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RCT on the Combined Modality Treatment of Squamous Cell Carcinoma of the Esophagus

Phase 3
Terminated
Conditions
Esophageal Neoplasms
Squamous Cell Cancer
Interventions
Procedure: transthoracic esophagectomy 2-field extended lymphadenectomy
Drug: neoadjuvant chemotherapy (cisplatin, 5-fluorouracil)
Radiation: neoadjuvant chemoradiotherapy
Registration Number
NCT00559351
Lead Sponsor
Ministry of Scientific Research and Information Technology, Poland
Brief Summary

The purpose of the study was to test a null hypothesis that a combined modality treatment of esophageal cancer with neoadjuvant chemotherapy or chemoradiotherapy is equivalent to surgery alone and what are the benefits from adding irradiation to chemotherapy in neoadjuvant treatment of esophageal cancer.

Detailed Description

The choice of the most beneficial method of treatment in esophageal cancer remains controversial and is the subject of vigorous debate. Surgery is still regarded as the principle modality among treatment strategies, with longterm survival achieved mainly in less advanced cases. More advanced cases, diagnosed more frequently, are more problematic in selection of the optimal therapeutic method. One of the options for improving treatment outcome in patients with advanced esophageal cancer is combined modality treatment with chemo- and chemoradiotherapy. Currently available RCTs have tested preoperative chemotherapy or chemoradiotherapy separately in comparison to surgery alone. Moreover, we do not know from these trials what is the added value of irradiation in a combined modality therapy over a preoperative chemotherapy. Another drawback of available RCTs is combining 2 different biological cancer entities: adenocarcinoma and squamous cell carcinoma of the esophagus as well as carcinoma of the esophagus and gastro-esophageal junction. That were the reasons for designing our trial testing 3 principal modes of esophageal cancer therapy: surgery vs. chemotherapy + surgery vs. chemoradiotherapy + surgery on homogenous population of esophageal cancer patients with single pathological type - squamous cell carcinoma affecting thoracic esophagus.

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
84
Inclusion Criteria
  • Informed consent
  • Histopathologically proven, clinically stage II-III (cTNM according to AJCC/UICC classification), primary squamous cell carcinoma of the thoracic esophagus
  • Patients' age above 18 years
  • General condition with Karnofsky performance status of >70
  • Circulatory and pulmonary capacity at normal range (FEV1 >60%; FVC >60%, NYHA I-II, cardiac output >40%)
  • Normal function of the bone marrow (RBC >3,5 T/l; PLT >100 G/l)
  • Normal renal (creatinine <1.5 of the upper limit) and liver (AST or ALT <2,5 of the upper limit or bilirubin <1,5 of the upper limit) function
Exclusion Criteria
  • Metastatic disease
  • Synchronous malignancy
  • History of other cancer within 5 years prior to esophageal cancer treatment
  • History of allergic reaction to cisplatin of 5-fluorouracil
  • Systemic infection
  • Pregnancy or female patients in childbearing age without proper contraceptives.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Stransthoracic esophagectomy 2-field extended lymphadenectomyesophagectomy
CHTSneoadjuvant chemotherapy (cisplatin, 5-fluorouracil)neoadjuvant chemotherapy followed by esophagectomy
CHRTSneoadjuvant chemoradiotherapyneoadjuvant chemoradiotherapy followed by esophagectomy
Primary Outcome Measures
NameTimeMethod
mean, median, 1-year, 3-year, 5-year overall survival5 years
Secondary Outcome Measures
NameTimeMethod
toxicity-related morbidity and mortality30-day
postoperative morbidity and mortality30-day
clinical and pathological response rates60-day
curative resection rate30-day

Trial Locations

Locations (1)

2nd Department of General, Gastrointestinal Surgery & Surgical Oncology of the Digestive Tract, Medical University of Lublin, Poland

🇵🇱

Lublin, Lubelskie, Poland

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