No signs of cervical and subclavear lymph nodes or distal metastases * Patient's consent form obtained, signed and dated before beginning specific protocol procedures * Absence of any psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol and follow-up schedule; those conditions should be discussed with the patient before registration in the trial Exclusion Criteria: * Contraindications for any sort of appropriate chemotherapy according to local standards * Linitis plastica * Second uncontrolled malignant tumour (synchronous or metachronous (last 5 years) other than Cis or mucosal cancer * Neoplasms involving the esophago-gastric junction (Siewert types I and II) * Expected unresectability after neo-adjuvant treatment or progression in metastases * Emergency surgery due to bleeding or perforation * Uncontrolled infections * Other serious underlying medical conditions that could impair the ability of the patient to participate in the study * Pregnant or lactating women * Significant neurologic or psychiatric disorders * Severe cardiac illness (NYHA class IV) * Under treatment of systemic steroids * Participation in any other clinical trial that might interfere with the results of this trial * Lack of compliance * Inability to fill in questionnaires (insufficient command of language, dementia, lack of time)

Locations (1)

General and Surgical Oncology Department, University of Siena

Siena, Italy

RECRUITING

Outcomes

Primary Outcomes

Overall survival analysis

Overall survival analysis will be analysed during follow up visits

Time frame: This outcome measure will be estimated from the time of randomization to the date of death or last follow up visit, assessed approximately 5 years after the disease diagnosis.

Secondary Outcomes

Recurrence free-survival

That part will also be analysed during follow up visits. The recurrence has to be documented in radiological, endoscopic or pathological examination, when possible.

Time frame: This outcome measure will be estimated from the time of randomization to the date of recurrence, assessed approximately 5 years after the disease diagnosis.

Post-operative morbidity

Severity of post-operative complications will be analysed using Clavien-Dindo classification

Time frame: This outcome measure will be assessed approximately 3 month after the operation date.

Post-operative mortality

Deaths after surgery

Time frame: Within 30 days from operation or during the hospital stay

R0 resection

Absence of microscopic (R1) or macroscopic (R2) residual tumor after surgery

Time frame: This outcome measure will be assessed approximately 3 month after the operation date.

Percentage of completion of protocol treatment

Percentage of patients who will complete the protocol treatment, including adjuvant chemotherapy

Time frame: This outcome measure will be assessed approximately 12 month after the date of enrollment.

Central Contacts

Daniele Marrelli

CONTACT

+39577585157 daniele.marrelli@unisi.it

Data from ClinicalTrials.gov

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