Study of Simultaneous Modulated Accelerated Radiation Therapy Concurrent With Chemotherapy to Treat Esophageal Cancer
Primary Purpose
Esophageal Neoplasms
Status
Completed
Phase
Phase 2
Locations
China
Study Type
Interventional
Intervention
SMART
PF
Sponsored by
About this trial
This is an interventional treatment trial for Esophageal Neoplasms focused on measuring Esophageal squamous cell carcinoma, SMART, IMRT, Chemotherapy
Eligibility Criteria
Inclusion Criteria:
- pathological proven diagnosis of primary squamous cell carcinoma of the esophagus
- the primary disease located in cervical, upper or middle thoracic esophagus
- no distant metastases
- zubrod performance status: 0~2
- life expectancy > 6 months; -absence of another malignancy
- adequate liver, renal and bone marrow function
- women of childbearing potential and male participants must practice adequate contraception
- patient must provide study-specific informed consent prior to study entry
Exclusion Criteria:
- evidence of tracheoesophageal or Mediastinal-esophageal fistula
- prior invasive malignancy (except non-melanomatous skin cancer) unless disease free for a minimum of 2 years
- prior radiation therapy that would result in overlap of planned radiation therapy fields; - Severe, active comorbidity
- pregnancy or women of childbearing potential and men who are sexually active and not willing/able to use medically acceptable forms of contraception
- women who are nursing
Sites / Locations
- Cancer Hospital, Shantou University Medical College
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
SMART combined with PF chemotherpay
Arm Description
SMART-base IMRT with concurrent and adjuvant chemotherapy(cisplatin and 5-fluorouracil)
Outcomes
Primary Outcome Measures
Toxicities
The probabilities of grade ≥ 3 acute toxicities and 2-year late toxicities of esophagus and lungs as assessed by CTCAE 4.0
Secondary Outcome Measures
Local control rate
The percentage of patients without locoregional tumor recurrence 2 years after treatment
overall survival rate
The percentage of patients that are alive 2 years after treatment
Complete blood count
The complete blood count as assessed by a Coulter (LH 750 Haematology Analyzer)
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT01670409
Brief Title
Study of Simultaneous Modulated Accelerated Radiation Therapy Concurrent With Chemotherapy to Treat Esophageal Cancer
Official Title
A Phase II Study of Simultaneous Modulated Accelerated Radiation Therapy Concurrent With Chemotherapy in Patients With Esophageal Squamous Cell Carcinoma
Study Type
Interventional
2. Study Status
Record Verification Date
December 2021
Overall Recruitment Status
Completed
Study Start Date
August 2012 (undefined)
Primary Completion Date
August 2015 (Actual)
Study Completion Date
August 2015 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Chuangzhen Chen
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this study is to evaluate the acute and 2-year late toxicities, the 2-year local control and overall survival rates in patients with esophageal squamous cell carcinoma receiving simultaneous modulated accelerated radiation therapy concurrent with chemotherapy.
Detailed Description
Esophageal cancer is one of the most common malignant diseases in China, especially in Chaoshan region. Concurrent chemoradiotherapy is the standard non-surgical treatment method for this disease and the radiation schedule is about 50.4~60 Gray (Gy) in total, 1.8~2Gy per fraction generally. However, although with such comprehensive method, noncontrol of local disease or recurrence is still the main reason of failure.
Most patients with esophageal cancer suffer from malnutrition. A number of factors including hypoxic, inflammation, radioresistance and accelerated repopulation may contribute to local failures of disease after treatment; therefore a higher radiation biological equivalent dose (BED) will improve the local control probability. Although the intergroup 0123 (INT123) trial had shown that simply increasing total radiation dose could not gain better local control or overall survival rate, however, the ability of this trial to test the potential benefits of higher radiation dose could be compromized by the deficiencies within them, such as, observation bias,large radiated target volume and usage of conventional radiation technique. In other words, the probability that increasing radiation may help improving the control of disease should not be denied.
