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

Ministry of Scientific Research and Information Technology, Poland

Status and phase: Terminated; Phase 3

Conditions: Squamous Cell Cancer; Esophageal Neoplasms

Treatments: Drug: neoadjuvant chemotherapy (cisplatin, 5-fluorouracil); Procedure: transthoracic esophagectomy 2-field extended lymphadenectomy; Radiation: neoadjuvant chemoradiotherapy

Study type: Interventional

Funder types: Other

Identifiers

NCT00559351

PL SCSR 6P05C01320

6P05C01320

Details and patient eligibility

About

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.

Full 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.

Enrollment: 84 patients

Sex: All

Ages: 18 to 75 years old

Volunteers: No Healthy Volunteers

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.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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84 participants in 3 patient groups

S

Active Comparator group

Description:

esophagectomy

Treatment:

Procedure: transthoracic esophagectomy 2-field extended lymphadenectomy

CHTS

Experimental group

Description:

neoadjuvant chemotherapy followed by esophagectomy

Treatment:

Drug: neoadjuvant chemotherapy (cisplatin, 5-fluorouracil)

CHRTS

Experimental group

Description:

neoadjuvant chemoradiotherapy followed by esophagectomy

Treatment:

Radiation: neoadjuvant chemoradiotherapy