Real-world Study on Comprehensive Treatment of Esophageal Cancer Based on Precision Radiotherapy

Sponsor
Zefen Xiao (Other)
Overall Status
Recruiting
CT.gov ID
NCT05543057
Collaborator
(none)
150
1
72
2.1

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Radiation: 3DCRT

Detailed Description

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.

Study Design

Study Type:
Observational [Patient Registry]
Anticipated Enrollment :
150 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Real-world Study on Comprehensive Treatment of Esophageal Cancer Based on Precision Radiotherapy
Actual Study Start Date :
Jan 1, 2020
Anticipated Primary Completion Date :
Jan 1, 2026
Anticipated Study Completion Date :
Jan 1, 2026

Outcome Measures

Primary Outcome Measures

  1. 1-, 2-, 3-year overall survival [From treatment initiation to death from any cause or censor, assessed up to 36 months]

    Overall survival

Secondary Outcome Measures

  1. 1-, 2-, 3-year progression-free survival [From treatment initiation to first documented progression or death or censor, assessed up to 36 months]

    Progression-free survival

  2. Rate of acute toxicity (any and above grade 3) [From enrollment to 3 months after treatment]

    Toxicities according to CTCAE criteria

  3. Rate of acute/late toxicity (any and above grade 3) [After 3 months of enrollment]

    Toxicities of chemoradiation therapy

  4. 1-month short-term efficacy [Assessed 1-month after radiotherapy (short-term) according to RECIST 1.1]

    Short-term efficacy

  5. Quality of Life change, QoL [1/3/6/12/24 months after radiotherapy]

    measurement basing on EORTC (Quality of life of patients with oesophageal cancer) QLQ-C30 tables

  6. Quality of life of patients with oesophageal cancer [1/3/6/12/24 months after radiotherapy]

    measurement basing on EORTC (Quality of life of patients with oesophageal cancer) QLQ-OES18 tables

Other Outcome Measures

  1. Biomarkers to predict radiotherapy efficacy [baseline/through study completion, an average of 2 year]

    potential biomarkers in tumor samples and blood samples

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 90 Years
Sexes Eligible for Study:
All
Inclusion Criteria:
  • Pathology proved esophageal cancer

  • ECOG PS ≤3

  • Signed Informed consent

Exclusion Criteria:
  • Pregnant and lactating women

  • Others that researchers consider inappropriate

Contacts and Locations

Locations

Site City State Country Postal Code
1 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) Beijing Beijing China 100021

Sponsors and Collaborators

  • Zefen Xiao

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Zefen Xiao, Professor, Chinese Academy of Medical Sciences
ClinicalTrials.gov Identifier:
NCT05543057
Other Study ID Numbers:
  • 22/036-3237
First Posted:
Sep 16, 2022
Last Update Posted:
Sep 16, 2022
Last Verified:
Sep 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Zefen Xiao, Professor, Chinese Academy of Medical Sciences
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 16, 2022