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Early Esophageal Cancer Treated With Carbon Ion Radiotherapy

Early Esophageal Cancer Treated With Carbon Ion Radiotherapy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100048809
Enrollment
Unknown
Registered
2021-07-16
Start date
2021-07-17
Completion date
Unknown
Last updated
2022-03-28

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

Conditions

Esophageal Cancer

Interventions

Sponsors

Wuwei Tumor Hospital Heavy Ion Center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. The pathology confirmed squamous or adenocarcinoma ; 2. AJCC 2017 8th Edition CT1-4 any N M0; 3. No distant metastasis to solid organs; 4. Never received radiation therapy for esophageal cancer; 5. No history of other malignant tumors (except cured skin cancer and stage zero cervical cancer); 6. Renal function, liver function and bone marrow function were basically normal (serum creatinine9.5 g/dL; White blood cell count>=3000 /ml; Platelet count>= 100,000 /mL); 7. Aged from 18 to 80 years; 8. Good physical condition, ECOG (Eastern United States Collaborative Oncology Group) =6 months. 10. Prior to radiotherapy, the patient or his/her legal representative has signed the informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with esophageal tracheal fistula or who have been judged by physicians to be at high risk of esophageal tracheal fistula; 2. Weight loss of more than 20% within six months; 3. Pregnancy (confirmed by serum or urine ß-HCG test) or lactation period; 4. Drug or alcohol abuse; 5. AIDS patients; 6. Concomitant with uncontrolled systemic, pulmonary or heart disease; 7. Concomitant serious comorbidities, including uncontrolled comorbidities (pulmonary insufficiency, cardiovascular, lung, liver, kidney, diabetes, etc.), addiction, and/or mental illness that prevent the trial regimen from proceeding smoothly; 8. Implant pacemaker or other metal prosthesis enough to affect radiotherapy; 9. Patients with poor compliance, including the possibility of failing to complete the treatment plan or receiving the required follow-up and testing check; 10. Previous experience with other malignant tumors (except non-malignant melanoma skin cancer or non-invasive cervical cancer); 11. Simultaneously receiving systemic immunotherapy or corticosteroid therapy; 12. Serum creatinine clearance rate < 30ml/ min; 13. Contraindications to radiotherapy; 14. Participated in other drug clinical trials within 30 days prior to inclusion in this study; 15. Incapacity or limited capacity for civil conduct; 16. Any medical history that, in the investigator's judgment, may interfere with trial results or increase patient risk; 17. Any circumstances in which the physician deems it inappropriate to participate in the trial.

Design outcomes

Primary

MeasureTime frame
Local control rate of tumor;Tumor response rate;

Secondary

MeasureTime frame
Progression-free survival;Overall survival;Distant metastasis rate;

Contacts

Public ContactZhang Yanshan

Wuwei Tumor Hospital Heavy Ion Center

13830510999@163.com+86 13830510999

Outcome results

None listed

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