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Treatment of non-operable esophageal cancers is based on radiochemotherapy, or exclusive radiotherapy.
The cardiac toxicity of radiotherapy in the treatment of thoracic tumor localizations is well documented, however, more and more studies are calling for the use of dosimetric parameters related to cardiac sub-structures to be integrated into clinical practice, rather than considering the heart as a whole.
With this in mind, the aim of this study is to define the parameters, particularly dosimetric ones linked to cardiac sub-structures, influencing survival in patients treated with exclusive radiotherapy or radiochemotherapy for esophageal cancer.
Treatment of non-operable esophageal cancers is based on radiochemotherapy, or exclusive radiotherapy.
The cardiac toxicity of radiotherapy in the treatment of thoracic tumor localizations is well documented, however, more and more studies are calling for the use of dosimetric parameters related to cardiac sub-structures to be integrated into clinical practice, rather than considering the heart as a whole.
Although most of these data have been studied in populations with long-term follow-up, such as breast cancer, cardiac toxicity and the reduced survival it entails are also found in diseases such as esophageal cancer.
With this in mind, the aim of this study is to define the parameters, particularly dosimetric ones linked to cardiac sub-structures, influencing survival in patients treated with exclusive radiotherapy or radiochemotherapy for esophageal cancer.
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| Measure | Description | Time Frame |
|---|---|---|
| Overall survival (OS) | OS is defined as the time elapsed between inclusion and death, whatever the cause. | through study completion, an average of 1 year |
| Measure | Description | Time Frame |
|---|---|---|
| The rate of cardiac events. | The rate of cardiac events. | through study completion, an average of 1 year |
| Response rate. | Response rate. |
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Inclusion Criteria:
Exclusion Criteria:
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Non-operated adult patients with localized or locally advanced esophageal cancer treated with radiochemotherapy or radiotherapy alone for curative purposes.
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Vincent BOURBONNE, MD, PhD | Contact | +33298223398 | vincent.bourbonne@chu-brest.fr |
| Name | Affiliation | Role |
|---|---|---|
| Vincent Bourbonne, MD, PhD | Radiation Oncology Department, Brest University Hospital | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Chu Brest | Recruiting | Brest | 29609 | France |
All collected data that underlie results in a publication
Data will be available beginning three years and ending fifteen years following the final study report completion
Data access requests will be reviewed by the internal committee of Brest UH. Requestors will be required to sign and complete a data access agreement
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| ID | Term |
|---|---|
| D004938 | Esophageal Neoplasms |
| D066126 | Cardiotoxicity |
| ID | Term |
|---|---|
| D005770 | Gastrointestinal Neoplasms |
| D004067 | Digestive System Neoplasms |
| D009371 | Neoplasms by Site |
| D009369 | Neoplasms |
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| through study completion, an average of 1 year |
| Progression-free survival (PFS). | PFS is defined as the time elapsed between inclusion and tumor progression assessed by an expert panel according to RECIST v1.1 criteria, or death from any cause. | through study completion, an average of 1 year |
| D006258 |
| Head and Neck Neoplasms |
| D004066 | Digestive System Diseases |
| D004935 | Esophageal Diseases |
| D005767 | Gastrointestinal Diseases |
| D006331 | Heart Diseases |
| D002318 | Cardiovascular Diseases |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D064420 | Drug-Related Side Effects and Adverse Reactions |
| D064419 | Chemically-Induced Disorders |
| D011832 | Radiation Injuries |
| D014947 | Wounds and Injuries |