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Efficacy of stereotactic boost radiotherapy ( SBRT-SIB ) with or without immune check point inhibitors in the treatment of advanced cancer

Efficacy of stereotactic boost radiotherapy ( SBRT-SIB ) with or without immune check point inhibitors in the treatment of advanced cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500101684
Enrollment
Unknown
Registered
2025-04-28
Start date
2025-06-01
Completion date
Unknown
Last updated
2025-05-05

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

Conditions

advanced solid tumor

Interventions

A(SBRT):None
B(SBRT-SIB):None

Sponsors

Hainan Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 95 Years

Inclusion criteria

Inclusion criteria: 1, >=18 years of age; 2. malignant tumors confirmed by cells or pathology; 3. Primary, recurrent or metastatic tumors, >= 5 cm in diameter, or involving important organs, in patients who cannot undergo surgery, failed first-line treatment, or refused chemotherapy; 4. KPS >=60 points; 5. Survival is expected to be >=3 months; 6. No serious comorbidities (bone marrow, liver and kidney function, coagulation function, heart function) (WBC>=3.0×10^9/L, ANC>=1.5 ×10^9/L, PLT>=90×10^9/L, HGB>=8g/dL; TBIL4 weeks; 8. sign written informed consent; 9. agree to collect biological specimens of tissue or blood) for standby;

Exclusion criteria

Exclusion criteria: 1, received radiotherapy at the same site within 3 months; 2. in pregnancy or lactation; 3. Diffuse metastases of the central nervous system (brain, meninges, spinal cord); 4. severe comorbidities (severe infection, bone marrow depression, cardio-cerebrovascular disease, persistent or intractable epilepsy; severe cardiac insufficiency, coagulation disorder, active hemorrhage, electrolyte disturbances); 5. KPS <60 points; 6. Any arterial thrombosis, embolism, or ischemia that occurred within; 6 months before enrollment, such as myocardial infarction, unstable angina, cerebrovascular accident, or transient ischemic attack; 7. previous history of mental illness, alcohol abuse, drug use, or substance abuse;

Design outcomes

Primary

MeasureTime frame
objective respone rate (ORR);local control rate (LCR);

Secondary

MeasureTime frame
physical parameters of radiotherapy planning;progress-free survival (PFS);overall survival (OS);Correlation between lymphocyte subsets response and treatment;toxico-complications;

Countries

China

Contacts

Public ContactLuo Yunxiu

Hainan Cancer Hospital

luoyunxiu@hnszlyy.wecom.work+86 898 3637 9999

Outcome results

None listed

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