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Completed

NCT Number: NCT01711242

Trial of Adjuvant XELOX Chemotherapy and Concurrent Capecitabine and Radiotherapy for Resected Gastric Carcinoma

The objective of the trial is to compare disease-free survival between adjuvant XELOX alone vs XELOX with concurrent capecitabine and radiotherapy in curatively resected gastric cancer patients with D2 dissection.

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

The First Affiliated Hospital of Wenzhou Medical College

Wenzhou, Zhejiang, 325000, China

About this study

Gastric cancer is one of the most common malignancies in China. Complete surgical resection is the only potentially curative therapy available to patients with gastric cancer. However, the overall survival results remain unsatisfactory. The main factor accounting for high mortality rate is the relapse after surgical resection. During the past few decades, the principle of combined modality treatment has been developed and applied in gastric cancer. Radiation therapy plus concurrent chemotherapy had demonstrated to be able to achieve a significant improvement in overall and disease-free survival according to Intergroup Trial 0116/Southwest Oncology Group 9008. Nevertheless, the result from Intergroup Trial 0116 study had been challenged by the fact that the surgical treatment applied in the trial was gastrectomy with limited lymph node dissection (D0 or D1) in 90% of cases. Therefore, it is debatable whether adjuvant chemoradiation therapy can confer survival benefit in patients with extensive lymph node dissection. In ARTIST study, the addition of concurrent capecitabine and radiotherapy to capecitabine and cisplatin chemotherapy did not significantly reduce recurrence after curative resection and D2 lymph node dissection in gastric cancer. In subgroup analysis of patients with positive pathologic lymphnodes, there was a statistically significant prolongation in disease-free survival in the concurrent treatment arm when compared with the chemotherapy alone arm. Furthermore, CLASSIC study showed that XELOX (oxaliplatin/capecitabine) combination given as adjuvant chemotherapy for stage II or III patients after D2 surgery could achieve a significant survival benefit. The standard treatment modality in gastric cancer after D2 dissection is still disputable. Thus, the assessment of the effect of adjuvant sequence chemoradiotherapy in D2 resected gastric cancer is essential.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Histologically proven gastric cancer; ≥ D2 resection
  • Stage T1-4, N+
  • 18 ≤ age ≤ 75
  • Eastern Cooperative Oncology Group 0-2
  • No distant metastasis
  • Adequate bone marrow functions (absolute neutrophil count≥ 1,500/ul, blood platelet≥ 100,000/ul, haemoglobin≥ 10g/dl)
  • Adequate renal functions(serum creatinine ≤ 1.5mg/dl)
  • Adequate liver functions (serum bilirubin ≤ 1.5mg/dl, aspartate aminotransferase/alanine aminotransferase ≤ 3 times(normal value)
  • Written informed consent

Exclusion criteria

  • Previous history of immunotherapy, chemotherapy, radiotherapy for gastric cancer;
  • Active infection requiring antibiotics;
  • Pregnant, lactating women;
  • Psychiatric illness, epileptic disorders;
  • Concurrent systemic illness not appropriate for chemotherapy;
  • Resection margin (+);
  • History of other malignancy within 5 years except for non-melanoma skin cancer, cervix in situ carcinoma;
  • D0, D1 resection;

Treatment and study plan

Capecitabine

Drug

Oxaliplatin

Drug

Radiotherapy

Radiation

Primary outcomes

  1. disease free survival

    Time frame: 3-year

Secondary outcomes

  1. 5 year Overall Survival

    Time frame: 5 years

Other outcomes

  1. Health-related quality of life

    Time frame: five years after enrollment

    assessed by the Functional Assessment of Cancer Therapy-Esophageal (FACT-E)

  2. Number of participants with adverse events as a measure of safety and tolerability

    Time frame: during treatment

    assessed by NCI Common Terminology Criteria v3.0

Sponsors and collaborators

Lead sponsor

xie congying

Other

Registry information

Official study title

Phase II Randomized Trial of Adjuvant XELOX Chemotherapy and XELOX With Concurrent Capecitabine and Radiotherapy for Gastric Adenocarcinoma With D2 Dissection

Important dates

Study start
2012
Primary completion
2020
Study completion
2021
First posted
Oct 22, 2012
Registry last updated
May 5, 2022

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.

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