Clinical Trial

Spatially Fractionated Radiotherapy Combined With Immunotherapy for Advanced Solid Tumors

Study acronym: SFRT-IM-P2
Recruiting Phase 2
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Record status
This record was last updated April 29, 2026 (before its estimated July 1, 2026 completion). Its status may not reflect the trial's current state.
Summary
Lattice radiation therapy (LRT) is a spatially fractionated radiotherapy technique that creates alternating high - and low - dose areas within a tumor to enhance local control and reduce toxicity to surrounding tissues. This study aims to evaluate the effectiveness and safety of combining LRT with immunotherapy in patients with advanced or metastatic solid tumors, through a Phase II clinical trial. Patients will receive specific - dose irradiation using a medical linear accelerator. Within the GTV of the largest tumor, spheres (0.5 - 3 cm in diameter) will be created as high - dose targets (LRT targets), spaced 2.0 - 5.0 cm apart. The LRT targets must be drawn within the GTV, avoiding blood vessels, with a margin of at least 1 cm from the GTV margin, and a volume ratio of 1% - 10% of the GTV. For a single lesion, the D95 of the GTV will be ≥1 Gy/fraction, and the D95 of the LRT target will be 8 - 12 Gy/fraction, with minimal possible single - fraction doses to organs at risk. All other irradiated metastases will receive low - dose radiotherapy (100 - 300 cGy × 5 fractions), except for brain and bone metastases, which will be treated with palliative radiotherapy as per clinical routine. Immunotherapy will be administered during or within one week after radiotherapy.
Protocol Amendment History 2 amendments
This ClinicalTrials.gov record has been amended 2 times since 2025-07-01; most recent amendment 2026-04-27.
Status change: Not Yet Recruiting → Recruiting 2025-07-13
Trial Details
NCT Number NCT07058948
Lead Sponsor Tianjin Medical University Cancer Institute and Hospital
Conditions Solid Cancers, Radiotherapy, Immune Checkpoint Inhibitor, Lung Cancer
Enrollment 30 participants
Start Date 2025-07-01
Primary Completion 2026-07-01 (estimated)
Study Completion 2027-07-01 (estimated)
Updated on ClinicalTrials.gov 2026-04-29