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NCT Number: NCT03734952

Postoperative Radiotherapy in Thoracic Esophageal Squamous Cell Carcinoma With Neoadjuvant Chemoradiotherapy

The primary objective is to compare surgery with postoperative radiotherapy (PORT) versus surgery, in terms of the overall survival time (OS) in Stage II or III squamous cell esophageal carcinoma with neoadjuvant chemoradiotherapy(nCRT).

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Key information

Conditions

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Fujian Medical University Union Hospital

Fuzhou, Fujian, 350000, China

Location status: Recruiting

Location contact

Benhua Xu

CONTACT

About this study

Esophageal squamous cell carcinoma (ESCC) is a common type of esophageal carcinoma in China, which is characterized by rapid development and fatal prognosis in most patients. Neoadjuvant chemoradiotherapy (nCRT) has been explored for many years in western countries and Japan, and proved to get survival benefit, especially for locally advanced esophageal cancer. However, the recurrence is the major cause of treatment failure in patients with ESCC. Our hypothesis is that inadequate radiation dose leads to recurrence of ESCC with nCRT and PORT lower recurrence rate and improved OS. As is known, there are no any studies concentrating on PORT in ESCC with nCRT. Patients are randomly assigned to PORT (Group A) or without PORT (Group B) with a 1:1 allocation ratio. The primary outcome is OS assessed with a minimum follow-up of 60 months. Secondary outcomes are progression-free survival (PFS), recurrence-free survival (RFS).

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients must not have received any prior anticancer therapy Histologically-confirmed squamous cell carcinoma of the esophagus;
  • Tumors of the esophagus are located in the thoracic cavity;
  • Pre-treatment stageⅡ-Ⅲ (AJCC/UICC 8th Edition)
  • Male or non pregnant female
  • Age is between 18 years and 65 years,
  • Eastern Cooperative Oncology Group (ECOG) performance status 0-1 or Karnofsky performance status (KPS) of 70 or more;
  • Adequate bone marrow function (White Blood Cells ≥4x109 /L; Neutrophil ≥1.5×109 /L; Hemoglobin≥ 90 g/L; platelets≥100x109 /L);
  • Adequate liver function (Total bilirubin, Aspartate transaminase(AST) and Alanine transaminase (ALT) ≤2x Upper Level of Normal (ULN));
  • Adequate renal function (serum creatinine (SCr) ≤1.5 x ULN);
  • The patient has provided written informed consent and is able to understand and comply with the study.

Exclusion criteria

  • Patients with non-squamous cell carcinoma histology;
  • Patients with advanced inoperable or metastatic esophageal cancer;
  • Patients with another previous or current malignant disease;
  • Any patient with a significant medical condition which is thought unlikely to tolerate the therapies. Such as cardiac disease;
  • Age >65 years;
  • Pregnant or lactating female or people during the birth-period who refused to take contraceptives;
  • Uncontrolled seizures or psychiatric diseases, loss of control over their own behavior;
  • Patients who refuse surgery after neoadjuvant chemotherapy;
  • Unsuitable to be enrolled in the trial in the opinion of the investigators

Treatment and study plan

Neoadjuvant Radiotherapy Program:

Radiation

Gross tumor volume (GTV) should include the primary tumor and involved regional lymph nodes as identified on pre-treatment diagnostic studies. Clinical target volume (CTV) is defined as the primary tumor plus 3cm expansion superiorly and inferiorly along the length of the esophagus and a 1cm radial expansion.The nodal CTV should be defined by a 0.5cm expansion from the nodal GTV.CTV should also include coverage the nodal region(s) in which the involved lymph node(s). A total dose of 45 Gy in 25 fractions is delivered 5 days per week on workdays with intensity modulated radiotherapy (IMRT).

Neoadjuvant chemotherapy Program

Drug

Chemotherapy is delivered concomitantly and composed of two cycles of Docetaxel 60mg per square meter of body-surface area and cisplatin 75mg per square meter of body-surface area every 21 days at the intervals of neoadjuvant radiotherapy.

Esophagectomy program:

Procedure

Patients receive esophagectomy in 4-6 weeks after neoadjuvant neoadjuvant chemotherapy

Postoperative radiotherapy program

Radiation

A total dose of 18 Gy in10 fractions is delivered 5 days per week on workdays with IMRT.

Primary outcomes

  1. overall survival

    Time frame: From enrollment to 5 years after the end of treatment

    The length of time from enrollment until the time of death

Secondary outcomes

  1. disease free survival

    Time frame: From enrollment to 5 years after the end of treatment

    The length of time from enrollment until the time of progression of disease

  2. local recurrence rate

    Time frame: From enrollment to 5 years after the end of treatment

    The percent of the patient with local recurrence

  3. Side effects

    Time frame: From enrollment to 12 weeks after end of the treatment

    adverse events according to NCI CTCAE 4.0 criteria

Study contacts

Contact information is provided by the study sponsor or research team.

Benhua Xu, doctor

CONTACT

[email protected]

+86-13696884375

Jianyuan Song, doctor

CONTACT

[email protected]

+86-13625045732

Sponsors and collaborators

Lead sponsor

Fujian Medical University Union Hospital

Other

Registry information

Official study title

Prospective Randomized Controlled Trial of Postoperative Radiotherapy in Thoracic Esophageal Squamous Cell Carcinoma With Neoadjuvant Chemoradiotherapy

Important dates

Study start
2023
Primary completion
2029
Study completion
2029
First posted
Nov 8, 2018
Registry last updated
Sep 25, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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