Improve the Treatment of Thoracic Esophageal Cancer
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Purpose
The purpose of this study is
- To compare the effects of the three types of thoracic esophageal cancer lymphadenectomy on the staging and prognosis of resectable esophageal cancer, which defined by the International Association of esophageal disease(ISDE) - standard mediastinal lymphadenectomy,total mediastinal lymphadenectomy and three field lymphadenectomy,and to find out reasonable range of lymphadenectomy.
- To compare the effects of Chemotherapy Group (Docetaxel + Nedaplatin) with Control Group on the prognosis of resectable thoracic esophageal cancer,and to explore the indications of adjuvant chemotherapy.
| Condition | Intervention | Phase |
|---|---|---|
|
Thoracic Esophageal Squamous Cell Carcinoma |
Drug: adjuvant chemotherapy Procedure: standard two field Lymphadenectomy Procedure: Total two field Lymphadenectomy Procedure: three field Lymphadenectomy |
Phase 3 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Factorial Assignment Masking: Single Blind (Outcomes Assessor) Primary Purpose: Treatment |
| Official Title: | A Prospective Clinical Trial of Improving the Treatment of Thoracic Esophageal Cancer |
- survival rate [ Time Frame: 5 years ] [ Designated as safety issue: Yes ]
- Disease-free survival
- overall survival
| Estimated Enrollment: | 2615 |
| Study Start Date: | April 2010 |
| Estimated Study Completion Date: | September 2016 |
| Estimated Primary Completion Date: | January 2013 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
| Active Comparator: standard two field +follow-up |
Procedure: standard two field Lymphadenectomy
Standard two field lymphadenectomy is standard mediastinal lymphadenectomy which defined by the International Association of esophageal disease(ISDE) of thoracic esophageal cancer.
Other Name: two field(S)
|
| Experimental: standard two field +adjuvant chemotherapy |
Drug: adjuvant chemotherapy
Docetaxel 75mg/m2 +Nedaplatin 75mg/m2,IV drip on day 1 of each 21 day cycle. Number of cycles: till unacceptable toxicity develops and no more than 4 cycles.
Procedure: standard two field Lymphadenectomy
Standard two field lymphadenectomy is standard mediastinal lymphadenectomy which defined by the International Association of esophageal disease(ISDE) of thoracic esophageal cancer.
Other Name: two field(S)
|
| Experimental: total two field+follow-up |
Procedure: Total two field Lymphadenectomy
Total two field Lymphadenectomy is total mediastinal lymphadenectomy which defined by the International Association of esophageal disease(ISDE) of thoracic esophageal cancer.
Other Name: two field(T)
|
| Experimental: total two field+adjuvant chemotherapy |
Drug: adjuvant chemotherapy
Docetaxel 75mg/m2 +Nedaplatin 75mg/m2,IV drip on day 1 of each 21 day cycle. Number of cycles: till unacceptable toxicity develops and no more than 4 cycles.
Procedure: Total two field Lymphadenectomy
Total two field Lymphadenectomy is total mediastinal lymphadenectomy which defined by the International Association of esophageal disease(ISDE) of thoracic esophageal cancer.
Other Name: two field(T)
|
| Experimental: three field+follow-up |
Procedure: three field Lymphadenectomy
Three field Lymphadenectomy includes abdominal,mediastinal and cervical lymphadenectomy.
Other Name: three field
|
| Experimental: three field+adjuvant chemotherapy |
Drug: adjuvant chemotherapy
Docetaxel 75mg/m2 +Nedaplatin 75mg/m2,IV drip on day 1 of each 21 day cycle. Number of cycles: till unacceptable toxicity develops and no more than 4 cycles.
Procedure: three field Lymphadenectomy
Three field Lymphadenectomy includes abdominal,mediastinal and cervical lymphadenectomy.
