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Radiotherapy is one of the main treatments for locally advanced esophageal carcinoma (EC). The accuracy of the existing imaging methods in diagnosing and predicting therapeutic efficacy is disappointing, which increases the difficulty in clinical decision-making. In this study, based on a continuous cohort of EC treated with radiotherapy, the clinical and pathological factors of the patients are used to classify them into the appropriate therapeutic group. By multiple liquid biopsy technologies, combining with radiomics, we intend to construct prediction models of prognosis, therapeutic effect and toxicity. The aim of this RWS is to provide appropriate individualized regimen, further optimize the treatment mode based on precision radiotherapy and improve the outcome and quality of life of EC patients.
Radiotherapy is one of the main treatments for locally advanced esophageal squamous cell carcinoma (ESCC). The guidelines recommend neoadjuvant concurrent chemoradiotherapy plus surgery for resectable or potentially resectable patients; for unresectable patients, definitive chemoradiotherapy is the standard treatment. However, due to the complexity of the biological behavior of esophageal cancer (EC) and individual differences, fully complying with guideline recommendations in clinical practice is difficult and idealized. The results of prospective clinical trials are difficult to meet the demand of clinical diagnosis and treatment, thus, carrying out high-quality real-world study (RWS) is necessary.
Three-dimensional conformal radiotherapy (3DCRT) for unresectable EC yields 5-year OS rates of 34%-45.6%, which is an improvement over the rates reported in the RTOG 85-01 and 94-05 studies. Even so, there is still room for improvement of local control rate and overall survival. The accuracy of the existing imaging methods [computed tomography (CT), magnetic resonance imaging (MRI), endoscopic ultrasonography (EUS), endoscopic ultrasonography (EUS), as well as positron-emission tomography (PET)-CT, etc.] in diagnosing and predicting therapeutic efficacy is disappointing, which increases the difficulty in clinical decision-making. It is worthy to investigate an appropriate individualized radiation regimen based on different treatment sensitivity.
In this study, based on a continuous cohort of EC treated with radiotherapy, the clinical and pathological factors of the patients are used to classify them into the appropriate therapeutic group. Collect the blood and saliva samples before, during and after radiotherapy; the remaining diagnostic biopsy tissue samples. By using multiple liquid biopsy technologies [microbial flora, circulating tumor DNA (ctDNA), genome, RNA, and immunophenotype, ect.], combining with radiomics, construct prediction models of prognosis, therapeutic effect and toxicity. The aim of this RWS is to provide appropriate individualized regimen, further optimize the treatment mode based on precision radiotherapy and improve the outcome and quality of life of EC patients.
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| 3DCRT | Radiation | Three-dimensional conformal radiotherapy (3DCRT) |
| Measure | Description | Time Frame |
|---|---|---|
| 1-, 2-, 3-year overall survival | Overall survival | From treatment initiation to death from any cause or censor, assessed up to 36 months |
| Measure | Description | Time Frame |
|---|---|---|
| 1-, 2-, 3-year progression-free survival | Progression-free survival | From treatment initiation to first documented progression or death or censor, assessed up to 36 months |
| Rate of acute toxicity (any and above grade 3) |
| Measure | Description | Time Frame |
|---|---|---|
| Biomarkers to predict radiotherapy efficacy | potential biomarkers in tumor samples and blood samples | baseline/through study completion, an average of 2 year |
Inclusion Criteria:
Exclusion Criteria:
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Patients with esophageal cancer who are acceptable and tolerable to radiotherapy
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Department of Radiation Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences (CAMS) and Peking Union Medical College (PUMC) | Recruiting | Beijing | Beijing Municipality | 100021 |
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| ID | Term |
|---|---|
| D004938 | Esophageal Neoplasms |
| ID | Term |
|---|---|
| D005770 | Gastrointestinal Neoplasms |
| D004067 | Digestive System Neoplasms |
| D009371 | Neoplasms by Site |
| D009369 | Neoplasms |
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The blood and saliva samples before, during and after radiotherapy; the remaining diagnostic biopsy tissue samples.
Toxicities according to CTCAE criteria
| From enrollment to 3 months after treatment |
| Rate of acute/late toxicity (any and above grade 3) | Toxicities of chemoradiation therapy | After 3 months of enrollment |
| 1-month short-term efficacy | Short-term efficacy | Assessed 1-month after radiotherapy (short-term) according to RECIST 1.1 |
| Quality of Life change, QoL | measurement basing on EORTC (Quality of life of patients with oesophageal cancer) QLQ-C30 tables | 1/3/6/12/24 months after radiotherapy |
| Quality of life of patients with oesophageal cancer | measurement basing on EORTC (Quality of life of patients with oesophageal cancer) QLQ-OES18 tables | 1/3/6/12/24 months after radiotherapy |
| China |
|
| D006258 |
| Head and Neck Neoplasms |
| D004066 | Digestive System Diseases |
| D004935 | Esophageal Diseases |
| D005767 | Gastrointestinal Diseases |