: The mechanisms governing the abscopal effects of local radiotherapy in cancer patients remain an open conundrum. Here, we show that off-target intestinal low-dose irradiation (ILDR) increases the clinical benefits of immune checkpoint inhibitors or chemotherapy in eight retrospective cohorts of cancer patients and in tumor-bearing mice. The abscopal effects of ILDR depend on dosimetry (≥1 and ≤3 Gy) and on the metabolic and immune host-microbiota interaction at baseline allowing CD8+ T cell activation without exhaustion. Various strains of Christensenella minuta selectively boost the anti-cancer efficacy of ILDR and PD-L1 blockade, allowing emigration of intestinal PD-L1-expressing dendritic cells to tumor-draining lymph nodes. An interventional phase 2 study provides the proof-of-concept that ILDR can circumvent resistance to first- or second-line immunotherapy in cancer patients. Prospective clinical trials are warranted to define optimal dosimetry and indications for ILDR to maximize its therapeutic potential.

Low-dose irradiation of the gut improves the efficacy of PD-L1 blockade in metastatic cancer patients / Chen, J., Levy, A., Tian, A., Huang, X., Cai, G., Fidelle, M., Rauber, C., Ly, P., Pizzato, E., Sitterle, L., Piccinno, G., Liu, P., Durand, S., Mao, M., Zhao, L., Iebba, V., Felchle, H., Mallard de La Varende, A., Fischer, J.C., Thomas, S., et al.. - In: CANCER CELL. - ISSN 1878-3686. - ELETTRONICO. - 43:(2025), pp. 361-379. [10.1016/j.ccell.2025.02.010]

Low-dose irradiation of the gut improves the efficacy of PD-L1 blockade in metastatic cancer patients

Mangoni, Monica;Di Cataldo, Vanessa;Arilli, Chiara;Galluzzi, Lorenzo;
2025

Abstract

: The mechanisms governing the abscopal effects of local radiotherapy in cancer patients remain an open conundrum. Here, we show that off-target intestinal low-dose irradiation (ILDR) increases the clinical benefits of immune checkpoint inhibitors or chemotherapy in eight retrospective cohorts of cancer patients and in tumor-bearing mice. The abscopal effects of ILDR depend on dosimetry (≥1 and ≤3 Gy) and on the metabolic and immune host-microbiota interaction at baseline allowing CD8+ T cell activation without exhaustion. Various strains of Christensenella minuta selectively boost the anti-cancer efficacy of ILDR and PD-L1 blockade, allowing emigration of intestinal PD-L1-expressing dendritic cells to tumor-draining lymph nodes. An interventional phase 2 study provides the proof-of-concept that ILDR can circumvent resistance to first- or second-line immunotherapy in cancer patients. Prospective clinical trials are warranted to define optimal dosimetry and indications for ILDR to maximize its therapeutic potential.
2025
43
361
379
Chen, Jianzhou; Levy, Antonin; Tian, Ai-Ling; Huang, Xuehan; Cai, Guoxin; Fidelle, Marine; Rauber, Conrad; Ly, Pierre; Pizzato, Eugénie; Sitterle, Lis...espandi
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Utilizza questo identificatore per citare o creare un link a questa risorsa: https://hdl.handle.net/2158/1450773
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