Laparoscopic vs. Open Distal Gastrectomy After Neoadjuvant Chemotherapy

Official title

A Multicenter Prospective Phase II Comparative Study of Laparoscopic Versus Open Distal Gastrectomy After Neoadjuvant Chemotherapy for the Treatment of Locally Advanced Gastric Cancer Patients

Overview

The study was designed as single-country, multi-center, open-labelled, randomized (1:1), phase II trial. 238 patients with medically and technically operable advanced gastric adenocarcinoma in middle or distal 1/3 of stomach are enrolled and randomly assigned to laparoscopic gastrectomy group and open gastrectomy group. 4 cycles of mFLOT chemotherapy will be conducted before and after gastrectomy. The primary objective of this study is comparison of D2 lymph node dissection compliance rate between open surgery group and laparoscopic surgery group after neoadjuvant chemotherapy.

Detailed description

The effect of neoadjuvant chemotherapy on locally advanced gastric cancer was confirmed from a prospective clinical trial. Oncologic safety and excellence of the laparoscopic gastrectomy surgery was recently established for locally advanced gastric cancer.

However, neither technical nor oncologic stability was established for laparoscopic gastrectomy surgery after neoadjuvant chemotherapy. Anticipated benefits from laparoscopic gastrectomy surgery after neoadjuvant chemotherapy are as follows: 1) Reduced postoperative complications; 2) Reduced intra- or postoperative transfusion and patient's pain after surgery; 3) Enhance postoperative recovery (shortened hospitalization duration); 4) Facilitate completion rate of adjuvant chemotherapy.

The study was designed as single-country, multi-center, open-labelled, randomized (1:1), phase II trial.

238 patients with medically and technically operable advanced gastric adenocarcinoma in middle or distal 1/3 of stomach are enrolled and randomly assigned to laparoscopic gastrectomy group and open gastrectomy group. 4 cycles of mFLOT chemotherapy will be conducted before and after gastrectomy.

The primary objective of this study is comparison of D2 lymph node dissection compliance rate between open surgery group and laparoscopic surgery group after neoadjuvant chemotherapy.

Interventions

• Procedure Laparoscopic versus open distal gastrectomy
  Laparoscopic versus open distal gastrectomy after neoadjuvant chemotherapy for locally advanced gastric cancer

Primary outcome measures

• Number of harvested lymph nodes in D2 lymph node dissection [Time frame: 2 weeks after operation when the pathologic report is available]

Secondary outcome measures (5)

• 3 year progression free survival [Time frame: 3 years after randomization]
• 3 year relapse free survival [Time frame: 3 years after randomization]
• Comparison of postoperative morbidity and mortality [Time frame: 90 days after operation]
• Curative resection rate [Time frame: 2 weeks after operation when the pathologic report is available]
• Conversion to open surgery [Time frame: 1 day]

Eligibility criteria

Inclusion criteria

• Patients who voluntarily expressed their consent to participate in this trial by signing a written 'Subject Consent Form.'
• Patients whose gastric adenocarcinoma located in the middle or lower part of the stomach is histologically confirmed and deemed possible to perform a radical distal gastrectomy surgery.
• Patients who come under T2/N(+)M0, T3\~4a/N(- or +) M0 according to the 8th edition of the TNM classification.

Exclusion criteria

• Methodologies

• Patients less than 20 years old or older than 80 years old
• Eastern Cooperative Oncology Group(ECOG) ≥ 2
• Patients with a surgery experience due to a neoplasm in the stomach.
• Patients with complications due to gastric cancer (acute hemorrhage, gastric outlet obstruction or perforation)
• Patients with distant metastases (M1) including distant lymph nodes (Retropancreatic, para-aortic, periportal, retroperitoneal, or mesenteric lymph nodes)
• Patients without distant metastases but who are, according to a surgeon's judgment, unqualified for radical gastrectomy because of invasions to adjacent organs (T4b).
• In the case of localized conglomerated metastatic lymph nodes
• Patients who received surgery or radiation therapy for a primary cancer developed in another organ or those with active/synchronous double cancer in recent 5 years.
• Patients who participated in another clinical trial or was administered with a different investigational drug in 30 days prior to randomization.
• Patients who had any of the following in 6 months before the trial recruitment: myocardial infarction, severe/unstable angina pectoris, coronary/peripheral artery bypass surgery, NYHA class III or IV congestive heart failure, stroke or transient ischemic attack.
• Patients with a previous experience of uncontrolled seizure, central nervous system or psychological disorders whose conditions are clinically significant to the extent that they are unable to express consent to participate in the trial and oral drug administration is not possible.
• Patients with uncontrolled active infection or sepsis.
• Patients who had deep vein thrombosis in recent 4 weeks before the beginning of the trial recruitment.
• Patients with serious acute or chronic disease that can degrade the patient's ability to participate in the trial or impede the interpretation of the trial results.
• Pregnant or breast-feeding patients. Fertile female patients who are positive in pregnancy test.

Drug Administration for Neoadjuvant Chemotherapy

• Inadequate functions of marrow or organs:

I. Absolute Neutrophil Count (ANC) < 1.5 x 109/L II. Platelet (PLT) < 100 x 109/L III. Hemoglobin (Hb) ≤ 9 g/dL IV. AST> 2.5 x ULN, ALT> 2.5 x ULN V. ALP > 2.5 x ULN VI. Total Bilirubin (T. Bil) > 1.5 x ULN VII. Serum creatinine (Cr) > 1.5 x ULN

• Patients who have peripheral neuropathy with clinical signs of Grade≥2 (NCI CTCAE v4.03) or with absence of deep tension reflex (DTR).
• Patients with hypersensitivity history of the investigational drug (5-FU, Oxaliplatin, Docetaxel).
• Patients who are on treatment with warfarin or coumarin anticoagulants.
• Patients who are on immunosuppressive therapy.
• Patients who are receiving co-medication with Cytochrome P450 2A6 inducer, inhibitor, and substrate.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation

Randomized

Model

Parallel assignment

Masking

Open label

Primary purpose

Treatment

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT04658589 · H2020-0407

Primary sources (government registries)

• ClinicalTrials.gov (US NIH)

View this study on ClinicalTrials.gov ↗