Esophageal Neoplasms
Conditions
Keywords
Locally advanced esophageal cancer, Radiotherapy and nimotuzumab, Concurrent chemoradiotherapy
Brief summary
This prospective, non-randomized phase II study aims to compare radiotherapy and concurrent nimotuzumab with concurrent chemoradiotherapy to obtain a non-inferior pCR rate and pathological lymph node metastases rate in premise of lower toxicities in locally advanced esophageal cancer.
Detailed description
In the era of IMRT and concurrent chemoradiotherapy, the 5-year overall survival of esophageal cancer increase from 10% to about 20%-40%, recurrence rate decrease from 80% to 50%-60%, and local recurrence remains to be the most important type of failure. What called for is to enhance local control without increasing toxicity to improve survival. The investigators have found effective and safe regimen of simultaneously integrated boost radiotherapy in previous study, which can achieve high dose in tumor area with avoid of normal tissues. However, a recent prospective study reported that neoadjuvant chemoradiotherapy resulted in much higher toxicities compares to neoadjuvant chemotherapy (46% vs. 15%, p= 0.04). Although chemoradiotherapy reached a higher pCR rate (28% vs. 9%, p=0.002), patients did not differ in survival in two groups. Nimotuzumab is an humanized monoclonal antibody against EGFR. Radiotherapy combines Nimotuzumab reveals synergistic effect in head and neck cancers with lower toxicities as compared to concurrent chemoradiotherapy. Our previous study showed that EGFR expression rate were similar in esophageal cancer and head and neck cancers. Based on above results, the investigators design this study which aims to obtain a non-inferior pCR rate and pathological lymph node metastases rate in premise of lower toxicities.
Interventions
To achieve a prophylactic dosage and radical dosage of 1.8Gy and 2.14Gy once respectively
nimotuzumab 400mg per week which start from 1 week before radiotherapy and in the following 4 weeks
Paclitaxel from 45 to 60 mg/m2 per week which start from 1 week before radiotherapy and in the following 4 weeks
Nedaplatin 25mg/m2 per week which start from 1 week before radiotherapy and in the following 4 weeks
Radical esophagectomy 4-6 weeks after neoadjuvant therapy
Sponsors
Study design
Eligibility
Inclusion criteria
* Diagnosis of clinical stage T1-4aN0-1M1a untreated squamous esophageal carcinoma * KPS≥70 * Adequate organ function * No known history of drug allergy
Exclusion criteria
* Known drug allergy * Insufficient hepatorenal function * Severe cardiovascular diseases, diabetes with uncontrolled blood sugar, mental disorders, uncontrolled severe infection, active ulceration which need intervention.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pathological response rate | Up to 1 year |
| Pathological lymph node metastases rate | Up to 1 year |
| R0 resection rate | Up to 1 year |
| Adverse events | Up to 2 years |
Secondary
| Measure | Time frame |
|---|---|
| Overall survival (OS) | Up to 2 years |
| Recurrence rate | Up to 2 years |
| Disease-free survival (DFS) | Up to 2 years |
Countries
China