Modern radiation techniques, such as intensity modulation radiation therapy (IMRT), specially, are able to improve the coverage of target volumes and sparing of critical structures, while increase the total radiation dose. By using simultaneous modulated accelerated radiation therapy (SMART) technique, the doses to the relevant normal organs per fraction could be reduced significantly, while the doses to tumor could be increased to higher than 2Gy. Thus reach the double goal of protection of normal tissues, increasing total radiation Equivalent Uniform Dose (EUD). Dosimetric study has proven the feasibility and superiority of SMART-base IMRT in radiation treatment of esophageal cancer, compared with conventional technique.
Overall, SMART-base IMRT concurrent with chemotherapy may improve the local control and overall survival rate of patients with esophageal cancer; Meanwhile, the acute and late toxicities would be tolerable and slighter than that of conventional technique.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Esophageal Neoplasms
Keywords
Esophageal squamous cell carcinoma, SMART, IMRT, Chemotherapy
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
85 (Actual)
8. Arms, Groups, and Interventions
Arm Title
SMART combined with PF chemotherpay
Arm Type
Experimental
Arm Description
SMART-base IMRT with concurrent and adjuvant chemotherapy(cisplatin and 5-fluorouracil)
Intervention Type
Radiation
Intervention Name(s)
SMART
Intervention Description
The PTV (planning target volume) of gross tumor will receive radiation dose of 66Gy, 2.2Gy per fraction and the PTV of subclinical disease will receive 54Gy, 1.8Gy per fraction,5 fraction per week.
Intervention Type
Drug
Intervention Name(s)
PF
Other Intervention Name(s)
cisplatin plus 5fluorouracil
Intervention Description
Concurrent and adjuvant chemotherapy: Cisplatin, 80mg/m2, intravenous on day 1, 5fluorouracil 0.5/m2, intravenous on d1 to d4. Two cycles during radiation treatment on d1 and d28. Two additional cycles after radiation treatment, 4 weeks per cycle.
Primary Outcome Measure Information:
Title
Toxicities
Description
The probabilities of grade ≥ 3 acute toxicities and 2-year late toxicities of esophagus and lungs as assessed by CTCAE 4.0
Time Frame
The period during treatment and the 2 years after treatment
Secondary Outcome Measure Information:
Title
Local control rate
Description
The percentage of patients without locoregional tumor recurrence 2 years after treatment
Time Frame
2 years after treatment
Title
overall survival rate
Description
The percentage of patients that are alive 2 years after treatment
Time Frame
2 years after treatment
Title
Complete blood count
Description
The complete blood count as assessed by a Coulter (LH 750 Haematology Analyzer)
Time Frame
before radiation treatment and after every 5 fraction of radiotherapy (7 time points in total)
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
pathological proven diagnosis of primary squamous cell carcinoma of the esophagus
the primary disease located in cervical, upper or middle thoracic esophagus
no distant metastases
zubrod performance status: 0~2
life expectancy > 6 months; -absence of another malignancy
adequate liver, renal and bone marrow function
women of childbearing potential and male participants must practice adequate contraception
patient must provide study-specific informed consent prior to study entry
Exclusion Criteria:
evidence of tracheoesophageal or Mediastinal-esophageal fistula
prior invasive malignancy (except non-melanomatous skin cancer) unless disease free for a minimum of 2 years
prior radiation therapy that would result in overlap of planned radiation therapy fields; - Severe, active comorbidity
pregnancy or women of childbearing potential and men who are sexually active and not willing/able to use medically acceptable forms of contraception
women who are nursing
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Chuangzhen Chen, MD
Organizational Affiliation
Cancer Hospital, Shantou University Medical College
Official's Role
Principal Investigator
Facility Information:
Facility Name
Cancer Hospital, Shantou University Medical College
City
Shantou
State/Province
Guangdong
ZIP/Postal Code
515031
Country
China
12. IPD Sharing Statement
Citations:
PubMed Identifier
25320535
Citation
Zhang WZ, Chen JZ, Li DR, Chen ZJ, Guo H, Zhuang TT, Li DS, Zhou MZ, Chen CZ. Simultaneous modulated accelerated radiation therapy for esophageal cancer: a feasibility study. World J Gastroenterol. 2014 Oct 14;20(38):13973-80. doi: 10.3748/wjg.v20.i38.13973.
Results Reference
derived
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Study of Simultaneous Modulated Accelerated Radiation Therapy Concurrent With Chemotherapy to Treat Esophageal Cancer
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