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Multi-omics sequencing analysis of esophageal squamous cell carcinoma gene expression and its clinical characteristics, clinical research on the relationship between radiotherapy efficacy

Multi-omics sequencing analysis of esophageal squamous cell carcinoma gene expression and its clinical characteristics, clinical research on the relationship between radiotherapy efficacy

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100043052
Enrollment
Unknown
Registered
2021-02-04
Start date
2021-02-01
Completion date
Unknown
Last updated
2021-05-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

esophageal squamous cell carcinoma

Interventions

Sponsors

Shanxi Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Patients with stage Ib~?a esophageal squamous cell carcinoma (ESCC) who are unresectable or have surgical contraindications or refuse surgery; 2. Have not received any treatment before; 3. Age 18-75 years old, both male and female; 4. ECOG: 0~2; 5. The estimated survival time exceeds 6 months; 6. The functions of vital organs meet the following requirements (no blood components and cell growth factors are allowed to be used 2 weeks before the start of research and treatment): a. Absolute neutrophil count (ANC) >= 1.5 x 10^9/L; b. Platelets >= 100 x 10^9/L; c. Hemoglobin >= 9 g/dL; d. Serum albumin >= 2.8 g/dL; e. Bilirubin = 50mL/min; 6. Female subjects with fertility should undergo a urine or serum pregnancy test within 72 hours before receiving the first study drug administration and prove to be negative, and are willing to use effective methods of contraception during the trial. For male subjects whose partners are women of childbearing age, effective methods of contraception should be used during the trial; 7. The researcher determined that the patient can receive radiotherapy without contraindications to radiotherapy; 8. The subjects voluntarily joined the study, signed an informed consent form, had good compliance, and cooperated with the follow-up.

Exclusion criteria

Exclusion criteria: 1. Other malignant tumors have been diagnosed within 5 years before the first use of the research drug, except for effectively treated skin basal cell carcinoma, skin squamous cell carcinoma, and/or effectively resected in situ cervical cancer and/or breast cancer; 2. Symptomatic brain metastases; 3. Have received other anti-tumor drug treatment in the past; 4. Poor general condition, accompanied by cachexia, poor cardiopulmonary function or serious diseases of other vital organ systems, and cannot tolerate radiotherapy; 5. There are signs of esophageal hemorrhage or hemorrhage; 6. Esophageal fistula combined with severe infection; 7. Women during pregnancy or lactation; 8. The blood or tissue sample is unqualified; According to the judgment of the investigator, the subject has other factors that may cause him to be forced to terminate the study, such as suffering from other serious diseases (including mental illness) requiring combined treatment, severely abnormal laboratory test values, family or social factors, which may affect to the safety of subjects or the collection of experimental data.

Design outcomes

Primary

MeasureTime frame
Full exome and transcriptome information;

Countries

China

Contacts

Public ContactHongwei Li

Shanxi Cancer Hospital

15140200212@163.com+86 15140200212

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026