International journal of radiation oncology, biology, physics · 2026
External Beam Radiation Therapy Primes Programmed Death-Ligand 1, Targeted Radionuclide Therapy in Preclinical Colorectal Cancer Model.
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Bellaye Pierre-Simon, Tavares Alexia, Ladjohounlou Riad, Moreau Mathieu, Bernhard Claire, Dias Alexandre, Claron Michael, Froidurot Lisa, Guillemin Mélanie, Collin Bertrand, Denat Franck, Truc Gilles, Cochet Alexandre, Baude Jérémy, Mirjolet Céline
Аннотация
PURPOSE: Colorectal cancer remains one of the most prevalent and lethal malignancies worldwide. Although external beam radiation therapy (RT) plays a growing role in primary and metastatic colorectal cancer, dose escalation may remain limited due to the high dose received by neighboring organs, which may cause toxicity. Targeted radionuclide therapy (TRT) selectively delivers cytotoxic radiation to tumor cells through a molecular vector that targets a specific protein overexpressed by cancer cells and that is linked to a therapeutic radionuclide. The present study aims to provide proof-of-concept for combining in vivo RT with anti-Programmed Death-Ligand 1 (PDL1)-targeted TRT delivered via an anti-PDL1 antibody.
METHODS AND MATERIALS: An anti-PDL1 monoclonal antibody (mAb) was bioconjugated with a DOTAGA (2,2',2"-(10-(2,6-dioxotetrahydro-2H-pyran-3-yl)-1,4,7,10-tetraazacyclododecane-1,4,7-triyl) triacetic acid) chelating agent and radiolabeled with either indium-111 (111In) for imaging purposes (single-photon emission computed tomography [SPECT] imaging) or lutetium-177 (177Lu) for therapeutic purposes (TRT). 111In-mAb-PDL1 biodistribution and TRT evaluation were performed in CT26 tumor-bearing mice 6 days after RT (8 Gy) by i.v. injection of 111In-mAb-PDL1 or 177Lu-mAb-PDL1. An epitope-saturation assay was performed by co-administering an excess of unconjugated mAb-PDL1.
RESULTS: RT induced a significant increase in PDL1 expression in colon tumors in vivo, enhancing the intratumoral uptake of radiolabeled anti-PDL1 mAb with 111In or 177Lu. A high uptake of radiolabeled anti-PDL1 mAb was found in the spleen, which hampered the efficacy of the combination of RT with anti-PDL1 TRT by inducing a significant decrease in CD8+ T lymphocytes infiltration in tumors. Epitope-saturation with a 15-fold excess of unlabeled anti-PDL1 mAb significantly reduced the spleen uptake of 111In-mAb-PDL1 while preserving tumor uptake. This restored the efficacy of the combination of RT with 177Lu-mAb-PDL1, compared with both treatments alone.
CONCLUSIONS: The combination of RT and anti-PDL1 TRT shows promising synergistic effects, but it requires the blockade of anti-PDL1 mAb uptake in the spleen.
METHODS AND MATERIALS: An anti-PDL1 monoclonal antibody (mAb) was bioconjugated with a DOTAGA (2,2',2"-(10-(2,6-dioxotetrahydro-2H-pyran-3-yl)-1,4,7,10-tetraazacyclododecane-1,4,7-triyl) triacetic acid) chelating agent and radiolabeled with either indium-111 (111In) for imaging purposes (single-photon emission computed tomography [SPECT] imaging) or lutetium-177 (177Lu) for therapeutic purposes (TRT). 111In-mAb-PDL1 biodistribution and TRT evaluation were performed in CT26 tumor-bearing mice 6 days after RT (8 Gy) by i.v. injection of 111In-mAb-PDL1 or 177Lu-mAb-PDL1. An epitope-saturation assay was performed by co-administering an excess of unconjugated mAb-PDL1.
RESULTS: RT induced a significant increase in PDL1 expression in colon tumors in vivo, enhancing the intratumoral uptake of radiolabeled anti-PDL1 mAb with 111In or 177Lu. A high uptake of radiolabeled anti-PDL1 mAb was found in the spleen, which hampered the efficacy of the combination of RT with anti-PDL1 TRT by inducing a significant decrease in CD8+ T lymphocytes infiltration in tumors. Epitope-saturation with a 15-fold excess of unlabeled anti-PDL1 mAb significantly reduced the spleen uptake of 111In-mAb-PDL1 while preserving tumor uptake. This restored the efficacy of the combination of RT with 177Lu-mAb-PDL1, compared with both treatments alone.
CONCLUSIONS: The combination of RT and anti-PDL1 TRT shows promising synergistic effects, but it requires the blockade of anti-PDL1 mAb uptake in the spleen.