Related Experiment Video
Updated: May 29, 2026

Inducing Targeted Mild Hyperthermia in Murine Tumor Models through Photothermal Conversion of Near-infrared Light by Intratumoral Gold Nanorods
Published on: October 10, 2025
Beneficial Effects of Combining an Immune Checkpoint Inhibitor With Proton Radiation, OXi4503, or Hyperthermia in a
Priyanshu Manojkumar Sinha1, Charlemagne Asonganyi Folefac2, Mateusz Sitarz3
1Experimental Clinical Oncology-Department of Oncology, Aarhus University Hospital, Aarhus, Denmark; prianshusinha@hotmail.com priyanshusinha@oncology.au.dk.
Background/Aim:
This pre-clinical study investigated the combination of various treatments with a checkpoint blocker in an immunologically unresponsive tumor.
Materials And Methods:
Experiments were performed using C3H mammary carcinoma mice, where tumors of various sizes (44-467 mm3) were treated with either proton radiation (up to 20 Gy), OXi4503 (4×50 mg/kg), or hyperthermia (42.5°C for 60 min), with or without anti-CTLA-4 (4×10 mg/kg). The endpoint was the time to reach 1,000 mm3. Mechanistic studies focused on CD4/CD8 expression, assessed in histological sections up to 10 days after irradiation.
Results:
The median time for untreated tumors to reach 1,000 mm3 was unaffected by anti-CTLA-4 alone. Proton radiation, OXi4503, or hyperthermia alone increased the tumor growth time at all tumor sizes when compared to untreated tumors. Combining proton radiation or OXi4503 with anti-CTLA-4 resulted in additional tumor inhibition, which was more pronounced in smaller tumors (44-131 mm3). Anti-CTLA-4 had no additional effect on tumor response to hyperthermia regardless of tumor size at treatment. Expression of CD4/CD8 levels decreased 1 day after irradiation before recovering to pre-treatment levels on day 5.
Conclusion:
Overall, combining anti-CTLA-4 with either proton radiation or OXi4503, but not with hyperthermia, enhanced growth inhibition of C3H mammary carcinoma compared to that seen with each treatment alone, suggesting potential clinical relevance.
More Related Videos
Related Concept Videos
Tumor Immunotherapy
Cancer Therapies
However, cancer treatments can pose several challenges, as therapies used to kill cancer cells are generally also toxic to normal cells. Moreover, cancer cells mutate rapidly and can develop resistance to chemical agents or radiation therapy. Besides, all types of cancer cells may not respond to the same therapy. Some cancer cells respond to one...

