Skip to main content
OpenTrials
Completed

NCT Number: NCT03399110

XELOX for 4 Months Versus 6 Months in Gastric Cancer (LOMAC)

Our study aims to compare 4 months versus 6 months of adjuvant capecitabine plus oxaliplatin after D2 gastrectomy in patients with gastric cancer.

Hypothesis: We hypothesize that a 4-month regimen of capecitabine plus oxaliplatin is noninferior to a 6-month regimen with respect to DFS and is associated with lower treatment-related toxicity.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Sun Yat-sen University Cancer Center, Guangzhou, China

Loading trial locations.

About this study

Surgical resection is the cornerstone of treatment for patients with localized gastric cancer. In the CLASSIC trial, capecitabine plus oxaliplatin for 6 months following D2 gastrectomy has been established as a standard postoperative adjuvant treatment for patients with operable stage II or III gastric cancer. However, due to adverse events, chemotherapy was discontinued in 50 patients (10%), primarily due to nausea, neutropenia, decreased appetite, peripheral neuropathy, diarrhea, and vomiting. At the 2017 ASCO Annual Meeting, Grothey et al. reported the results of the IDEA trial. For patients with lymph node-positive colon cancer (stage III), some patients may benefit from a shorter duration of postoperative chemotherapy. An analysis of six clinical trials involving over 12,800 patients showed that 3 months of chemotherapy was nearly as effective as 6 months for patients with a lower recurrence risk, while also causing fewer side effects, particularly nerve damage. Based on the findings from the IDEA trial, we hypothesize that a 4-month regimen of capecitabine plus oxaliplatin may also benefit patients following D2 gastrectomy while reducing adverse events compared with the standard 6-month regimen.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Age between 18 and 80 years.
  • Histologically confirmed adenocarcinoma of the stomach or gastroesophageal junction, staged as II, IIIA, or IIIB according to the American Joint Committee on Cancer classification system, eighth edition.
  • Underwent R0 gastrectomy with D2 lymphadenectomy.
  • No other concurrent malignancies.
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1
  • No contraindications to chemotherapy.

Exclusion criteria

  • Receipt of preoperative treatment, including radiation therapy, chemotherapy, or immunotherapy.
  • Patients with stage I, IIIC, or IV gastric cancer.
  • Severe cardiac, pulmonary, neurologic, hepatic, or other major organ dysfunction.
  • Known or suspected drug allergies.
  • Pregnant or lactating women.

Treatment and study plan

Oxaliplatin

Drug

Oxaliplatin 130 mg/m2

Other names: Eloxatin

Capecitabine

Drug

Capecitabine 1000 mg/m2

Other names: Xeloda

Primary outcomes

  1. DFS

    Time frame: 3 years

    Disease-free survival, defined as the time from randomization to the first occurrence of disease recurrence or death from any cause.

Secondary outcomes

  1. Adverse Events

    Time frame: 6 months

    Adverse Events of Chemotherapy

  2. OS

    Time frame: 3 years

    Overall survival, defined as the time from randomization to death from any cause.

Sponsors and collaborators

Lead sponsor

Fudan University

Other

Registry information

Official study title

XELOX for 4 Months Versus 6 Months as Adjuvant Chemotherapy in Gastric Cancer After D2 Resection (LOMAC)

Important dates

Study start
2018
Primary completion
2026
Study completion
2026
First posted
Jan 16, 2018
Registry last updated
Aug 24, 2026

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.