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Completed

NCT Number: NCT00578201

FOLFOX-Cetuximab-radiotherapy for the Treatment of Esophageal Cancer

This phase II trial is studying the effects of oxaliplatin, leucovorin and fluorouracil-when given together with Cetuximab and radiation therapy and radiation therapy to see how they work in treating patients with stage III esophageal cancer.

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Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Clinique Saint Jean

Lyon, 69008, France

About this study

Cetuximab is a monoclonal antibody which can block the ability of tumor cells to grow and spread Cetuximab may also make tumor cells more sensitive to radiation therapy. Drug used in chemotherapy such as oxaliplatin leucovorin and Fluorouracil work in different way to stop the growth of tumor cells either by killing the cells or by stopping them form dividing. Radiation therapy uses high energy X rays to kill tumor cells. Giving cetuximab could improve the efficacy of chemotherapy and radiation therapy and may make the tumor smaller This phase II trial is studying the effects of oxaliplatin, leucovorin and fluorouracil-when given together with Cetuximab and radiation therapy and radiation therapy to see how they work in treating patients with stage III esophageal cancer.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Histologically confirmed squamous cell carcinoma of the esophagus stage III (according to UICC classification)
  • Measurable disease according to the RECIST criteria
  • WHO performance status of 0 or 1
  • Age 18-80 years old
  • Reference imaging within the 2 weeks prior to the treatment
  • Hematological and biochemical assessment within the 2 weeks prior to the treatment
  • Neutrophils >1.5 10 9/L, platelets >150.10 9/L, Haemoglobin ≥10g/dL, Bilirubin ≤ 1.25 ULN, Aspartate Aminotransferase (AST) and Alanine aminotransferase (ALT) ≤ 3 ULN Woman of childbearing potential must use effective contraception methods Written informed consent obtained No prior chemotherapy or radiation therapy for esophageal cancer

Exclusion criteria

  • Stage I, II or IV (according to UICC classification)
  • Esophageal carcinoma with small cells or endocrine cells or esophageal stromal tumor
  • visceral metastasis
  • orotracheal fistula weight loss >15% within the previous 6 months Pregnancy or breast feeding Contra indication to the study treatment History of coronary heart disease uncontrolled, or myocardial necrosis within the previous 6 months
  • Peripheral Neuropathy NCI >1
  • Liver Failure
  • Prior thoracic radiation therapy
  • history of cancer within the previous 5 years (except removed skin carcinoma, removed local melanoma located, and carcinoma cervix of uterus Esophageal Endoprosthesis

Treatment and study plan

radiochemotherapy,combination Cetuximab-FOLFOX

Drug

objective response rate at 12 weeks with radiochemotherapy then combination Cetuximab-FOLFOX

Other names: objective response rate,combination Cetuximab-FOLFOX

Primary outcomes

  1. objective response rate (ORR) at 12 weeks with radiochemotherapy (first evaluation), and if applicable, within 2 to 4 weeks following the end of additional treatment with the combination Cetuximab-FOLFOX (second evaluation)

    Time frame: at 12 weeks and within 2 to 4 weeks following the end of additionnal treatment

Secondary outcomes

  1. Progression free survival Quality of life Dysphagia score Overall survival toxicity of this regimen

    Time frame: during the study

Sponsors and collaborators

Lead sponsor

Assistance Publique - Hôpitaux de Paris

Other

Collaborators

  • GERCOR - Multidisciplinary Oncology Cooperative Group

Registry information

Official study title

Phase II Trial of FOLFOX in Combination With Cetuximab and Concomitant Radiotherapy in the Treatment of Esophageal Cancer Stage III

Acronym: FOLFOX

Important dates

Study start
2007
Primary completion
2011
Study completion
2011
First posted
Dec 21, 2007
Registry last updated
Mar 31, 2011

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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