NCT06840067 Clinical Study of Carbon Ion Radiotherapy for Pancreatic Cancer.
| NCT ID | NCT06840067 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Gansu Wuwei Tumor Hospital |
| Condition | Pancreatic Cancer Metastatic |
| Study Type | INTERVENTIONAL |
| Enrollment | 62 participants |
| Start Date | 2025-03-01 |
| Primary Completion | 2027-12-31 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 62 participants in total. It began in 2025-03-01 with a primary completion date of 2027-12-31.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
The objective is to evaluate the efficacy and safety of carbon ion radiotherapy (CIRT) combined with nituzumab and gemcitabine in the treatment of locally advanced and metastatic pancreatic cancer.
Eligibility Criteria
Inclusion Criteria: 1. Age ≥18 years and ≤80 years; 2. Indications: patients with locally advanced or metastatic pancreatic adenocarcinoma confirmed by histopathology or cytology (stage III - IV). 3. At least one measurable lesion was present according to RECIST version 1.1 evaluation criteria. 4. Suitable for one cycle of gemcitabine combined with nituzumab. 5. No history of other malignant tumors (except cured skin cancer and stage 0 cervical cancer); 6. Liver function, kidney function and bone marrow function were basically normal (ALT and AST \< 1.5 times of high normal value (ULN), bilirubin \< 1.5×ULN; Adult endogenous creatinine clearance rate of 60ml/min or serum creatinine SCR≤140μmoI/L, BUN≤6.8mmol/L; Hemoglobin level \>9 g/dL; White blood cell count ≥3.0\*109/L; Platelet count ≥100\*109/L;) 7. Good physical condition, i.e. ECOG (Eastern United States Oncology Collaboration Group) 0\~2; There were no complications such as severe pulmonary hypertension, cardiovascular disease, peripheral vascular disease, and severe chronic heart disease that may affect radiotherapy. Cardiac function grade 1. (According to the New York College of Cardiology Cardiac Function Scale (NYHA) 8. Adequate functions of major organs; 9. Predicted survival (after treatment) ≥3 months; 10. Informed consent has been signed by the patient or his legal representative before radiotherapy. Exclusion Criteria: 1. Patients who have received monoclonal antibodies, EGFR-TKI therapy, anti-angiogenic drugs, and immunosuppressants within six months. 2. Patients with uncontrolled, cancerous pleural effusion requiring frequent drainage, pericardial effusion, or ascites (allowing for cytological confirmation of effusion), gastrointestinal bleeding, or those identified by the investigator as having a high blood risk within 14 days prior to admission. 3. Participated in other interventional clinical trials within 30 days prior to screening. 4. The dose limit for organs at risk cannot reach the preset safe dose limit. 5. Being on chronic steroid hormone therapy for more than 6 months (e.g., prednisone dose \> 10 mg/ day or equivalent). 6. People who are allergic to the drugs or their ingredients used in this program. 7. Pregnancy (confirmed by serum or urine β-HCG test) or lactation 8. Persons with AIDS, including those who have received antiretroviral therapy; Active stage of syphilis; 9. Accompanied by serious comorbiditions, including uncontrolled systemic or co-existing diseases (pulmonary insufficiency, cardiovascular, pulmonary, liver, kidney, diabetes, etc.), drug or alcohol abuse, dependence, addiction, and/or mental illness that prevent the successful implementation of the trial protocol; 10. Patients with poor compliance, including those who may not be able to complete the treatment plan or receive prescribed follow-up and examination; 11. Patients had other malignant neoplasms (except cured skin cancer and stage 0 cervical cancer); 12. There are contraindications to radiotherapy; 13. having no or limited capacity for civil conduct; 14. Any medical history that, in the investigator's judgment, might interfere with the trial results or increase the patient's risk; 15. Any condition in which the physician considers that participation in the trial is not appropriate, the physician determines that the patient will not benefit from carbon ion radiotherapy, or that there are other co-existing conditions or other factors that may affect carbon ion therapy. 16. Inability to understand the purpose of treatment or unwillingness/inability to sign treatment consent.
Contact & Investigator
Xiaojun Li
STUDY DIRECTOR
Gansu Wuwei Tumor Hospital
Frequently Asked Questions
Who can join the NCT06840067 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, up to 80 Years, studying Pancreatic Cancer Metastatic. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT06840067 currently recruiting?
Yes, NCT06840067 is actively recruiting participants. Contact the research team at anglweli@qq.com for enrollment information.
Where is the NCT06840067 trial being conducted?
This trial is being conducted at Wuwei, China.
Who is sponsoring the NCT06840067 clinical trial?
NCT06840067 is sponsored by Gansu Wuwei Tumor Hospital. The principal investigator is Xiaojun Li at Gansu Wuwei Tumor Hospital. The trial plans to enroll 62 participants.
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