Phase III Study of Neo-adjuvant Chemoradiotherapy Followed by Surgery for Squamous Cell Esophageal Cancer

Sponsor
Sun Yat-sen University (Other)
Overall Status
Unknown status
CT.gov ID
NCT01216527
Collaborator
Affiliated Cancer Hospital of Shantou University Medical College (Other), Shanghai Chest Hospital (Other), Fudan University (Other), Zhejiang Cancer Hospital (Other), Taizhou Hospital (Other), The Second People's Hospital of Sichuan (Other), Tianjin Medical University Cancer Institute and Hospital (Other)
430
2
2
150
215
1.4

Study Details

Study Description

Brief Summary

The primary objective is to compare neo-adjuvant chemoradiotherapy followed by surgery versus surgery, in terms of the overall survival time (OS) in patients with Stage IIB or III squamous cell esophageal carcinoma.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Neo-adjuvant Chemoradiotherapy followed by Surgery
  • Procedure: surgery
Phase 3

Detailed Description

Esophageal cancer (EC) is the eighth most common cancers in the world, with more than 480,000 new cases and 400,000 deaths occurred annually worldwide. In China, every year, no matter new cases or deaths account for more than half of the world. Besides, over 90% of Chinese patients have esophageal squamous cell carcinoma (ESCC).

Surgery is the main treatment of this disease, but the prognosis of patients with locally advanced esophageal cancer is rather poor. As a result of surgery alone, the 5-year survival rate of about 25% has not changed significantly in several decades.

Preoperative chemoradiotherapy followed by surgery seems to hopefully improve the survival of EC. Nevertheless, the results of different studies were inconsistent. Recently, the CROSS trial has demonstrated that preoperative chemoradiotherapy can significantly increased the overall survival of patients with EC compared with surgery alone. It should be noticed that only 84 cases(23%) of ESCC were enrolled in this trial with potential minimal follow-up of 2 years, which may be not perfect to evaluate the effect of this combined therapy for this tumor type.

Up till now, vinorelbine has no indications for esophageal cancer, although, some studied have reported its effect and feasibility to the therapy of EC. Vinorelbine has similar mechanism with paclitaxel and docetaxel, which are recommended for the chemotherapy of EC by NCCN. They are all classified as antimicrotubule agents, which cause mitotic arrest and eventual cell death through inhibition of microtubule dynamics. In comparison with the taxanes, vinorelbine has obvious advantage of few cardiac toxicity. This should be beneficial to prevent cardiac side effects of chemoradiotherapy, especially for the middle or lower thoracic EC, which account for over 70% of thoracic EC in China. For this group of patients, radiotherapy can hardly avoid cardiac toxicity.

Based on our preliminary study, we have demonstrated the validity and safety of vinorelbine and cisplatin-based neoadjuvant chemoradiotherapy.

We are to carry out a phased III clinical trial to investigate the effect of this multidisciplinary therapy for the overall survival of patients with locally advanced ESCC.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
430 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
A Phase III, Multicenter Randomized Controlled Study of Neo-adjuvant Chemoradiotherapy Followed by Surgery Versus Surgery for Locally Advanced Squamous Cell Esophageal Carcinoma
Study Start Date :
Jun 1, 2007
Anticipated Primary Completion Date :
Dec 1, 2019
Anticipated Study Completion Date :
Dec 1, 2019

Arms and Interventions

Arm Intervention/Treatment
Experimental: experimental group

Neo-adjuvant Chemoradiotherapy followed by Surgery

Procedure: Neo-adjuvant Chemoradiotherapy followed by Surgery
Radiotherapy combined with concomitant chemotherapy: Radiotherapy Program:External radiation with a total dose of 40.0Gy is given in 20 fractions of 2.0Gy,5 fractions a week. neo-chemotherapy program: Vinorelbine 25mg/m2, IV (in the vein) on day 1 and day 8 of each 21 day cycle. Cisplatin 75mg/m2,IV DRIP on day 1 of each 21 day cycle;or Cisplatin 25mg/m2,IV DRIP on day 1 to day 4 of each 21 day cycle. Number of cycles:two surgery:Mckeown Modification Surgery and total two-field lymphadenectomy

Active Comparator: control group

only Surgery

Procedure: surgery
two field lymphadenectomy

Outcome Measures

Primary Outcome Measures

  1. Overall survival rate [3 and 5 years]

Secondary Outcome Measures

  1. toxicities of neo-adjuvant chemoradiotherapy [56 days]

    Evaluate the toxicities of neo-adjuvant chemoradiotherapy,according to National Cancer Institute Common Terminology Criteria for Adverse Event,Version 3.0(CTC AE3.0).

  2. assessment in perioperation [perioperative period]

    Removal rate, Time of operation, Quantity of bleeding, Thoracic Drainage, Days of Hospitalization, Rate of Operative Complication, Mortality of perioperation,

  3. efficacy of neo-adjuvant chemoradiotherapy [4 weeks after completion of radiotherapy]

    Criteria:Response Evaluation Criteria in Solid Tumors,RECIST

  4. Disease free survival rate [5 years]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 70 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Histologic diagnosis of squamous cell thoracic esophageal carcinoma of Stage IIB or III, which is potentially resectable.

  2. Patients must not have received any prior anticancer therapy.

  3. More than 6 months of expected survival.

  4. Age ranges from 18 to 70 years.

  5. Absolute white blood cells count ≥4.0×109/L, neutrophil ≥1.5×109/L, platelets ≥100.0×109/L, hemoglobin ≥90g/L, and normal functions of liver and kidney.

  6. Karnofsky performance status (KPS) of 90 or more.

  7. Signed informed consent document on file.

Exclusion Criteria:
  1. Patients are diagnosed or suspected to be allergic to cisplatin or vinorelbine.

  2. Patients with concomitant hemorrhagic disease.

  3. Pregnant or breast feeding.

  4. Inability to use gastric conduit after esophagectomy because of a prior surgery.

  5. Patients with concomitant peripheral neuropathy, whose CTC status is 2 or even more.

  6. Have a prior malignancy other than esophageal carcinoma, carcinoma in situ of the cervix, nonmelanoma skin cancer or cured early stage of prostate cancer.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Sun Yat-sen Uniersity Cancer Center GuangZhou Guangdong China 510060
2 Cancer Hospital of Shantou University Medical College Shantou Guangdong China 515000

Sponsors and Collaborators

  • Sun Yat-sen University
  • Affiliated Cancer Hospital of Shantou University Medical College
  • Shanghai Chest Hospital
  • Fudan University
  • Zhejiang Cancer Hospital
  • Taizhou Hospital
  • The Second People's Hospital of Sichuan
  • Tianjin Medical University Cancer Institute and Hospital

Investigators

  • Principal Investigator: Jian-hua Fu, Professor, Sun Yat-sen University

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Jianhua Fu, Professor, Sun Yat-sen University
ClinicalTrials.gov Identifier:
NCT01216527
Other Study ID Numbers:
  • 2007048
First Posted:
Oct 7, 2010
Last Update Posted:
Feb 27, 2017
Last Verified:
Feb 1, 2017
Keywords provided by Jianhua Fu, Professor, Sun Yat-sen University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 27, 2017