Other Name: three field
|
Detailed Description:
According to different location of the primary lesion,the subject can be allocated to two sub-groups:
The patient with upper or middle thoracic esophageal cancer may be assigned to two field(T)-total mediastinal lymphadenectomy group,which is control group in this study or three field lymphadenectomy-Abdominal + mediastinal + cervical lymphadenectomy group,which is study group in this study randomly.
The patient with lower thoracic esophageal cancer may be assigned to three different groups:two field(S)-standard mediastinal lymphadenectomy group, which is control group in this study,or two field(T)-total mediastinal lymphadenectomy,which is the first study group in this study,or three field lymphadenectomy group which is the second study group in this study randomly.
After the operation,the patient whose primary lesion is completely(R0) resected will be assigned to adjuvant chemotherapy group or interview group randomly.
Eligibility| Ages Eligible for Study: | up to 70 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Age≤70 years old;
- Karnofsky Performance Status(KPS)≥80;
- Pathological diagnosis is squamous cell carcinoma of thoracic esophageal which is treated initially;
- Clinical stage is c T 1 ~ 3 N 0 ~ 1 according to the results of endoscopic ultrasonography,chest and abdomen CT and neck ultrasonic.
- The preoperative evaluation of organ function is tolerant of surgery and chemotherapy;
- The subject can understand and sign the informed consent form (ICF);
- The following laboratory tests, made in 4 weeks before first medication, confirmed that bone marrow, liver and kidney function in line with the requirements to participate in research; Hemoglobin(HGB)≥9.0g/L; absolute neutrophils count(ANC)≥1.5×109/L; platelet count(PLT)≥100×109/L; total bilirubin(TBIL)≤1.5N;aspartate aminotransferase (AST)≤2.5N;alanine aminotransferase(ALT)≤2.5N;prothrombin time(PT)≤1.5N, and activated partial thromboplastin time(APTT) is in normal range;endogenous creatinine clearance rate(CRE)≤1.5N.
Exclusion Criteria:
- Cervical esophageal cancer and Non-squamous cell carcinoma of thoracic esophageal cancer;
- Advanced Esophageal Cancer;
- Prior malignancy in 5 years recently;
- History of previous chest radiotherapy;
- History of cardio-cerebral vascular accident in 6 months lately;
- The subject can not understand and sign the informed consent form(ICF).
Contacts and Locations| Contact: Peng Ling, professor | +86-20-87343314 | linpeng@sysucc.org.cn |
| Contact: Tan Zi Hui | +86-20-87343736 | tanzh@sysucc.org.cn |
| China, Guangdong | |
| Sun Yat-sen Uniersity Cancer Center | Recruiting |
| GuangZhou, Guangdong, China, 510060 | |
| Contact: Peng Lin, Professor +86-20-87343314 linpeng@sysucc.org.cn | |
| Contact: Jun Zeng +86-20-87343736 zengjun@sysucc.org.cn | |
| Principal Investigator: Peng Lin, Professor | |
| Principal Investigator: | Peng Lin, Professor | 651, Dongfeng Road East, Guangzhou, P. R. China |
More Information
Publications:
| Responsible Party: | Peng Lin, Sun Yat-sen University Cancer Center |
| ClinicalTrials.gov Identifier: | NCT01137123 History of Changes |
| Other Study ID Numbers: | 2007044 |
| Study First Received: | June 3, 2010 |
| Last Updated: | October 19, 2012 |
| Health Authority: | China: Ethics Committee |
Keywords provided by Sun Yat-sen University:
|
esophageal squamous cell carcinoma |
Additional relevant MeSH terms:
|
Carcinoma Carcinoma, Squamous Cell Esophageal Diseases Esophageal Neoplasms Neoplasms, Glandular and Epithelial Neoplasms by Histologic Type Neoplasms Neoplasms, Squamous Cell Gastrointestinal Diseases |
Digestive System Diseases Gastrointestinal Neoplasms Digestive System Neoplasms Neoplasms by Site Head and Neck Neoplasms Adjuvants, Immunologic Immunologic Factors Physiological Effects of Drugs Pharmacologic Actions |
ClinicalTrials.gov processed this record on May 19, 2013