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Low-dose Radiotherapy Combined with Chemotherapy and immunotherapy for Relapsed Refractory Tumors

Efficacy of low dose radiotherapy combined with chemotherapy and immunotherapyin the treatment of relapsed or refractory tumors

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500109755
Enrollment
Unknown
Registered
2025-09-24
Start date
2025-09-25
Completion date
Unknown
Last updated
2025-09-29

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

Conditions

relapse, metastatic refractory tumors

Interventions

low-dose radiotherapy group:None

Sponsors

Hainan Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. >=18 years of age; 2. Confirmed malignant tumor by cells or pathology; 3. Patients with primary, relapsed or metastatic tumors, or involvement of vital organs, who refuse or cannot tolerate surgery, who fail first-line treatment, who cannot tolerate or refuse systemic treatment; 4. Patients with locally advanced or advanced tumors who have received previous radiotherapy and have difficulty in further radiotherapy; 5. ECOG >=60 points; 6. Expected survival >=3 months; 7. No serious comorbidities (bone marrow, liver and kidney function, coagulation function, heart function) Blood routine: WBC >= 3.0×10^9/L, ANC >= 1.5×10^9/L, PLT >= 90×10^9/L, HGB >= 8g/dL; 1 Liver function: TBIL =55%, QTCF interval 4 weeks; 9. Sign informed consent in writing; 10, consent to collect biological specimens of tissue or blood) for backup;

Exclusion criteria

Exclusion criteria: 1. during pregnancy or lactation; 2. Diffuse metastases of the central nervous system (>=10 brain metastases, meninges, spinal cord); 3. Severe Comorbidities (severe infection, bone marrow suppression, cardiac Cerebrovascular disease, persistent or intractable epilepsy; severe cardiac dysfunction, Coagulation Disorder, active bleeding, electrolyte disorders); 4. KPS <60 points; 5. Any arterial thrombosis, embolism or ischemia occurred within the 6 months before enrollment, such as myocardial infarction, unstable angina, cerebrovascular accident or transient ischemic attack; 6. a history of psychiatric illness, alcoholism, drug use, or drug abuse;

Design outcomes

Primary

MeasureTime frame
Local control rate;Objective response rate;

Secondary

MeasureTime frame
Correlation of Lymphocytes Subsets with Immunotherapy;Progression-Free-Survival;safety and tolerability;Overall Survival;

Countries

China

Contacts

Public ContactYunxiu Luo

Hainan Cancer Hospital

luoyunxiu@hnszlyy.wecom.work+86 898 36379999

Outcome results

None listed

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