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Simultaneous Integrated Boost Radiotherapy and Concurrent Nimotuzumab or Chemotherapy for Esophageal Carcinoma

Prospective, Non-randomised Phase Ⅱ Study of Simultaneous Integrated Boost Radiotherapy and Concurrent Nimotuzumab or Chemotherapy for Locally Advanced Esophageal Carcinoma

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02858206
Enrollment
120
Registered
2016-08-08
Start date
2016-06-30
Completion date
2021-11-30
Last updated
2019-07-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Esophageal Neoplasms

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

DRUGNimotuzumab

nimotuzumab 400mg per week which start from 1 week before radiotherapy and in the following 4 weeks

DRUGPaclitaxel

Paclitaxel from 45 to 60 mg/m2 per week which start from 1 week before radiotherapy and in the following 4 weeks

DRUGNedaplatin

Nedaplatin 25mg/m2 per week which start from 1 week before radiotherapy and in the following 4 weeks

PROCEDUREEsophagectomy

Radical esophagectomy 4-6 weeks after neoadjuvant therapy

Sponsors

Hebei Medical University Fourth Hospital
CollaboratorOTHER
Affiliated Hospital of Hebei University
CollaboratorOTHER
Beijing Army General Hospital
CollaboratorOTHER_GOV
Beijing Hospital
CollaboratorOTHER_GOV
Peking University First Hospital
CollaboratorOTHER
Tianjin Medical University Cancer Institute and Hospital
CollaboratorOTHER
Henan Cancer Hospital
CollaboratorOTHER_GOV
The Affiliated Hospital of Inner Mongolia Medical University
CollaboratorOTHER
The First Affiliated Hospital with Nanjing Medical University
CollaboratorOTHER
Fujian Cancer Hospital
CollaboratorOTHER_GOV
Chinese Academy of Medical Sciences
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 69 Years
Healthy volunteers
No

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

MeasureTime frame
Pathological response rateUp to 1 year
Pathological lymph node metastases rateUp to 1 year
R0 resection rateUp to 1 year
Adverse eventsUp to 2 years

Secondary

MeasureTime frame
Overall survival (OS)Up to 2 years
Recurrence rateUp to 2 years
Disease-free survival (DFS)Up to 2 years

Countries

China

Contacts

Primary ContactZefen Xiao, MD
xiaozefen@sina.com8610-87787643
Backup ContactWei Deng, MD
sherrydw@126.com+8618813019080

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026